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    Results: 1 to 50 of 113

    1.

    The Type I Diabetes Genetics Consortium 'Rapid Response' family-based candidate gene study: strategy, genes selection, and main outcome.

    Julier C, Akolkar B, Concannon P, Morahan G, Nierras C, Pugliese A; the Type I Diabetes Genetics Consortium.

    Genes Immun. 2009 Dec;10(s1):S121-S127.PMID: 19956109 [PubMed - as supplied by publisher]Related articles

    2.

    Evaluation of IL12B as a candidate type I diabetes susceptibility gene using data from the Type I Diabetes Genetics Consortium.

    Morahan G, McKinnon E, Berry J, Browning B, Julier C, Pociot F, James I.

    Genes Immun. 2009 Dec;10(S1):S64-S68.PMID: 19956104 [PubMed - as supplied by publisher]Related articles

    3.

    Evidence for association of the TCF7 locus with type I diabetes.

    Erlich HA, Valdes AM, Julier C, Mirel D, Noble JA.

    Genes Immun. 2009 Dec;10(S1):S54-S59.PMID: 19956102 [PubMed - as supplied by publisher]Related articles

    4.

    Association analysis of SNPs in the IL4R locus with type I diabetes.

    Erlich HA, Lohman K, Mack SJ, Valdes AM, Julier C, Mirel D, Noble JA, Morahan GE, Rich SS; for the Type I Diabetes Genetics Consortium.

    Genes Immun. 2009 Dec;10(S1):S33-S41.PMID: 19956098 [PubMed - as supplied by publisher]Related articles

    5.

    rs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.

    Steck AK, Baschal EE, Jasinski JM, Boehm BO, Bottini N, Concannon P, Julier C, Morahan G, Noble JA, Polychronakos C, She JX, Eisenbarth GS.

    Genes Immun. 2009 Dec;10(S1):S21-S26.PMID: 19956096 [PubMed - as supplied by publisher]Related articles

    6.

    Current status and the future for the genetics of type I diabetes.

    Rich SS, Akolkar B, Concannon P, Erlich H, Hilner JE, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA.

    Genes Immun. 2009 Dec;10(S1):S128-S131.PMID: 19956094 [PubMed - as supplied by publisher]Related articles

    7.

    Overview of the Type I Diabetes Genetics Consortium.

    Rich SS, Akolkar B, Concannon P, Erlich H, Hilner JE, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA.

    Genes Immun. 2009 Dec;10(S1):S1-S4.PMID: 19956093 [PubMed - as supplied by publisher]Related articles

    8.

    Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.

    Barrett JC, Clayton DG, Concannon P, Akolkar B, Cooper JD, Erlich HA, Julier C, Morahan G, Nerup J, Nierras C, Plagnol V, Pociot F, Schuilenburg H, Smyth DJ, Stevens H, Todd JA, Walker NM, Rich SS; The Type 1 Diabetes Genetics Consortium.

    Nat Genet. 2009 May 10. [Epub ahead of print]PMID: 19430480 [PubMed - as supplied by publisher]Related articles

    9.

    Results of the MHC fine mapping workshop.

    Rich SS, Akolkar B, Concannon P, Erlich H, Hilner J, Julier C, Morahan G, Nerup J, Nierras C, Pociot F, Todd JA.

    Diabetes Obes Metab. 2009 Feb;11 Suppl 1:108-9. No abstract available. PMID: 19143823 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Genome-wide scan for linkage to type 1 diabetes in 2,496 multiplex families from the Type 1 Diabetes Genetics Consortium.

    Concannon P, Chen WM, Julier C, Morahan G, Akolkar B, Erlich HA, Hilner JE, Nerup J, Nierras C, Pociot F, Todd JA, Rich SS; Type 1 Diabetes Genetics Consortium.

    Diabetes. 2009 Apr;58(4):1018-22. Epub 2009 Jan 9.PMID: 19136655 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    The large form of human 2',5'-Oligoadenylate Synthetase (OAS3) exerts antiviral effect against Chikungunya virus.

    Bréhin AC, Casadémont I, Frenkiel MP, Julier C, Sakuntabhai A, Desprès P.

    Virology. 2009 Feb 5;384(1):216-22. Epub 2008 Dec 3.PMID: 19056102 [PubMed - indexed for MEDLINE]Related articles

    12.

    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.

    Hum Mol Genet. 2008 Dec 15;17(24):4012-21. Epub 2008 Sep 20.PMID: 18806274 [PubMed - indexed for MEDLINE]Related articles

    13.

    A human type 1 diabetes susceptibility locus maps to chromosome 21q22.3.

    Concannon P, Onengut-Gumuscu S, Todd JA, Smyth DJ, Pociot F, Bergholdt R, Akolkar B, Erlich HA, Hilner JE, Julier C, Morahan G, Nerup J, Nierras CR, Chen WM, Rich SS; Type 1 Diabetes Genetics Consortium.

    Diabetes. 2008 Oct;57(10):2858-61. Epub 2008 Jul 22.PMID: 18647951 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Genetic determination and linkage mapping of Plasmodium falciparum malaria related traits in Senegal.

    Sakuntabhai A, Ndiaye R, Casadémont I, Peerapittayamongkol C, Rogier C, Tortevoye P, Tall A, Paul R, Turbpaiboon C, Phimpraphi W, Trape JF, Spiegel A, Heath S, Mercereau-Puijalon O, Dieye A, Julier C.

    PLoS One. 2008 Apr 23;3(4):e2000. Erratum in: PLoS ONE. 2008;3(4). doi: 10.1371/annotation/d0a416fa-b683-4721-88c1-3f6dc9a04d8d. Peerapittayamonkol, Chayanon [corrected to Peerapittayamongkol, Chayanon]. PMID: 18431485 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    FCRL3 -169CT functional polymorphism in type 1 diabetes and autoimmunity traits.

    Duchatelet S, Caillat-Zucman S, Dubois-Laforgue D, Blanc H, Timsit J, Julier C.

    Biomed Pharmacother. 2008 Mar;62(3):153-7. Epub 2007 Oct 8.PMID: 17961971 [PubMed - indexed for MEDLINE]Related articles

    16.

    Severe FOXP3+ and naïve T lymphopenia in a non-IPEX form of autoimmune enteropathy combined with an immunodeficiency.

    Zuber J, Viguier M, Lemaitre F, Senée V, Patey N, Elain G, Geissmann F, Fakhouri F, Ferradini L, Julier C, Bandeira A.

    Gastroenterology. 2007 May;132(5):1694-704. Epub 2007 Feb 21.PMID: 17484867 [PubMed - indexed for MEDLINE]Related articles

    17.

    PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits.

    Chelala C, Duchatelet S, Joffret ML, Bergholdt R, Dubois-Laforgue D, Ghandil P, Pociot F, Caillat-Zucman S, Timsit J, Julier C.

    Diabetes. 2007 Feb;56(2):522-6.PMID: 17259401 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    The Type 1 Diabetes Genetics Consortium.

    Rich SS, Concannon P, Erlich H, Julier C, Morahan G, Nerup J, Pociot F, Todd JA.

    Ann N Y Acad Sci. 2006 Oct;1079:1-8. Review.PMID: 17130525 [PubMed - indexed for MEDLINE]Related articles

    19.

    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.

    Neurogenetics. 2006 Nov;7(4):259-63. Epub 2006 Sep 14.PMID: 16972080 [PubMed - indexed for MEDLINE]Related articles

    20.

    Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism.

    Senée V, Chelala C, Duchatelet S, Feng D, Blanc H, Cossec JC, Charon C, Nicolino M, Boileau P, Cavener DR, Bougnères P, Taha D, Julier C.

    Nat Genet. 2006 Jun;38(6):682-7. Epub 2006 May 21.PMID: 16715098 [PubMed - indexed for MEDLINE]Related articles

    21.

    [A variant in the CD209 (DC-SIGN) promoter is associated with severity of dengue disease]

    Desprès P, Sakuntabhai A, Julier C.

    Med Sci (Paris). 2005 Nov;21(11):905-6. French. No abstract available. PMID: 16274635 [PubMed - indexed for MEDLINE]Related articles

    22.

    Crohn's disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes.

    Ghandil P, Chelala C, Dubois-Laforgue D, Senée V, Caillat-Zucman S, Kockum I, Luthman H, Nerup J, Pociot F, Timsit J, Julier C.

    Mol Genet Metab. 2005 Nov;86(3):379-83. Epub 2005 Sep 28.PMID: 16198136 [PubMed - indexed for MEDLINE]Related articles

    23.

    Type 1 diabetes: evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.

    Concannon P, Erlich HA, Julier C, Morahan G, Nerup J, Pociot F, Todd JA, Rich SS; Type 1 Diabetes Genetics Consortium.

    Diabetes. 2005 Oct;54(10):2995-3001.PMID: 16186404 [PubMed - indexed for MEDLINE]Related articlesFree article

    24.

    Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases?

    Cadet E, Capron D, Gallet M, Omanga-Léké ML, Boutignon H, Julier C, Robson KJ, Rochette J.

    J Med Genet. 2005 May;42(5):390-5.PMID: 15863667 [PubMed - indexed for MEDLINE]Related articlesFree article

    25.

    Genetic study of ICAM1 in clinical malaria in Senegal.

    Ndiaye R, Sakuntabhai A, Casadémont I, Rogier C, Tall A, Trape JF, Spiegel A, Dieye A, Julier C.

    Tissue Antigens. 2005 May;65(5):474-80.PMID: 15853902 [PubMed - indexed for MEDLINE]Related articles

    26.

    A variant in the CD209 promoter is associated with severity of dengue disease.

    Sakuntabhai A, Turbpaiboon C, Casadémont I, Chuansumrit A, Lowhnoo T, Kajaste-Rudnitski A, Kalayanarooj SM, Tangnararatchakit K, Tangthawornchaikul N, Vasanawathana S, Chaiyaratana W, Yenchitsomanus PT, Suriyaphol P, Avirutnan P, Chokephaibulkit K, Matsuda F, Yoksan S, Jacob Y, Lathrop GM, Malasit P, Desprès P, Julier C.

    Nat Genet. 2005 May;37(5):507-13. Epub 2005 Apr 17.PMID: 15838506 [PubMed - indexed for MEDLINE]Related articles

    27.

    Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes.

    Duchatelet S, Ostergaard E, Cortes D, Lemainque A, Julier C.

    Hum Mol Genet. 2005 Jan 1;14(1):1-5. Epub 2004 Nov 3.PMID: 15525660 [PubMed - indexed for MEDLINE]Related articlesFree article

    28.

    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.

    Diabetes. 2004 Jul;53(7):1876-83.PMID: 15220213 [PubMed - indexed for MEDLINE]Related articlesFree article

    29.

    Genetic and functional evaluation of an interleukin-12 polymorphism (IDDM18) in families with type 1 diabetes.

    Bergholdt R, Ghandil P, Johannesen J, Kristiansen OP, Kockum I, Luthman H, Rønningen KS, Nerup J, Julier C, Pociot F.

    J Med Genet. 2004 Apr;41(4):e39. No abstract available. PMID: 15060115 [PubMed - indexed for MEDLINE]Related articlesFree article

    30.

    Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein.

    Vickers MA, Green FR, Terry C, Mayosi BM, Julier C, Lathrop M, Ratcliffe PJ, Watkins HC, Keavney B.

    Cardiovasc Res. 2002 Mar;53(4):1029-34.PMID: 11922913 [PubMed - indexed for MEDLINE]Related articlesFree article

    31.

    Lost in translation.

    Julier C.

    Nat Genet. 2001 Dec;29(4):358-9. No abstract available. PMID: 11726916 [PubMed - indexed for MEDLINE]Related articles

    32.

    Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE).

    McKenzie CA, Abecasis GR, Keavney B, Forrester T, Ratcliffe PJ, Julier C, Connell JM, Bennett F, McFarlane-Anderson N, Lathrop GM, Cardon LR.

    Hum Mol Genet. 2001 May 1;10(10):1077-84.PMID: 11331618 [PubMed - indexed for MEDLINE]Related articlesFree article

    33.

    [Genomics and type I diabetes]

    Julier C.

    Bull Acad Natl Med. 2000;184(7):1393-404; discussion 1404-7. Review. French. PMID: 11261246 [PubMed - indexed for MEDLINE]Related articles

    34.

    Linkage mapping for hypertension susceptibility genes.

    Kato N, Julier C.

    Curr Hypertens Rep. 1999 Feb-Mar;1(1):15-24. Review.PMID: 10981038 [PubMed - indexed for MEDLINE]Related articles

    35.

    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.

    Nat Genet. 2000 Aug;25(4):406-9.PMID: 10932183 [PubMed - indexed for MEDLINE]Related articles

    36.

    Screening for hereditary hemochromatosis.

    Rochette J, Capron D, Capron JP, Julier C.

    Am J Gastroenterol. 2000 May;95(5):1368-9. No abstract available. PMID: 10811362 [PubMed - indexed for MEDLINE]Related articles

    37.

    Screening for the GRA mutation in Jamaica.

    McKenzie CA, Keavney B, Forrester T, Julier C, Ratcliffe PJ.

    J Hum Hypertens. 2000 Feb;14(2):157-8. No abstract available. PMID: 10723126 [PubMed - indexed for MEDLINE]Related articles

    38.

    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.

    Diabetes. 1998 Nov;47(11):1797-9. No abstract available. PMID: 9792551 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Measured haplotype analysis of the angiotensin-I converting enzyme gene.

    Keavney B, McKenzie CA, Connell JM, Julier C, Ratcliffe PJ, Sobel E, Lathrop M, Farrall M.

    Hum Mol Genet. 1998 Oct;7(11):1745-51.PMID: 9736776 [PubMed - indexed for MEDLINE]Related articlesFree article

    40.

    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.

    Hum Mol Genet. 1997 Nov;6(12):2077-85.PMID: 9328471 [PubMed - indexed for MEDLINE]Related articlesFree article

    41.

    Comparative mapping of novel simple sequence repeat markers in a hypertension-related region on rat chromosome 1.

    Nabika T, Ito T, Kitada K, Serikawa T, Mashimo T, Soubrier F, Julier C, Ohno Y, Saruta T, Tanase H, Masuda J, Yamori Y, Nara Y.

    Mamm Genome. 1997 Mar;8(3):215-7. No abstract available. PMID: 9069124 [PubMed - indexed for MEDLINE]Related articles

    42.

    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.

    Am J Hum Genet. 1997 Jan;60(1):174-87.PMID: 8981961 [PubMed - indexed for MEDLINE]Related articlesFree article

    43.

    Genetics of insulin-dependent diabetes mellitus.

    Julier C, Hashimoto L, Lathrop GM.

    Curr Opin Genet Dev. 1996 Jun;6(3):354-60. Review.PMID: 8791512 [PubMed - indexed for MEDLINE]Related articles

    44.

    Contribution of genes of the major histocompatibility complex to susceptibility and disease phenotype in inflammatory bowel disease.

    Satsangi J, Welsh KI, Bunce M, Julier C, Farrant JM, Bell JI, Jewell DP.

    Lancet. 1996 May 4;347(9010):1212-7.PMID: 8622450 [PubMed - indexed for MEDLINE]Related articles

    45.

    Distribution of HLA-DQA1 and -DQB1 alleles and DQA1-DQB1 genotypes among Senegalese patients with insulin-dependent diabetes mellitus.

    Cissé A, Chauffert M, Chevenne D, Parfait B, Julier C, Assouline Z, Michel S, Trivin F.

    Tissue Antigens. 1996 Apr;47(4):333-7.PMID: 8773324 [PubMed - indexed for MEDLINE]Related articles

    46.

    [HLA-DR:DQ genotypes and insulin-dependent diabetes in Senegal]

    Cisse A, Chauffert M, Julier C, Chevenne D, Michel S, Trivin F, Diop SN, Sidibe EH, Sow AM.

    Dakar Med. 1996;41(2):75-8. French. PMID: 9827098 [PubMed - indexed for MEDLINE]Related articles

    47.

    Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci.

    McKenzie CA, Julier C, Forrester T, McFarlane-Anderson N, Keavney B, Lathrop GM, Ratcliffe PJ, Farrall M.

    Am J Hum Genet. 1995 Dec;57(6):1426-35. Erratum in: Am J Hum Genet 1996 Mar;58(3):648. PMID: 8533773 [PubMed - indexed for MEDLINE]Related articlesFree article

    48.

    Regulation of insulin gene expression by the IDDM associated, insulin locus haplotype.

    Lucassen AM, Screaton GR, Julier C, Elliott TJ, Lathrop M, Bell JI.

    Hum Mol Genet. 1995 Apr;4(4):501-6.PMID: 7633396 [PubMed - indexed for MEDLINE]Related articles

    49.

    A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus.

    Hager J, Hansen L, Vaisse C, Vionnet N, Philippi A, Poller W, Velho G, Carcassi C, Contu L, Julier C, et al.

    Nat Genet. 1995 Mar;9(3):299-304.PMID: 7773293 [PubMed - indexed for MEDLINE]Related articles

    50.

    Evaluation of the SA locus in human hypertension.

    Nabika T, Bonnardeaux A, James M, Julier C, Jeunemaitre X, Corvol P, Lathrop M, Soubrier F.

    Hypertension. 1995 Jan;25(1):6-13.PMID: 7843754 [PubMed - indexed for MEDLINE]Related articlesFree article

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