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Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

Nature genetics, 2009-02, Vol.41 (2), p.157-159

2009

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A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

Nature genetics, 2009-01, Vol.41 (1), p.89-94

2009

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Variation in FTO contributes to childhood obesity and severe adult obesity

Nature genetics, 2007-06, Vol.39 (6), p.724-726

2007

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R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population

Human molecular genetics, 2008-06, Vol.17 (12), p.1798-1802

2008

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Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Human molecular genetics, 2008-07, Vol.17 (13), p.1916-1921

2008

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Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene

PloS one, 2012-06, Vol.7 (6), p.e37423-e37423

2012

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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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Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome

PloS one, 2010-10, Vol.5 (10), p.e13630-e13630

2010

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Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

PLoS genetics, 2010-04, Vol.6 (4), p.e1000916-e1000916

2010

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TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment

Brain (London, England : 1878), 2014-10, Vol.137 (Pt 10), p.2657-2663

2014

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Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population

Obesity (Silver Spring, Md.), 2012-02, Vol.20 (2), p.389-395

2012

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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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Type 2 Diabetes Whole-Genome Association Study in Four Populations: The DiaGen Consortium

American journal of human genetics, 2007-08, Vol.81 (2), p.338-345

2007

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Tissue Distribution and Evolution of Fructosamine 3-Kinase and Fructosamine 3-Kinase-related Protein

The Journal of biological chemistry, 2004-11, Vol.279 (45), p.46606-46613

2004

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The gene MAPK8IP1 , encoding islet-brain-1, is a candidate for type 2 diabetes

Nature genetics, 2000-03, Vol.24 (3), p.291-295

2000

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Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Nature genetics, 2010-02, Vol.42 (2), p.142-148

2010

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Tryptophan metabolism activation by indoleamine 2,3-dioxygenase in adipose tissue of obese women: an attempt to maintain immune homeostasis and vascular tone

American journal of physiology. Regulatory, integrative and comparative physiology, 2012-07, Vol.303 (2), p.R135-R143

2012

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A Rare Variant in the Visfatin Gene ( ) Is Associated With Protection From Obesity

Obesity (Silver Spring, Md.), 2009-08, Vol.17 (8), p.1549-1553

2009

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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Human molecular genetics, 2002-08, Vol.11 (17), p.1997-2004

2002

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Variation in FTO contributes to childhood obesity and severe adult obesity

Nature genetics, 2007, Vol.39 (6), p.726-728

2007

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New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Nature genetics, 2010-05, Vol.42 (5), p.464

2010

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Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups: e1000916

PLoS genetics, 2010-04, Vol.6 (4)

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.803-11

2004

Volltextzugriff (PDF)

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Human molecular genetics, 2002-08, Vol.11 (17), p.1997-2004

2002

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Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations

A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk

Variation in FTO contributes to childhood obesity and severe adult obesity

R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene

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

Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value

TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment

Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population

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

Type 2 Diabetes Whole-Genome Association Study in Four Populations: The DiaGen Consortium

Tissue Distribution and Evolution of Fructosamine 3-Kinase and Fructosamine 3-Kinase-related Protein

The gene MAPK8IP1 , encoding islet-brain-1, is a candidate for type 2 diabetes

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Tryptophan metabolism activation by indoleamine 2,3-dioxygenase in adipose tissue of obese women: an attempt to maintain immune homeostasis and vascular tone

A Rare Variant in the Visfatin Gene ( ) Is Associated With Protection From Obesity

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Variation in FTO contributes to childhood obesity and severe adult obesity

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study Groups: e1000916

A genome-wide scan for childhood obesity-associated traits in French families shows significant linkage on chromosome 6q22.31-q23.2

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

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