A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data.
A knowledge-driven interaction analysis reveals potential neurodegenerative mechanism of multiple sclerosis susceptibility.
A small number of candidate gene SNPs reveal continental ancestry in African Americans.
Alex’s Lemonade Stand Foundation Infant and Childhood Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2007-2011.
Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction.
American Brain Tumor Association Adolescent and Young Adult Primary Brain and Central Nervous System Tumors Diagnosed in the United States in 2008-2012.
Antiepileptic activity of preferential inhibitors of persistent sodium current.
Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts?
Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study.
Associations between KCNJ6 (GIRK2) gene polymorphisms and pain-related phenotypes.
Automated extraction of clinical traits of multiple sclerosis in electronic medical records.
Automated quantification of pancreatic β-cell mass.
Bioinformatics challenges in genome-wide association studies (GWAS).
Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project.
Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.
Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium.
eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants.
eMERGEing progress in genomics-the first seven years.
Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study.
Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.
Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models.
Evidence for polygenic susceptibility to multiple sclerosis–the shape of things to come.
Gene expression in cell lines from propionic acidemia patients, carrier parents, and controls.
Genetic analysis of biological pathway data through genomic randomization.
Genetic and clinical risk prediction model for postoperative atrial fibrillation.
Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network.
Genome simulation approaches for synthesizing in silico datasets for human genomics.
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Human islet preparations distributed for research exhibit a variety of insulin-secretory profiles.
ICD-9 tobacco use codes are effective identifiers of smoking status.
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies.
Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study.
Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests.
LD-spline: mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium.
Molecular Profiling Reveals Biologically Discrete Subsets and Pathways of Progression in Diffuse Glioma.
Multivariate analysis of regulatory SNPs: empowering personal genomics by considering cis-epistasis and heterogeneity.
Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene-gene interactions.
Pathway analysis by randomization incorporating structure-PARIS: an update.
Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia.
Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia.
Population Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide Data.
Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data.
Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists.
Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study.
SecureMA: protecting participant privacy in genetic association meta-analysis.
Sex-Specific Parental Effects on Offspring Lipid Levels.
The phenotypic legacy of admixture between modern humans and Neandertals.
The somatic genomic landscape of glioblastoma.
Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry.
Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.
Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus.