Potential etiologic and functional implications of genome-wide association loci for human diseases and traits - Wikidata - wikimedia - TriplyDB

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

http://www.wikidata.org/entity/Q22066284

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Ensembl variation resources Swedish population substructure revealed by genome-wide single nucleotide polymorphism data A user's guide to the encyclopedia of DNA elements (ENCODE)Circ2Traits: a comprehensive database for circular RNA potentially associated with disease and traits Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits Fast association tests for genes with FAST Shared molecular and functional frameworks among five complex human disorders: a comparative study on interactomes linked to susceptibility genes Pervasive transcription of the human genome produces thousands of previously unidentified long intergenic noncoding RNAs Comparison of family history and SNPs for predicting risk of complex disease A genome-wide screen for genetic variants that modify the recruitment of REST to its target genes Phased whole-genome genetic risk in a family quartet using a major allele reference sequence A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease Chapter 11: Genome-wide association studies Discovery of active enhancers through bidirectional expression of short transcripts Human genetics and genomics a decade after the release of the draft sequence of the human genome Quantitative genetics of CTCF binding reveal local sequence effects and different modes of X-chromosome association Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS Integrative annotation of variants from 1092 humans: application to cancer genomics Defining functional DNA elements in the human genome Enhancers: five essential questions An integrated encyclopedia of DNA elements in the human genome An integrated map of genetic variation from 1,092 human genomes Finding the missing heritability of complex diseases Crohn's disease risk alleles on the NOD2 locus have been maintained by natural selection on standing variation Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease Revealing the genetic basis of multiple sclerosis: are we there yet?Genetic studies of body mass index yield new insights for obesity biology Genome-wide association study identifies novel loci associated with diisocyanate-induced occupational asthma Identifying genetic variation for alcohol dependence This I believe in genetics: discovery can be a nuisance, replication is science, implementation matters Multilocus genetic analysis of brain images A critical review of the first 10 years of candidate gene-by-environment interaction research in psychiatry Knowledge Integration in Cancer: Current Landscape and Future Prospects Personalized medicine: hope or hype?Data-driven integration of epidemiological and toxicological data to select candidate interacting genes and environmental factors in association with disease MR-PheWAS: hypothesis prioritization among potential causal effects of body mass index on many outcomes, using Mendelian randomization The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus A proteome-scale map of the human interactome network

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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Lucia A Hindorff

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Praveen Sethupathy

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A map of recent positive selection in the human genome

Heritability in the genomics era — concepts and misconceptions

Genome-wide detection and characterization of positive selection in human populations

The human genome browser at UCSC

Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"?

Genetic determinants of hair, eye and skin pigmentation in Europeans

Multiple newly identified loci associated with prostate cancer susceptibility

Transcriptional regulation of the human hepatic lipase (LIPC) gene promoter

Hepatocyte nuclear factor 4alpha (nuclear receptor 2A1) is essential for maintenance of hepatic gene expression and lipid homeostasis

Multiple loci identified in a genome-wide association study of prostate cancer

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genome-wide association study

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