Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population. - Wikidata - awgldk - TriplyDB

Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population.

Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population.

http://www.wikidata.org/entity/Q37322218

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Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians Etiology of Obesity Over the Life Span: Ecological and Genetic Highlights from Asian Countries.Chromosome 16p11.2 deletions: another piece in the genetic puzzle of childhood obesity CONAN: copy number variation analysis software for genome-wide association studies From monogenic to polygenic obesity: recent advances.Evolution in health and medicine Sackler colloquium: Genomic disorders: a window into human gene and genome evolution.Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians.Analysis of genome-wide copy number variations in Chinese indigenous and western pig breeds by 60 K SNP genotyping arrays Ancestral paternal genotype controls body weight and food intake for multiple generations Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.A comprehensive survey of copy number variation in 18 diverse pig populations and identification of candidate copy number variable genes associated with complex traits.Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.Identification of both copy number variation-type and constant-type core elements in a large segmental duplication region of the mouse genome.Molecular basis of obesity: current status and future prospects Investigation of modifier genes within copy number variations in Rett syndrome Apolipoprotein A-II polymorphism: relationships to behavioural and hormonal mediators of obesity Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV Identification and computational analysis of gene regulatory elements.Interactions between obesity-related copy number variants and dietary behaviors in childhood obesity.Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.Genome Wide Distributions and Functional Characterization of Copy Number Variations between Chinese and Western Pigs.Large copy-number variations are enriched in cases with moderate to extreme obesity.CNV Analysis Associates AKNAD1 with Type-2 Diabetes in Jordan Subpopulations Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity.Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease.Implications of gene copy-number variation in health and diseases.Obesity and genomics: role of technology in unraveling the complex genetic architecture of obesity.Genome-wide analysis of copy number variations reveals that aging processes influence body fat distribution in Korea Associated Resource (KARE) cohorts.CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity.Ethnic and population differences in the genetic predisposition to human obesity.Low copy number of the salivary amylase gene predisposes to obesity.Copy number of pancreatic polypeptide receptor gene NPY4R correlates with body mass index and waist circumference.The evolution and population diversity of human-specific segmental duplications.

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Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population.

http://www.wikidata.org/entity/Q37322218

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bilimsel makale

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scientific article published on 20 February 2009

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Genome-wide association study ...... dex in the Chinese population.

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Genome-wide association study ...... dex in the Chinese population.

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Genome-wide association study ...... dex in the Chinese population.

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Genome-wide association study ...... dex in the Chinese population.

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Genome-wide association study ...... dex in the Chinese population.

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Genome-wide association study ...... dex in the Chinese population.

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Journal of Human Genetics

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Genome-wide association study ...... dex in the Chinese population.

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Bao-Yong Sha

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Feng Pan

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Lan-Juan Zhao

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Shan-Shan Dong

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Xiang-Ding Chen

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Xiang-Hong Xu

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Yuan Chen

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Zhi-Xin Zhang

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P2860

Predictive values of body mass index and waist circumference for risk factors of certain related diseases in Chinese adults: study on optimal cut-off points of body mass index and waist circumference in Chinese adults

Inference of population structure using multilocus genotype data

Structural variation of chromosomes in autism spectrum disorder

Global variation in copy number in the human genome

GAD2 on chromosome 10p12 is a candidate gene for human obesity

Pancreatic polypeptide reduces appetite and food intake in humans

Neuropeptide Y receptors as targets for anti-obesity drug development: perspective and current status

Neuropeptide y receptor selective ligands in the treatment of obesity

Large-scale copy number polymorphism in the human genome

Genomic control for association studies

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10.1038/JHG.2009.10

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4

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54

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genome-wide association study

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