434 articles – 313 Notices  [english version]
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fulltext access On the use of sibling recurrence risks to select environmental factors liable to interact with genetic risk factors.
Kazma R., Bonaïti-Pellié C., Norris J. M., Génin E.
Eur J Hum Genet 18, 1 (2010) 88-94 [inserm-00446027 - version 1]
ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study.
Meyre D., Bouatia-Naji N., Vatin V., Veslot J., Samson C., Tichet J., Marre M., Balkau B., Froguel P.
Diabetologia / Diabetologica 50, 10 (2007) 2090-6 [hal-00172953 - version 1]
Analysis of KLF transcription factor family gene variants in type 2 diabetes.
Gutierrez-Aguilar R., Benmezroua Y., Vaillant E., Balkau B., Marre M., Charpentier G., Sladek R., Froguel P., Neve B.
BMC Medicine Genet 8, 1 (2007) 53 [hal-00172970 - version 1]
Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene.
Stutzmann F., Vatin V., Cauchi S., Morandi A., Jouret B., Landt O., Tounian P., Levy-Marchal C., Buzzetti R., Pinelli L. et al
Human Molecular Genetics 16, 15 (2007) 1837-44 [hal-00172976 - version 1]
Variation in FTO contributes to childhood obesity and severe adult obesity.
Dina C., Meyre D., Gallina S., Durand E., Körner A., Jacobson P., Carlsson L. M. S., Kiess W., Vatin V., Lecoeur C. et al
Nature Genetics 39, 6 (2007) 724-6 [hal-00173651 - version 1]
No contribution of angiotensin-converting enzyme (ACE) gene variants to severe obesity: a model for comprehensive case/control and quantitative cladistic analysis of ACE in human diseases.
Bell C. G., Meyre D., Petretto E., Levy-Marchal C., Hercberg S., Charles M.-A., Boyle C., Weill J., Tauber M., Mein C. A. et al
European Journal of Human Genetics 15, 3 (2007) 320-7 [hal-00173842 - version 1]
Single nucleotide polymorphisms in the neuropeptide Y2 receptor (NPY2R) gene and association with severe obesity in French white subjects.
Siddiq A., Gueorguiev M., Samson C., Hercberg S., Heude B., Levy-Marchal C., Jouret B., Weill J., Meyre D., Walley A. et al
Diabetologia / Diabetologica 50, 3 (2007) 574-84 [hal-00173827 - version 1]
A genome-wide association study identifies novel risk loci for type 2 diabetes.
Sladek R., Rocheleau G., Rung J., Dina C., Shen L., Serre D., Boutin P., Vincent D., Belisle A., Hadjadj S. et al
Nature 445, 7130 (2007) 881-5 [hal-00173692 - version 1]
Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity.
Bouatia-Naji N., Vatin V., Lecoeur C., Heude B., Proença C., Veslot J., Jouret B., Tichet J., Charpentier G., Marre M. et al
BMC Medicine Genet 8 (2007) 44 [hal-00173645 - version 1]
Bardet-Biedl syndrome gene variants are associated with both childhood and adult common obesity in French Caucasians.
Benzinou M., Walley A., Lobbens S., Charles M.-A., Jouret B., Fumeron F., Balkau B., Meyre D., Froguel P.
Diabetes 55, 10 (2006) 2876-82 [hal-00174354 - version 1]