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Subject Areas on Research
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1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.
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A Common Polymorphism in SCN2A Predicts General Cognitive Ability through Effects on PFC Physiology.
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A Pragmatic, Randomized Controlled Trial of Oral Antivirals for the Treatment of Chronic Hepatitis C: The PRIORITIZE Study.
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A Review and Update on Papillary Immature Metaplasia of the Uterine Cervix: A Distinct Subset of Low-Grade Squamous Intraepithelial Lesion, Proposing a Possible Cell of Origin.
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A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes.
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Aldose Reductase Polymorphisms, Fasting Blood Glucose, and Age-Related Cortical Cataract.
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An effective tool for identifying HIV-1 subtypes B, C, CRF01_AE, their recombinant forms, and dual infections in Southeast Asia by the multi-region subtype specific PCR (MSSP) assay.
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Association of CYP2C19 polymorphisms and lansoprazole-associated respiratory adverse effects in children.
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Blood glucose levels and cortical thinning in cognitively normal, middle-aged adults.
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Cell-free DNA diagnostics in transplantation utilizing next generation sequencing.
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Clinical pharmacogenetics implementation consortium guideline (CPIC) for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants: 2016 update.
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Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.
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Combinations of DIPs and Dprs control organization of olfactory receptor neuron terminals in Drosophila.
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Combined genotype and haplotype tests for region-based association studies.
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Common Genetic Variation and Susceptibility to Ovarian Cancer: Current Insights and Future Directions.
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Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse.
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Content and Performance of the MiniMUGA Genotyping Array: A New Tool To Improve Rigor and Reproducibility in Mouse Research.
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Cost-effectiveness analysis of genotyping for HLA-B*5801 and an enhanced safety program in gout patients starting allopurinol in Singapore.
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Detailed genetic characteristics of an international large cohort of patients with Stargardt disease: ProgStar study report 8.
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Efficient Genome-Wide Sequencing and Low-Coverage Pedigree Analysis from Noninvasively Collected Samples.
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Endogenous Tagging at the cdh1 Locus for Live Visualization of E-Cadherin Dynamics.
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Ethnic variation in early age-related macular degeneration lesions between white Australians and Singaporean Asians.
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Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.
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Factors influencing uptake of pharmacogenetic testing in a diverse patient population.
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Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus.
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Gene variants in angiogenesis and lymphangiogenesis and cutaneous melanoma progression.
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Genetic Dissection of Heritable Traits in Yeast Using Bulk Segregant Analysis.
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Genetic architecture of gene expression traits across diverse populations.
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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis.
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Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.
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Genome Sequencing of Arabidopsis abp1-5 Reveals Second-Site Mutations That May Affect Phenotypes.
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Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.
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Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.
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Global and regional molecular epidemiology of HIV-1, 1990-2015: a systematic review, global survey, and trend analysis.
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High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.
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Human disturbance causes the formation of a hybrid swarm between two naturally sympatric fish species.
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Interlaboratory study to validate a STR profiling method for intraspecies identification of mouse cell lines.
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Leveraging Phylogenetics to Understand HIV Transmission and Partner Notification Networks.
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Matrix metalloproteinase-9 genetic polymorphisms and the risk for advanced pelvic organ prolapse.
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Measures of linkage disequilibrium among neighbouring SNPs indicate asymmetries across the house mouse hybrid zone.
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Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations.
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MicroRNA-196A-2 polymorphisms and hepatocellular carcinoma in patients with chronic hepatitis B.
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Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.
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Molecular Detection and Typing of Pathogenic Leptospira in Febrile Patients and Phylogenetic Comparison with Leptospira Detected among Animals in Tanzania.
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Multiplexed shotgun genotyping resolves species relationships within the North American genus Penstemon.
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Next-generation genotyping of hypervariable loci in many individuals of a non-model species: technical and theoretical implications.
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Overlap Extension Barcoding for the Next Generation Sequencing and Genotyping of Plasmodium falciparum in Individual Patients in Western Kenya.
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Prolonged tenofovir treatment of macaques infected with K65R reverse transcriptase mutants of SIV results in the development of antiviral immune responses that control virus replication after drug withdrawal.
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Quantitative Trait Locus Analysis of SIX1-SIX6 With Retinal Nerve Fiber Layer Thickness in Individuals of European Descent.
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RNA-Seq optimization with eQTL gold standards.
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Rapid Molecular Diagnostics, Antibiotic Treatment Decisions, and Developing Approaches to Inform Empiric Therapy: PRIMERS I and II.
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SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma.
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Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma.
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Simultaneous Detection of Major Drug Resistance Mutations of HIV-1 Subtype B Viruses from Dried Blood Spot Specimens by Multiplex Allele-Specific Assay.
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Single-Nucleotide Polymorphisms Associated With Age-Related Macular Degeneration and Lesion Phenotypes in the Comparison of Age-Related Macular Degeneration Treatments Trials.
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Specific combinations of donor and recipient KIR-HLA genotypes predict for large differences in outcome after cord blood transplantation.
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Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.
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TOMM40'523 variant and cognitive decline in older persons with APOE ε3/3 genotype.
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The genetic architecture of type 2 diabetes.
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The significance of single nucleotide polymorphism rs2070770 in CD20 gene in Chinese patients with diffuse large B-cell lymphoma.
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Unisexual reproduction drives meiotic recombination and phenotypic and karyotypic plasticity in Cryptococcus neoformans.
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Using ERDS to infer copy-number variants in high-coverage genomes.
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Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.
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Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study.
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Keywords of People