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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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TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups : a global meta-analysis

Journal of molecular medicine (Berlin, Germany), 2007-07, Vol.85 (7), p.777-782

2007

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Prevalence of Melanocortin-4 Receptor Deficiency in Europeans and Their Age-Dependent Penetrance in Multigenerational Pedigrees

Diabetes (New York, N.Y.), 2008-09, Vol.57 (9), p.2511-2518

2008

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The Common P446L Polymorphism in GCKR Inversely Modulates Fasting Glucose and Triglyceride Levels and Reduces Type 2 Diabetes Risk in the DESIR Prospective General French Population

Diabetes (New York, N.Y.), 2008-08, Vol.57 (8), p.2253-2257

2008

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Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retention

Diabetes (New York, N.Y.), 2010-03, Vol.59 (3), p.653-661

2010

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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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Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study

Diabetes (New York, N.Y.), 2008-01, Vol.57 (1), p.244-254

2008

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Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians

Diabetes (New York, N.Y.), 2009-11, Vol.58 (11), p.2703-2708

2009

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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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Combined effects of MC4R and FTO common genetic variants on obesity in European general populations

Journal of molecular medicine (Berlin, Germany), 2009-05, Vol.87 (5), p.537-546

2009

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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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Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations

Diabetes care, 2012-02, Vol.35 (2), p.248-251

2012

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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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ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity

Diabetes (New York, N.Y.), 2006-02, Vol.55 (2), p.545-550

2006

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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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Long-Term Follow-Up of Oral Glucose Tolerance Test-Derived Glucose Tolerance and Insulin Secretion and Insulin Sensitivity Indexes in Subjects With Glucokinase Mutations (MODY2)

Diabetes care, 2008-07, Vol.31 (7), p.1321-1323

2008

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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 mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Nature (London), 1998-03, Vol.392 (6674), p.398-401

1998

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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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Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in French Caucasians

Diabetes (New York, N.Y.), 2006-10, Vol.55 (10), p.2876-2882

2006

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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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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

TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups : a global meta-analysis

Prevalence of Melanocortin-4 Receptor Deficiency in Europeans and Their Age-Dependent Penetrance in Multigenerational Pedigrees

The Common P446L Polymorphism in GCKR Inversely Modulates Fasting Glucose and Triglyceride Levels and Reduces Type 2 Diabetes Risk in the DESIR Prospective General French Population

Insulin Gene Mutations Resulting in Early-Onset Diabetes: Marked Differences in Clinical Presentation, Metabolic Status, and Pathogenic Effect Through Endoplasmic Reticulum Retention

Genetics of obesity and the prediction of risk for health

Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study

Common Genetic Variation Near Melatonin Receptor MTNR1B Contributes to Raised Plasma Glucose and Increased Risk of Type 2 Diabetes Among Indian Asians and European Caucasians

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

Combined effects of MC4R and FTO common genetic variants on obesity in European general populations

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

Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations

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

ACDC/Adiponectin Polymorphisms Are Associated With Severe Childhood and Adult Obesity

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

Long-Term Follow-Up of Oral Glucose Tolerance Test-Derived Glucose Tolerance and Insulin Secretion and Insulin Sensitivity Indexes in Subjects With Glucokinase Mutations (MODY2)

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 mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

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

Bardet-Biedl Syndrome Gene Variants Are Associated With Both Childhood and Adult Common Obesity in French Caucasians

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

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