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Rapid SNP allele frequency determination in genomic DNA pools by pyrosequencing

Philippe Froguel
Biotechniques, 2002, 35, pp.1138-1142
Journal articles hal-00093655v1

Identification of two missense mutations in glucokinase linked to early-onset non-insulin-dependent diabetes mellitus

M. Stoffel , Ph. Froguel , J. Takeda , H. Zouali , N. Vionnet et al.
Proceedings of the National Academy of Sciences of the United States of America, 1992, 89, pp.7698-7702
Journal articles hal-00094195v1

Common Polymorphisms In The Adiponectin Gene Acdc Are Not Associated Withdiabetes In Pima Indians.

De Courten Bv , Hanson Rl , T. Funahashi , Lindsay Rs , Y. Matsuzawa et al.
Diabetes, 2005, 54, pp.284-289
Journal articles hal-00094168v1

Lack of association between the Pro(12)Ala polymorphism of the PPAR-gamma2 gene and type 2 diabetes mellitus in the Qatari consanguineous population.

Ramin Badii , Abdulbari Bener , Mahmoud Zirie , Ammar Al-Rikabi , Mehmet Simsek et al.
Acta Diabetologica, 2007, epub ahead of print. ⟨10.1007/s00592-007-0013-8⟩
Journal articles hal-00172941v1

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

Benjamin G Challis , Lynn E Pritchard , John W M Creemers , Jerome Delplanque , Julia M Keogh et al.
Human Molecular Genetics, 2002, 11 (17), pp.1997-2004
Journal articles hal-00174706v1

Expanding the cardiac spectrum of Noonan syndrome with RIT1 variant: Left main coronary artery atresia causing sudden death

Francis Ramond , Sébastien Duband , Pierre Croisille , Hélène Cavé , Georges Teyssier et al.
European Journal of Medical Genetics, 2017, 60 (6), pp.299-302. ⟨10.1016/j.ejmg.2017.03.009⟩
Journal articles hal-02071037v1

A CD36 nonsense mutation associated with insulin resistance and familial type 2 diabetes.

F. Lepretre , F. Vasseur , M. Vaxillaire , Scherer Pe , S. Ali et al.
Human Mutation, 2004, 24, pp.104
Journal articles hal-00094124v1

In vivo calibration of a subcutaneous sensor for determination of subcutaneous glucose kinetics

G. Velho , P. Froguel , Daniel R. Thevenot , G. Reach
Diab., Nutr. Metab, 1988, 1, pp.227-233
Journal articles hal-00094172v1

No evidence of linkage or diabetes-associated mutations in the transcription factors BETA2/NEUROD1 and PAX4 in Type II diabetes in France

Samuel Dupont , N. Vionnet , C. Chèvre , Sophie Gallina , C. Dina et al.
Diabetologia, 1999, 42 (4), pp.480 - 484. ⟨10.1007/s001250051182⟩
Journal articles hal-01655342v1
Image document

Le récepteur 4 aux mélanocortines, un paradigme de la génétique de l'obésité

Fanny Stutzmann
Sciences du Vivant [q-bio]. Université du Droit et de la Santé - Lille II, 2009. Français. ⟨NNT : ⟩
Theses tel-00422165v1

Preadipocyte response and impairment of differentiation in an inflammatory environment.

Odile Poulain-Godefroy , Philippe Froguel
Biochemical and Biophysical Research Communications, 2007, 356 (3), pp.662-7. ⟨10.1016/j.bbrc.2007.03.053⟩
Journal articles istex hal-00173683v1

Adiponectin gene polymorphisms and adiponectin levels are independently associated with the development of hyperglycemia during a 3-year period: the epidemiologic data on the insulin resistance syndrome prospective study.

Frédéric Fumeron , Roberte Aubert , Afshan Siddiq , Dina Betoulle , Frank Péan et al.
Diabetes, 2004, 53 (4), pp.1150-7. ⟨10.2337/diabetes.53.4.1150⟩
Journal articles hal-00174545v1

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

Fanny Stutzmann , Vincent Vatin , Stéphane Cauchi , Anita Morandi , Béatrice Jouret et al.
Human Molecular Genetics, 2007, 16 (15), pp.1837-44. ⟨10.1093/hmg/ddm132⟩
Journal articles hal-00172976v1

Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses.

Tetsuo Tsuchiya , Schwarz Pe , Bosque-Plata Ld , Geoffrey Hayes M , C. Dina et al.
Mol Genet Metab, 2006, 89, pp.174-84
Journal articles hal-00093643v1

Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.

Nabila Bouatia-Naji , Vincent Vatin , Cécile Lecoeur , Barbara Heude , Christine Proença et al.
BMC Medical Genetics, 2007, 8, pp.44. ⟨10.1186/1471-2350-8-44⟩
Journal articles hal-00173645v1

Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French Caucasians.

Fernando Gibson , Serge Hercberg , Philippe Froguel
Diabetes, 2005, 54 (10), pp.3040-2
Journal articles hal-00174470v1

[ENPP1, the first example of common genetic link between childhood and adult obesity and type 2 diabetes]

David Meyre , Philippe Froguel
médecine/sciences, 2006, 22 (3), pp.308-12
Journal articles hal-00174458v1

Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France.

M. Vaxillaire , C. Samson , H. Cavé , C. Metz , P. Froguel et al.
Diabetologia, 2002, 45 (3), pp.454-5. ⟨10.1007/s00125-001-0741-1⟩
Journal articles hal-00174747v1

Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in caucasian families.

J. Delplanque , M. Barat-Houari , C. Dina , P. Gallina , K. Clément et al.
Diabetologia, 2000, 43 (12), pp.1554-7
Journal articles hal-00174921v1

Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects.

A. Siddiq , M. Gueorguiev , C. Samson , S. Hercberg , Barbara Heude et al.
Diabetologia, 2007, 50 (3), pp.574-84. ⟨10.1007/s00125-006-0555-2⟩
Journal articles hal-00173827v1

No major contribution of TCF7L2 sequence variants to maturity onset of diabetes of the young (MODY) or neonatal diabetes mellitus in French white subjects.

S. Cauchi , M. Vaxillaire , H. Choquet , E. Durand , A. Duval et al.
Diabetologia, 2007, 50 (1), pp.214-6. ⟨10.1007/s00125-006-0505-z⟩
Journal articles hal-00126948v1

Role of the DGAT gene C79T single-nucleotide polymorphism in French obese subjects.

Sylvie Kipfer Coudreau , Patrick Tounian , Geneviève Bonhomme , Philippe Froguel , Jean-Philippe Girardet et al.
Obesity Research, 2003, 11 (10), pp.1163-7
Journal articles hal-00174573v1

Understanding the rising incidence of type 2 diabetes in adolescence.

J. Weill , S. Vanderbecken , P. Froguel
Archives of Disease in Childhood, 2004, 89 (6), pp.502-4
Journal articles hal-00174531v1

Hypoadiponectinaemia and high risk of type 2 diabetes are associated with adiponectin-encoding (ACDC) gene promoter variants in morbid obesity: evidence for a role of ACDC in diabesity.

F. Vasseur , N. Helbecque , S. Lobbens , V. Vasseur-Delannoy , C. Dina et al.
Diabetologia, 2005, 48 (5), pp.892-9. ⟨10.1007/s00125-005-1729-z⟩
Journal articles hal-00174484v1

Unexpected genetic associations with human longevity at the Apo E and ACE loci

F. Schachter , L. Faure-Delanef , H. Rouger , F. Guenot , Ph. Froguel et al.
Nature Genetics, 1994, 6, pp.29-32
Journal articles hal-00094419v1

Genetic variation in the gene encoding adiponectin is associated with an increased risk of type 2 diabetes in the Japanese population

Philippe Froguel
Diabetes, 2002, 51, pp.536-540
Journal articles hal-00093667v1

Mutation screening of the urocortin gene: identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians

Philippe Froguel
Journal of Clinical Endocrinology and Metabolism, 2002, 87, pp.867-869
Journal articles hal-00093661v1

Two Taq 1 RFLPs at the Glut-2 locus in French Caucasian population

Ph. Froguel , N. Vionnet , S. Lesage , D. Cohen
Nucleic Acids Research, 1991, 19, pp.5799
Journal articles hal-00094186v1

EIF4A2 Is a Positional Candidate Gene at the 3q27 Locus Linked to Type 2 Diabetes in French Families

C. Cheyssac , C. Dina , F. Lepretre , V. Vasseur-Delannoy , A. Dechaume et al.
Diabetes, 2006, 55, pp.1171-6
Journal articles hal-00093807v1

A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children

Philippe Froguel
Journal of Clinical Endocrinology and Metabolism, 2002, 87, pp.4005-4008
Journal articles hal-00093604v1