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Subject Areas on Research
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"Good enough solutions" and the genetics of complex diseases.
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172G>T variant in the 5' untranslated region of DNA repair gene RAD51 reduces risk of squamous cell carcinoma of the head and neck and interacts with a P53 codon 72 variant.
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2μ plasmid in Saccharomyces species and in Saccharomyces cerevisiae.
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50 Years of Emmonsia Disease in Humans: The Dramatic Emergence of a Cluster of Novel Fungal Pathogens.
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50 million years of genomic stasis in endosymbiotic bacteria.
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A Genocentric Approach to Discovery of Mendelian Disorders.
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A Germline Variant at 8q24 Contributes to Familial Clustering of Prostate Cancer in Men of African Ancestry.
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A KRAS-variant in ovarian cancer acts as a genetic marker of cancer risk.
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A NEIL1 single nucleotide polymorphism (rs4462560) predicts the risk of radiation-induced toxicities in esophageal cancer patients treated with definitive radiotherapy.
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A Quantitative Analysis of Growth and Size Regulation in Manduca sexta: The Physiological Basis of Variation in Size and Age at Metamorphosis.
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A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay.
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A biometrical genome search in rats reveals the multigenic basis of blood pressure variation.
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A common variant near TGFBR3 is associated with primary open angle glaucoma.
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A common variant on chromosome 9p21 affects the risk of myocardial infarction.
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A comprehensive mutation analysis of RP2 and RPGR in a North American cohort of families with X-linked retinitis pigmentosa.
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A conservative test of genetic drift in the endosymbiotic bacterium Buchnera: slightly deleterious mutations in the chaperonin groEL.
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A copy number variation morbidity map of developmental delay.
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A cystic fibrosis transmembrane conductance regulator splice variant with partial penetrance associated with variable cystic fibrosis presentations.
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A functional polymorphism in the ATP-Binding Cassette B1 transporter predicts pharmacologic response to combination of nortriptyline and morphine in neuropathic pain patients.
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A functional variant (-1304T>G) in the MKK4 promoter contributes to a decreased risk of lung cancer by increasing the promoter activity.
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A generalized least-squares estimate for the origin of sporophytic self-incompatibility.
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A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence
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A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
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A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.
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A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans.
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A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.
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A genome-wide in vitro bacterial-infection screen reveals human variation in the host response associated with inflammatory disease.
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A genome-wide investigation of SNPs and CNVs in schizophrenia.
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A genome-wide scan for common alleles affecting risk for autism.
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A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.
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A global meta-analysis of Tuber ITS rDNA sequences: species diversity, host associations and long-distance dispersal.
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A global reference for human genetic variation.
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A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response.
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A longitudinal study of epigenetic variation in twins.
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A mechanistic study of evolvability using the mitogen-activated protein kinase cascade.
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A molecular phylogeny of the fern family Pteridaceae: assessing overall relationships and the affinities of previously unsampled genera
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A multilocus sequence survey in Arabidopsis thaliana reveals a genome-wide departure from a neutral model of DNA sequence polymorphism.
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A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS.
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A novel 2-oxoacid-dependent dioxygenase involved in the formation of the goiterogenic 2-hydroxybut-3-enyl glucosinolate and generalist insect resistance in Arabidopsis,.
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A novel functional variant (-842G>C) in the PIN1 promoter contributes to decreased risk of squamous cell carcinoma of the head and neck by diminishing the promoter activity.
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A novel variant marking HLA-DP expression levels predicts recovery from hepatitis B virus infection.
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A pharmacogenetic study of aldehyde oxidase I in patients treated with XK469.
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A phylogeographically distinct and deep divergence in the widespread Neotropical turnip-tailed gecko, Thecadactylus rapicauda.
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A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.
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A public resource facilitating clinical use of genomes.
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A re-evaluation of 12S ribosomal RNA variability in Drosophila pseudoobscura.
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A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis.
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A regulatory variant of the human tryptophan hydroxylase-2 gene biases amygdala reactivity.
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A stochastic evolutionary model for protein structure alignment and phylogeny.
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A strong effect of AT mutational bias on amino acid usage in Buchnera is mitigated at high-expression genes.
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A susceptibility gene for affective disorders and the response of the human amygdala.
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A three-generation approach in biodemography is based on the developmental profiles and the epigenetics of female gametes.
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A variant of the DNA repair gene XRCC3 and risk of squamous cell carcinoma of the head and neck: a case-control analysis.
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APOL1 Kidney Risk Variants and Cardiovascular Disease: An Individual Participant Data Meta-Analysis.
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APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy.
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APOL1-G0 protects podocytes in a mouse model of HIV-associated nephropathy.
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Absence of mitochondrial progesterone receptor polymorphisms in women with spontaneous preterm birth.
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Abundance and diversity of Schizophyllum commune spore clouds in the Caribbean detected by selective sampling.
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Abundance and genetic diversity of aerobic anoxygenic phototrophic bacteria of coastal regions of the pacific ocean.
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Acute-phase CD8 T cell responses that select for escape variants are needed to control live attenuated simian immunodeficiency virus.
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Adaptive Radiation Genomics of Two Ecologically Divergent Hawai'ian Honeycreepers: The 'akiapōlā'au and the Hawai'i 'amakihi.
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Adaptive divergence in plasticity in natural populations of Impatiens capensis and its consequences for performance in novel habitats.
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Adaptive interactions between HLA and HIV-1: highly divergent selection imposed by HLA class I molecules with common supertype motifs.
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Adding pharmacogenetics information to drug labels: lessons learned.
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African-American HLA class II allele and haplotype diversity.
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African-American HLA class II allele and haplotype diversity.
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Age at maturity in wild baboons: genetic, environmental and demographic influences.
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Age at natural menopause genetic risk score in relation to age at natural menopause and primary open-angle glaucoma in a US-based sample.
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Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population.
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Allele-specific assay reveals functional variation in the chalcone synthase promoter of Arabidopsis thaliana that is compatible with neutral evolution.
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Allele-specific gene expression in a wild nonhuman primate population.
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Allelic Imbalance Is a Prevalent and Tissue-Specific Feature of the Mouse Transcriptome.
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Allelic and locus heterogeneity in inherited venous malformations.
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Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.
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Allelic diversity and gene genealogy at the self-incompatibility locus in the Solanaceae.
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Allelic diversity in the TGFB1 regulatory region: characterization of novel functional single nucleotide polymorphisms.
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Allelic variants of the human glutathione S-transferase P1 gene confer differential cytoprotection against anticancer agents in Escherichia coli.
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Allelic variation in human gene expression.
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Allotetraploid Mimulus sookensis are highly interfertile despite independent origins.
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Alternative Splicing of Opioid Receptor Genes Shows a Conserved Pattern for 6TM Receptor Variants.
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Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise.
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Amplification of a complete simian immunodeficiency virus genome from fecal RNA of a wild chimpanzee.
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An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease.
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An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis.
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An activated factor VII variant with enhanced tissue factor-independent activity speeds wound healing in a mouse hemophilia B model.
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An active site tyrosine influences the ability of the dimethyl sulfoxide reductase family of molybdopterin enzymes to reduce S-oxides.
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An atlas of genetic influences on human blood metabolites.
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An epigenetic pathway in rice connects genetic variation to anaerobic germination and seedling establishment.
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An integrated encyclopedia of DNA elements in the human genome.
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An integrated map of genetic variation from 1,092 human genomes.
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An introgression analysis of quantitative trait loci that contribute to a morphological difference between Drosophila simulans and D. mauritiana.
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Analyses of pediatric isolates of Cryptococcus neoformans from South Africa.
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Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.
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Analysis of shared heritability in common disorders of the brain.
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Analysis of the T-cell receptor beta-chain variable-region (V beta) repertoire in monozygotic twins discordant for human immunodeficiency virus: evidence for perturbations of specific V beta segments in CD4+ T cells of the virus-positive twins.
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Analysis of the protein products encoded by variant glucokinase transcripts via expression in bacteria.
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Analytical DNA fingerprinting in lions: parentage, genetic diversity, and kinship.
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Ancestral population genomics: the coalescent hidden Markov model approach.
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Ancient and recent positive selection transformed opioid cis-regulation in humans.
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Androgen receptor variant-driven prostate cancer: clinical implications and therapeutic targeting.
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Anther-stigma separation is associated with inbreeding depression in Datura stramonium, a predominantly self-fertilizing annual.
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Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load.
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Antigenicity and immunogenicity of HIV-1 consensus subtype B envelope glycoproteins.
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Apolipoprotein E and Alzheimer's disease.
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Apolipoprotein L1 gene variants in deceased organ donors are associated with renal allograft failure.
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Assessing genetic association with human survival at multi-allelic loci.
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Assessing the Role of Rare Genetic Variation in Patients With Heart Failure.
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Assessment of genetic relatedness of vaginal isolates of Candida albicans from different geographical origins.
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Assessment of the genetic variance of late-onset Alzheimer's disease.
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Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses.
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Association between ICAM-1 Gly-Arg polymorphism and renal parenchymal scarring following childhood urinary tract infection.
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Association between chromosome 2p16.3 variants and glaucoma in populations of African descent.
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Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.
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Association between genetic variation at the porphobilinogen deaminase gene and schizophrenia.
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Association of Rare CYP39A1 Variants With Exfoliation Syndrome Involving the Anterior Chamber of the Eye.
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Association of a cystatin C gene variant with cystatin C levels, CKD, and risk of incident cardiovascular disease and mortality.
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Association of a functional tandem repeats in the downstream of human telomerase gene and lung cancer.
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Association of angiotensinogen gene T235 variant with increased risk of coronary heart disease.
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Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.
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Association of gene variants of the renin-angiotensin system with accelerated hippocampal volume loss and cognitive decline in old age.
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Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease.
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Association of genetic variants of FBXO32 and FOXO6 in the FOXO pathway with breast cancer risk.
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Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children.
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Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
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Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
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Association of misexpression with sterility in hybrids of Drosophila simulansand D. mauritiana.
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Association of tumor necrosis factor-alpha promoter variants with risk of HPV-associated oral squamous cell carcinoma.
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Association of uridine diphosphate-glucuronosyltransferase 2B gene variants with serum glucuronide levels and prostate cancer risk.
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Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore.
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Association study of genetic polymorphisms of SLC2A10 gene and type 2 diabetes in the Taiwanese population.
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Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.
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Associations, populations, and the truth: recommendations for genetic association studies in Arthritis & Rheumatism.
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Autism and developmental disability caused by KCNQ3 gain-of-function variants.
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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
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AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
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BAG3 (Bcl-2-Associated Athanogene-3) Coding Variant in Mice Determines Susceptibility to Ischemic Limb Muscle Myopathy by Directing Autophagy.
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BCR sequences essential for transformation by the BCR-ABL oncogene bind to the ABL SH2 regulatory domain in a non-phosphotyrosine-dependent manner.
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Balancing selection and trans-specific polymorphisms.
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Balancing selection maintains hyper-divergent haplotypes in Caenorhabditis elegans.
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Bcr-Abl variants: biological and clinical aspects.
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Better together: Thinking anthropologically about genetics.
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Between-site differences in the scale of dispersal and gene flow in red oak.
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Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
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Biodemographic trajectories of longevity.
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Biologic and clinical significance of androgen receptor variants in castration resistant prostate cancer.
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Biological diversity: where is it?
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Biotic interactions. Genomics and coevolution.
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Boechera, a model system for ecological genomics.
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CCL3L1 and HIV/AIDS susceptibility.
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CD4 receptor diversity in chimpanzees protects against SIV infection.
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COMT gene locus: new functional variants.
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CYP2C19 variation and citalopram response.
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Calcium and calcium receptor CAS promote Arabidopsis thaliana de-etiolation.
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Can Genetics Predict Response to Complex Behavioral Interventions? Evidence from a Genetic Analysis of the Fast Track Randomized Control Trial
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Candida virulence properties and adverse clinical outcomes in neonatal candidiasis.
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Captivity humanizes the primate microbiome.
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Car8 dorsal root ganglion expression and genetic regulation of analgesic responses are associated with a cis-eQTL in mice.
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Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.
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Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population.
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Catechol O-methyltransferase haplotype predicts immediate musculoskeletal neck pain and psychological symptoms after motor vehicle collision.
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Causal Genetic Variants in Stillbirth.
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Causal effects of cardiovascular risk factors on onset of major age-related diseases: A time-to-event Mendelian randomization study.
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Cell-type-specific effects of genetic variation on chromatin accessibility during human neuronal differentiation.
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Centralized immunogens as a vaccine strategy to overcome HIV-1 diversity.
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Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
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Changing the paradigm from 'race' to human genome variation.
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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery.
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Characterization of alpha-toxin hla gene variants, alpha-toxin expression levels, and levels of antibody to alpha-toxin in hemodialysis and postsurgical patients with Staphylococcus aureus bacteremia.
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Characterization of long G4-rich enhancer-associated genomic regions engaging in a novel loop:loop 'G4 Kissing' interaction.
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Characterization of primary isolate-like variants of simian-human immunodeficiency virus.
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Characterization of the G protein-coupled receptor kinase GRK4. Identification of four splice variants.
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Characterization of the Transmitted Virus in an Ongoing HIV-1 Epidemic Driven by Injecting Drug Use.
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Child μ-opioid receptor gene variant influences parent-child relations.
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Chromatin and DNA replication.
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Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.
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Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration.
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Circulating vitamin D concentration and risk of seven cancers: Mendelian randomisation study.
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Cis-regulatory evolution of chalcone-synthase expression in the genus Arabidopsis.
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Classifying the evolutionary and ecological features of neoplasms.
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Clinical interpretation and implications of whole-genome sequencing.
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Clonality and recombination in genetically differentiated subgroups of Cryptococcus gattii.
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Cloning, characterization, and expression of two angiotensin receptor (AT-1) isoforms from the mouse genome.
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Clopidogrel for coronary stenting: response variability, drug resistance, and the effect of pretreatment platelet reactivity.
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Coalescent Theory of Migration Network Motifs.
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Combination of exome sequencing and immune testing confirms Aicardi-Goutières syndrome type 5 in a challenging pediatric neurology case.
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Combinatorial and synergistic properties of CaMV 35S enhancer subdomains.
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Combined effects of the p53 and p73 polymorphisms on lung cancer risk.
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Commentary: When does understanding phenotypic evolution require identification of the underlying genes?
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Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk.
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Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease.
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Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.
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Common genetic variants on 5p14.1 associate with autism spectrum disorders.
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Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.
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Common genetic variation and performance on standardized cognitive tests.
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Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.
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Common genetic variation and the control of HIV-1 in humans.
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Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.
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Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.
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Common human ANK2 variant confers in vivo arrhythmia phenotypes.
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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
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Common variants in Mendelian kidney disease genes and their association with renal function.
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Common variation in the BRCA1 gene and prostate cancer risk.
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Community engagement and informed consent in the International HapMap project.
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Comparative RNA sequencing reveals substantial genetic variation in endangered primates.
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Comparative Serum Challenges Show Divergent Patterns of Gene Expression and Open Chromatin in Human and Chimpanzee.
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Comparative analyses of clinical and environmental populations of Cryptococcus neoformans in Botswana.
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Comparative analysis of quantitative trait loci controlling glucosinolates, myrosinase and insect resistance in Arabidopsis thaliana.
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Comparative evolutionary analysis of chalcone synthase and alcohol dehydrogenase loci in Arabidopsis, Arabis, and related genera (Brassicaceae).
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Comparative gene genealogical analyses of strains of serotype AD identify recombination in populations of serotypes A and D in the human pathogenic yeast Cryptococcus neoformans.
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Comparative genome sequencing of Drosophila pseudoobscura: chromosomal, gene, and cis-element evolution.
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Comparative genomics and regulatory evolution: conservation and function of the Chs and Apetala3 promoters.
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Comparative genomics provides new insights into the diversity, physiology, and sexuality of the only industrially exploited tremellomycete: Phaffia rhodozyma.
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Comparative genomics reveals insights into avian genome evolution and adaptation.
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Comparative genomics search for losses of long-established genes on the human lineage.
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Comparative hybridization reveals extensive genome variation in the AIDS-associated pathogen Cryptococcus neoformans.
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Comparative population structure of two deep-sea hydrothermal-vent-associated decapods (Chorocaris sp. 2 and Munidopsis lauensis) from southwestern Pacific back-arc basins.
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Comparative quantitative trait loci mapping of aliphatic, indolic and benzylic glucosinolate production in Arabidopsis thaliana leaves and seeds.
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Comparative structural analysis of HLA-A2 antigens distinguishable by cytotoxic T lymphocytes: variants M7 and DR1.
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Comparison of ribosomal DNA ITS regions among geographic isolates of Cenococcum geophilum.
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Comparison of viral Env proteins from acute and chronic infections with subtype C human immunodeficiency virus type 1 identifies differences in glycosylation and CCR5 utilization and suggests a new strategy for immunogen design.
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Competition in oxygen-linked anion binding to normal and variant human hemoglobins.
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Complement factor H variant increases the risk of age-related macular degeneration.
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Complete genomic screen for disease susceptibility loci in nuclear families.
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Complex selection on a regulator of social cognition: Evidence of balancing selection, regulatory interactions and population differentiation in the prairie vole Avpr1a locus.
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Complex-trait analysis in plants.
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Complexity of the msp2 locus and the severity of childhood malaria, in south-western Nigeria.
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Comprehensive analysis of ADA2 genetic variants and estimation of carrier frequency driven by a function-based approach.
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Comprehensive identification of mRNA isoforms reveals the diversity of neural cell-surface molecules with roles in retinal development and disease.
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Computational tools for understanding sequence variability in recombination signals.
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Conceptualizing human variation.
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Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry.
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Connecting genetic risk to disease end points through the human blood plasma proteome.
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Connecting recombination, nucleotide diversity and species divergence in Drosophila.
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Consensus and ancestral state HIV vaccines.
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Consensus statement on transcultural issues in depression and anxiety from the International Consensus Group on Depression and Anxiety.
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Conservation and diversification of SCARECROW in maize.
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Conservation genomic analysis reveals ancient introgression and declining levels of genetic diversity in Madagascar's hibernating dwarf lemurs.
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Conserved sequence and structural elements in the HIV-1 principal neutralizing determinant.
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Conserved sequence and structural elements in the HIV-1 principal neutralizing determinant: further clarifications.
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Cooperation and functional diversification of two closely related galactolipase genes for jasmonate biosynthesis.
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Coping with viral diversity in HIV vaccine design: a response to Nickle et al.
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Copy number variation contributes to cryptic genetic variation in outbreak lineages of Cryptococcus gattii from the North American Pacific Northwest.
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Correlation between env V1/V2 region diversification and neutralizing antibodies during primary infection by simian immunodeficiency virus sm in rhesus macaques.
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Country Level Diversity of the HIV-1 Pandemic between 1990 and 2015.
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Critical weight in the development of insect body size.
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Cross-species microsatellite markers for elucidating population genetic structure in Arabidopsis and Arabis (Brassicaeae).
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Cross-subtype T-cell immune responses induced by a human immunodeficiency virus type 1 group m consensus env immunogen.
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Cryptic variation in butterfly eyespot development: the importance of sample size in gene expression studies
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Cryptococcus neoformans shows a remarkable genotypic diversity in Brazil.
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DNA Methylation Analysis Identifies Loci for Blood Pressure Regulation.
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DNA copy number evolution in Drosophila cell lines.
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DNA repair gene polymorphisms and risk of pancreatic cancer.
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DNA- and PCR-fingerprinting in fungi.
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DNase I sensitivity QTLs are a major determinant of human expression variation.
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DOG1 expression is predicted by the seed-maturation environment and contributes to geographical variation in germination in Arabidopsis thaliana.
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Darwinian genomics and diversity in the tree of life.
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De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae.
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De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorder.
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Decoupling of genome size and sequence divergence in a symbiotic bacterium.
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Deep Sequencing of 71 Candidate Genes to Characterize Variation Associated with Alcohol Dependence.
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Deep Sequencing of Influenza A Virus from a Human Challenge Study Reveals a Selective Bottleneck and Only Limited Intrahost Genetic Diversification.
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Deep Sequencing of Three Loci Implicated in Large-Scale Genome-Wide Association Study Smoking Meta-Analyses.
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Deep whole-genome sequencing of 100 southeast Asian Malays.
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Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual Inheritance.
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Defining the role of common variation in the genomic and biological architecture of adult human height.
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Deleterious mutations and genetic variation for flower size in Mimulus guttatus.
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Density dependence and population differentiation of genetic architecture in Impatiens capensis in natural environments.
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Detangling red hair from pain: phenotype-specific contributions from different genetic variants in melanocortin-1 receptor.
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Detection of allelic variations of human gene expression by polymerase colonies.
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Detection of diverse variants of human immunodeficiency virus-1 groups M, N, and O and simian immunodeficiency viruses from chimpanzees by using generic pol and env primer pairs.
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Detection of phylogenetically diverse human immunodeficiency virus type 1 groups M and O from plasma by using highly sensitive and specific generic primers.
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Determinants of CD4 independence for a human immunodeficiency virus type 1 variant map outside regions required for coreceptor specificity.
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Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation.
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Developing a synthetic psychosocial stress measure and harmonizing CVD-risk data: a way forward to GxE meta- and mega-analyses.
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Developmental mediation of genetic variation in response to the Fast Track prevention program.
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Different evolutionary pathways of HIV-1 between fetus and mother perinatal transmission pairs indicate unique immune selection in fetuses.
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Differential susceptibility to adolescent externalizing trajectories: examining the interplay between CHRM2 and peer group antisocial behavior.
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Diploid apomicts of the Boechera holboellii complex display large-scale chromosome substitutions and aberrant chromosomes.
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Direct allelic variation scanning of the yeast genome.
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Discordant and heterogeneous clinically relevant genomic alterations in circulating tumor cells vs plasma DNA from men with metastatic castration resistant prostate cancer.
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Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.
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Distinctive variation in the U3R region of the 5' Long Terminal Repeat from diverse HIV-1 strains.
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Distribution and medical impact of loss-of-function variants in the Finnish founder population.
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Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma.
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Distribution, ecology, life history, genetic variation, and risk of extinction of nonhuman primates from Costa Rica.
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Divergent effects of genetic variation in endocannabinoid signaling on human threat- and reward-related brain function.
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Diverse genetic causes of polymicrogyria with epilepsy.
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Diversification before the most recent glaciation in Balanus glandula.
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Diversification of phytochrome contributions to germination as a function of seed-maturation environment.
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Diversity and host range of foliar fungal endophytes: are tropical leaves biodiversity hotspots?
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Diversity and selectivity in mRNA translation on the endoplasmic reticulum.
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Diversity considerations in HIV-1 vaccine selection.
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Diversity in the realm of eukaryotic microbe form and function.
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Diversity of ankyrins in the brain.
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Diversity of full-length subtype E HIV type 1 env sequences in early seroconvertors from northern Thailand.
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Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
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Dramatic Response After Lamotrigine in a Patient With Epileptic Encephalopathy and a De NovoCACNA1A Variant.
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Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale.
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Dynamics of microsatellite divergence under stepwise mutation and proportional slippage/point mutation models.
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Dysregulation of dopamine transporters via dopamine D2 autoreceptors triggers anomalous dopamine efflux associated with attention-deficit hyperactivity disorder.
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EGFR and EGFRvIII interact with PUMA to inhibit mitochondrial translocalization of PUMA and PUMA-mediated apoptosis independent of EGFR kinase activity.
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Early onset prostate cancer has a significant genetic component.
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Early-onset of symptoms and clinical course of Pompe disease associated with the c.-32-13 T > G variant.
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Ecological reproductive isolation of coast and inland races of Mimulus guttatus.
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Education influences the association between genetic variants and refractive error: a meta-analysis of five Singapore studies.
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Effect of Genetic African Ancestry on eGFR and Kidney Disease.
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Effect of Human Genetic Variability on Gene Expression in Dorsal Root Ganglia and Association with Pain Phenotypes.
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Effect of allelic variation at the NACP-Rep1 repeat upstream of the alpha-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system.
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Effect of genetic variation in the nicotinic receptor genes on risk for posttraumatic stress disorder.
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Effect of vertical sleeve gastrectomy in melanocortin receptor 4-deficient rats.
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Effects of genetic variation in protease activated receptor 4 after an acute coronary syndrome: Analysis from the TRACER trial.
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Effects of selection and mutation on mitochondrial variation and inferences of historical population expansion in a Caribbean reef fish.
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Effects of sequence variation on differential allelic transcription factor occupancy and gene expression.
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Effects of variation at the flower-colour A locus on mating system parameters in Ipomoea purpurea.
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Efficacy of the pharmacologic chaperone migalastat in a subset of male patients with the classic phenotype of Fabry disease and migalastat-amenable variants: data from the phase 3 randomized, multicenter, double-blind clinical trial and extension study.
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Elevated cerebrospinal fluid cytokine levels in tuberculous meningitis predict survival in response to dexamethasone.
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Elucidation of the transcription network governing mammalian sex determination by exploiting strain-specific susceptibility to sex reversal.
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Engineering a BCR-ABL-activated caspase for the selective elimination of leukemic cells.
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Enlarged Dural Sac in Idiopathic Bronchiectasis Implicates Heritable Connective Tissue Gene Variants.
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Envelope diversity, coreceptor usage and syncytium-inducing phenotype of HIV-1 variants in saliva and blood during primary infection.
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Envelope-specific B-cell populations in African green monkeys chronically infected with simian immunodeficiency virus.
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Environmental and genetic influences on the germination of Arabidopsis thaliana in the field.
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Epigenetic alterations in cytochrome P450 oxidoreductase (Por) in sperm of rats exposed to tetrahydrocannabinol (THC).
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Epigenome-wide association study of kidney function identifies trans-ethnic and ethnic-specific loci.
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Epstein-Barr Virus Genomes Reveal Population Structure and Type 1 Association with Endemic Burkitt Lymphoma.
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Erythrocyte Webb-type glycophorin C variant lacks N-glycosylation due to an asparagine to serine substitution.
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Escape from homeostasis.
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Estimating the heritability of cognitive traits across dog breeds reveals highly heritable inhibitory control and communication factors.
-
Evaluation of the Genetic Variance of Alzheimer's Disease Explained by the Disease-Associated Chromosomal Regions.
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Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.
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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
-
Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients.
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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index.
-
Evidence from opsin genes rejects nocturnality in ancestral primates.
-
Evidence of sexual recombination among Cryptococcus neoformans serotype A isolates in sub-Saharan Africa.
-
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.
-
Evidence that structural variants within the human delta-globin protein may reflect genetic interactions between the delta- and beta-globin genes.
-
Evolution and diversity in human herpes simplex virus genomes.
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Evolution of a polyphenism by genetic accommodation.
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Evolution of host range in Coleosporium ipomoeae, a plant pathogen with multiple hosts.
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Evolution of king crabs from hermit crab ancestors.
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Evolution of plant resistance at the molecular level: ecological context of species interactions.
-
Evolution of the MHC class I genes of a New World primate from ancestral homologues of human non-classical genes.
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Evolution of the gene encoding mitochondrial intermediate peptidase and its cosegregation with the A mating-type locus of mushroom fungi.
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Evolution, interactions, and biological networks.
-
Evolution. Chaperones as buffering agents?
-
Evolutionary analysis of the well characterized endo16 promoter reveals substantial variation within functional sites.
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Evolutionary biology: significance of primate sexual swellings.
-
Evolutionary design on a budget: robustness and optimality of bacteriophage T7.
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Evolutionary dissociations between homologous genes and homologous structures.
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Evolutionary dynamics of an Arabidopsis insect resistance quantitative trait locus.
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Evolutionary genetics and acclimatization in nephrology.
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Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.
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Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease.
-
Exome sequencing identifies gene variants and networks associated with extreme respiratory outcomes following preterm birth.
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Exome-Based Rare-Variant Analyses in CKD.
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Expanding the diversity of DNA base modifications with N⁶-methyldeoxyadenosine.
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Experimental analysis of sources of error in evolutionary studies based on Roche/454 pyrosequencing of viral genomes.
-
Experimental habitat fragmentation increases linkage disequilibrium but does not affect genetic diversity or population structure in the Amazonian liverwort Radula flaccida.
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Explaining the heritability of an ecologically significant trait in terms of individual quantitative trait loci.
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Exploiting expression patterns across multiple tissues to map expression quantitative trait loci.
-
Exploring molecular diversity with combinatorial shape libraries.
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Extended ORF8 Gene Region Is Valuable in the Epidemiological Investigation of Severe Acute Respiratory Syndrome-Similar Coronavirus.
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Extensive chloroplast haplotype variation indicates Pleistocene hybridization and radiation of North American Arabis drummondii, A. x divaricarpa, and A. holboellii (Brassicaceae).
-
Extensive haplotype diversity in African American mothers and their cord blood units.
-
Extensive junctional diversity of rearranged human T cell receptor delta genes.
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Extensive recombination due to heteroduplexes generates large amounts of artificial gene fragments during PCR.
-
Extracellular superoxide dismutase haplotypes are associated with acute lung injury and mortality.
-
Extreme selective sweeps independently targeted the X chromosomes of the great apes.
-
FOXP2 variation in great ape populations offers insight into the evolution of communication skills.
-
Factors affecting harp seal (Pagophilus groenlandicus) strandings in the Northwest Atlantic.
-
Factors associated with the diversification of the gut microbial communities within chimpanzees from Gombe National Park.
-
Failure to replicate two mate preference QTLs across multiple strains of Drosophila pseudoobscura.
-
Family-based association tests for rare variants with censored traits.
-
Favorable and unfavorable HLA class I alleles and haplotypes in Zambians predominantly infected with clade C human immunodeficiency virus type 1.
-
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.
-
Fine-scale crossover rate heterogeneity in Drosophila pseudoobscura.
-
Fine-scale mapping of recombination rate in Drosophila refines its correlation to diversity and divergence.
-
Fine-scale phylogenetic architecture of a complex bacterial community.
-
Fine-scale population genetic structure in a fission-fusion society.
-
Fine-scale variation in meiotic recombination in Mimulus inferred from population shotgun sequencing.
-
Flow cytometric analysis of fluorescence resonance energy transfer: a tool for high-throughput screening of molecular interactions in living cells.
-
Flux control in a plant defense pathway is robust to environmental perturbations and controls variation in adaptive traits
-
Formalizing morphologically cryptic biological entities: new insights from DNA taxonomy, hybridization, and biogeography in the leafy liverwort Porella platyphylla (Jungermanniopsida, Porellales).
-
Frequent circumarctic and rare transequatorial dispersals in the lichenised agaric genus Lichenomphalia (Hygrophoraceae, Basidiomycota).
-
From genome-wide to candidate gene: an investigation of variation at the major histocompatibility complex in common bottlenose dolphins exposed to harmful algal blooms.
-
From genotype to phenotype: systems biology meets natural variation.
-
From man to fish: What can Zebrafish tell us about ApoL1 nephropathy?
-
Functional FLT1 Genetic Variation is a Prognostic Factor for Recurrence in Stage I-III Non-Small-Cell Lung Cancer.
-
Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma.
-
Functional analysis of intra-allelic variation at NACP-Rep1 in the alpha-synuclein gene.
-
Functional analysis of novel SNPs and mutations in human and mouse genomes.
-
Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex.
-
Functional consequences of natural sequence variation in the activation domain of HIV-1 Rev.
-
Functional divergence in tandemly duplicated Arabidopsis thaliana trypsin inhibitor genes.
-
Functional diversity of notch family genes in fetal lung development.
-
Functional genetic screen of human diversity reveals that a methionine salvage enzyme regulates inflammatory cell death.
-
Functional neuroimaging of genetic variation in serotonergic neurotransmission.
-
Functional polymorphisms in the promoter regions of the FAS and FAS ligand genes and risk of bladder cancer in south China: a case-control analysis.
-
Functional polymorphisms of matrix metalloproteinase-9 are associated with risk of occurrence and metastasis of lung cancer.
-
Functional variants in DCAF4 associated with lung cancer risk in European populations.
-
Fungal community analysis by large-scale sequencing of environmental samples.
-
Fungal mating: Candida albicans flips a switch to get in the mood.
-
Further evidence for the involvement of EFL1 in a Shwachman-Diamond-like syndrome and expansion of the phenotypic features.
-
Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association.
-
G protein-coupled receptor kinase 5 gene polymorphisms are associated with postoperative atrial fibrillation after coronary artery bypass grafting in patients receiving β-blockers.
-
GAA variants and phenotypes among 1,079 patients with Pompe disease: Data from the Pompe Registry.
-
GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium.
-
GWAS or Gee Whiz, PSAS or Pshaw: elucidating the biologic and clinical significance of genetic variation in cardiovascular disease.
-
Gene expression and adaptive noncoding changes during human evolution.
-
Gene expression divergence and the origin of hybrid dysfunctions.
-
General olfactory sensitivity database (GOSdb): candidate genes and their genomic variations.
-
Generation of high-affinity human antibodies by combining donor-derived and synthetic complementarity-determining-region diversity.
-
Generators of phenotypic diversity in the evolution of pathogenic microorganisms.
-
Genes and environment in neonatal intraventricular hemorrhage.
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Genetic Consequences of Biologically Altered Environments.
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Genetic Differences in the Immediate Transcriptome Response to Stress Predict Risk-Related Brain Function and Psychiatric Disorders.
-
Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians.
-
Genetic Regulation of Fibroblast Activation and Proliferation in Cardiac Fibrosis.
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Genetic Variants Associated With Vincristine-Induced Peripheral Neuropathy in Two Populations of Children With Acute Lymphoblastic Leukemia.
-
Genetic Variants Associated with Circulating Parathyroid Hormone.
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Genetic Variants Predict Optimal Timing of Radiotherapy to Reduce Side-effects in Breast Cancer Patients.
-
Genetic Variants in WNT2B and BTRC Predict Melanoma Survival.
-
Genetic Variants of the MDM2 Gene Are Predictive of Treatment-Related Toxicities and Overall Survival in Patients With Advanced NSCLC.
-
Genetic Variation Associated with Longer Telomere Length Increases Risk of Chronic Lymphocytic Leukemia.
-
Genetic Variation in Surfactant Protein-A2 Delays Resolution of Eosinophilia in Asthma.
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Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction.
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Genetic analysis of the beta-tubulin gene, TUBB, in non-small-cell lung cancer.
-
Genetic and 'cultural' similarity in wild chimpanzees.
-
Genetic and environmental influences on functional abilities in Danish twins aged 75 years and older.
-
Genetic and evolutionary correlates of fine-scale recombination rate variation in Drosophila persimilis.
-
Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium.
-
Genetic and nongenetic covariates of pain severity in patients with adenocarcinoma of the pancreas: assessing the influence of cytokine genes.
-
Genetic and physiological basis of adaptive salt tolerance divergence between coastal and inland Mimulus guttatus.
-
Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing.
-
Genetic architecture of human pain perception.
-
Genetic association between endothelial nitric oxide synthase and Alzheimer disease.
-
Genetic association study of adiposity and melanocortin-4 receptor (MC4R) common variants: replication and functional characterization of non-coding regions.
-
Genetic basis and consequences of niche construction: plasticity-induced genetic constraints on the evolution of seed dispersal in Arabidopsis thaliana.
-
Genetic control of blood pressure and the angiotensinogen locus.
-
Genetic correlations of psychiatric traits with body composition and glycemic traits are sex- and age-dependent.
-
Genetic determinants in HIV-1 Gag and Env V3 are related to viral response to combination antiretroviral therapy with a protease inhibitor.
-
Genetic determinants of renal transplant outcome: where do we stand?
-
Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
-
Genetic determinants of variable metabolism have little impact on the clinical use of leading antipsychotics in the CATIE study.
-
Genetic dissection of interspecific differences in yeast thermotolerance.
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Genetic divergence causes parallel evolution of flower color in Chilean Mimulus.
-
Genetic diversity among Mycobacterium avium complex strains recovered from children with and without human immunodeficiency virus infection.
-
Genetic diversity does not explain variation in extra-pair paternity in multiple populations of a songbird.
-
Genetic diversity fuels gene discovery for tobacco and alcohol use.
-
Genetic diversity in the Mycobacterium tuberculosis complex based on variable numbers of tandem DNA repeats.
-
Genetic diversity of coastal bottlenose dolphins revealed by structurally and functionally diverse hemoglobins.
-
Genetic diversity of human immunodeficiency virus type 2: evidence for distinct sequence subtypes with differences in virus biology.
-
Genetic diversity of the Cryptococcus species complex suggests that Cryptococcus gattii deserves to have varieties.
-
Genetic diversity of the msp-1 locus and symptomatic malaria in south-west Nigeria.
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Genetic effects on mating success and partner choice in a social mammal.
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Genetic evidence and integration of various data sources for classifying uncertain variants into a single model.
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Genetic evidence for long-term population decline in a savannah-dwelling primate: inferences from a hierarchical bayesian model.
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Genetic evidence reveals temporal change in hybridization patterns in a wild baboon population.
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Genetic factors in susceptibility to death: a comparative analysis of bivariate survival models.
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Genetic heterogeneity of diffuse large B-cell lymphoma.
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Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes.
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Genetic influence of CCR5, CCR2, and SDF1 variants on human immunodeficiency virus 1 (HIV-1)-related disease progression and neurological impairment, in children with symptomatic HIV-1 infection.
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Genetic isolation by distance in Arabidopsis thaliana: biogeography and postglacial colonization of Europe.
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Genetic mechanisms and evolutionary significance of natural variation in Arabidopsis.
-
Genetic modifier loci affecting survival and cardiac function in murine dilated cardiomyopathy.
-
Genetic nature of individual frailty: comparison of two approaches.
-
Genetic organization, length conservation, and evolution of RNA polymerase II carboxyl-terminal domain.
-
Genetic polymorphisms and the risk of stroke after cardiac surgery.
-
Genetic polymorphisms modify bladder cancer recurrence and survival in a USA population-based prognostic study.
-
Genetic polymorphisms of p21 are associated with risk of squamous cell carcinoma of the head and neck.
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Genetic recombination of poliovirus in a cell-free system.
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Genetic relationships and evolution of genotypes of yellow fever virus and other members of the yellow fever virus group within the Flavivirus genus based on the 3' noncoding region.
-
Genetic screen of African Americans with Fuchs endothelial corneal dystrophy.
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Genetic structure of typical and atypical populations of Candida albicans from Africa.
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Genetic studies of human neuropathic pain conditions: a review.
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Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia.
-
Genetic variability of Bacillus anthracis and related species.
-
Genetic variability of the U5 and downstream sequence of major HIV-1 subtypes and circulating recombinant forms.
-
Genetic variance and covariance for physiological traits in Lobelia: are there constraints on adaptive evolution?
-
Genetic variance in fitness indicates rapid contemporary adaptive evolution in wild animals.
-
Genetic variant in DNA repair gene GTF2H4 is associated with lung cancer risk: a large-scale analysis of six published GWAS datasets in the TRICL consortium.
-
Genetic variant of IRAK2 in the toll-like receptor signaling pathway and survival of non-small cell lung cancer.
-
Genetic variant rs16430 6bp > 0bp at the microRNA-binding site in TYMS and risk of sporadic breast cancer risk in non-Hispanic white women aged ≤ 55 years.
-
Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach.
-
Genetic variants and associations of 25-hydroxyvitamin D concentrations with major clinical outcomes.
-
Genetic variants and disease: correlate or cause?
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Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.
-
Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.
-
Genetic variants in 5-HTTLPR, BDNF, HTR1A, COMT, and FKBP5 and risk for treated depression after cancer diagnosis.
-
Genetic variants in ERCC1 and XPC predict survival outcome of non-small cell lung cancer patients treated with platinum-based therapy.
-
Genetic variants in Hippo pathway genes YAP1, TEAD1 and TEAD4 are associated with melanoma-specific survival.
-
Genetic variants in RORA and DNMT1 associated with cutaneous melanoma survival.
-
Genetic variants in SLC9A9 are associated with measures of attention-deficit/hyperactivity disorder symptoms in families.
-
Genetic variants in TNF-α promoter are predictors of recurrence in patients with squamous cell carcinoma of oropharynx after definitive radiotherapy.
-
Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival.
-
Genetic variants in microRNA-binding sites of DNA repair genes as predictors of recurrence in patients with squamous cell carcinoma of the oropharynx.
-
Genetic variants in nucleotide excision repair pathway predict survival of esophageal squamous cell cancer patients receiving platinum-based chemotherapy.
-
Genetic variants in peroxisome proliferator-activated receptor-gamma gene are associated with risk of lung cancer in a Chinese population.
-
Genetic variants in the H2AFX promoter region are associated with risk of sporadic breast cancer in non-Hispanic white women aged
-
Genetic variants in the MDM2 promoter and lung cancer risk in a Chinese population.
-
Genetic variants in the PIWI-piRNA pathway gene DCP1A predict melanoma disease-specific survival.
-
Genetic variants in the TEP1 gene are associated with prostate cancer risk and recurrence.
-
Genetic variants in the platelet-derived growth factor subunit B gene associated with pancreatic cancer risk.
-
Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.
-
Genetic variants near PDGFRA are associated with corneal curvature in Australians.
-
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.
-
Genetic variants of JNK and p38α pathways and risk of non-small cell lung cancer in an Eastern Chinese population.
-
Genetic variants of SDCCAG8 and MAGI2 in mitosis-related pathway genes are independent predictors of cutaneous melanoma-specific survival.
-
Genetic variants of genes in the NER pathway associated with risk of breast cancer: A large-scale analysis of 14 published GWAS datasets in the DRIVE study.
-
Genetic variants of p21 and p27 and pancreatic cancer risk in non-Hispanic Whites: a case-control study.
-
Genetic variants of the ADPRT, XRCC1 and APE1 genes and risk of cutaneous melanoma.
-
Genetic variants of the vitamin D receptor gene alter risk of cutaneous melanoma.
-
Genetic variation across the human olfactory receptor repertoire alters odor perception.
-
Genetic variation at MHC class II loci influences both olfactory signals and scent discrimination in ring-tailed lemurs.
-
Genetic variation at a single locus and age of onset for Alzheimer's disease.
-
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.
-
Genetic variation in MAOA modulates ventromedial prefrontal circuitry mediating individual differences in human personality.
-
Genetic variation in SP-A2 leads to differential binding to Mycoplasma pneumoniae membranes and regulation of host responses.
-
Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association Consortium.
-
Genetic variation in a human odorant receptor alters odour perception.
-
Genetic variation in adiponectin (ADIPOQ) and the type 1 receptor (ADIPOR1), obesity and prostate cancer in African Americans.
-
Genetic variation in aldosterone synthase predicts plasma glucose levels.
-
Genetic variation in components of dopamine neurotransmission impacts ventral striatal reactivity associated with impulsivity.
-
Genetic variation in dopamine neurotransmission and motor development of infants born extremely-low-birthweight.
-
Genetic variation in horizontally transmitted fungal endophytes of pine needles reveals population structure in cryptic species.
-
Genetic variation in human NPY expression affects stress response and emotion.
-
Genetic variation in surfactant protein-A2 alters responses to ozone.
-
Genetic variation in the 3' non-coding region of dengue viruses.
-
Genetic variation in the leptin receptor gene and obesity in survivors of childhood acute lymphoblastic leukemia: a report from the Childhood Cancer Survivor Study.
-
Genetic variation in the odorant receptor OR2J3 is associated with the ability to detect the "grassy" smelling odor, cis-3-hexen-1-ol.
-
Genetic variation in the one-carbon transfer pathway and ovarian cancer risk.
-
Genetic variation in the spread of Drosophila subobscura from a nonequilibrium population.
-
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.
-
Genetic variation of DNA methyltransferase-3A contributes to protection against persistent MRSA bacteremia in patients.
-
Genetic variation of HIV type 1 in four World Health Organization-sponsored vaccine evaluation sites: generation of functional envelope (glycoprotein 160) clones representative of sequence subtypes A, B, C, and E. WHO Network for HIV Isolation and Characterization.
-
Genetic variation of an odorant receptor OR7D4 and sensory perception of cooked meat containing androstenone.
-
Genetic variation within and among populations of the threatened lichen Lobaria pulmonaria in Switzerland and implications for its conservation.
-
Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck.
-
Genetic variations of the ADIPOQgene and risk of prostate cancer in Chinese Han men.
-
Genetic-based dosing in orthopedic patients beginning warfarin therapy.
-
Genetically determined height and coronary artery disease.
-
Genetically divergent strains of human immunodeficiency virus type 2 use multiple coreceptors for viral entry.
-
Genetics of dispersal.
-
Genetics of drought adaptation in Arabidopsis thaliana: I. Pleiotropy contributes to genetic correlations among ecological traits.
-
Genetics of emotional regulation: the role of the serotonin transporter in neural function.
-
Genetics of incipient speciation in Drosophila mojavensis. I. Male courtship song, mating success, and genotype x environment interactions.
-
Genetics of incipient speciation in Drosophila mojavensis. III. Life-history divergence in allopatry and reproductive isolation.
-
Genetics. FDA races in wrong direction.
-
Genic intolerance to functional variation and the interpretation of personal genomes.
-
Genome Evolution and Innovation across the Four Major Lineages of Cryptococcus gattii.
-
Genome diversity in Brachypodium distachyon: deep sequencing of highly diverse inbred lines.
-
Genome organization and three kinds of heritable changes: general description and stochastic factors (a review).
-
Genome sequence of Blochmannia pennsylvanicus indicates parallel evolutionary trends among bacterial mutualists of insects.
-
Genome variation in Cryptococcus gattii, an emerging pathogen of immunocompetent hosts.
-
Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types.
-
Genome-wide architecture of reproductive isolation in a naturally occurring hybrid zone between Mus musculus musculus and M. m. domesticus.
-
Genome-wide association analysis of clinical vs. nonclinical origin provides insights into Saccharomyces cerevisiae pathogenesis.
-
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.
-
Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.
-
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.
-
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.
-
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.
-
Genome-wide meta-analyses of smoking behaviors in African Americans.
-
Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry.
-
Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
-
Genomes and gene expression across light and productivity gradients in eastern subtropical Pacific microbial communities.
-
Genomewide ancestry and divergence patterns from low-coverage sequencing data reveal a complex history of admixture in wild baboons.
-
Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.
-
Genomic acquisition of a capsular polysaccharide virulence cluster by non-pathogenic Burkholderia isolates.
-
Genomic approaches for understanding the genetics of complex disease.
-
Genomic features that predict allelic imbalance in humans suggest patterns of constraint on gene expression variation.
-
Genomic impacts of chromosomal inversions in parapatric Drosophila species.
-
Genomic medicine: genetic variation and its impact on the future of health care.
-
Genomic profiling to promote a healthy lifestyle: not ready for prime time.
-
Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
-
Genomic signatures of near-extinction and rebirth of the crested ibis and other endangered bird species.
-
Genomics and hypertension: concepts, potentials, and opportunities.
-
Genomics: Lessons in complexity from yeast.
-
Genotypic analysis of B cell colonies by in situ hybridization. Stoichiometric expression of three VH families in adult C57BL/6 and BALB/c mice.
-
Genotypic and Phenotypic Diversity among Human Isolates of Akkermansia muciniphila.
-
Genotypic diversity and clinical outcome of cryptococcosis in renal transplant recipients in Brazil.
-
Genotypic diversity of anaerobic isolates from bloodstream infections.
-
Genotypic diversity within a natural coastal bacterioplankton population.
-
Geographic and evolutionary diversification of glucosinolates among near relatives of Arabidopsis thaliana (Brassicaceae).
-
Geographic patterns of microsatellite variation in Boechera stricta, a close relative of Arabidopsis.
-
Geographic variation in algal partners of Cladonia subtenuis (Cladoniaceae) highlights the dynamic nature of a lichen symbiosis.
-
Global Survey of Variation in a Human Olfactory Receptor Gene Reveals Signatures of Non-Neutral Evolution.
-
Global and gene-specific DNA methylation across multiple tissues in early infancy: implications for children's health research.
-
Global and regional epidemiology of HIV-1 recombinants in 1990-2015: a systematic review and global survey.
-
Global and regional molecular epidemiology of HIV-1, 1990-2015: a systematic review, global survey, and trend analysis.
-
Global distribution, diversity hot spots and niche transitions of an astaxanthin-producing eukaryotic microbe.
-
Global patterns in peatmoss biodiversity.
-
Glucose metabolism gene variants modulate the risk of pancreatic cancer.
-
Gnao1 (G alphaO protein) is a likely genetic contributor to variation in physical dependence on opioids in mice.
-
Great ape genetic diversity and population history.
-
Growth of nutritionally variant streptococci on common laboratory and 10 commercial blood culture media.
-
HBV whole-genome mutation profile in HIV-1/HBV coinfected patients in a long-term follow-up study.
-
HER2 testing in metastatic colorectal cancer: ready for prime time?
-
HIV quasispecies and resampling.
-
HIV-1 Envelope Glycoproteins from Diverse Clades Differentiate Antibody Responses and Durability among Vaccinees.
-
HLA class I allelic diversity and progression of fibrosis in patients with chronic hepatitis C.
-
HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.
-
Half of the variation in susceptibility to mortality is genetic: findings from Swedish twin survival data.
-
Haplotype of signal transducer and activator of transcription 3 gene predicts cardiovascular disease in dialysis patients.
-
Haplotypes spanning the complement factor H gene are protective against age-related macular degeneration.
-
Hb Catonsville (glutamic acid inserted between Pro-37(C2)alpha and Thr-38(C3)alpha). Nonallelic gene conversion in the globin system?
-
Heritability estimates of endophenotypes of long and health life: the Long Life Family Study.
-
Heritable individual-specific and allele-specific chromatin signatures in humans.
-
Heritable resistance to tyrosine kinase inhibitors.
-
Heterogeneous polymerase fidelity and mismatch repair bias genome variation and composition.
-
Heteroplasmic mitochondrial DNA mutations in normal and tumour cells.
-
High Multiplicity Infection by HIV-1 in Men Who Have Sex with Men.
-
High genetic diversity in a remote island population system: sans sex.
-
High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.
-
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
-
High-frequency actionable pathogenic exome variants in an average-risk cohort.
-
High-resolution deep sequencing reveals biodiversity, population structure, and persistence of HIV-1 quasispecies within host ecosystems.
-
Historical effects on beta diversity and community assembly in Amazonian trees.
-
History and evolution of alpine plants endemic to the Qinghai-Tibetan Plateau: Aconitum gymnandrum (Ranunculaceae).
-
Homeostasis and dynamic stability of the phenotype link robustness and plasticity.
-
Honest olfactory ornamentation in a female-dominant primate.
-
Hormonal characteristics of free-ranging female lions (Panthera leo) of the Serengeti Plains and Ngorongoro Crater.
-
Host Genetic Variant in CXCL16 May Be Associated With Hepatitis B Virus-Related Acute Liver Failure.
-
Host genetic variation in susceptibility to Punta Toro virus.
-
Host lifestyle affects human microbiota on daily timescales.
-
Host-pathogen genetic interactions underlie tuberculosis susceptibility in genetically diverse mice.
-
How hot are drosophila hotspots? examining recombination rate variation and associations with nucleotide diversity, divergence, and maternal age in Drosophila pseudoobscura.
-
Human B cell alloantigens; alpha subunit variability.
-
Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants.
-
Human choline transporter gene variation is associated with corticolimbic reactivity and autonomic-cholinergic function.
-
Human genetic admixture through the lens of population genomics.
-
Human genetic admixture.
-
Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia.
-
Human genetic variation in VAC14 regulates Salmonella invasion and typhoid fever through modulation of cholesterol.
-
Human histocompatibility antigen mutants immunoselected in vitro. Biochemical analysis of a mutant which synthesizes an altered HLA-A2 heavy chain.
-
Human infection by genetically diverse SIVSM-related HIV-2 in west Africa.
-
Human pain genetics database: a resource dedicated to human pain genetics research.
-
Hybrid origin of SIV in chimpanzees.
-
Hypertension Susceptibility Loci are Associated with Anthracycline-related Cardiotoxicity in Long-term Childhood Cancer Survivors.
-
Hypothalamic-pituitary-adrenal axis genetic variation and early stress moderates amygdala function.
-
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.
-
Ice-age survival of Atlantic cod: agreement between palaeoecology models and genetics.
-
Identification and Quantitation of Coding Variants and Isoforms of Pulmonary Surfactant Protein A.
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
-
Identification and characterization of transmitted and early founder virus envelopes in primary HIV-1 infection.
-
Identification and utilization of arbitrary correlations in models of recombination signal sequences.
-
Identification of ENV determinants in V3 that influence the molecular anatomy of CCR5 utilization.
-
Identification of HIV-1 genitourinary tract compartmentalization by analyzing the env gene sequences in urine.
-
Identification of a new variant of PDE1A calmodulin-stimulated cyclic nucleotide phosphodiesterase expressed in mouse sperm.
-
Identification of a novel risk variant in the FUS gene in essential tremor.
-
Identification of a region of genetic variability among Bacillus anthracis strains and related species.
-
Identification of a structurally distinct CD101 molecule encoded in the 950-kb Idd10 region of NOD mice.
-
Identification of asteroid genera with species capable of larval cloning.
-
Identification of genetic variants in base excision repair pathway and their associations with risk of esophageal squamous cell carcinoma.
-
Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia.
-
Identification of the single base change causing the callipyge muscle hypertrophy phenotype, the only known example of polar overdominance in mammals.
-
Identification of variants in CNGA3 as cause for achromatopsia by exome sequencing of a single patient.
-
Identifying susceptibility genes for prostate cancer--a family-based association study of polymorphisms in CYP17, CYP19, CYP11A1, and LH-beta.
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Idiopathic pain disorders--pathways of vulnerability.
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IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis.
-
Imaging genetics and the neurobiological basis of individual differences in vulnerability to addiction.
-
Imaging genetics: perspectives from studies of genetically driven variation in serotonin function and corticolimbic affective processing.
-
Impact of BDNF Val66Met and 5-HTTLPR polymorphism variants on neural substrates related to sadness and executive function.
-
Impact of Bacterial and Human Genetic Variation on Staphylococcus aureus Infections.
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Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program.
-
Impact of ancestry and common genetic variants on QT interval in African Americans.
-
Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.
-
Impact of psychological stress on the associations between apolipoprotein E variants and metabolic traits: findings in an American sample of caregivers and controls.
-
Implementing a cumulative supermatrix approach for a comprehensive phylogenetic study of the Teloschistales (Pezizomycotina, Ascomycota).
-
Implementing genome-driven personalized cardiology in clinical practice.
-
In vitro kinetics of immunoglobulin synthesis and secretion by nonsecretory human myeloma cells.
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In vivo Modeling Implicates APOL1 in Nephropathy: Evidence for Dominant Negative Effects and Epistasis under Anemic Stress.
-
In vivo genetic variability of the human immunodeficiency virus type 2 V3 region.
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Incidentally identified genetic variants in arrhythmogenic right ventricular cardiomyopathy-associated genes among children undergoing exome sequencing reflect healthy population variation.
-
Incongruence between genetic and morphological diversity in Microcebus griseorufus of Beza Mahafaly.
-
Incorporating external information to improve sparse signal detection in rare-variant gene-set-based analyses.
-
Increased risk of low birth weight in women with placental malaria associated with P. falciparum VAR2CSA clade.
-
Independent variation and positive selection in env V1 and V2 domains within maternal-infant strains of human immunodeficiency virus type 1 in vivo.
-
Individual variation in inbreeding depression: the roles of inbreeding history and mutation.
-
Individualized therapy for hepatitis C infection: focus on the interleukin-28B polymorphism in directing therapy.
-
Infant transmitted/founder HIV-1 viruses from peripartum transmission are neutralization resistant to paired maternal plasma.
-
Inference of tumor evolution during chemotherapy by computational modeling and in situ analysis of genetic and phenotypic cellular diversity.
-
Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability.
-
Influence of interleukin-28B single-nucleotide polymorphisms on progression to liver cirrhosis in human immunodeficiency virus-hepatitis C virus-coinfected patients receiving antiretroviral therapy.
-
Influence of nociception and stress-induced antinociception on genetic variation in isoflurane anesthetic potency among mouse strains.
-
Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration.
-
Initial sequencing and comparative analysis of the mouse genome.
-
Insect sodium channels and insecticide resistance.
-
Insight into the phenotype of infants with Pompe disease identified by newborn screening with the common c.-32-13T>G "late-onset" GAA variant.
-
Integrating ethics and science in the International HapMap Project.
-
Integrative analyses reveal signaling pathways underlying familial breast cancer susceptibility.
-
Integrative annotation of variants from 1092 humans: application to cancer genomics.
-
Interaction of FKBP5 gene variants and adverse life events in predicting depression onset: results from a 10-year prospective community study.
-
Intergenic and genic sequence lengths have opposite relationships with respect to gene expression.
-
Interindividual variation in serum sodium and longitudinal blood pressure tracking in the Framingham Heart Study.
-
Interleukin 12B (IL12B) genetic variation and pulmonary tuberculosis: a study of cohorts from The Gambia, Guinea-Bissau, United States and Argentina.
-
Interleukin-10 promoter variants predict HPV-positive tumors and survival of squamous cell carcinoma of the oropharynx.
-
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals.
-
Intraspecific Genetic Variation for Behavioral Isolation Loci in Drosophila.
-
Intraspecific variation in symbiont genomes: bottlenecks and the aphid-buchnera association.
-
Intrinsic GTP hydrolysis is observed for a switch 1 variant of Cdc42 in the presence of a specific GTPase inhibitor.
-
Investigating Conservation of the Cell-Cycle-Regulated Transcriptional Program in the Fungal Pathogen, Cryptococcus neoformans.
-
Is epigenetic inheritance a counterexample to the central dogma?
-
Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults.
-
Is the aneuploid chromosome in an apomictic Boechera holboellii a genuine B chromosome?
-
Is there a dose-dependent effect of genetic susceptibility loci for gastric cancer on prognosis of the patients?
-
Is there protective haplotype of dysbindin gene (DTNBP1) 3 polymorphisms for major depressive disorder.
-
Joint influence of small-effect genetic variants on human longevity.
-
KCNJ11 variants and their effect on the association between serum potassium and diabetes risk in the Atherosclerosis Risk in Communities (ARIC) Study and Jackson Heart Study (JHS) cohorts.
-
Kidney Disease-Associated APOL1 Variants Have Dose-Dependent, Dominant Toxic Gain-of-Function.
-
Lack of association of mutations in optineurin with disease in patients with adult-onset primary open-angle glaucoma.
-
Lack of genetic differentiation between two geographically diverse samples of Candida albicans isolated from patients infected with human immunodeficiency virus.
-
Lack of variation in voltage-gated sodium channels of common bottlenose dolphins (Tursiops truncatus) exposed to neurotoxic algal blooms.
-
Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome.
-
Large-scale gene-centric analysis identifies novel variants for coronary artery disease.
-
Large-scale genetic investigation reveals genetic liability to multiple complex traits influencing a higher risk of ADHD.
-
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair.
-
Large-scale identification and analysis of genome-wide single-nucleotide polymorphisms for mapping in Arabidopsis thaliana.
-
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome.
-
Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.
-
Leaf-level gas-exchange uniformity and photosynthetic capacity among loblolly pine (Pinus taeda L.) genotypes of contrasting inherent genetic variation.
-
Letter by Gurbel et al regarding article, "Cytochrome 2C19*17 allelic variant, platelet aggregation, bleeding events, and stent thrombosis in clopidogrel-treated patients with coronary stent placement".
-
Letting the gene out of the bottle: OPRM1 interactions.
-
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
-
Leveraging population information in family-based rare variant association analyses of quantitative traits.
-
Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease.
-
Life, diversity and the pursuit of haplotypes.
-
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.
-
Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.
-
Local-scale genetic structure in the peatmoss Sphagnum fuscum.
-
Long-distance dispersal and genetic structure of natural populations: an assessment of the inverse isolation hypothesis in peat mosses.
-
Longitudinal Antigenic Sequences and Sites from Intra-Host Evolution (LASSIE) Identifies Immune-Selected HIV Variants.
-
Low genetic variation and no detectable population structure in aspergillus fumigatus compared to closely related Neosartorya species.
-
Low-dose mucosal simian immunodeficiency virus infection restricts early replication kinetics and transmitted virus variants in rhesus monkeys.
-
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
-
Lymph node metastases develop through a wider evolutionary bottleneck than distant metastases.
-
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
-
MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms.
-
Macroecological patterns of genetic structure and diversity in the aquatic moss Platyhypnidium riparioides.
-
Maintenance Poly (ADP-ribose) Polymerase Inhibitor Therapy for Ovarian Cancer: Precision Oncology or One Size Fits All?
-
Major flowering time gene, flowering locus C, regulates seed germination in Arabidopsis thaliana.
-
Major histocompatibility complex variation and evolution at a single, expressed DQA locus in two genera of elephants.
-
Major-gene resistance to the rust pathogen Coleosporium ipomoeae is common in natural populations of Ipomoea purpurea.
-
Many globally isolated AD hybrid strains of Cryptococcus neoformans originated in Africa.
-
Mapping and characterization of structural variation in 17,795 human genomes.
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
-
Mapping the proteo-genomic convergence of human diseases.
-
Massively parallel quantification of the regulatory effects of noncoding genetic variation in a human cohort.
-
Massively parallel sequencing of patients with intellectual disability, congenital anomalies and/or autism spectrum disorders with a targeted gene panel.
-
Maternal Broadly Neutralizing Antibodies Can Select for Neutralization-Resistant, Infant-Transmitted/Founder HIV Variants.
-
Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41.
-
Maximum-likelihood estimation of rates of recombination within mating-type regions.
-
Medical genomics: Gather and use genetic data in health care.
-
Melanocortin-1 receptor gene variants affect pain and mu-opioid analgesia in mice and humans.
-
Membranomyces species are common ectomycorrhizal symbionts in Northern Hemisphere forests
-
Mendelian randomisation study of the relationship between vitamin D and risk of glioma.
-
Mendelian randomization provides support for obesity as a risk factor for meningioma.
-
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.
-
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
-
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomes.
-
Meta-analysis of loci associated with age at natural menopause in African-American women.
-
Metabolism of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) by human CYP1B1 genetic variants.
-
Metagenomic and small-subunit rRNA analyses reveal the genetic diversity of bacteria, archaea, fungi, and viruses in soil.
-
Methicillin-resistant Staphylococcus aureus: an overview of basic and clinical research.
-
Metronidazole Metabolism in Neonates and the Interplay Between Ontogeny and Genetic Variation.
-
MicroRNA regulation and interspecific variation of gene expression.
-
Microgeographic patterns of genetic divergence and adaptation across natural environments in Boechera stricta (Brassicaceae)
-
Microsatellite analysis of genetic diversity among clinical and nonclinical Saccharomyces cerevisiae isolates suggests heterozygote advantage in clinical environments.
-
Microsatellite variation in populations of Drosophila pseudoobscura and Drosophila persimilis.
-
Mismatched dsRNA (ampligen) induces protection against genomic variants of the human immunodeficiency virus type 1 (HIV-1) in a multiplicity of target cells.
-
Missing genetic risk in neural tube defects: can exome sequencing yield an insight?
-
Mistaken Identity: Another Bias in the Use of Relative Genetic Divergence Measures for Detecting Interspecies Introgression.
-
Mitochondrial DNA variant in COX1 subunit significantly alters energy metabolism of geographically divergent wild isolates in Caenorhabditis elegans.
-
Mitochondrial DNA variation in human metabolic rate and energy expenditure.
-
Modeling Diversity: Do Homogeneous Laboratory Strains Limit Discovery?
-
Modeling the influence of genetic and environmental variation on the expression of plant life cycles across landscapes.
-
Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTR.
-
Molecular cloning, characterization, and expression in Escherichia coli of full-length cDNAs of three human glutathione S-transferase Pi gene variants. Evidence for differential catalytic activity of the encoded proteins.
-
Molecular evolution of a Drosophila homolog of human BRCA2.
-
Molecular evolutionary dynamics of cytochrome b in strepsirrhine primates: the phylogenetic significance of third-position transversions.
-
Molecular genetics of AMD and current animal models.
-
Molecular genetics of successful smoking cessation: convergent genome-wide association study results.
-
Molecular markers reveal that population structure of the human pathogen Candida albicans exhibits both clonality and recombination.
-
Molecular phylogeny of the kinesin family of microtubule motor proteins.
-
Molecular phylogeny, biogeography and speciation of the mushroom species Pleurotus cystidiosus and allied taxa.
-
Molecular phylogeography and cryptic speciation in the mosses, Mielichhoferia elongata and M. mielichhoferiana (Bryaceae).
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Molecular signatures of selection on reproductive character displacement of flower color in Phlox drummondii.
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Molecular surveillance for drug-resistant Plasmodium falciparum in clinical and subclinical populations from three border regions of Burma/Myanmar: cross-sectional data and a systematic review of resistance studies.
-
Monoclonal antibodies to malignant human gliomas.
-
Montagnard ethnicity and genetic relations in northern Cameroon: comment on "The Peopling of Sub-Saharan Africa: The Case Study of Cameroon," by G. Spedini et al.
-
Morphological and genetic differentiation and reproductive isolation among closely related taxa in the Ipomoea series Batatas.
-
Morphological and molecular characterization of variation in common bean (Phaseolus vulgaris L.) germplasm from Azad Jammu and Kashmir, Pakistan.
-
Mu Opioid Splice Variant MOR-1K Contributes to the Development of Opioid-Induced Hyperalgesia.
-
Multicentre search for genetic susceptibility loci in sporadic epilepsy syndrome and seizure types: a case-control study.
-
Multilocus analysis of variation and speciation in the closely related species Arabidopsis halleri and A. lyrata.
-
Multilocus coalescent analyses reveal the demographic history and speciation patterns of mouse lemur sister species.
-
Multilocus patterns of nucleotide diversity, population structure and linkage disequilibrium in Boechera stricta, a wild relative of Arabidopsis.
-
Multilocus phylogenetic and geospatial analyses illuminate diversification patterns and the biogeographic history of Malagasy endemic plated lizards (Gerrhosauridae: Zonosaurinae).
-
Multilocus sequence typing of serially collected isolates of Cryptococcus from HIV-infected patients in South Africa.
-
Multilocus sequence typing suggests the chytrid pathogen of amphibians is a recently emerged clone.
-
Multiple Functional Variants in cis Modulate PDYN Expression.
-
Multiple gene genealogies reveal recent dispersion and hybridization in the human pathogenic fungus Cryptococcus neoformans.
-
Multiple origins of hybrid strains of Cryptococcus neoformans with serotype AD.
-
Multiple paternity and sporophytic inbreeding depression in a dioicous moss species.
-
Multiple paths to similar germination behavior in Arabidopsis thaliana.
-
Multiple regions within 8q24 independently affect risk for prostate cancer.
-
Murine noroviruses comprising a single genogroup exhibit biological diversity despite limited sequence divergence.
-
Muscle trade-offs in a power-amplified prey capture system.
-
Mutation and evolution of microsatellites in Drosophila melanogaster.
-
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
-
Mutational analysis of the coding regions of the genes encoding protein kinase B-alpha and -beta, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients.
-
Mutational origin of new mating type specificities in flowering plants.
-
Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review.
-
Mutations that confer resistance to broadly-neutralizing antibodies define HIV-1 variants of transmitting mothers from that of non-transmitting mothers.
-
Myocilin and optineurin coding variants in Hispanics of Mexican descent with POAG.
-
Nager acrofacial dysostosis.
-
Natural allelic variation of the IL-21 receptor modulates ischemic stroke infarct volume.
-
Natural positive selection and north-south genetic diversity in East Asia.
-
Natural selection on a leaf-shape polymorphism in the ivyleaf morning glory (Ipomoea hederacea).
-
Natural selection on extrafloral nectar production in Chamaecrista fasciculata: the costs and benefits of a mutualism trait.
-
Natural variation in CDC28 underlies morphological phenotypes in an environmental yeast isolate.
-
Natural variation in HIV-1 protease, Gag p7 and p6, and protease cleavage sites within gag/pol polyproteins: amino acid substitutions in the absence of protease inhibitors in mothers and children infected by human immunodeficiency virus type 1.
-
Natural variation in MAM within and between populations of Arabidopsis lyrata determines glucosinolate phenotype.
-
Natural variation in germination responses of Arabidopsis to seasonal cues and their associated physiological mechanisms.
-
Natural variation, differentiation, and genetic trade-offs of ecophysiological traits in response to water limitation in Brachypodium distachyon and its descendent allotetraploid B. hybridum (Poaceae).
-
Near-Absent Levels Of Segregational Variation Suggest Limited Opportunities For The introduction of genetic variation via homeologous chromosome pairing In synthetic neoallotetraploid Mimulus.
-
Nearshore fish (Pholis gunnellus) persists across the North Atlantic through multiple glacial episodes.
-
Neutral evolution of the nonbinding region of the anthocyanin regulatory gene Ipmyb1 in Ipomoea.
-
Neutralizing antibodies in sera from macaques infected with chimeric simian-human immunodeficiency virus containing the envelope glycoproteins of either a laboratory-adapted variant or a primary isolate of human immunodeficiency virus type 1.
-
New nitrogen-fixing microorganisms detected in oligotrophic oceans by amplification of Nitrogenase (nifH) genes.
-
Niche partitioning and biogeography of high light adapted Prochlorococcus across taxonomic ranks in the North Pacific.
-
No Evidence That Genetic Variation in the Myeloid-Derived Suppressor Cell Pathway Influences Ovarian Cancer Survival.
-
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
-
No evidence of association of heterozygous NTF4 mutations in patients with primary open-angle glaucoma.
-
Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese population.
-
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.
-
Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.
-
Nuclear ribosomal DNA sequence variation and evolution of spotted marsh-orchids (Dactylorhiza maculata group)
-
Nucleotide variation at the myrosinase-encoding locus, TGG1, and quantitative myrosinase enzyme activity variation in Arabidopsis thaliana.
-
OPRM1 SNP (A118G): involvement in disease development, treatment response, and animal models.
-
Oceanic islands are not sinks of biodiversity in spore-producing plants.
-
Of cardiovascular illness and diversity of biological response.
-
Olfactory Receptor Subgenomes Linked with Broad Ecological Adaptations in Sauropsida.
-
On the evolution of genetic incompatibility systems. III. Introduction of weak gametophytic self-incompatibility under partial inbreeding.
-
One haploid parent contributes 100% of the gene pool for a widespread species in northwest North America.
-
Origin and evolution of HIV-1 in breast milk determined by single-genome amplification and sequencing.
-
Origin, fate, and architecture of ecologically relevant genetic variation.
-
Orion: Detecting regions of the human non-coding genome that are intolerant to variation using population genetics.
-
Outbreak of Invasive Wound Mucormycosis in a Burn Unit Due to Multiple Strains of Mucor circinelloides f. circinelloides Resolved by Whole-Genome Sequencing.
-
Oxidative stress survival in a clinical Saccharomyces cerevisiae isolate is influenced by a major quantitative trait nucleotide.
-
PCSK9 Loss-of-Function Variants, Low-Density Lipoprotein Cholesterol, and Risk of Coronary Heart Disease and Stroke: Data From 9 Studies of Blacks and Whites.
-
Parallel evolution of drug resistance in HIV: failure of nonsynonymous/synonymous substitution rate ratio to detect selection.
-
Paraoxonase 1 (PON1) gene variants are not associated with clopidogrel response.
-
Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
-
Patterns and mechanisms of genetic and phenotypic differentiation in marine microbes.
-
Patterns of evolutionary rate variation among genes of the anthocyanin biosynthetic pathway.
-
Patterns of mandibular variation in Pan and Gorilla and implications for African ape taxonomy.
-
Patterns of nucleotide diversity in two species of Mimulus are affected by mating system and asymmetric introgression.
-
Patterns of nucleotide variation and reproductive isolation between a Mimulus allotetraploid and its progenitor species.
-
Patterns of transcriptional parallelism and variation in the developing olfactory system of Drosophila species.
-
Patterns of variation within self-incompatibility loci.
-
Persistence of multiple maternal genotypes of human immunodeficiency virus type I in infants infected by vertical transmission.
-
Persistent tetrodotoxin-sensitive sodium current resulting from U-to-C RNA editing of an insect sodium channel.
-
Personalized medicine and human genetic diversity.
-
Pharmacogenetic testing: not as simple as it seems.
-
Pharmacogenetics: Ethical Issues and Policy Options
-
Pharmacogenomics and end-organ susceptibility to injury in the perioperative period.
-
Pharmacogenomics in cancer therapy: is host genome variability important?
-
Pharmacogenomics of adverse drug reactions: implementing personalized medicine.
-
PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.
-
Phenome-Wide Association Study of Severe COVID-19 Genetic Risk Variants.
-
Phenotype analysis of patients with the risk variant LOC387715 (A69S) in age-related macular degeneration.
-
Phenotypic Variability Correlates with Clinical Outcome in Cryptococcus Isolates Obtained from Botswanan HIV/AIDS Patients.
-
Phylogenetic diversity of 200+ isolates of the ectomycorrhizal fungus Cenococcum geophilum associated with Populus trichocarpa soils in the Pacific Northwest, USA and comparison to globally distributed representatives.
-
Phylogenetic relationships in the mushroom genus Coprinus and dark-spored allies based on sequence data from the nuclear gene coding for the large ribosomal subunit RNA: divergent domains, outgroups, and monophyly.
-
Phylogenetic relationships of agaric fungi based on nuclear large subunit ribosomal DNA sequences.
-
Phylogenetic relationships, morphological incongruence, and geographic speciation in the fontinalaceae (Bryophyta).
-
Phylogenomic inferences from reference-mapped and de novo assembled short-read sequence data using RADseq sequencing of California white oaks (Quercus section Quercus).
-
Phylogeny and biogeography of the American live oaks (Quercus subsection Virentes): a genomic and population genetics approach.
-
Phylogeographic structure and cryptic speciation in the trans-Antarctic moss Pyrrhobryum mnioides.
-
Phylogeography of a Morphologically Cryptic Golden Mole Assemblage from South-Eastern Africa.
-
Phylogeography of the Solanaceae-infecting Basidiomycota fungus Rhizoctonia solani AG-3 based on sequence analysis of two nuclear DNA loci.
-
Phylogeography of the arid-adapted Malagasy bullfrog, Laliostoma labrosum, influenced by past connectivity and habitat stability.
-
Phytochrome diversity in green plants and the origin of canonical plant phytochromes
-
Pioneering paradigms and magnificent manifestos--Leigh Van Valen's priceless contributions to evolutionary biology.
-
Plasmodium falciparum Genetic Diversity in Coincident Human and Mosquito Hosts.
-
Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.
-
Pleiotropy in developmental regulation by flowering-pathway genes: is it an evolutionary constraint?
-
Pneumococcal Colonization and the Nasopharyngeal Microbiota of Children in Botswana.
-
Pollen limitation and natural selection on floral characters in the yellow monkeyflower, Mimulus guttatus.
-
Pollinator-mediated selection on flower color allele drives reinforcement.
-
Polygenic risk, rapid childhood growth, and the development of obesity: evidence from a 4-decade longitudinal study.
-
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
-
Polymerase chain reaction fingerprinting in fungi using single primers specific to minisatellites and simple repetitive DNA sequences: strain variation in Cryptococcus neoformans.
-
Polymorphic TP53BP1 and TP53 gene interactions associated with risk of squamous cell carcinoma of the head and neck.
-
Polymorphism at the ribosomal DNA spacers and its relation to breeding structure of the widespread mushroom Schizophyllum commune.
-
Polymorphism of angiotensin converting enzyme gene is associated with circulating levels of plasminogen activator inhibitor-1.
-
Polymorphisms in transforming growth factor-beta-related genes ALK1 and ENG are associated with sporadic brain arteriovenous malformations.
-
Polymorphisms of DNA repair gene XRCC3 Thr241Met and risk of gastric cancer in a Chinese population.
-
Polymorphisms of p21 and p27 jointly contribute to an earlier age at diagnosis of pancreatic cancer.
-
Polymorphisms of the FAS and FAS ligand genes associated with risk of cutaneous malignant melanoma.
-
Polymorphisms of thymidylate synthase in the 5'- and 3'-untranslated regions associated with risk of gastric cancer in South China: a case-control analysis.
-
Polyvalent vaccines for optimal coverage of potential T-cell epitopes in global HIV-1 variants.
-
Population differentiation and plasticity in vegetative ontogeny: effects on life-history expression in Erysimum capitatum (Brassicaceae).
-
Population genetic analyses reveal the African origin and strain variation of Cryptococcus neoformans var. grubii.
-
Population genetic structure of Arabidopsis lyrata in Europe.
-
Population genetics of a trochid gastropod broadens picture of Caribbean Sea connectivity.
-
Population genetics of tandem trypsin inhibitor genes in Arabidopsis species with contrasting ecology and life history.
-
Population genomics in South East Asia captures unexpectedly high carrier frequency for treatable inherited disorders.
-
Population history in Arabidopsis halleri using multilocus analysis.
-
Population perspectives on functional genomic variation in yeast.
-
Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer.
-
Positive selection driving diversification in plant secondary metabolism.
-
Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
-
Potentially functional single nucleotide polymorphisms in the core nucleotide excision repair genes and risk of squamous cell carcinoma of the head and neck.
-
Potentially functional variants of ERAP1, PSMF1 and NCF2 in the MHC-I-related pathway predict non-small cell lung cancer survival.
-
Predictable patterns of constraint among anthocyanin-regulating transcription factors in Ipomoea.
-
Predictors of consent to pharmacogenomics testing in the IDEAL study.
-
Predictors of variation in serum IGF1 and IGFBP3 levels in healthy African American and white men.
-
Presence of diverse human immunodeficiency virus type 1 viral variants in Cameroon.
-
Prevalence of chemokine and chemokine receptor polymorphisms in seroprevalent children with symptomatic HIV-1 infection in the United States.
-
Prevalence of clinical isolates of Cryptococcus gattii serotype C among patients with AIDS in Sub-Saharan Africa.
-
Prevalence of hepatitis B antiviral drug resistance variants in North American patients with chronic hepatitis B not receiving antiviral treatment.
-
Programmed evolution for optimization of orthogonal metabolic output in bacteria.
-
Prospective dosing of warfarin based on cytochrome P-450 2C9 genotype.
-
Prostate cancer in men of African origin.
-
Prostatic alpha-linolenic acid (ALA) is positively associated with aggressive prostate cancer: a relationship which may depend on genetic variation in ALA metabolism.
-
Protective effect of CRHR1 gene variants on the development of adult depression following childhood maltreatment: replication and extension.
-
Protein Quantitative Trait Loci Analysis Identifies Genetic Variation in the Innate Immune Regulator TOLLIP in Post-Lung Transplant Primary Graft Dysfunction Risk.
-
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
-
Puzzling role of genetic risk factors in human longevity: "risk alleles" as pro-longevity variants.
-
QTL mapping in a mouse model of cardiomyopathy reveals an ancestral modifier allele affecting heart function and survival.
-
Quality control in the flow cytometric measurement of T-lymphocyte subsets: the multicenter AIDS cohort study experience. The Multicenter AIDS Cohort Study Group.
-
Quantifying effects of environmental and geographical factors on patterns of genetic differentiation.
-
Quantitating the multiplicity of infection with human immunodeficiency virus type 1 subtype C reveals a non-poisson distribution of transmitted variants.
-
Quantitation of hepatitis B viremia and emergence of YMDD variants in patients with chronic hepatitis B treated with lamivudine.
-
Quantitative genetic variation in CD19 expression correlates with autoimmunity.
-
RNA Splicing of the BHC80 Gene Contributes to Neuroendocrine Prostate Cancer Progression.
-
RNA sequencing of isolated cell populations expressing human APOL1 G2 risk variant reveals molecular correlates of sickle cell nephropathy in zebrafish podocytes.
-
RNase 1 genes from the family Sciuridae define a novel rodent ribonuclease cluster.
-
Race, common genetic variation, and therapeutic response disparities in heart failure.
-
Rapid changes in the gut microbiome during human evolution.
-
Rare Things Being Common: Implications for Common Genetic Variants in Rare Diseases Like Long-QT Syndrome.
-
Rare and low-frequency coding variants alter human adult height
-
Rare coding variants and X-linked loci associated with age at menarche.
-
Rare functional genetic variants in COL7A1, COL6A5, COL1A2 and COL5A2 frequently occur in Chiari Malformation Type 1.
-
Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
-
Rare-variant collapsing analyses for complex traits: guidelines and applications.
-
Reactivity of avian RNA tumor viruses with lectins.
-
Real-Time Genomic Profiling of Pancreatic Ductal Adenocarcinoma: Potential Actionability and Correlation with Clinical Phenotype.
-
Reaper-induced dissociation of a Scythe-sequestered cytochrome c-releasing activity.
-
Receptor Switching in Newly Evolved Adeno-associated Viruses.
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Recognition of HLA-A2 mutant and variant target cells by an HLA-A2 allospecific human cytotoxic T lymphocyte line.
-
Recombination modulates how selection affects linked sites in Drosophila.
-
Recombining without Hotspots: A Comprehensive Evolutionary Portrait of Recombination in Two Closely Related Species of Drosophila.
-
Reconciling extreme branch length differences: decoupling time and rate through the evolutionary history of filmy ferns
-
Recurrent polyploid origins and chloroplast phylogeography in the Arabis holboellii complex (Brassicaceae).
-
Reduced expression of brain-enriched microRNAs in glioblastomas permits targeted regulation of a cell death gene.
-
Reduced selective constraint in endosymbionts: elevation in radical amino acid replacements occurs genome-wide.
-
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.
-
Refugial isolation and range expansions drive the genetic structure of Oxyria sinensis (Polygonaceae) in the Himalaya-Hengduan Mountains.
-
Relationship between CYP2A6 and CHRNA5-CHRNA3-CHRNB4 variation and smoking behaviors and lung cancer risk.
-
Relationship of disease-associated gene expression to cardiac phenotype is buffered by genetic diversity and chromatin regulation.
-
Relationship of genetic variability and depressive symptoms to adverse events after coronary artery bypass graft surgery.
-
Relaxed selection among duplicate floral regulatory genes in Lamiales.
-
Remaining flexible in old alliances: functional plasticity in constrained mutualisms.
-
Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection.
-
Repeated phenotypic changes highlight molecular targets of convergent evolution.
-
Repeated range expansion and glacial endurance of Potentilla glabra (Rosaceae) in the Qinghai-Tibetan plateau.
-
Replicated Landscape Genomics Identifies Evidence of Local Adaptation to Urbanization in Wood Frogs.
-
Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon.
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Review of evidence for genetic testing for CYP450 polymorphisms in management of patients with nonpsychotic depression with selective serotonin reuptake inhibitors.
-
Risk Analysis of Prostate Cancer in PRACTICAL, a Multinational Consortium, Using 25 Known Prostate Cancer Susceptibility Loci.
-
S-allele diversity in a natural population of Physalis crassifolia (Solanaceae) (ground cherry) assessed by RT-PCR.
-
SIV infection duration largely determines broadening of neutralizing antibody response in macaques.
-
SLC6A4 variation and citalopram response.
-
SMRTER, a Drosophila nuclear receptor coregulator, reveals that EcR-mediated repression is critical for development.
-
SNiPA: an interactive, genetic variant-centered annotation browser.
-
Saccharomyces cerevisiae: population divergence and resistance to oxidative stress in clinical, domesticated and wild isolates.
-
Searching for causal relationships of glioma: a phenome-wide Mendelian randomisation study.
-
Secrets of the perioptome: new tools for a new concept.
-
Seed after-ripening and dormancy determine adult life history independently of germination timing.
-
Selection for character displacement is constrained by the genetic architecture of floral traits in the ivyleaf morning glory.
-
Selection of HIV Envelope Strains for Standardized Assessments of Vaccine-Elicited Antibody-Dependent Cellular Cytotoxicity-Mediating Antibodies.
-
Selective sweeps and intercontinental migration in the cosmopolitan moss Ceratodon purpureus (Hedw.) Brid.
-
Semi-automated assembly of high-quality diploid human reference genomes.
-
Sequence context of indel mutations and their effect on protein evolution in a bacterial endosymbiont.
-
Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
-
Sequence divergence of coiled coils--structural rods, myosin filament packing, and the extraordinary conservation of cohesins.
-
Sequence requirements for ligand binding and cell surface expression of the Tac antigen, a human interleukin-2 receptor.
-
Sequence signatures of a recent chromosomal rearrangement in Drosophila mojavensis.
-
Sequence variants in the transforming growth beta-induced factor (TGIF) gene are not associated with high myopia.
-
Sequence variation in the mitochondrial gene cytochrome c oxidase subunit I and prostate cancer in African American men.
-
Sequence variations at I260 and A1731 contribute to persistent currents in Drosophila sodium channels.
-
Sequence variations in DNA repair gene XPC is associated with lung cancer risk in a Chinese population: a case-control study.
-
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
-
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity.
-
Sequencing studies in human genetics: design and interpretation.
-
Serotonin transporter gene moderates the development of emotional problems among children following bullying victimization.
-
Serotonin transporter genetic variation and the response of the human amygdala.
-
Serotonin.
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Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5q.
-
Sex-biased admixture and assortative mating shape genetic variation and influence demographic inference in admixed Cabo Verdeans.
-
Sex-dependent effect of APOE on Alzheimer's disease and other age-related neurodegenerative disorders.
-
SgD-CNV, a database for common and rare copy number variants in three Asian populations.
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Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians.
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Shift in S-layer protein expression responsible for antigenic variation in Campylobacter fetus.
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Signature Patterns of MHC Diversity in Three Gombe Communities of Wild Chimpanzees Reflect Fitness in Reproduction and Immune Defense against SIVcpz.
-
Signatures of demography and recombination at coding genes in naturally-distributed populations of Arabidopsis lyrata subsp. petraea.
-
Simian immunodeficiency virus (SIV) envelope quasispecies transmission and evolution in infant rhesus macaques after oral challenge with uncloned SIVmac251: increased diversity is associated with neutralizing antibodies and improved survival in previously immunized animals.
-
Simple models of genomic variation in human SNP density.
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Single origin and subsequent diversification of central Andean endemic Umbilicaria species.
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Single-cell RNA-seq highlights intratumoral heterogeneity in primary glioblastoma.
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Smooth nonparametric maximum likelihood estimation for population pharmacokinetics, with application to quinidine.
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Snapshot of the allele-specific variation in human gene expression.
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Social behavior shapes the chimpanzee pan-microbiome
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Sources of variability in John Henryism.
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Spatial Genetic Structure of the Abundant and Widespread Peatmoss Sphagnum magellanicum Brid.
-
Spatial models for hybrid zones.
-
Spatially and temporally varying selection on intrapopulation quantitative trait loci for a life history trade-off in Mimulus guttatus.
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Speciation on a local geographic scale: the evolution of a rare rock outcrop specialist in Mimulus.
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Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate-binding region.
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Sphagnum physiology in the context of changing climate: emergent influences of genomics, modelling and host-microbiome interactions on understanding ecosystem function.
-
Spontaneous deletions and duplications of sequences in the genome of cowpox virus.
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Sporadic, Global Linkage Disequilibrium Between Unlinked Segregating Sites.
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Statistical analysis of antigen receptor spectratype data.
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Statistical genetics of an annual plant, Impatiens capensis. I. Genetic basis of quantitative variation.
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Stereoselective Ketamine Metabolism by Genetic Variants of Cytochrome P450 CYP2B6 and Cytochrome P450 Oxidoreductase.
-
Streamlined Subpopulation, Subtype, and Recombination Analysis of HIV-1 Half-Genome Sequences Generated by High-Throughput Sequencing.
-
Stress: a possible link between genetics, epigenetics, and childhood asthma.
-
Structural analysis of an HLA-B7 antigen variant detected by cytotoxic T lymphocytes.
-
Structural variants can be more informative for disease diagnostics, prognostics and translation than current SNP mapping and exon sequencing.
-
Structure and immune recognition of trimeric pre-fusion HIV-1 Env.
-
Structure of the human allelic glutathione S-transferase-pi gene variant, hGSTP1 C, cloned from a glioblastoma multiforme cell line.
-
Studying genetic resilience to improve human health.
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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
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Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8.
-
Survey of variation in human transcription factors reveals prevalent DNA binding changes.
-
Survival prediction in patients with glioblastoma multiforme by human telomerase genetic variation.
-
Systematic detection of positive selection in the human-pathogen interactome and lasting effects on infectious disease susceptibility.
-
Systems Biology of Phenotypic Robustness and Plasticity.
-
Systems biology of robustness and homeostatic mechanisms.
-
T-Cell receptor Vbeta repertoire CDR3 length diversity differs within CD45RA and CD45RO T-cell subsets in healthy and human immunodeficiency virus-infected children.
-
T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection.
-
TERC is not a major gene in human neural tube defects.
-
TGFβ1 Genetic Variants Predict Clinical Outcomes of HPV-Positive Oropharyngeal Cancer Patients after Definitive Radiotherapy.
-
TOMM40'523 variant and cognitive decline in older persons with APOE ε3/3 genotype.
-
TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study.
-
Taking cardiovascular genetic association studies to the next level.
-
Tamoxifen pharmacogenomics: the role of CYP2D6 as a predictor of drug response.
-
Tandemly arranged variant 5S ribosomal RNA genes in the yeast Saccharomyces cerevisiae.
-
Targeted sequencing in chromosome 17q linkage region identifies familial glioma candidates in the Gliogene Consortium.
-
Telomere structure and maintenance gene variants and risk of five cancer types.
-
Temporal Stability of Molecular Diversity Measures in Natural Populations of Drosophila pseudoobscura and Drosophila persimilis.
-
Testing Rare-Variant Association without Calling Genotypes Allows for Systematic Differences in Sequencing between Cases and Controls.
-
Testing morphological concepts of orders of pleurocarpous mosses (Bryophyta) using phylogenetic reconstructions based on TRNL-TRNF and RPS4 sequences.
-
The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory.
-
The DNA sequence and biological annotation of human chromosome 1.
-
The Effect of Propofol Versus Isoflurane Anesthesia on Human Cerebrospinal Fluid Markers of Alzheimer's Disease: Results of a Randomized Trial.
-
The Influenza B Virus Hemagglutinin Head Domain Is Less Tolerant to Transposon Mutagenesis than That of the Influenza A Virus.
-
The International HapMap Project.
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The Intolerance of Regulatory Sequence to Genetic Variation Predicts Gene Dosage Sensitivity.
-
The North Carolina Experience with Mucopolysaccharidosis Type I Newborn Screening.
-
The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers.
-
The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal Variants.
-
The Snail's Charm.
-
The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
-
The Time Scale of Recombination Rate Evolution in Great Apes.
-
The beta3 subunit of the Na+,K+-ATPase mediates variable nociceptive sensitivity in the formalin test.
-
The case for strategic international alliances to harness nutritional genomics for public and personal health.
-
The clinical significance of tenascin-C splice variant expression in chondrosarcoma.
-
The cloning of a receptor-type protein tyrosine phosphatase expressed in the central nervous system.
-
The contribution of admixture to primate evolution.
-
The contribution of common CYP2A6 alleles to variation in nicotine metabolism among European-Americans.
-
The effect of SNCA 3' region on the levels of SNCA-112 splicing variant.
-
The effects of quantitative fecundity in the haploid stage on reproductive success and diploid fitness in the aquatic peat moss Sphagnum macrophyllum.
-
The evolution of transcriptional regulation in eukaryotes.
-
The evolutionary forest algorithm.
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The extent of amino-terminal heterogeneity in rabbit fast skeletal muscle troponin T.
-
The functional consequences of genetic variation on tyrosine hydroxylase (TH) expression
-
The genetic architecture of biofilm formation in a clinical isolate of Saccharomyces cerevisiae.
-
The genetic architecture of the human cerebral cortex.
-
The genetic architecture of type 2 diabetes.
-
The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease.
-
The genetic structure and diversity of the A and B mating-type genes from the tropical oyster mushroom, Pleurotus djamor.
-
The genomics of speciation in Drosophila: diversity, divergence, and introgression estimated using low-coverage genome sequencing.
-
The geography of malaria genetics in the Democratic Republic of Congo: A complex and fragmented landscape.
-
The impact of caspase-12 on susceptibility to candidemia.
-
The importance of dynamic re-analysis in diagnostic whole exome sequencing.
-
The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes.
-
The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes.
-
The meaning of genetic research results: reflections from individuals with and without a known genetic disorder.
-
The missense of smell: functional variability in the human odorant receptor repertoire.
-
The molecular basis of quantitative genetic variation in central and secondary metabolism in Arabidopsis.
-
The neurobiology of individual differences in complex behavioral traits.
-
The origin and evolution of animal appendages.
-
The origin of helping: the role of variability in reproductive potential.
-
The origins and genomic diversity of American Civil War Era smallpox vaccine strains.
-
The phylogeography and incidence of multi-drug resistant typhoid fever in sub-Saharan Africa.
-
The quick and the dead: microbial demography at the yeast thermal limit.
-
The rise of genomic profiling in ovarian cancer.
-
The role of CD4-Lck in T-cell receptor antagonism: evidence for negative signaling.
-
The roles of positive and negative selection in the molecular evolution of insect endosymbionts.
-
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
-
The spatial scale of genetic subdivision in populations of Ifremeria nautilei, a hydrothermal-vent gastropod from the southwest Pacific.
-
The tRNA-Tyr gene family of Saccharomyces cerevisiae: agents of phenotypic variation and position effects on mutation frequency.
-
The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group.
-
The transcriptional landscape of Shh medulloblastoma.
-
Theoretical and practical advances in genome halving.
-
Three crocodilian genomes reveal ancestral patterns of evolution among archosaurs.
-
Tissue-specific expression from CaMV 35S enhancer subdomains in early stages of plant development.
-
Toward a Wolbachia multilocus sequence typing system: discrimination of Wolbachia strains present in Drosophila species.
-
Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus.
-
Tracking HIV-1 recombination to resolve its contribution to HIV-1 evolution in natural infection.
-
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
-
Transcriptional diversity during lineage commitment of human blood progenitors.
-
Transcriptome analysis reveals novel patterning and pigmentation genes underlying Heliconius butterfly wing pattern variation.
-
Transforming single DNA molecules into fluorescent magnetic particles for detection and enumeration of genetic variations.
-
Transient compartmentalization of simian immunodeficiency virus variants in the breast milk of african green monkeys.
-
Transmission of Multiple HIV-1 Subtype C Transmitted/founder Viruses into the Same Recipients Was not Determined by Modest Phenotypic Differences.
-
Tuberculosis Susceptibility and Vaccine Protection Are Independently Controlled by Host Genotype.
-
Type 2 diabetes: evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs.
-
U1 small nuclear RNA variants differentially form ribonucleoprotein particles in vitro.
-
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study.
-
Understanding human variation in infectious disease susceptibility through clinical and cellular GWAS.
-
Unique expression of a sporophytic character on the gametophytes of notholaenid ferns (Pteridaceae).
-
Unisexual and heterosexual meiotic reproduction generate aneuploidy and phenotypic diversity de novo in the yeast Cryptococcus neoformans.
-
Use of Pharmacogenetic Information in the Treatment of Cardiovascular Disease.
-
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
-
Uterine Fibroids: Burden and Unmet Medical Need.
-
Vaccine development for HIV infection.
-
Vaccine-induced neutralizing antibodies directed in part to the simian immunodeficiency virus (SIV) V2 domain were unable to protect rhesus monkeys from SIV experimental challenge.
-
Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).
-
Variable apoptotic response of NSCLC cells to inhibition of the MEK/ERK pathway by small molecules or dominant negative mutants.
-
Variable phenotypic expression of mutations in genes of the immune system.
-
Variant genotypes of CDKN1A and CDKN1B are associated with an increased risk of breast cancer in Chinese women.
-
Variant of Bartter's syndrome with a distal tubular rather than loop of Henle defect.
-
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level.
-
Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans.
-
Variation and fitness costs for tolerance to different types of herbivore damage in Boechera stricta genotypes with contrasting glucosinolate structures.
-
Variation and selection in neural function.
-
Variation at 8q24 and 9p24 and risk of epithelial ovarian cancer.
-
Variation in Recombination Rate: Adaptive or Not?
-
Variation in olfactory neuron repertoires is genetically controlled and environmentally modulated.
-
Variation in the fitness effects of mutations with population density and size in Escherichia coli.
-
Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening.
-
Variations in Prkdc and susceptibility to benzene-induced toxicity in mice.
-
Variations of cardiovascular disease associated genes exhibit sex-dependent influence on human longevity.
-
VarioWatch: providing large-scale and comprehensive annotations on human genomic variants in the next generation sequencing era.
-
Virulence attributes and hyphal growth of C. neoformans are quantitative traits and the MATalpha allele enhances filamentation.
-
Virulence genes of poxviruses and reoviruses.
-
What can patterns of differentiation across plant genomes tell us about adaptation and speciation?
-
When two is better than one.
-
Which evolutionary processes influence natural genetic variation for phenotypic traits?
-
Whole-genome analysis informs breast cancer response to aromatase inhibition.
-
Wide variation in the multiplicity of HIV-1 infection among injection drug users.
-
Within- and between- subject variability of indices from the closing volume and flow volume traces.
-
Yeast diversity sampling on the San Juan Islands reveals no evidence for the spread of the Vancouver Island Cryptococcus gattii outbreak to this locale.
-
[Analysis of genetic heterogeneity of bronchial asthma in relation with the age at the onset of disease]
-
[Genetic structure of geographically different populations of candida albicans].
-
alpha AD alpha hybrids of Cryptococcus neoformans: evidence of same-sex mating in nature and hybrid fitness.
-
alpha-Synuclein gene haplotypes are associated with Parkinson's disease.
-
apex: phylogenetics with multiple genes.
-
gsSKAT: Rapid gene set analysis and multiple testing correction for rare-variant association studies using weighted linear kernels.
-
optix Drives the Repeated Convergent Evolution of Butterfly Wing Pattern Mimicry
-
rbcL and matK earn two thumbs up as the core DNA barcode for ferns
-
rqt: an R package for gene-level meta-analysis.
-
α satellite DNA variation and function of the human centromere.
-
Keywords of People
-
Abbruzzese, James,
D. C. I. Distinguished Professor of Medical Oncology,
Medicine, Medical Oncology
-
Alberts, Susan C.,
Robert F. Durden Distinguished Professor of Biology,
Duke Science & Society
-
Bennett, Vann,
George Barth Geller Distinguished Professor of Molecular Biology,
Duke Cancer Institute
-
Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
-
Erickson, Harold Paul,
Professor Emeritus of Cell Biology,
Cell Biology
-
Grambow, Steven C.,
Associate Professor of Biostatistics & Bioinformatics,
Biostatistics & Bioinformatics
-
Hartemink, Alexander J.,
Professor in the Department of Computer Science,
Biology
-
Kelsoe, Garnett H.,
James B. Duke Distinguished Professor of Immunology,
Immunology
-
Krangel, Michael S.,
George Barth Geller Distinguished Professor of Immunology,
Immunology
-
Liu, Yutao,
Adjunct Assistant Professor in the Department of Medicine,
Medicine, Medical Genetics
-
Luftig, Micah Alan,
Associate Professor of Molecular Genetics and Microbiology,
Cell Biology
-
Magwene, Paul Mitaari,
Professor of Biology,
Biology
-
Mitchell-Olds, Thomas,
Newman Ivey White Distinguished Professor of Biology,
Biology
-
Moorman, Patricia Gripka,
Professor Emeritus in Family Medicine and Community Health,
Duke Cancer Institute
-
Noor, Mohamed A. F.,
Professor of Biology,
Duke Science & Society
-
O'Connor, Christopher Michael,
Richard Sean Stack, M.D. Distinguished Professor,
Medicine, Clinical Pharmacology
-
Orlando, Lori Ann,
Professor of Medicine,
Medicine, General Internal Medicine
-
Reddy, Timothy E,
Associate Professor of Biostatistics & Bioinformatics,,
Molecular Genetics and Microbiology
-
Schultz, Thomas F.,
Assistant Professor of the Practice of Marine Molecular Conservation,
Marine Science and Conservation
-
Shinohara, Mari L.,
Associate Professor of Immunology,
Cell Biology
-
Soderling, Scott Haydn,
George Barth Geller Distinguished Professor of Molecular Biology,
Cell Biology
-
Tung, Jenny,
Associate Professor of Evolutionary Anthropology,
Duke Science & Society
-
Wernegreen, Jennifer Jo,
Lee Hill Snowdon Associate Professor,
Environmental Sciences and Policy
-
Wray, Gregory Allan,
Professor of Biology,
Evolutionary Anthropology
-
Yan, Hai,
Adjunct Professor of Pathology,
Pathology
-
Yoder, Anne Daphne,
Braxton Craven Distinguished Professor of Evolutionary Biology,
Duke Science & Society