A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants - Wikidata - awgldk - TriplyDB

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

http://www.wikidata.org/entity/Q29547210

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Polymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell function Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution The genetic signatures of noncoding RNAs Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus Genetic variation in an individual human exome Data and theory point to mainly additive genetic variance for complex traits Enrichment of sequencing targets from the human genome by solution hybridization Isolated populations and complex disease gene identification A genome-wide association study of the metabolic syndrome in Indian Asian men INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis Common inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traits Fine mapping of five loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability Structural Properties of Gene Promoters Highlight More than Two Phenotypes of Diabetes Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders Personal history of diabetes, genetic susceptibility to diabetes, and risk of brain glioma: a pooled analysis of observational studies Prevalence in the United States of selected candidate gene variants. Third National Health and Nutrition Examination Survey, 1991- 1994 Genome-wide association studies: a primer Meta-analysis in genome-wide association studies Is replication the gold standard for validating genome-wide association findings?Replication in Genome-Wide Association Studies Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors ALKBH4-dependent demethylation of actin regulates actomyosin dynamics.N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase ALKBH5 is a mammalian RNA demethylase that impacts RNA metabolism and mouse fertility Oxidative demethylation of 3-methylthymine and 3-methyluracil in single-stranded DNA and RNA by mouse and human FTO GRM7 variants confer susceptibility to age-related hearing impairment Evidence that the gene encoding insulin degrading enzyme influences human lifespan Glucokinase regulatory protein gene polymorphism affects postprandial lipemic response in a dietary intervention study Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls Common variants at 30 loci contribute to polygenic dyslipidemia Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study Epigenetic regulation of the INK4b-ARF-INK4a locus: in sickness and in health Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis Association between a literature-based genetic risk score and cardiovascular events in women

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

http://www.wikidata.org/entity/Q29547210

description

2007 nî lūn-bûn

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2007 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2007年の論文

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P2860

A family of insulin-like growth factor II mRNA-binding proteins represses translation in late development

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

Identification of a neuronal Cdk5 activator-binding protein as Cdk5 inhibitor

Identification and cloning of a beta-cell-specific zinc transporter, ZnT-8, localized into insulin secretory granules

In vivo expression and functional characterization of the zinc transporter ZnT8 in glucose-induced insulin secretion

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

A haplotype map of the human genome

Global prevalence of diabetes: estimates for the year 2000 and projections for 2030

Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in beta-islet cell hyperplasia

A genome-wide association study identifies novel risk loci for type 2 diabetes

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