V. Vatin

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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

Tanya M. Teslovich, Ayellet V. Segrè, P. Elliott, 2010 .

Positional candidate gene analysis of Lim domain homeobox gene (Isl-1) on chromosome 5q11-q13 in a French morbidly obese population suggests indication for association with type 2 diabetes.

K. Clément, C. Dina, P. Froguel, 2002, Diabetes.

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

Barbara Heude, Jean Tichet, Beverley Balkau, 2009, Nature Genetics.

Differential co-expression analysis of obesity-associated networks in human subcutaneous adipose tissue

S. Richardson, S. Richardson, L. Bottolo, 2011, International Journal of Obesity.

Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index

Henrik, Tanya M. Teslovich, Jennie, 2012 .

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

Raimund Erbel, Barbara Heude, Mark I. McCarthy, 2010, PLoS genetics.

Contribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications

D. Meyre, P. Froguel, K. Linton, 2019, Scientific Reports.

Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene.

F. Horber, B. Balkau, D. Meyre, 2007, Human molecular genetics.

Estimation of Newborn Risk for Child or Adolescent Obesity: Lessons from Longitudinal Birth Cohorts

Philippe Froguel, David Meyre, Ken Kleinman, 2012, PloS one.

The Imprinted Gene Neuronatin Is Regulated by Metabolic Status and Associated With Obesity

P. J. Larsen, D. Meyre, H. Deng, 2010, Obesity.

Proposal for Standardization of Optimized Mycobacterial Interspersed Repetitive Unit-Variable-Number Tandem Repeat Typing of Mycobacterium tuberculosis

Nalin Rastogi, Stefan Niemann, Philip Supply, 2006, Journal of Clinical Microbiology.

Genome-Wide Search for Type 2 Diabetes in Japanese Affected Sib-Pairs Confirms Susceptibility Genes on 3 q , 15 q , and 20 q and Identifies Two New Candidate Loci on 7 p and 11 p

C. Dina, P. Boutin, P. Froguel, 2002 .

Genetic analysis of ADIPOR1 and ADIPOR2 candidate polymorphisms for type 2 diabetes in the Caucasian population.

C. Dina, P. Boutin, G. Charpentier, 2006, Diabetes.

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

S. O’Rahilly, F. Horber, C. Dina, 2008, Diabetes.

Variation in FTO contributes to childhood obesity and severe adult obesity

Beverley Balkau, Philippe Froguel, Sophie Gallina, 2007, Nature Genetics.

INS VNTR Is Not Associated With Childhood Obesity in 1,023 Families: A Family‐based Study

B. Heude, D. Meyre, P. Froguel, 2008, Obesity.

Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population.

B. Lyoussi, D. Meyre, Y. El achhab, 2009, Diabetes & metabolism.

Study of TNFalpha -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population.

D. Meyre, P. Froguel, M. Vaxillaire, 2010, Clinical biochemistry.

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2

P. Elliott, M. Jarvelin, L. Coin, 2009, Nature.

Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue

L. Bottolo, E. Petretto, M. Petteni, 2018 .

Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population

C. Bogardus, B. Heude, D. Meyre, 2010, Obesity.

Genetic study of the CD36 gene in a French diabetic population.

C. Dina, P. Froguel, M. Chikri, 2004, Diabetes & metabolism.

Genetic studies of the leptin receptor gene in morbidly obese French Caucasian families

K. Clément, P. Behn, M. Permutt, 1997, Human Genetics.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2010, Nature Genetics.

Genome-wide search for type 2 diabetes in Japanese affected sib-pairs confirms susceptibility genes on 3q, 15q, and 20q and identifies two new candidate Loci on 7p and 11p.

C. Dina, P. Boutin, P. Froguel, 2002, Diabetes.

Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene

I. Fajardy, A. Vambergue, B. Balkau, 2012, PloS one.

A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature

B. Heude, D. Meyre, C. Mein, 2009, Annals of human genetics.

A Central Role for GRB10 in Regulation of Islet Function in Man

Mark I. McCarthy, Philippe Froguel, Jeffrey R. O'Connell, 2014, PLoS genetics.

A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10

K. Clément, C. Dina, P. Froguel, 1998, Nature Genetics.

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.

Beverley Balkau, Philippe Froguel, David Meyre, 2013, The Journal of clinical investigation.

A POMC variant implicates beta-melanocyte-stimulating hormone in the control of human energy balance.

S. O’Rahilly, D. Meyre, P. Froguel, 2006, Cell metabolism.

Analysis of sequence variability in the CART gene in relation to obesity in a Caucasian population

K. Clément, F. Horber, C. Dina, 2005, BMC Genetics.

Genetic evidence of assortative mating in humans

Tanya M. Teslovich, Ross M. Fraser, Brendan P. Zietsch, 2017, Nature Human Behaviour.

Short Technical Repor t Rapid SNP Allele Frequency Determination in Genomic DNA Pools by Pyrosequencin g

P. Boutin, P. Froguel, V. Vatin, 2002 .

Loss‐of‐Function Mutations in MC4R Are Very Rare in the Greek Severely Obese Adult Population

D. Meyre, P. Froguel, M. Marchand, 2012, Obesity.

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

D. Meyre, P. Froguel, S. Lobbens, 2012, Obesity.

Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity

P. Elliott, M. Jarvelin, F. Horber, 2012, Diabetes.

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

S. O’Rahilly, F. Horber, B. Balkau, 2009, Diabetes.

Effect of ENPP1/PC-1-K121Q and PPARgamma-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population.

D. Meyre, P. Froguel, M. Vaxillaire, 2008, Diabetes research and clinical practice.

Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

K. Clément, C. Dina, P. Boutin, 2005, Nature Genetics.

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

C. Dina, D. Meyre, P. Froguel, 2004, Diabetes.

A Genome-Wide Scan for Childhood Obesity – Associated Traits in French Families Shows Significant Linkage on Chromosome 6 q 22 . 31-q 23 . 2

C. Dina, D. Meyre, P. Froguel, 2004 .

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Thomas Meitinger, Inês Barroso, Peter Kraft, 2011, Nature Genetics.

Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing.

P. Boutin, P. Froguel, V. Vatin, 2002, BioTechniques.

A Rare Variant in the Visfatin Gene (NAMPT/PBEF1) Is Associated With Protection From Obesity

B. Balkau, D. Meyre, P. Froguel, 2009, Obesity.

Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity

B. Heude, D. Meyre, P. Froguel, 2009, Obesity.

Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1

P. Froguel, M. Vaxillaire, V. Vatin, 2005, Human Genetics.

Genetic study of the melanin-concentrating hormone receptor 2 in childhood and adulthood severe obesity.

B. Heude, D. Meyre, P. Froguel, 2007, The Journal of clinical endocrinology and metabolism.

Assessment of an Optimized Mycobacterial Interspersed Repetitive- Unit-Variable-Number Tandem-Repeat Typing System Combined with Spoligotyping for Population-Based Molecular Epidemiology Studies of Tuberculosis

Stefan Niemann, Philip Supply, Walter Haas, 2006, Journal of Clinical Microbiology.

Bmc Medical Genetics Secretory Granule Neuroendocrine Protein 1 (sgne1) Genetic Variation and Glucose Intolerance in Severe Childhood and Adult Obesity

B. Balkau, B. Heude, G. Charpentier, 2007 .

Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index

Henrik, Tanya M. Teslovich, Jennie, 2012 .

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Tanya M. Teslovich, P. Elliott, M. Jarvelin, 2011, Nature Genetics.

ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study

B. Balkau, D. Meyre, P. Froguel, 2007, Diabetologia.

Association analyses of 249 , 796 individuals reveal 18 new loci associated with body mass index

Tanya M. Teslovich, Eric, P. Elliott, 2012 .

A novel highly-penetrant form of obesity due to microdeletions on chromosome 16p11.2

P. Elliott, M. Jarvelin, L. Coin, 2009, Nature.

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

Tanya M. Teslovich, P. Elliott, M. Jarvelin, 2010, Nature Genetics.

Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index

Tanya M. Teslovich, M. Jarvelin, L. Coin, 2010, Nature genetics.

Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity

B. Heude, D. Meyre, P. Froguel, 2009, Obesity.

The Q121 Variant of ENPP1 May Protect From Childhood Overweight/obesity in the Italian Population

D. Meyre, P. Froguel, V. Vatin, 2009, Obesity.