Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. - Wikidata - awgldk - TriplyDB

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

http://www.wikidata.org/entity/Q30368157

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Over-expression of NYGGF4 inhibits glucose transport in 3T3-L1 adipocytes via attenuated phosphorylation of IRS-1 and Akt Analyses of shared genetic factors between asthma and obesity in children Beyond the fourth wave of genome-wide obesity association studies Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study The structure of full-length human CTNNBL1 reveals a distinct member of the armadillo-repeat protein family Exploring the Major Sources and Extent of Heterogeneity in a Genome-Wide Association Meta-Analysis Genetic risk factors for BMI and obesity in an ethnically diverse population: results from the population architecture using genomics and epidemiology (PAGE) study The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians Genotype imputation Genetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass.Toward objective monitoring of ingestive behavior in free-living population.Evaluation of the genetic overlap between osteoarthritis with body mass index and height using genome-wide association scan data Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.Uncovering Adaptation from Sequence Data: Lessons from Genome Resequencing of Four Cattle Breeds.Non-replication of genome-wide based associations between common variants in INSIG2 and PFKP and obesity in studies of 18,014 Danes Variations in the ghrelin receptor gene associate with obesity and glucose metabolism in individuals with impaired glucose tolerance Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.Studies of CTNNBL1 and FDFT1 variants and measures of obesity: analyses of quantitative traits and case-control studies in 18,014 Danes.Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche.Mutations in genes involved in nonsense mediated decay ameliorate the phenotype of sel-12 mutants with amber stop mutations in Caenorhabditis elegans The INSIG2 rs7566605 genetic variant does not play a major role in obesity in a sample of 24,722 individuals from four cohorts.Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study.Analyses and comparison of imputation-based association methods Recent progress in the genetics of common obesity Dietary ascorbic acid and subsequent change in body weight and waist circumference: associations may depend on genetic predisposition to obesity--a prospective study of three independent cohorts.Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.Replication of 6 obesity genes in a meta-analysis of genome-wide association studies from diverse ancestries.Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study.Linkage analysis of obesity phenotypes in pre- and post-menopausal women from a United States mid-western population Common Genetic Variant of insig2 Gene rs7566605 Polymorphism Is Associated with Severe Obesity in North India Do gene variants influencing adult adiposity affect birth weight? A population-based study of 24 loci in 4,744 Danish individuals.Metabolic syndrome components in murine models.Multilocus association testing of quantitative traits based on partial least-squares analysis.FTO genetic variation and association with obesity in West Africans and African Americans.Correcting for cryptic relatedness in population-based association studies of continuous traits.Genome wide association study identifies KCNMA1 contributing to human obesity Genetic association study of common mitochondrial variants on body fat mass Obesity-related genomic loci are associated with type 2 diabetes in a Han Chinese population.

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P2860

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

http://www.wikidata.org/entity/Q30368157

description

2008 nî lūn-bûn

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2008 թուականի Մարտին հրատարակուած գիտական յօդուած

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2008 թվականի մարտին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@ast

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@en

type

label

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@ast

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@en

prefLabel

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@ast

Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

@en

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Human Molecular Genetics

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Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.

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Betty M Drees

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Christian Dina

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Christopher J Papasian

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David Meyre

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Han Yan

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James J Hamilton

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Jerome Delplanque

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Lei Zhang

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Liang Wang

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Robert R Recker

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P2860

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

Inhibition of adipogenesis by Wnt signaling

A Bayesian measure of the probability of false discovery in genetic epidemiology studies

Sequence, gene structure, and expression pattern of CTNNBL1, a minor-class intron-containing gene--evidence for a role in apoptosis

An alternative to null-hypothesis significance tests

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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

A second generation human haplotype map of over 3.1 million SNPs

Statistical significance for genomewide studies

The structure of haplotype blocks in the human genome

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10.1093/HMG/DDN072

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12

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18325910

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genome-wide association study

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2900891

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