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The genetic contribution to non-syndromic human obesity

Nature reviews. Genetics, 2009-07, Vol.10 (7), p.431-442

2009

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

Nature, 2007-02, Vol.445 (7130), p.881-885

2007

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The genetics of human obesity

Nature reviews. Genetics, 2005-03, Vol.6 (3), p.221-234

2005

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Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

American journal of human genetics, 2009-07, Vol.85 (1), p.106-111

2009

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Genetics of obesity and the prediction of risk for health

Human molecular genetics, 2006-10, Vol.15 (suppl-2), p.R124-R130

2006

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Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

American journal of human genetics, 2000-12, Vol.67 (6), p.1470-1480

2000

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

Human molecular genetics, 2008-06, Vol.17 (12), p.1803-1813

2008

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Kir6.2 Mutations Are a Common Cause of Permanent Neonatal Diabetes in a Large Cohort of French Patients

Diabetes (New York, N.Y.), 2004-10, Vol.53 (10), p.2719-2722

2004

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Genetics of the APM1 Locus and Its Contribution to Type 2 Diabetes Susceptibility in French Caucasians

Diabetes (New York, N.Y.), 2004-11, Vol.53 (11), p.2977-2983

2004

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A Synonymous Coding Polymorphism in the α2-Heremans-Schmid Glycoprotein Gene Is Associated With Type 2 Diabetes in French Caucasians

Diabetes (New York, N.Y.), 2005-08, Vol.54 (8), p.2477-2481

2005

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Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals

Diabetes (New York, N.Y.), 2010-01, Vol.59 (1), p.311-318

2010

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A Genome-Wide Scan for Childhood Obesity–Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2

Diabetes (New York, N.Y.), 2004-03, Vol.53 (3), p.803-811

2004

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MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans

Diabetes (New York, N.Y.), 2010-06, Vol.59 (6), p.1539-1548

2010

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New ABCC8 Mutations in Relapsing Neonatal Diabetes and Clinical Features

Diabetes (New York, N.Y.), 2007-06, Vol.56 (6), p.1737-1741

2007

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Evaluation of the Association of IGF2BP2 Variants With Type 2 Diabetes in French Caucasians

Diabetes (New York, N.Y.), 2008-07, Vol.57 (7), p.1992-1995

2008

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Common Polymorphisms in the Adiponectin Gene ACDC Are Not Associated With Diabetes in Pima Indians

Diabetes (New York, N.Y.), 2005-01, Vol.54 (1), p.284-289

2005

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Molecular Genetics of Maturity-onset Diabetes of the Young

Trends in Endocrinology & Metabolism, 1999-05, Vol.10 (4), p.142-146

1999

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Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q

Diabetes (New York, N.Y.), 2004-07, Vol.53 (7), p.1857-1865

2004

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Hepatocyte Nuclear Factor-4α P2 Promoter Haplotypes Are Associated With Type 2 Diabetes in the Japanese Population

Diabetes (New York, N.Y.), 2006-05, Vol.55 (5), p.1260-1264

2006

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Activating Transcription Factor 6 (ATF6) Sequence Polymorphisms in Type 2 Diabetes and Pre-Diabetic Traits

Diabetes (New York, N.Y.), 2007-03, Vol.56 (3), p.856-862

2007

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Polymorphisms in the Glucokinase-Associated, Dual-Specificity Phosphatase 12 (DUSP12) Gene Under Chromosome 1q21 Linkage Peak Are Associated With Type 2 Diabetes

Diabetes (New York, N.Y.), 2006-09, Vol.55 (9), p.2631-2639

2006

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A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

Nature genetics, 1995-04, Vol.9 (4), p.418-423

1995

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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

Nature (London), 2012-03, Vol.483 (7389), p.350-354

2012

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Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children

Diabetes (New York, N.Y.), 2008-02, Vol.57 (2), p.494-502

2008

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Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus

The New England journal of medicine, 2006-08, Vol.355 (5), p.456-466

2006

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The genetic contribution to non-syndromic human obesity

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

The genetics of human obesity

Loss-of-Function Mutation in the Dioxygenase-Encoding FTO Gene Causes Severe Growth Retardation and Multiple Malformations

Genetics of obesity and the prediction of risk for health

Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

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

Kir6.2 Mutations Are a Common Cause of Permanent Neonatal Diabetes in a Large Cohort of French Patients

Genetics of the APM1 Locus and Its Contribution to Type 2 Diabetes Susceptibility in French Caucasians

A Synonymous Coding Polymorphism in the α2-Heremans-Schmid Glycoprotein Gene Is Associated With Type 2 Diabetes in French Caucasians

Prevalence of Loss-of-Function FTO Mutations in Lean and Obese Individuals

A Genome-Wide Scan for Childhood Obesity–Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2

MTNR1B G24E Variant Associates With BMI and Fasting Plasma Glucose in the General Population in Studies of 22,142 Europeans

New ABCC8 Mutations in Relapsing Neonatal Diabetes and Clinical Features

Evaluation of the Association of IGF2BP2 Variants With Type 2 Diabetes in French Caucasians

Common Polymorphisms in the Adiponectin Gene ACDC Are Not Associated With Diabetes in Pima Indians

Molecular Genetics of Maturity-onset Diabetes of the Young

Genome-wide Linkage Analysis for Severe Obesity in French Caucasians Finds Significant Susceptibility Locus on Chromosome 19q

Hepatocyte Nuclear Factor-4α P2 Promoter Haplotypes Are Associated With Type 2 Diabetes in the Japanese Population

Activating Transcription Factor 6 (ATF6) Sequence Polymorphisms in Type 2 Diabetes and Pre-Diabetic Traits

Polymorphisms in the Glucokinase-Associated, Dual-Specificity Phosphatase 12 (DUSP12) Gene Under Chromosome 1q21 Linkage Peak Are Associated With Type 2 Diabetes

A gene for maturity onset diabetes of the young (MODY) maps to chromosome 12q

Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children

Activating Mutations in the ABCC8 Gene in Neonatal Diabetes Mellitus

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