Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. - Wikidata - awgldk - TriplyDB

Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants.

Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants.

http://www.wikidata.org/entity/Q35518379

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APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans Heritability in the genome-wide association era The evolutionary genetics of the genes underlying phenotypic associations for loblolly pine (Pinus taeda, Pinaceae)Toward genomic prediction from whole-genome sequence data: impact of sequencing design on genotype imputation and accuracy of predictions.Gradient Boosting as a SNP Filter: an Evaluation Using Simulated and Hair Morphology Data.The effects of demography and long-term selection on the accuracy of genomic prediction with sequence data.Comprehensive genotyping of the USA national maize inbred seed bank.The impact of rare and low-frequency genetic variants in common disease The impact of population demography and selection on the genetic architecture of complex traits.Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.Genetic-epigenetic interactions in cis: a major focus in the post-GWAS era Applying compressed sensing to genome-wide association studies Haplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Conditions for the validity of SNP-based heritability estimation.The SNP rs961253 in 20p12.3 is associated with colorectal cancer risk: a case-control study and a meta-analysis of the published literature Cohen's h for detection of disease association with rare genetic variants.An integrated approach to reduce the impact of minor allele frequency and linkage disequilibrium on variable importance measures for genome-wide data.Gene-gene interaction and functional impact of polymorphisms on innate immune genes in controlling Plasmodium falciparum blood infection level.Progress in genetic association studies of plasma lipids.The UK10K project identifies rare variants in health and disease High trans-ethnic replicability of GWAS results implies common causal variants.The genetics of infectious disease susceptibility: has the evidence for epistasis been overestimated?Genetics of callous-unemotional behavior in children.Sex-specific trans-regulatory variation on the Drosophila melanogaster X chromosome.Genetic determinants influencing human serum metabolome among African Americans Asymmetry in family history implicates nonstandard genetic mechanisms: application to the genetics of breast cancer.Calcium, ARMS2 genotype, and Chlamydia pneumoniae infection in early age-related macular degeneration: a multivariate analysis from the Nagahama study.Rare and common variants: twenty arguments.Using Network Methodology to Infer Population Substructure.Enrichment of Minor Alleles of Common SNPs and Improved Risk Prediction for Parkinson's Disease.Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements.Association between IL7R polymorphisms and severe liver disease in HIV/HCV coinfected patients: a cross-sectional study An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies Exploiting biological priors and sequence variants enhances QTL discovery and genomic prediction of complex traits.The Fourth Law of Behavior Genetics.Explaining additional genetic variation in complex traits Improved heritability estimation from genome-wide SNPs.Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics Genomic risk models improve prediction of longitudinal lipid levels in children and young adults.Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation

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Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants.

http://www.wikidata.org/entity/Q35518379

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2011 nî lūn-bûn

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2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2011 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Distribution of allele frequen ...... netic susceptibility variants.

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PNAS.1114759108

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Proceedings of the National Academy of Sciences of the United States of America

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Distribution of allele frequen ...... netic susceptibility variants.

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P2093

Charles C Chung

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Clarice R Weinberg

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Joseph F Fraumeni

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Ju-Hyun Park

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Mitchell H Gail

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Raymond J Carroll

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P2860

Are rare variants responsible for susceptibility to complex diseases?

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

Biological, clinical and population relevance of 95 loci for blood lipids

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

Epidemiologic studies utilizing surveys: accounting for the sampling design

A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

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18026-18031

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10.1073/PNAS.1114759108

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44

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108

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Nilanjan Chatterjee

Stephen Chanock

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2011-10-14T00:00:00Z

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51720090

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22003128

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3207674

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