Delplanque J - Search Results

1

Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians.

Veiga-da-Cunha M, Delplanque J, Gillain A, Bonthron DT, Boutin P, Van Schaftingen E, Froguel P. Veiga-da-Cunha M, et al. Among authors: delplanque j. Diabetologia. 2003 May;46(5):704-11. doi: 10.1007/s00125-003-1083-y. Epub 2003 May 9. Diabetologia. 2003. PMID: 12739015

2

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

Delplanque J, Barat-Houari M, Dina C, Gallina P, Clément K, Guy-Grand B, Vasseur F, Boutin P, Froguel P. Delplanque J, et al. Diabetologia. 2000 Dec;43(12):1554-7. doi: 10.1007/s001250051568. Diabetologia. 2000. PMID: 11151766

3

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

Delplanque J, Vasseur F, Durand E, Abderrahmani A, Dina C, Waeber G, Guy-Grand B, Clement K, Weill J, Boutin P, Froguel P. Delplanque J, et al. J Clin Endocrinol Metab. 2002 Feb;87(2):867-9. doi: 10.1210/jcem.87.2.8259. J Clin Endocrinol Metab. 2002. PMID: 11836334

4

Tissue distribution and evolution of fructosamine 3-kinase and fructosamine 3-kinase-related protein.

Delplanque J, Delpierre G, Opperdoes FR, Van Schaftingen E. Delplanque J, et al. J Biol Chem. 2004 Nov 5;279(45):46606-13. doi: 10.1074/jbc.M407678200. Epub 2004 Aug 25. J Biol Chem. 2004. PMID: 15331600 Free article.

5

Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease.

Helbecque N, Abderrahamani A, Meylan L, Riederer B, Mooser V, Miklossy J, Delplanque J, Boutin P, Nicod P, Haefliger JA, Cottel D, Amouyel P, Froguel P, Waeber G. Helbecque N, et al. Among authors: delplanque j. Mol Psychiatry. 2003 Apr;8(4):413-22, 363. doi: 10.1038/sj.mp.4001344. Mol Psychiatry. 2003. PMID: 12740599

6

Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population.

Durand E, Lecoeur C, Delplanque J, Benzinou M, Degraeve F, Boutin P, Marre M, Balkau B, Charpentier G, Froguel P, Meyre D. Durand E, et al. Among authors: delplanque j. Obes Facts. 2008;1(6):305-9. doi: 10.1159/000178157. Epub 2008 Dec 12. Obes Facts. 2008. PMID: 20054193 Free PMC article.

7

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.

Philippe J, Stijnen P, Meyre D, De Graeve F, Thuillier D, Delplanque J, Gyapay G, Sand O, Creemers JW, Froguel P, Bonnefond A. Philippe J, et al. Among authors: delplanque j. Int J Obes (Lond). 2015 Feb;39(2):295-302. doi: 10.1038/ijo.2014.96. Epub 2014 Jun 3. Int J Obes (Lond). 2015. PMID: 24890885

8

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

Waeber G, Delplanque J, Bonny C, Mooser V, Steinmann M, Widmann C, Maillard A, Miklossy J, Dina C, Hani EH, Vionnet N, Nicod P, Boutin P, Froguel P. Waeber G, et al. Among authors: delplanque j. Nat Genet. 2000 Mar;24(3):291-5. doi: 10.1038/73523. Nat Genet. 2000. PMID: 10700186

9

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

Meyre D, Lecoeur C, Delplanque J, Francke S, Vatin V, Durand E, Weill J, Dina C, Froguel P. Meyre D, et al. Among authors: delplanque j. Diabetes. 2004 Mar;53(3):803-11. doi: 10.2337/diabetes.53.3.803. Diabetes. 2004. PMID: 14988267

10

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

Meyre D, Farge M, Lecoeur C, Proenca C, Durand E, Allegaert F, Tichet J, Marre M, Balkau B, Weill J, Delplanque J, Froguel P. Meyre D, et al. Among authors: delplanque j. Hum Mol Genet. 2008 Jun 15;17(12):1798-802. doi: 10.1093/hmg/ddn070. Epub 2008 Mar 5. Hum Mol Genet. 2008. PMID: 18325908

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