Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis. - Wikidata - wikimedia - TriplyDB

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

http://www.wikidata.org/entity/Q34505634

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Beyond the fourth wave of genome-wide obesity association studies Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches On the association of common and rare genetic variation influencing body mass index: a combined SNP and CNV analysis Sex bias in copy number variation of olfactory receptor gene family depends on ethnicity 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.Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions.Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants Identification of structural variation in mouse genomes.Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index.Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.Analysis of genome-wide copy number variations in Chinese indigenous and western pig breeds by 60 K SNP genotyping arrays Olfaction under metabolic influences.Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants.Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.Obesity gene NEGR1 associated with white matter integrity in healthy young adults Genetics of childhood obesity Molecular basis of obesity: current status and future prospects Interactions between obesity-related copy number variants and dietary behaviors in childhood obesity.Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.Genome Wide Distributions and Functional Characterization of Copy Number Variations between Chinese and Western Pigs.Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing.The Genetics of Pediatric Obesity.Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity.Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.Molecular genetic aspects of weight regulation.Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations A 680 kb duplication at the FTO locus in a kindred with obesity and a distinct body fat distribution.Copy Number Variations in Candidate Genes and Intergenic Regions Affect Body Mass Index and Abdominal Obesity in Mexican Children Programming towards childhood obesity.Integrating genomic and epigenomic information: a promising strategy for identifying functional DNA variants of human disease.Obesity and genomics: role of technology in unraveling the complex genetic architecture of obesity.The cilium: a cellular antenna with an influence on obesity risk.Aberrations of NEGR1 on 1p31 and MYEOV on 11q13 in neuroblastoma.CNV analysis and mutation screening indicate an important role for the NPY4R gene in human obesity.Olfactory receptor genes cooperate with protocadherin genes in human extreme obesity.

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P2860

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

http://www.wikidata.org/entity/Q34505634

description

2010 nî lūn-bûn

@nan

2010 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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type

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Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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prefLabel

Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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Novel common copy number varia ...... ied by a genome-wide analysis.

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Human Molecular Genetics

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Novel common copy number varia ...... ied by a genome-wide analysis.

@en

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Carla I G Vogel

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Helmut Schäfer

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Ivonne Jarick

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Susann Scherag

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P2860

Finding the missing heritability of complex diseases

The genetic contribution to non-syndromic human obesity

Large, rare chromosomal deletions associated with severe early-onset obesity

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Strong association of de novo copy number mutations with autism

Common variants near MC4R are associated with fat mass, weight and risk of obesity

Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

Large recurrent microdeletions associated with schizophrenia

Global variation in copy number in the human genome

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

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10.1093/HMG/DDQ518

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4

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20

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Johannes Hebebrand

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2010-12-02T00:00:00Z

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49658021

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