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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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(Session Introduction) Joint Learning from Multiple Types of Genomic Data
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A Bayesian hierarchical model to estimate DNA methylation conservation in colorectal tumors.
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A GWAS Study on Liver Function Test Using eMERGE Network Participants.
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A Genocentric Approach to Discovery of Mendelian Disorders.
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A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans.
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A Global Collaborative to Advance Genomic Medicine.
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A Guide for a Cardiovascular Genomics Biorepository: the CATHGEN Experience.
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A Multidimensional Bioinformatic Platform for the Study of Human Response to Surgery.
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A Roadmap for the Human Oral and Craniofacial Cell Atlas.
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A central support system can facilitate implementation and sustainability of a Classroom-based Undergraduate Research Experience (CURE) in Genomics.
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A chromosome-level reference genome and pangenome for barn swallow population genomics.
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A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease.
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A compendium of promoter-centered long-range chromatin interactions in the human genome.
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A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative.
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A computational framework to assess genome-wide distribution of polymorphic human endogenous retrovirus-K In human populations.
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A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network.
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A content analysis of the views of genetics professionals on race, ancestry, and genetics.
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A course-based research experience: how benefits change with increased investment in instructional time.
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A draft genome sequence of the elusive giant squid, Architeuthis dux.
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A functional genomics predictive network model identifies regulators of inflammatory bowel disease.
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A general integrative genomic feature transcription factor binding site prediction method applied to analysis of USF1 binding in cardiovascular disease.
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A genomic approach to colon cancer risk stratification yields biologic insights into therapeutic opportunities.
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A genomic approach to identify molecular pathways associated with chemotherapy resistance.
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A genomic approach to identify regulatory nodes in the transcriptional network of systemic acquired resistance in plants.
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A genomic approach to improve prognosis and predict therapeutic response in chronic lymphocytic leukemia.
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A genomic strategy to elucidate modules of oncogenic pathway signaling networks.
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A genomic- and proteomic-based hypothesis on the eclectic effects of systemic interleukin-2 administration in the context of melanoma-specific immunization.
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A genomic-augmented multivariate prognostic model for the survival of natural-killer/T-cell lymphoma patients from an international cohort.
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A global approach to tumor immunology.
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A global reference for human genetic variation.
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A haplotype-resolved genome assembly of the Nile rat facilitates exploration of the genetic basis of diabetes.
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A high-density screen for linkage in multiple sclerosis.
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A high-quality genome and comparison of short- versus long-read transcriptome of the palaearctic duck Aythya fuligula (tufted duck).
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A high-quality, long-read genome assembly of the endangered ring-tailed lemur (Lemur catta).
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A high-resolution map of human evolutionary constraint using 29 mammals.
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A hybrid bayesian approach for genome-wide association studies on related individuals.
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A joint analysis of metabolomics and genetics of breast cancer.
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A knowledge network for a dynamic taxonomy of psychiatric disease.
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A machine learning approach to radiogenomics of breast cancer: a study of 922 subjects and 529 DCE-MRI features.
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A national clinical decision support infrastructure to enable the widespread and consistent practice of genomic and personalized medicine.
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A network-heuristic approach to improve the impact of genomic data on drug discovery.
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A new analysis tool for individual-level allele frequency for genomic studies.
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A novel integrative risk index of papillary thyroid cancer progression combining genomic alterations and clinical factors.
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A pathway-based classification of human breast cancer.
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A personalized paradigm in the treatment of platinum-resistant ovarian cancer - A cost utility analysis of genomic-based versus cytotoxic therapy.
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A proposed approach to accelerate evidence generation for genomic-based technologies in the context of a learning health system.
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A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources.
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A sampling of methods to study chromosome and genome structure and function.
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A study of the repetitive structure and distribution of short motifs in human genomic sequences.
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A(r)Ray of hope in analysis of the function and diversity of microbial communities.
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AKT1 and neurocognition in schizophrenia.
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Abundant raw material for cis-regulatory evolution in humans.
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Active learning for computational chemogenomics.
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Activity-Dependent Transcription Collaborates with Local Dendritic Translation to Encode Stimulus-Specificity in the Genome Binding of NPAS4.
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Acute myeloid leukemia arising from polycythemia vera underwent reversion to chronic phase of myeloproliferative neoplasm status post chemotherapy: Biclonal myeloid neoplasms with genomic evidence of a common early hematopoietic progenitor.
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Adaptive evolution drives the diversification of zinc-finger binding domains.
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Adaptive sequence divergence forged new neurodevelopmental enhancers in humans.
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Addressing underrepresentation in genomics research through community engagement.
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Advances in understanding the evolution of fungal genome architecture.
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Advancing toxicology research using in vivo high throughput toxicology with small fish models.
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Affiliate network members as force amplifiers of genomic medicine research.
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American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
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An Exploration of Fern Genome Space
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An Integrated TCGA Pan-Cancer Clinical Data Resource to Drive High-Quality Survival Outcome Analytics.
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An algorithm for the reconstruction of consensus sequences of ancient segmental duplications and transposon copies in eukaryotic genomes.
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An encyclopedia of mouse DNA elements (Mouse ENCODE).
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An evaluation of copy number variation detection tools from whole-exome sequencing data.
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An integrated encyclopedia of DNA elements in the human genome.
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An integrated genomic-based approach to individualized treatment of patients with advanced-stage ovarian cancer.
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An integrated map of genetic variation from 1,092 human genomes.
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An overview of genomic data analysis.
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An overview of lung cancer genomics and proteomics.
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An unbiased in vivo functional genomics screening approach in mice identifies novel tumor cell-based regulators of immune rejection.
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Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis.
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Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
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Ancestry adjustment improves genome-wide estimates of regional intolerance.
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Ancient bacterial endosymbionts of insects: Genomes as sources of insight and springboards for inquiry.
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Application of an optimized annotation pipeline to the Cryptococcus deuterogattii genome reveals dynamic primary metabolic gene clusters and genomic impact of RNAi loss.
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Aquatic models, genomics and chemical risk management.
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Arabidopsis functional genomics.
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Architecture of the human regulatory network derived from ENCODE data.
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Assessing bioequivalence using genomic data.
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Assessing the utility of thermodynamic features for microRNA target prediction under relaxed seed and no conservation requirements.
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Assessing the utility of whole genome amplified DNA for next-generation molecular ecology.
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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 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 tumor genomic factors and efficacy for metastasis-directed stereotactic body radiotherapy for oligometastatic colorectal cancer.
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Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis.
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Author's Reply.
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Automated Nuclear Segmentation in Head and Neck Squamous Cell Carcinoma Pathology Reveals Relationships between Cytometric Features and ESTIMATE Stromal and Immune Scores.
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Automated next-generation profiling of genomic alterations in human cancers.
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Avian genomes. A flock of genomes. Introduction.
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Avianbase: a community resource for bird genomics.
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Baby Genomics: Tracing the Evolutionary Changes That Gave Rise to Placentation.
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Basic concepts and potential applications of genetics and genomics for cardiovascular and stroke clinicians: a scientific statement from the American Heart Association.
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Bayesian consensus clustering.
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Bayesian estimation of genomic distance.
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Bayesian joint analysis of heterogeneous genomics data.
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Bayesian quantitative electrophysiology and its multiple applications in bioengineering.
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Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium.
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Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.
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Bimodal age distribution at diagnosis in breast cancer persists across molecular and genomic classifications.
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Biomarkers for amyotrophic lateral sclerosis.
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Biomarkers for equine joint injury and osteoarthritis.
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Boechera, a model system for ecological genomics.
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Bone-associated gene evolution and the origin of flight in birds.
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Breast Cancer Radiogenomics: Current Status and Future Directions.
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Breast MRI radiogenomics: Current status and research implications.
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Broadening primate genomics: new insights into the ecology and evolution of primate gene regulation.
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Building evidence and measuring clinical outcomes for genomic medicine.
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Building the evidence base for decision making in cancer genomic medicine using comparative effectiveness research.
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Burkitt lymphoma: analysis of the genome.
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CANEapp: a user-friendly application for automated next generation transcriptomic data analysis.
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COUGER--co-factors associated with uniquely-bound genomic regions.
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CRISPR-based methods for high-throughput annotation of regulatory DNA.
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Cancer 2015: a longitudinal whole-of-system study of genomic cancer medicine.
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Cancer Informatics: New Tools for a Data-Driven Age in Cancer Research.
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Cancer genomics: integrating form and function.
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Cancer systems biology: exploring cancer-associated genes on cellular networks.
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Cardiac function and heart failure.
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Cardiovascular Disease: Impact of Biomarkers, Proteomics, and Genomics.
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Cascaded Multi-view Canonical Correlation (CaMCCo) for Early Diagnosis of Alzheimer's Disease via Fusion of Clinical, Imaging and Omic Features.
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Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.
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Cell cycle-regulated transcription: effectively using a genomics toolbox.
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Centromere scission drives chromosome shuffling and reproductive isolation.
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ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia.
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Challenges and Controversies in Hypertrophic Cardiomyopathy: Clinical, Genomic and Basic Science Perspectives.
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Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network.
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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 metastatic urothelial carcinoma via comprehensive genomic profiling of circulating tumor DNA.
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Chromosomal-Level Genome Assembly of the Sea Urchin Lytechinus variegatus Substantially Improves Functional Genomic Analyses.
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Chromosome-Level Reference Genomes for Two Strains of Caenorhabditis briggsae: An Improved Platform for Comparative Genomics.
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Circulating Tumor Cell Genomic Evolution and Hormone Therapy Outcomes in Men with Metastatic Castration-Resistant Prostate Cancer.
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Clinical Applications of the Genomic Landscape of Aggressive Non-Hodgkin Lymphoma.
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Clinical and genomic characterization of Low PSA Secretors: a unique subset of metastatic castration resistant prostate cancer.
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Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples.
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Clinical decisions surrounding genomic and proteomic testing among United States veterans treated for lung cancer within the Veterans Health Administration.
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Clinical genomic testing: getting it right.
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Clinical genomics in the world of the electronic health record.
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Clinical implications of genomic alterations in the tumour and circulation of pancreatic cancer patients.
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Clinical pharmacogenomic testing and reporting: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
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Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science.
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Clinicopathologic Features and Genomic Signature of De Novo CD5 + Diffuse Large B-Cell Lymphoma : A Multicenter Collaborative Study.
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Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.
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Communicating genetic and genomic information: health literacy and numeracy considerations.
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Comparative Analyses of Chromatin Landscape in White Adipose Tissue Suggest Humans May Have Less Beigeing Potential than Other Primates.
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Comparative Genomic Analysis of the Pheromone Receptor Class 1 Family (V1R) Reveals Extreme Complexity in Mouse Lemurs (Genus, Microcebus) and a Chromosomal Hotspot across Mammals.
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Comparative and population mitogenomic analyses of Madagascar's extinct, giant 'subfossil' lemurs.
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Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects.
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Comparative effectiveness research, genomics-enabled personalized medicine, and rapid learning health care: a common bond.
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Comparative genome-wide screening identifies a conserved doxorubicin repair network that is diploid specific in Saccharomyces cerevisiae.
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Comparative genomic analyses of multi-drug resistant Mycobacterium tuberculosis from Nepal and other geographical locations.
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Comparative genomic analysis of fungal genomes reveals intron-rich ancestors.
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Comparative genomics and regulatory evolution: conservation and function of the Chs and Apetala3 promoters.
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Comparative genomics applied to Mucor species with different lifestyles.
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Comparative genomics as a tool for gene discovery.
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Comparative genomics in the Brassicaceae: a family-wide perspective.
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Comparative genomics of mammalian hibernators using gene networks.
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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 dynamic genome evolution in host specialist ectomycorrhizal fungi.
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Comparative genomics reveals insights into avian genome evolution and adaptation.
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Comparative genomics reveals molecular features unique to the songbird lineage.
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Comparative genomics search for losses of long-established genes on the human lineage.
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Comparing methods for detecting multilocus adaptation with multivariate genotype-environment associations.
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Comparison of genomics and functional imaging from canine sarcomas treated with thermoradiotherapy predicts therapeutic response and identifies combination therapeutics.
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Complete genomic and epigenetic maps of human centromeres.
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Complete vertebrate mitogenomes reveal widespread repeats and gene duplications.
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Comprehensive Multi-omics Analysis Reveals Mitochondrial Stress as a Central Biological Hub for Spaceflight Impact.
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Comprehensive genomic characterization defines human glioblastoma genes and core pathways.
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Comprehensive genomic meta-analysis identifies intra-tumoural stroma as a predictor of survival in patients with gastric cancer.
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Comprehensive genomic profiling in advanced/metastatic colorectal cancer: number needed to test and budget impact of expanded first line use.
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Comprehensive genomic profiling of pancreatic acinar cell carcinomas identifies recurrent RAF fusions and frequent inactivation of DNA repair genes.
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Comprehensive genomic studies: emerging regulatory, strategic, and quality assurance challenges for biorepositories.
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Comprehensive molecular portraits of human breast tumours.
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Computational approach to radiogenomics of breast cancer: Luminal A and luminal B molecular subtypes are associated with imaging features on routine breast MRI extracted using computer vision algorithms.
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Computational approaches for inferring 3D conformations of chromatin from chromosome conformation capture data.
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Concordance Between Genomic Alterations Detected by Tumor and Germline Sequencing: Results from a Tertiary Care Academic Center Molecular Tumor Board.
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Consensus Statement on Circulating Biomarkers for Advanced Prostate Cancer.
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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 genomic collinearity as a source of broadly applicable, fast evolving, markers to resolve species complexes: A case study using the lichen-forming genus Peltigera section Polydactylon.
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Considering the Benefits and Risks of Research Participants' Access to Sequence Data.
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Contrasts between adaptive coding and noncoding changes during human evolution.
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Contributions from medical geneticists in clinical trials of genetic therapies: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
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Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.
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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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Cortical volume abnormalities in posttraumatic stress disorder: an ENIGMA-psychiatric genomics consortium PTSD workgroup mega-analysis.
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Cost-Effectiveness of Tumor Genomic Profiling to Guide First-Line Targeted Therapy Selection in Patients With Metastatic Lung Adenocarcinoma.
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Cross species genomic analysis identifies a mouse model as undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma.
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Cross-study projections of genomic biomarkers: an evaluation in cancer genomics.
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Cross-validation for linear model with unequal variances in genomic analysis.
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Cryptococcus neoformans Recovered From Olive Trees (Olea europaea) in Turkey Reveal Allopatry With African and South American Lineages.
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DNA patents and diagnostics: not a pretty picture.
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DNase-seq predicts regions of rotational nucleosome stability across diverse human cell types.
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DOK2 inhibits EGFR-mutated lung adenocarcinoma.
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Darwinian genomics and diversity in the tree of life.
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Data Harmonization for a Molecularly Driven Health System.
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Deciding among green plants for whole genome studies.
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Defending information-free genocentrism.
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Depside and Depsidone Synthesis in Lichenized Fungi Comes into Focus through a Genome-Wide Comparison of the Olivetoric Acid and Physodic Acid Chemotypes of Pseudevernia furfuracea.
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Design and implementation of high-throughput RNAi screens in cultured Drosophila cells.
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Design, Assembly, and Characterization of TALE-Based Transcriptional Activators and Repressors.
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Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
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Developing a common framework for evaluating the implementation of genomic medicine interventions in clinical care: the IGNITE Network's Common Measures Working Group.
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Development and application of a phylogenomic toolkit: resolving the evolutionary history of Madagascar's lemurs.
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Development of Competency-based Online Genomic Medicine Training (COGENT).
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Developmental single-cell transcriptomics in the Lytechinus variegatus sea urchin embryo.
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Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
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Diagnostic testing for uniparental disomy: a points to consider statement from the American College of Medical Genetics and Genomics (ACMG).
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DictyBase 2013: integrating multiple Dictyostelid species.
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Differential alternative RNA splicing and transcription events between tumors from African American and White patients in The Cancer Genome Atlas.
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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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Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome.
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Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise.
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Donor genomics influence graft events: the effect of donor polymorphisms on acute rejection and chronic allograft nephropathy.
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Drosophila genome-wide RNAi screens: are they delivering the promise?
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Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolution.
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Dynamic evolution of base composition: causes and consequences in avian phylogenomics.
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Ecological genomics of Boechera stricta: identification of a QTL controlling the allocation of methionine- vs branched-chain amino acid-derived glucosinolates and levels of insect herbivory.
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Educating future providers of personalized medicine.
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Educating healthcare providers in the delivery of genomic medicine.
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Embracing the complexity of genomic data for personalized medicine.
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Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example.
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Enabling functional genomics with genome engineering.
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Enhancing our brains: Genomic mechanisms underlying cortical evolution.
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Ensuring the safe use of genomic medicine in children.
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Environmental genomics: a key to understanding biology, pathophysiology and disease.
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Epigenetic Heterogeneity in Human Colorectal Tumors Reveals Preferential Conservation And Evidence of Immune Surveillance.
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Epigenome-wide association of PTSD from heterogeneous cohorts with a common multi-site analysis pipeline.
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Equity in Genomics: A Brief Report on Cardiovascular Health Disparities in African American Adults.
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Establishing the value of genomics in medicine: the IGNITE Pragmatic Trials Network.
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Estimating genomic coexpression networks using first-order conditional independence.
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Evaluating Chromatin Accessibility Differences Across Multiple Primate Species Using a Joint Modeling Approach.
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Evaluation of 122 advanced-stage cutaneous squamous cell carcinomas by comprehensive genomic profiling opens the door for new routes to targeted therapies.
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Evaluation of right and left ventricular diastolic filling.
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Evidence for a single loss of mineralized teeth in the common avian ancestor.
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Evidence for sexuality in the opportunistic fungal pathogen Aspergillus fumigatus.
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Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium.
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Evolution of genes and genomes on the Drosophila phylogeny.
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Evolutionary and biomedical insights from a marmoset diploid genome assembly.
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Evolutionary and ecological functional genomics.
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Evolutionary and phylogenetic insights from a nuclear genome sequence of the extinct, giant, "subfossil" koala lemur Megaladapis edwardsi.
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Evolutionary genomics and adaptive evolution of the Hedgehog gene family (Shh, Ihh and Dhh) in vertebrates.
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Evolving Roles of Histologic Evaluation and Molecular/Genomic Profiling in the Management of Endometrial Cancer.
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Exercise biology and medicine: innovative research to improve global health.
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Expanded Genomic Profiling of Circulating Tumor Cells in Metastatic Breast Cancer Patients to Assess Biomarker Status and Biology Over Time (CALGB 40502 and CALGB 40503, Alliance).
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Expanding studies of chromosome structure and function in the era of T2T genomics.
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Exploring syntenic conservation across genomes for phylogenetic studies of organisms subjected to horizontal gene transfers: A case study with Cyanobacteria and cyanolichens.
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Family history assessment significantly enhances delivery of precision medicine in the genomics era.
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Father Knows Best? Small RNA Pathway Controls Endosperm Response to Paternal Genomic Dosage.
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Feather development genes and associated regulatory innovation predate the origin of Dinosauria.
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Finding our way through phenotypes.
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First Responder to Genomic Information: A Guide for Primary Care Providers.
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For better or worse: genomic consequences of intracellular mutualism and parasitism.
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Four genomic clades of Candida auris identified in Canada, 2012-2019.
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From breast to the brain: unraveling the puzzle of metastasis organotropism.
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From diagnostic testing to precision medicine: the evolving role of genomics in cardiac channelopathies and cardiomyopathies in children.
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From genotype to phenotype: systems biology meets natural variation.
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Functional Genomic Analyses of Mendelian and Sporadic Disease Identify Impaired eIF2α Signaling as a Generalizable Mechanism for Dystonia.
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Functional analysis of novel SNPs and mutations in human and mouse genomes.
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Functional genomic analysis of phagocytosis and identification of a Drosophila receptor for E. coli.
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Functional genomics approach for the identification of human host factors supporting dengue viral propagation.
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Functional genomics identifies specific vulnerabilities in PTEN-deficient breast cancer.
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Functional genomics identifies type I interferon pathway as central for host defense against Candida albicans.
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Functional genomics of root growth and development in Arabidopsis.
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Functional genomics of the beta-cell: short-chain 3-hydroxyacyl-coenzyme A dehydrogenase regulates insulin secretion independent of K+ currents.
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Functional interaction between responses to lactic acidosis and hypoxia regulates genomic transcriptional outputs.
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Functional nanostructures from surface chemistry patterning.
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Fungal diagnostics in pneumonia.
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Fungal pathogenesis: gene clusters unveiled as secrets within the Ustilago maydis code.
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Future translational applications from the contemporary genomics era: a scientific statement from the American Heart Association.
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GOBASE--a database of organelle and bacterial genome information.
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GREAT improves functional interpretation of cis-regulatory regions.
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GenBlastA: enabling BLAST to identify homologous gene sequences.
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Gene expression and adaptive noncoding changes during human evolution.
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Gene loss, adaptive evolution and the co-evolution of plumage coloration genes with opsins in birds.
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Generating RNA Baits for Capture-Based Enrichment.
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Generation of full-length cDNA libraries enriched for differentially expressed genes for functional genomics.
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Genetic and Genomic Analyses Reveal Boundaries between Species Closely Related to Cryptococcus Pathogens.
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Genetic and genomic evolution of sexual reproduction: echoes from LECA to the fungal kingdom.
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Genetic and pharmacological relationship between P-glycoprotein and increased cardiovascular risk associated with clarithromycin prescription: An epidemiological and genomic population-based cohort study in Scotland, UK.
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Genetic architecture of gene expression traits across diverse populations.
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Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults.
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Genetic dissection of the mouse CNS using magnetic resonance microscopy.
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Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.
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Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota.
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Genetic markers: progress and potential for cardiovascular disease.
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Genetic simulation tools for post-genome wide association studies of complex diseases.
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Genome engineering: the next genomic revolution.
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Genome evolution in bacterial endosymbionts of insects.
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Genome-wide association studies in Africans and African Americans: expanding the framework of the genomics of human traits and disease.
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Genome-wide high-resolution mapping of chromosome fragile sites in Saccharomyces cerevisiae.
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Genome-wide identification and predictive modeling of tissue-specific alternative polyadenylation.
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Genome-wide mapping of DNase hypersensitive sites using massively parallel signature sequencing (MPSS).
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Genome-wide meta-analyses identifies novel taxane-induced peripheral neuropathy-associated loci.
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Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.
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Genomic Amplifications and Distal 6q Loss: Novel Markers for Poor Survival in High-risk Neuroblastoma Patients.
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Genomic Analysis of a Hospital-Associated Outbreak of Mycobacterium abscessus: Implications on Transmission.
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Genomic Approaches to Posttraumatic Stress Disorder: The Psychiatric Genomic Consortium Initiative.
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Genomic Characterization of the Evolutionary Potential of the Sea Urchin Strongylocentrotus droebachiensis Facing Ocean Acidification.
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Genomic Classification and Clinical Outcome in Rhabdomyosarcoma: A Report From an International Consortium.
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Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer.
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Genomic Landscape of Cell-Free DNA in Patients with Colorectal Cancer.
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Genomic Medicine: 'grand challenges' in the translation of genomics to human health.
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Genomic Scores are Independent of Disease Volume in Men with Favorable Risk Prostate Cancer: Implications for Choosing Men for Active Surveillance.
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Genomic Sequencing Should Not be Part of the Standard of Care for Most Urologic Cancers.
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Genomic Variation across a Clinical Cryptococcus Population Linked to Disease Outcome.
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Genomic Views of Transcriptional Enhancers: Essential Determinants of Cellular Identity and Activity-Dependent Responses in the CNS.
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Genomic analyses: a neonatology perspective.
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Genomic analysis defines clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancer.
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Genomic analysis demonstrates that histologically-defined astroblastomas are molecularly heterogeneous and that tumors with MN1 rearrangement exhibit the most favorable prognosis.
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Genomic analysis of "microphenotypes" in epilepsy.
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Genomic analysis of early-stage lung cancer reveals a role for TP53 mutations in distant metastasis.
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Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas.
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Genomic ancestry and somatic alterations correlate with age at diagnosis in Hispanic children with B-cell acute lymphoblastic leukemia.
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Genomic and Epigenomic Profiling of High-Risk Intestinal Metaplasia Reveals Molecular Determinants of Progression to Gastric Cancer.
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Genomic and Functional Approaches to Understanding Cancer Aneuploidy.
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Genomic and molecular profiling predicts response to temozolomide in melanoma.
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Genomic and outcome analysis of adult T-cell lymphoblastic lymphoma.
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Genomic approaches for understanding the genetics of complex disease.
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Genomic characterization of chronic lymphocytic leukemia (CLL) in radiation-exposed Chornobyl cleanup workers.
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Genomic complexity identifies patients with aggressive chronic lymphocytic leukemia.
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Genomic complexity is associated with epigenetic regulator mutations and poor prognosis in diffuse large B-cell lymphoma.
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Genomic determination of breeding systems and trans-specific evolution of HD MAT genes in suilloid fungi.
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Genomic dissection of conserved transcriptional regulation in intestinal epithelial cells.
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Genomic divergence and brain evolution: How regulatory DNA influences development of the cerebral cortex.
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Genomic erosion and extensive horizontal gene transfer in gut-associated Acetobacteraceae.
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Genomic insights into inter- and intraspecific mating system shifts in Primulina.
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Genomic landscape of the global oak phylogeny.
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Genomic map of candidate human imprint control regions: the imprintome.
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Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection.
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Genomic medicine: a decade of successes, challenges, and opportunities.
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Genomic medicine: bringing biomarkers to clinical medicine.
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Genomic medicine: genetic variation and its impact on the future of health care.
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Genomic profiling to promote a healthy lifestyle: not ready for prime time.
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Genomic resources for the endangered Hawaiian honeycreepers.
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Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
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Genomic sequencing is required for identification of tuberculosis transmission in Hawaii.
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Genomic signatures of diet-related shifts during human origins.
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Genomic stratification for the treatment of lymphomas.
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Genomic translational research: Paving the way to individualized cardiac functional analyses and personalized cardiology.
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Genomic, Pathway Network, and Immunologic Features Distinguishing Squamous Carcinomas.
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Genomics and clinical medicine: rationale for creating and effectively evaluating animal models.
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Genomics and expression profiles of the Hedgehog and Notch signaling pathways in sea urchin development.
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Genomics and the circulation.
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Genomics identifies medulloblastoma subgroups that are enriched for specific genetic alterations.
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Genomics in medicine: a novel elective rotation for internal medicine residents.
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Genomics of Cardiovascular Measures of Autonomic Tone.
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Genomics of human health and aging.
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Genomics of varicose veins and chronic venous insufficiency.
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Genomics reveals the role of admixture in the evolution of structure among sperm whale populations within the Mediterranean Sea.
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Genomics, clinical research, and learning health care systems: Strategies to improve patient care.
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Genomics-Inspired Biomarkers and Diagnostics-Where Are They?
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Genomics-based identification of a potential causal role for acylcarnitine metabolism in depression.
-
Genomics-enabled drug repositioning and repurposing: insights from an IOM Roundtable activity.
-
Genomics. Genomics, biobanks, and the trade-secret model.
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Genomics: Lessons in complexity from yeast.
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Germline genetic landscape of pediatric central nervous system tumors.
-
Getting to the root of plant biology: impact of the Arabidopsis genome sequence on root research.
-
Glioma through the looking GLASS: molecular evolution of diffuse gliomas and the Glioma Longitudinal Analysis Consortium.
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Global approaches to genomic medicine implementation.
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Global transcriptome profile of Cryptococcus neoformans during exposure to hydrogen peroxide induced oxidative stress.
-
Globally Relaxed Selection and Local Adaptation in Boechera stricta.
-
Going the distance: Neocentromeres make long-range contacts with heterochromatin.
-
Guidelines for Genome-Scale Analysis of Biological Rhythms.
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Hierarchical Convolutional Neural Networks for Segmentation of Breast Tumors in MRI With Application to Radiogenomics.
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High-frequency actionable pathogenic exome variants in an average-risk cohort.
-
High-resolution genome-wide in vivo footprinting of diverse transcription factors in human cells.
-
High-throughput interpretation of gene structure changes in human and nonhuman resequencing data, using ACE.
-
Histone lysine methyltransferase SDG8 is involved in brassinosteroid-regulated gene expression in Arabidopsis thaliana.
-
Histoplasmosis acquired in Alberta, Canada: an epidemiological and genomic study.
-
How nontraditional model systems can save us.
-
IMAGE: high-powered detection of genetic effects on DNA methylation using integrated methylation QTL mapping and allele-specific analysis.
-
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.
-
Identification and characterization of a new cross-reactive human immunodeficiency virus type 1-neutralizing human monoclonal antibody.
-
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis.
-
Identification of cis-suppression of human disease mutations by comparative genomics.
-
Identification of functional elements and regulatory circuits by Drosophila modENCODE.
-
Identifying branch-specific positive selection throughout the regulatory genome using an appropriate proxy neutral.
-
Identifying genomic and developmental causes of adverse drug reactions in children.
-
Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks.
-
IgA and IgG antineutrophil cytoplasmic antibody engagement of Fc receptor genetic variants influences granulomatosis with polyangiitis.
-
Imaging Genetics and Genomics in Psychiatry: A Critical Review of Progress and Potential.
-
Imaging genetics of brain longevity and mental wellness: the next frontier?
-
Imaging genomics.
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Impact of Genomic and Clinical Factors on Outcome of Children ≥18 Months of Age with Stage 3 Neuroblastoma with Unfavorable Histology and without MYCN Amplification: A Children's Oncology Group (COG) Report.
-
Impact of Therapy on Genomics and Transcriptomics in High-Risk Prostate Cancer Treated with Neoadjuvant Docetaxel and Androgen Deprivation Therapy.
-
Impact of a Genomic Test on Treatment Decision in a Predominantly African American Population With Favorable-Risk Prostate Cancer: A Randomized Trial.
-
Impact of delivery models on understanding genomic risk for type 2 diabetes.
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Impact of the Percepta Genomic Classifier on Clinical Management Decisions in a Multicenter Prospective Study.
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Implementing genomic medicine in the clinic: the future is here.
-
Implications of the first complete human genome assembly.
-
Improving the measurement of semantic similarity between gene ontology terms and gene products: insights from an edge- and IC-based hybrid method.
-
Independent ancient polyploidy events in the sister families Brassicaceae and Cleomaceae.
-
Induction of an immortalized songbird cell line allows for gene characterization and knockout by CRISPR-Cas9.
-
Information-seeking and sharing behavior following genomic testing for diabetes risk.
-
Initial sequencing and comparative analysis of the mouse genome.
-
Initiation of the Primate Genome Project.
-
Insights from a chimpanzee adipose stromal cell population: opportunities for adult stem cells to expand primate functional genomics.
-
Insights into the evolution of social systems and species from baboon studies.
-
Integrated Analysis of RNA and DNA from the Phase III Trial CALGB 40601 Identifies Predictors of Response to Trastuzumab-Based Neoadjuvant Chemotherapy in HER2-Positive Breast Cancer.
-
Integrated Genomic Analysis of the Ubiquitin Pathway across Cancer Types.
-
Integrated functional networks of process, tissue, and developmental stage specific interactions in Arabidopsis thaliana.
-
Integrated genomic analyses of ovarian carcinoma.
-
Integrated genomic analysis of survival outliers in glioblastoma.
-
Integrated genomic characterization of endometrial carcinoma.
-
Integrated genomic characterization of oesophageal carcinoma.
-
Integrated metabolomics and genomics: systems approaches to biomarkers and mechanisms of cardiovascular disease.
-
Integrated modeling of clinical and gene expression information for personalized prediction of disease outcomes.
-
Integrating ethics and science in the International HapMap Project.
-
Integrating genetic and gene expression evidence into genome-wide association analysis of gene sets.
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Integration of functional assay data results provides strong evidence for classification of hundreds of BRCA1 variants of uncertain significance.
-
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
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Integrative Omics: Harnessing the Proteome to Maximize the Potential of the Genome.
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Integrative annotation of variants from 1092 humans: application to cancer genomics.
-
Integrative biomechanics: A paradigm for clinical applications of fundamental mechanics
-
Integrative genomic approaches identify IKBKE as a breast cancer oncogene.
-
Integrative genomic approaches to understanding cancer.
-
Integrative genomics identifies RAB23 as an invasion mediator gene in diffuse-type gastric cancer.
-
Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease.
-
Integrative metabolomics-genomics approach reveals key metabolic pathways and regulators of Alzheimer's disease.
-
Integrative systems biology: an attempt to describe a simple weed.
-
Interdisciplinary Models for Research and Clinical Endeavors in Genomic Medicine: A Scientific Statement From the American Heart Association.
-
Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG).
-
Interpreting the genomic landscape of speciation: a road map for finding barriers to gene flow.
-
Knowledge about genomic recurrence risk testing among breast cancer survivors.
-
Label propagation defines signaling networks associated with recurrently mutated cancer genes.
-
Laboratory analysis of acylcarnitines, 2020 update: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
-
Laboratory analysis of amino acids, 2018 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
-
Laboratory diagnosis of creatine deficiency syndromes: a technical standard and guideline of the American College of Medical Genetics and Genomics.
-
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.
-
Letter to the editor: Standardization of genetic association studies, pros and cons, reaffirmed.
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Letting the genome out of the bottle.
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Leveraging Genome and Phenome-Wide Association Studies to Investigate Genetic Risk of Acute Lymphoblastic Leukemia.
-
Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium.
-
Linking Genes to Cardiovascular Diseases: Gene Action and Gene-Environment Interactions.
-
Linking Genes to Molecules in Eukaryotic Sources: An Endeavor to Expand Our Biosynthetic Repertoire.
-
Liver genomic responses to ciguatoxin: evidence for activation of phase I and phase II detoxification pathways following an acute hypothermic response in mice.
-
Localizing Post-Admixture Adaptive Variants with Object Detection on Ancestry-Painted Chromosomes.
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Making Personalized Health Care Even More Personalized: Insights From Activities of the IOM Genomics Roundtable.
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Managing incidental genomic findings: legal obligations of clinicians.
-
Manifestations of Alzheimer's disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90.
-
Mapping genomic loci implicates genes and synaptic biology in schizophrenia.
-
Mapping nucleosome positions using DNase-seq.
-
Mapping the proteo-genomic convergence of human diseases.
-
Medical genomics: Gather and use genetic data in health care.
-
Medulloblastoma Down Under 2013: a report from the third annual meeting of the International Medulloblastoma Working Group.
-
Merfin: improved variant filtering, assembly evaluation and polishing via k-mer validation.
-
Merging Electronic Health Record Data and Genomics for Cardiovascular Research: A Science Advisory From the American Heart Association.
-
Mesenchymal stem cells use integrin beta1 not CXC chemokine receptor 4 for myocardial migration and engraftment.
-
Metabolomics applied to diabetes research: moving from information to knowledge.
-
Methionine metabolism influences genomic architecture and gene expression through H3K4me3 peak width.
-
Mining the Gene Wiki for functional genomic knowledge.
-
Molecular Biology and Evolution of Cancer: From Discovery to Action.
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Molecular Imaging and Precision Medicine in Head and Neck Cancer.
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Molecular Tools for Carotenogenesis Analysis in the Mucoral Mucor circinelloides.
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Molecular and genetic markers in thoracic surgery.
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Molecular biomarkers in glaucoma.
-
Molecular medicine tumor board: whole-genome sequencing to inform on personalized medicine for a man with advanced prostate cancer.
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Molecular pathology of prostate cancer revealed by next-generation sequencing: opportunities for genome-based personalized therapy.
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Morning glory as a powerful model in ecological genomics: tracing adaptation through both natural and artificial selection.
-
Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies.
-
Multi-marker strategies in heart failure: clinical and statistical approaches.
-
Multi-omics integration in biomedical research - A metabolomics-centric review.
-
Multicenter study of acetaminophen hepatotoxicity reveals the importance of biological endpoints in genomic analyses.
-
Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function.
-
Multilocus patterns of nucleotide diversity, population structure and linkage disequilibrium in Boechera stricta, a wild relative of Arabidopsis.
-
Multiple regions within 8q24 independently affect risk for prostate cancer.
-
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility.
-
Multiregional Radiogenomic Assessment of Prostate Microenvironments with Multiparametric MR Imaging and DNA Whole-Exome Sequencing of Prostate Glands with Adenocarcinoma.
-
NEIBank: genomics and bioinformatics resources for vision research.
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Neptune: an environment for the delivery of genomic medicine.
-
Network-assisted genetic dissection of pathogenicity and drug resistance in the opportunistic human pathogenic fungus Cryptococcus neoformans.
-
New insights into gestational glucose metabolism: lessons learned from 21st century approaches.
-
New paradigms in cardiovascular medicine: emerging technologies and practices: perioperative genomics.
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Next-Generation Sequencing Concordance Analysis of Comprehensive Solid Tumor Profiling between a Centralized Specialty Laboratory and the Decentralized Personal Genome Diagnostics elio Tissue Complete Kitted Solution.
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Next-generation sequencing for constitutional variants in the clinical laboratory, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
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Non-canonical genomic driver mutations of urethane carcinogenesis.
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Obesity Genomics and Metabolomics: a Nexus of Cardiometabolic Risk.
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Omics approaches to discover pathophysiological pathways contributing to human pain.
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Omics meet networks - using systems approaches to infer regulatory networks in plants.
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Only connect: personal genomics and the future of American medicine.
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Open Chromatin Profiling in Adipose Tissue Marks Genomic Regions with Functional Roles in Cardiometabolic Traits.
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Open window: when easily identifiable genomes and traits are in the public domain.
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Operationalizing Precision Cardiovascular Medicine: Three Innovations.
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Opportunities to implement a sustainable genomic medicine program: lessons learned from the IGNITE Network.
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Opportunities, resources, and techniques for implementing genomics in clinical care.
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Opportunities-and hard work-ahead.
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Organellar phylogenomics of an emerging model system: Sphagnum (peatmoss).
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Organizational improvements to enhance modern clinical epidemiology.
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Origins of MERS-CoV, and lessons for 2019-nCoV.
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OrthoClusterDB: an online platform for synteny blocks.
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Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience.
-
PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice.
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PROMISE: a real-world clinical-genomic database to address knowledge gaps in prostate cancer.
-
Palo: spatially aware color palette optimization for single-cell and spatial data.
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Pan-cancer Alterations of the MYC Oncogene and Its Proximal Network across the Cancer Genome Atlas.
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Pan-cancer analysis of whole genomes.
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Parallel Multi-Omics in High-Risk Subjects for the Identification of Integrated Biomarker Signatures of Type 1 Diabetes.
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Parallel assay of oxygen equilibria of hemoglobin.
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Partial shotgun sequencing of the Boechera stricta genome reveals extensive microsynteny and promoter conservation with Arabidopsis.
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Participant choices for return of genomic results in the eMERGE Network.
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Pathogenesis of varicose veins.
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Pathophysiology of the blood-brain barrier: animal models and methods.
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Patterns of somatic mutation in human cancer genomes.
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Performance assessment of promoter predictions on ENCODE regions in the EGASP experiment.
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Performance of repeat cytology with reflex ThyroSeq genomic classifier for indeterminant thyroid cytology.
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Personalized Prediction Model to Risk Stratify Patients With Myelodysplastic Syndromes.
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Personalized health care in 2013: a status report on the impact of genomics.
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Personalized health care: from theory to practice.
-
Personalized targeted therapy for esophageal squamous cell carcinoma.
-
Perspective on Oncogenic Processes at the End of the Beginning of Cancer Genomics.
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Perspective: Prospective health care and the role of academic medicine: lead, follow, or get out of the way.
-
Perspectives from the Avian Phylogenomics Project: Questions that Can Be Answered with Sequencing All Genomes of a Vertebrate Class.
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Pharmacogenomics and end-organ susceptibility to injury in the perioperative period.
-
Pharmacogenomics study of thiazide diuretics and QT interval in multi-ethnic populations: the cohorts for heart and aging research in genomic epidemiology.
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Pharmacometabolomics reveals racial differences in response to atenolol treatment.
-
PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.
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PhyloOncology: Understanding cancer through phylogenetic analysis.
-
Phylogenetic and Phylogenomic Definition of Rhizopus Species.
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Phylogenetic, genomic, and biogeographic characterization of a novel and ubiquitous marine invertebrate-associated Rickettsiales parasite, Candidatus Aquarickettsia rohweri, gen. nov., sp. nov.
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Phylogenomic analyses data of the avian phylogenomics project.
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Phylogenomic analyses provide insights into primate evolution.
-
Phylogeny and evolution of aldehyde dehydrogenase-homologous folate enzymes.
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Phylogeography's past, present, and future: 10 years after Avise, 2000.
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Physiological Genomics: Who we are and where we're going.
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Physiological genomics of cardiac disease: quantitative relationships between gene expression and left ventricular hypertrophy.
-
Physiological genomics of human arteries: quantitative relationship between gene expression and arterial stiffness.
-
Pioneering geneticist Mary-Claire King receives the 2014 Lasker~Koshland Special Achievement Award in Medical Science.
-
Platelets from genome to proteome and beyond.
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Plug-and-Play Protein Modification Using Homology-Independent Universal Genome Engineering.
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Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
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Polymorphisms and evolutionary history of retrotransposon insertions in rice promoters.
-
Population perspectives on functional genomic variation in yeast.
-
Population-genomic inference of the strength and timing of selection against gene flow.
-
Positive selection in noncoding genomic regions of vocal learning birds is associated with genes implicated in vocal learning and speech functions in humans.
-
Posttranslational, translational, and transcriptional responses to nitric oxide stress in Cryptococcus neoformans: implications for virulence.
-
Preanalytical Variables for the Genomic Assessment of the Cellular and Acellular Fractions of the Liquid Biopsy in a Cohort of Breast Cancer Patients.
-
Precision Medicine: From Science To Value.
-
Predicting clinical outcome of therapy-resistant prostate cancer.
-
Prediction of a time-to-event trait using genome wide SNP data.
-
Preface to the special issue: ecological and evolutionary genomics of populations in nature.
-
Primary role for endoplasmic reticulum-bound ribosomes in cellular translation identified by ribosome profiling.
-
Prognostic modeling in early stage lung cancer: an evolving process from histopathology to genomics.
-
Progressive Cactus is a multiple-genome aligner for the thousand-genome era.
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Prospective care: a personalized, preventative approach to medicine.
-
Prospective health care: the second transformation of medicine.
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Prospective medicine: the role for genomics in personalized health planning.
-
Prospects for personalized cardiovascular medicine: the impact of genomics.
-
Proteomic profiling of patient-derived glioblastoma xenografts identifies a subset with activated EGFR: implications for drug development.
-
PseudoBase: a genomic visualization and exploration resource for the Drosophila pseudoobscura
subgroup.
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Psychiatric disease in the genomic era: rational approach.
-
Public health. Genomics and medicine at a crossroads in Chernobyl.
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Public knowledge of and attitudes toward genetics and genetic testing.
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Public perspectives on returning genetics and genomics research results.
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Public perspectives regarding data-sharing practices in genomics research.
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Purine synthesis promotes maintenance of brain tumor initiating cells in glioma.
-
QBiC-Pred: quantitative predictions of transcription factor binding changes due to sequence variants.
-
Qualitative study of system-level factors related to genomic implementation.
-
Quantum computing at the frontiers of biological sciences.
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Radiogenomic analysis of breast cancer: luminal B molecular subtype is associated with enhancement dynamics at MR imaging.
-
Radiogenomics: what it is and why it is important.
-
Randomized trial of personal genomics for preventive cardiology: design and challenges.
-
Real-Time Genomic Profiling of Pancreatic Ductal Adenocarcinoma: Potential Actionability and Correlation with Clinical Phenotype.
-
Realising the Value of Linked Data to Health Economic Analyses of Cancer Care: A Case Study of Cancer 2015.
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Realizing the Full Potential of Precision Medicine in Health and Health Care.
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Realizing the opportunities of genomics in health care.
-
Reclassification of cardiovascular risk using integrated clinical and molecular biosignatures: Design of and rationale for the Measurement to Understand the Reclassification of Disease of Cabarrus and Kannapolis (MURDOCK) Horizon 1 Cardiovascular Disease Study.
-
Reconstruction of gross avian genome structure, organization and evolution suggests that the chicken lineage most closely resembles the dinosaur avian ancestor.
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Redefining Genomic Privacy: Trust and Empowerment
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Redefining heart failure: the utility of genomics.
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Regeneration Genetics.
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Regulation: The FDA is Overcautious on Consumer Genetics
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Reinvestigation of the Saccharomyces cerevisiae genome annotation by comparison to the genome of a related fungus: Ashbya gossypii.
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Relative contribution of clinicopathological variables, genomic markers, transcriptomic subtyping and microenvironment features for outcome prediction in stage II/III colorectal cancer.
-
Replicated Landscape Genomics Identifies Evidence of Local Adaptation to Urbanization in Wood Frogs.
-
Reply to A. Dalla Volta et al.
-
Report on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, Cameroon.
-
Research capacity. Enabling the genomic revolution in Africa.
-
Residual dipolar couplings: synergy between NMR and structural genomics.
-
Response to Rosenberg et al.
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Returning integrated genomic risk and clinical recommendations: The eMERGE study.
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Revolution and renaissance.
-
Robust regression analysis of copy number variation data based on a univariate score.
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Role of natural product diversity in chemical biology.
-
SMARCA4 and Other SWItch/Sucrose NonFermentable Family Genomic Alterations in NSCLC: Clinicopathologic Characteristics and Outcomes to Immune Checkpoint Inhibition.
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SMRT Sequencing for Parallel Analysis of Multiple Targets and Accurate SNP Phasing.
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SNiPA: an interactive, genetic variant-centered annotation browser.
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Sacrifice, individuation, and the economies of genomics.
-
Sample type bias in the analysis of cancer genomes.
-
Scalable Open Science Approach for Mutation Calling of Tumor Exomes Using Multiple Genomic Pipelines.
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Searching for genes that matter in acute kidney injury: a systematic review.
-
Secrets of the perioptome: new tools for a new concept.
-
Selection of optimal reference genes for normalization in quantitative RT-PCR.
-
Semi-automated assembly of high-quality diploid human reference genomes.
-
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program.
-
Showcasing Fungal Genetics & Genomics with the Genetics Society of America.
-
SigProfilerMatrixGenerator: a tool for visualizing and exploring patterns of small mutational events.
-
Signatures of neutral evolution in exponentially growing tumors: A theoretical perspective.
-
Single-cell genomics identifies cell type-specific molecular changes in autism.
-
Single-cell genomics revolutionizes plant development studies across scales.
-
Six reference-quality genomes reveal evolution of bat adaptations.
-
Small but Mighty: Functional Peptides Encoded by Small ORFs in Plants.
-
Speciation genetics: evolving approaches.
-
Sphagnum physiology in the context of changing climate: emergent influences of genomics, modelling and host-microbiome interactions on understanding ecosystem function.
-
Sphingolipid Metabolic Pathway Impacts Thiazide Diuretics Blood Pressure Response: Insights From Genomics, Metabolomics, and Lipidomics.
-
Standards recommendations for the Earth BioGenome Project.
-
Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browser.
-
Statistical challenges in preprocessing in microarray experiments in cancer.
-
Strengthening the reporting of Genetic RIsk Prediction Studies (GRIPS): explanation and elaboration.
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Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.
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Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.
-
Stringent comparative sequence analysis reveals SOX10 as a putative inhibitor of glial cell differentiation.
-
Structural and transcriptional analyses of a purine nucleotide-binding protein from Pyrococcus furiosus: a component of a novel, membrane-bound multiprotein complex unique to this hyperthermophilic archaeon.
-
Structural genomics of Pyrococcus furiosus: X-ray crystallography reveals 3D domain swapping in rubrerythrin.
-
Subgroup-specific structural variation across 1,000 medulloblastoma genomes.
-
Summary of the OA biomarkers workshop 2010 - genetics and genomics: new targets in OA.
-
Suppression of ABHD2, identified through a functional genomics screen, causes anoikis resistance, chemoresistance and poor prognosis in ovarian cancer.
-
Synthetic lethal analysis of Caenorhabditis elegans posterior embryonic patterning genes identifies conserved genetic interactions.
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Systems Genetics for Mechanistic Discovery in Heart Diseases.
-
TBestDB: a taxonomically broad database of expressed sequence tags (ESTs).
-
Taking the first steps towards a standard for reporting on phylogenies: Minimum Information About a Phylogenetic Analysis (MIAPA).
-
Test-Retest Reliability of the Genetics and Genomics in Nursing Practice Survey Instrument.
-
The 17-Gene Genomic Prostate Score Test Is Prognostic for Outcomes After Primary External Beam Radiation Therapy in Men With Clinically Localized Prostate Cancer.
-
The ABC's of comparative genomics in the Brassicaceae: building blocks of crucifer genomes.
-
The Bioinformatics Open Source Conference (BOSC) 2013.
-
The DNA sequence and biological annotation of human chromosome 1.
-
The DNA sequence of the human X chromosome.
-
The ENCODE (ENCyclopedia Of DNA Elements) Project.
-
The Earth BioGenome Project 2020: Starting the clock.
-
The Gene Ontology (GO) database and informatics resource.
-
The Gene Ontology in 2010: extensions and refinements.
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The Gene Ontology project in 2008.
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The Genome 10K Project: a way forward.
-
The Genomic Medicine Integrative Research Framework: A Conceptual Framework for Conducting Genomic Medicine Research.
-
The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system.
-
The Global Synanthrome Project: A Call for an Exhaustive Study of Human Associates.
-
The Human Pangenome Project: a global resource to map genomic diversity.
-
The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution.
-
The IGNITE network: a model for genomic medicine implementation and research.
-
The Immune Landscape of Cancer.
-
The International HapMap Project.
-
The MetJ regulon in gammaproteobacteria determined by comparative genomics methods.
-
The NEXT-1 (Next generation pErsonalized tX with mulTi-omics and preclinical model) trial: prospective molecular screening trial of metastatic solid cancer patients, a feasibility analysis.
-
The National Academies' Roundtable on Genomics and Precision Health: Where we have been and where we are heading.
-
The Psychiatric Genomics Consortium Posttraumatic Stress Disorder Workgroup: Posttraumatic Stress Disorder Enters the Age of Large-Scale Genomic Collaboration.
-
The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal Variants.
-
The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
-
The Sphagnome Project: enabling ecological and evolutionary insights through a genus-level sequencing project.
-
The Trait Repertoire Enabling Cyanobacteria to Bloom Assessed through Comparative Genomic Complexity and Metatranscriptomics.
-
The accessible chromatin landscape of the human genome.
-
The case for strategic international alliances to harness nutritional genomics for public and personal health.
-
The comparative genomics and complex population history of Papio
baboons.
-
The dangers of diagnostic monopolies.
-
The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG).
-
The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.
-
The ecological, genetic and genomic architecture of local adaptation and population differentiation in Boechera stricta
.
-
The enduring importance of family health history in the era of genomic medicine and risk assessment.
-
The era of reference genomes in conservation genomics.
-
The future of Physiological Genomics.
-
The genetic landscape of gliomas arising after therapeutic radiation.
-
The genome of the green anole lizard and a comparative analysis with birds and mammals.
-
The genomic analysis of erythrocyte microRNA expression in sickle cell diseases.
-
The genomic analysis of lactic acidosis and acidosis response in human cancers.
-
The genomic epidemiology of multi-drug resistant invasive non-typhoidal Salmonella in selected sub-Saharan African countries.
-
The genomic landscape of TERT promoter wildtype-IDH wildtype glioblastoma.
-
The genomic landscape of familial glioma.
-
The genomic landscape of mantle cell lymphoma is related to the epigenetically determined chromatin state of normal B cells.
-
The genomic, biochemical, and cellular responses of the retina in inherited photoreceptor degenerations and prospects for the treatment of these disorders.
-
The genomics education partnership: successful integration of research into laboratory classes at a diverse group of undergraduate institutions.
-
The genomics of speciation in Drosophila: diversity, divergence, and introgression estimated using low-coverage genome sequencing.
-
The host response as a tool for infectious disease diagnosis and management.
-
The impact of disregarding family structure on genome-wide association analysis of complex diseases in cohorts with simple pedigrees.
-
The impact of genomics on the biotechnology industry.
-
The integrated genomic and epigenomic landscape of brainstem glioma.
-
The integrated landscape of driver genomic alterations in glioblastoma.
-
The integration of molecular diagnostics with therapeutics. Implications for drug development and pathology practice.
-
The lemur revolution starts now: the genomic coming of age for a non-model organism.
-
The naturalist in a world of genomics.
-
The new age of medical genomics.
-
The origin of extracellular DNA during the clearance of dead and dying cells.
-
The performance of ZDOCK and ZRANK in rounds 6-11 of CAPRI.
-
The rise of genomic profiling in ovarian cancer.
-
The routinisation of genomics and genetics: implications for ethical practices.
-
The teleost anatomy ontology: anatomical representation for the genomics age.
-
The value of population-based studies in the genomic era.
-
The virulence of human pathogenic fungi: notes from the South of France.
-
The whole-genome landscape of medulloblastoma subtypes.
-
These Are the Genes You're Looking For: Finding Host Resistance Genes.
-
Thousands of small, novel genes predicted in global phage genomes.
-
Toward clinical genomics in everyday medicine: perspectives and recommendations.
-
Towards integrated clinico-genomic models for personalized medicine: combining gene expression signatures and clinical factors in breast cancer outcomes prediction.
-
Towards structural genomics of RNA: rapid NMR resonance assignment and simultaneous RNA tertiary structure determination using residual dipolar couplings.
-
Transcriptome analysis reveals novel patterning and pigmentation genes underlying Heliconius butterfly wing pattern variation.
-
Translating genomic biomarkers into clinically useful diagnostics.
-
Translating genomics into clinical practice: applications in lung cancer.
-
Translating the genomics revolution: the need for an international gene therapy consortium for monogenic diseases.
-
Translational Bioinformatics: Past, Present, and Future.
-
Uncoupling of genomic and epigenetic signals in the maintenance and inheritance of heterochromatin domains in fission yeast.
-
Uncovering the HARbingers of human brain evolution.
-
Uncovering the genomic signature of ancient introgression between white oak lineages (Quercus).
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Understanding Mucor circinelloides pathogenesis by comparative genomics and phenotypical studies.
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Understanding the biological basis of psychiatric disease: What's next?
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Unisexual reproduction drives meiotic recombination and phenotypic and karyotypic plasticity in Cryptococcus neoformans.
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Unlocking the secrets of the genome.
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Unraveling the dynamic transcriptome.
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Update on Chronic Kidney Disease Mineral and Bone Disorder in Cardiovascular Disease.
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Update on the genetics of primary open-angle glaucoma.
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Updates and Critical Evaluation on Novel Biomarkers for the Malignant Progression of Intraductal Papillary Mucinous Neoplasms of the Pancreas.
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Urine as a high-quality source of host genomic DNA from wild populations.
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Use of integrative epigenetic and cytogenetic analyses to identify novel tumor-suppressor genes in malignant melanoma.
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Using context to improve protein domain identification.
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Validation of a genomic classifier for prediction of metastasis and prostate cancer-specific mortality in African-American men following radical prostatectomy in an equal access healthcare setting.
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Very low mutation burden is a feature of inflamed recurrent glioblastomas responsive to cancer immunotherapy.
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Visual annotation of the gene database.
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We are the genes we've been waiting for: rational responses to the gathering storm of personal genomics.
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What can patterns of differentiation across plant genomes tell us about adaptation and speciation?
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What can you do with 0.1x genome coverage? A case study based on a genome survey of the scuttle fly Megaselia scalaris (Phoridae).
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What was old is new again: using the host response to diagnose infectious disease.
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What will it take to implement genomics in practice? Lessons from the IGNITE Network.
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Who owns the genome?
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Whole Genomic Copy Number Alterations in Circulating Tumor Cells from Men with Abiraterone or Enzalutamide-Resistant Metastatic Castration-Resistant Prostate Cancer.
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Whole blood gene expression analyses in patients with single versus recurrent venous thromboembolism.
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Whole-Genome Analysis Illustrates Global Clonal Population Structure of the Ubiquitous Dermatophyte Pathogen Trichophyton rubrum.
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Whole-Slide Cytometric Feature Mapping for Distinguishing Tumor Genomic Subtypes in Head and Neck Squamous Cell Carcinoma Whole-Slide Images.
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Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
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Whole-genome reconstruction and mutational signatures in gastric cancer.
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Why sequence all eukaryotes?
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Widespread false gene gains caused by duplication errors in genome assemblies.
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YbiV from Escherichia coli K12 is a HAD phosphatase.
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cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.
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dictyBase, the model organism database for Dictyostelium discoideum.
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dictyBase--a Dictyostelium bioinformatics resource update.
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dictyBase: a new Dictyostelium discoideum genome database.
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minotaur: A platform for the analysis and visualization of multivariate results from genome scans with R Shiny.
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siRNA-based approaches in cancer therapy.
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Keywords of People
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-
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Acharya, Chaitanya,
Research Associate, Senior,
Surgery
-
Baugh, L. Ryan,
Associate Professor of Biology,
Biology
-
Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
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Cho, Alex Han,
Associate Professor of Medicine,
Medicine, General Internal Medicine
-
Guevara, Elaine Elizabeth Gomez,
Lecturer in Evolutionary Anthropology,
Evolutionary Anthropology
-
Haase, Steven B.,
Professor of Biology,
Biology
-
Hartemink, Alexander J.,
Professor in the Department of Computer Science,
Biology
-
Ji, Zhicheng,
Assistant Professor of Biostatistics & Bioinformatics,
Biostatistics & Bioinformatics
-
Knisely, Mitchell,
Associate Professor in the School of Nursing,
School of Nursing
-
Landstrom, Andrew Paul,
Associate Professor of Pediatrics,
Cell Biology
-
Liu, Yongmei,
Professor of Medicine,
Medicine, Cardiology
-
Magwene, Paul Mitaari,
Professor of Biology,
Biology
-
Mangan, Riley,
Student,
Basic Science Departments
-
McLendon, Roger Edwin,
Professor of Pathology,
Pathology
-
Mitchell-Olds, Thomas,
Newman Ivey White Distinguished Professor of Biology,
Biology
-
O'Connor, Christopher Michael,
Adjunct Professor in the Department of Medicine,
Medicine, Clinical Pharmacology
-
Orlando, Lori Ann,
Professor of Medicine,
Medicine, General Internal Medicine
-
Osterberg, Joshua Samuel,
Adjunct Assistant Professor in the Marine Science and Conservation Division,
Marine Science and Conservation
-
Patel, Uptal Dinesh,
Adjunct Professor in the Department of Medicine,
Medicine, Nephrology
-
Reddy, Timothy E,
Associate Professor of Biostatistics & Bioinformatics,,
Molecular Genetics and Microbiology
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Reitman, Zachary James,
Assistant Professor of Radiation Oncology,
Pathology
-
Swain Lenz, Devi,
Research Scientist,
Biology
-
Tsalik, Ephraim,
Adjunct Associate Professor in the Department of Medicine,
Medicine, Infectious Diseases
-
Wald, Priscilla,
R. Florence Brinkley Distinguished Professor of English,
Duke Science & Society
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Wernegreen, Jennifer Jo,
Lee Hill Snowdon Associate Professor,
Environmental Sciences and Policy
-
Wray, Gregory Allan,
Professor of Biology,
Evolutionary Anthropology
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Yoder, Anne Daphne,
Braxton Craven Distinguished Professor of Evolutionary Biology,
Duke Science & Society