Delepine M - Search Results

1

Multiple DNA variant association analysis: application to the insulin gene region in type I diabetes.

Julier C, Lucassen A, Villedieu P, Delepine M, Levy-Marchal C, Danzé PM, Bianchi F, Boitard C, Froguel P, Bell J, et al. Julier C, et al. Among authors: delepine m. Am J Hum Genet. 1994 Dec;55(6):1247-54. Am J Hum Genet. 1994. PMID: 7977386 Free PMC article.

2

Evidence of a non-MHC susceptibility locus in type I diabetes linked to HLA on chromosome 6.

Delépine M, Pociot F, Habita C, Hashimoto L, Froguel P, Rotter J, Cambon-Thomsen A, Deschamps I, Djoulah S, Weissenbach J, Nerup J, Lathrop M, Julier C. Delépine M, et al. Am J Hum Genet. 1997 Jan;60(1):174-87. Am J Hum Genet. 1997. PMID: 8981961 Free PMC article.

3

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

Julier C, Delépine M, Keavney B, Terwilliger J, Davis S, Weeks DE, Bui T, Jeunemaître X, Velho G, Froguel P, Ratcliffe P, Corvol P, Soubrier F, Lathrop GM. Julier C, et al. Among authors: delepine m. Hum Mol Genet. 1997 Nov;6(12):2077-85. doi: 10.1093/hmg/6.12.2077. Hum Mol Genet. 1997. PMID: 9328471

4

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon.

Zalloua PA, Azar ST, Delépine M, Makhoul NJ, Blanc H, Sanyoura M, Lavergne A, Stankov K, Lemainque A, Baz P, Julier C. Zalloua PA, et al. Among authors: delepine m. Hum Mol Genet. 2008 Dec 15;17(24):4012-21. doi: 10.1093/hmg/ddn304. Epub 2008 Sep 20. Hum Mol Genet. 2008. PMID: 18806274

5

EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome.

Delépine M, Nicolino M, Barrett T, Golamaully M, Lathrop GM, Julier C. Delépine M, et al. Nat Genet. 2000 Aug;25(4):406-9. doi: 10.1038/78085. Nat Genet. 2000. PMID: 10932183

6

Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.

Senée V, Vattem KM, Delépine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC, Julier C. Senée V, et al. Among authors: delepine m. Diabetes. 2004 Jul;53(7):1876-83. doi: 10.2337/diabetes.53.7.1876. Diabetes. 2004. PMID: 15220213

7

Genetic mapping of a susceptibility locus for insulin-dependent diabetes mellitus on chromosome 11q.

Hashimoto L, Habita C, Beressi JP, Delepine M, Besse C, Cambon-Thomsen A, Deschamps I, Rotter JI, Djoulah S, James MR, et al. Hashimoto L, et al. Among authors: delepine m. Nature. 1994 Sep 8;371(6493):161-4. doi: 10.1038/371161a0. Nature. 1994. PMID: 8072544

8

Genetic analysis of chromosome 2 in type 1 diabetes: analysis of putative loci IDDM7, IDDM12, and IDDM13 and candidate genes NRAMP1 and IA-2 and the interleukin-1 gene cluster. IMDIAB Group.

Esposito L, Hill NJ, Pritchard LE, Cucca F, Muxworthy C, Merriman ME, Wilson A, Julier C, Delepine M, Tuomilehto J, Tuomilehto-Wolf E, Ionesco-Tirgoviste C, Nistico' L, Buzzetti R, Pozzilli P, Ferrari M, Bosi E, Pociot F, Nerup J, Bain SC, Todd JA. Esposito L, et al. Among authors: delepine m. Diabetes. 1998 Nov;47(11):1797-9. doi: 10.2337/diabetes.47.11.1797. Diabetes. 1998. PMID: 9792551 No abstract available.

9

Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus.

de Wit MC, de Coo IF, Julier C, Delépine M, Lequin MH, van de Laar I, Sibbles BJ, Bruining GJ, Mancini GM. de Wit MC, et al. Among authors: delepine m. Neurogenetics. 2006 Nov;7(4):259-63. doi: 10.1007/s10048-006-0061-1. Epub 2006 Sep 14. Neurogenetics. 2006. PMID: 16972080

10

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

Magré J, Delépine M, Khallouf E, Gedde-Dahl T Jr, Van Maldergem L, Sobel E, Papp J, Meier M, Mégarbané A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon-Chevalier A, Polak M, Robert JJ, Tric P, Tubiana-Rufi N, Vigouroux C, Weissenbach J, Savasta S, Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J; BSCL Working Group. Magré J, et al. Among authors: delepine m. Nat Genet. 2001 Aug;28(4):365-70. doi: 10.1038/ng585. Nat Genet. 2001. PMID: 11479539

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