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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

http://www.wikidata.org/entity/Q24607677

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Development of biomarkers to optimize pediatric patient management: what makes children different?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 The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes.Obesity and diabetes: from genetics to epigenetics.Proceedings of the Tenth Annual UT-ORNL-KBRIN Bioinformatics Summit 2011.Another tool in the genome-wide association study arsenal: population-based detection of somatic gene conversion dbPTB: a database for preterm birth.A bioinformatics approach to preterm birth.The impact of errors in copy number variation detection algorithms on association results.Identification and analysis of genome-wide SNPs provide insight into signatures of selection and domestication in channel catfish (Ictalurus punctatus).Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss.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.Genomic structure and marker-derived gene networks for growth and meat quality traits of Brazilian Nelore beef cattle The impact of genomics on pediatric research and medicine.Genetic variance of body mass index from childhood to early adulthood.Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.Phylogenetic ANOVA: The Expression Variance and Evolution Model for Quantitative Trait Evolution.The Genetics of Pediatric Obesity.Copy number variations associated with obesity-related traits in African Americans: a joint analysis between GENOA and HyperGEN.Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study Pathway-based genetic analysis of preterm birth.Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.Mouse model implicates GNB3 duplication in a childhood obesity syndrome.Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.The Role of Copy Number Variation in African Americans with Type 2 Diabetes-Associated End Stage Renal Disease.Programming towards childhood obesity.ParseCNV integrative copy number variation association software with quality tracking.Obesity and genomics: role of technology in unraveling the complex genetic architecture of obesity.A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape Kernel-Based Aggregation of Marker-Level Genetic Association Tests Involving Copy-Number Variation Genome-wide analysis of copy number variations reveals that aging processes influence body fat distribution in Korea Associated Resource (KARE) cohorts.Genome-wide assessment of the association of rare and common copy number variations to testicular germ cell cancer.Lack of relationship between mitochondrial heteroplasmy or variation and childhood obesity.The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion.

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P2860

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

http://www.wikidata.org/entity/Q24607677

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2010 nî lūn-bûn

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2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին 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

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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J.AJHG.2010.09.014

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American Journal of Human Genetics

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A genome-wide study reveals copy number variants exclusive to childhood obesity cases

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Cecilia E Kim

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Cuiping Hou

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Edward C Frackelton

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F George Otieno

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Frank D Mentch

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Haitao Zhang

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Hakon Hakonarson

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Jianhua Zhao

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Jonathan P Bradfield

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Kai Wang

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P2860

A functional genetic link between distinct developmental language disorders

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

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

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

FOXC2 is a winged helix gene that counteracts obesity, hypertriglyceridemia, and diet-induced insulin resistance

Variation in FTO contributes to childhood obesity and severe adult obesity

Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

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Joseph D. Buxbaum

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