PubMed

The V16A polymorphism in SOD2 is associated with increased risk of diabetic nephropathy and cardiovascular disease in type 1 diabetes.

Möllsten A, Jorsal A, Lajer M, Vionnet N, Tarnow L.

Diabetologia. 2009 Oct 16. [Epub ahead of print]PMID: 19834686 [PubMed - as supplied by publisher]Related articles

Functional annotations of diabetes nephropathy susceptibility loci through analysis of genome-wide renal gene expression in rat models of diabetes mellitus.

Hu Y, Kaisaki PJ, Argoud K, Wilder SP, Wallace KJ, Woon PY, Blancher C, Tarnow L, Groop PH, Hadjadj S, Marre M, Parving HH, Farrall M, Cox RD, Lathrop M, Vionnet N, Bihoreau MT, Gauguier D.

BMC Med Genomics. 2009 Jul 9;2:41.PMID: 19586551 [PubMed - in process]Related articlesFree article

G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.

Trégouet DA, Groop PH, McGinn S, Forsblom C, Hadjadj S, Marre M, Parving HH, Tarnow L, Telgmann R, Godefroy T, Nicaud V, Rousseau R, Parkkonen M, Hoverfält A, Gut I, Heath S, Matsuda F, Cox R, Kazeem G, Farrall M, Gauguier D, Brand-Herrmann SM, Cambien F, Lathrop M, Vionnet N; EURAGEDIC Consortium.

Diabetes. 2008 Oct;57(10):2843-50. Epub 2008 Jul 15.PMID: 18633107 [PubMed - indexed for MEDLINE]Related articlesFree article

Serum adiponectin predicts all-cause mortality and end stage renal disease in patients with type I diabetes and diabetic nephropathy.

Jorsal A, Tarnow L, Frystyk J, Lajer M, Flyvbjerg A, Parving HH, Vionnet N, Rossing P.

Kidney Int. 2008 Sep;74(5):649-54. Epub 2008 May 21.PMID: 18496510 [PubMed - indexed for MEDLINE]Related articles

European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy.

Tarnow L, Groop PH, Hadjadj S, Kazeem G, Cambien F, Marre M, Forsblom C, Parving HH, Trégouët D, Thévard A, Farrall M, Gut I, Gauguier D, Cox R, Matsuda F, Lathrop M, Vionnet N; EURAGEDIC Consortium.

Nephrol Dial Transplant. 2008 Jan;23(1):161-8. Epub 2007 Aug 17.PMID: 17704113 [PubMed - indexed for MEDLINE]Related articles

Analysis of 14 candidate genes for diabetic nephropathy on chromosome 3q in European populations: strongest evidence for association with a variant in the promoter region of the adiponectin gene.

Vionnet N, Tregouët D, Kazeem G, Gut I, Groop PH, Tarnow L, Parving HH, Hadjadj S, Forsblom C, Farrall M, Gauguier D, Cox R, Matsuda F, Heath S, Thévard A, Rousseau R, Cambien F, Marre M, Lathrop M.

Diabetes. 2006 Nov;55(11):3166-74.PMID: 17065357 [PubMed - indexed for MEDLINE]Related articlesFree article

Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndrome.

Kaisaki PJ, Delépine M, Woon PY, Sebag-Montefiore L, Wilder SP, Menzel S, Vionnet N, Marion E, Riveline JP, Charpentier G, Schurmans S, Levy JC, Lathrop M, Farrall M, Gauguier D.

Diabetes. 2004 Jul;53(7):1900-4.PMID: 15220217 [PubMed - indexed for MEDLINE]Related articlesFree article

A quantitative trait locus influencing type 2 diabetes susceptibility maps to a region on 5q in an extended French family.

Martin LJ, Comuzzie AG, Dupont S, Vionnet N, Dina C, Gallina S, Houari M, Blangero J, Froguel P.

Diabetes. 2002 Dec;51(12):3568-72.PMID: 12453915 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic, pharmacological and functional analysis of cholecystokinin-1 and cholecystokinin-2 receptor polymorphism in type 2 diabetes and obese patients.

Marchal-Victorion S, Vionnet N, Escrieut C, Dematos F, Dina C, Dufresne M, Vaysse N, Pradayrol L, Froguel P, Fourmy D.

Pharmacogenetics. 2002 Jan;12(1):23-30.PMID: 11773861 [PubMed - indexed for MEDLINE]Related articles

Polymorphism screening of four genes encoding advanced glycation end-product putative receptors. Association study with nephropathy in type 1 diabetic patients.

Poirier O, Nicaud V, Vionnet N, Raoux S, Tarnow L, Vlassara H, Parving HH, Cambien F.

Diabetes. 2001 May;50(5):1214-8. Erratum in: Diabetes 2002 Jan;51(1):256. PMID: 11334430 [PubMed - indexed for MEDLINE]Related articlesFree article

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P.

Am J Hum Genet. 2000 Dec;67(6):1470-80. Epub 2000 Nov 6.PMID: 11067779 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Nat Genet. 2000 Mar;24(3):291-5.PMID: 10700186 [PubMed - indexed for MEDLINE]Related articles

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

Dupont S, Vionnet N, Chèvre JC, Gallina S, Dina C, Seino Y, Yamada Y, Froguel P.

Diabetologia. 1999 Apr;42(4):480-4.PMID: 10230653 [PubMed - indexed for MEDLINE]Related articles

[Genetic risk of non-insulin-dependent diabetes]

Vionnet N, Froguel P.

Journ Annu Diabetol Hotel Dieu. 1998:223-40. Review. French. No abstract available. PMID: 9773623 [PubMed - indexed for MEDLINE]Related articles

Mutation screening in 18 Caucasian families suggest the existence of other MODY genes.

Chèvre JC, Hani EH, Boutin P, Vaxillaire M, Blanché H, Vionnet N, Pardini VC, Timsit J, Larger E, Charpentier G, Beckers D, Maes M, Bellanné-Chantelot C, Velho G, Froguel P.

Diabetologia. 1998 Sep;41(9):1017-23.PMID: 9754819 [PubMed - indexed for MEDLINE]Related articles

No association between the Friedreich's ataxia gene and NIDDM in the French population.

Dupont S, Dubois D, Vionnet N, Boitard C, Caillat-Zucman S, Timsit J, Froguel P.

Diabetes. 1998 Oct;47(10):1654-6. No abstract available. PMID: 9753307 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic studies of polymorphisms in ten non-insulin-dependent diabetes mellitus candidate genes in Tamil Indians from Pondichery.

Leprêtre F, Vionnet N, Budhan S, Dina C, Powell KL, Génin E, Das AK, Nallam V, Passa P, Froguel P.

Diabetes Metab. 1998 Jun;24(3):244-50.PMID: 9690058 [PubMed - indexed for MEDLINE]Related articlesFree article

A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus.

Hani EH, Suaud L, Boutin P, Chèvre JC, Durand E, Philippi A, Demenais F, Vionnet N, Furuta H, Velho G, Bell GI, Laine B, Froguel P.

J Clin Invest. 1998 Feb 1;101(3):521-6.PMID: 9449683 [PubMed - indexed for MEDLINE]Related articlesFree article

A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene.

Zouali H, Hani EH, Philippi A, Vionnet N, Beckmann JS, Demenais F, Froguel P.

Hum Mol Genet. 1997 Sep;6(9):1401-8.PMID: 9285775 [PubMed - indexed for MEDLINE]Related articlesFree article

Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2q.

Hani EH, Hager J, Philippi A, Demenais F, Froguel P, Vionnet N.

Diabetes. 1997 Jul;46(7):1225-6. No abstract available. PMID: 9200659 [PubMed - indexed for MEDLINE]Related articles

Genetic studies of the renin-angiotensin system in arterial hypertension associated with non-insulin-dependent diabetes mellitus.

Lesage S, Velho G, Vionnet N, Chatelain N, Demenais F, Passa P, Soubrier F, Froguel P.

J Hypertens. 1997 Jun;15(6):601-6.PMID: 9218178 [PubMed - indexed for MEDLINE]Related articles

Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs.

Vionnet N, Hani EH, Lesage S, Philippi A, Hager J, Varret M, Stoffel M, Tanizawa Y, Chiu KC, Glaser B, Permutt MA, Passa P, Demenais F, Froguel P.

Diabetes. 1997 Jun;46(6):1062-8.PMID: 9166680 [PubMed - indexed for MEDLINE]Related articles

Genetic analyses of glucose transporter genes in French non-insulin-dependent diabetic families.

Lesage S, Zouali H, Vionnet N, Philippi A, Velho G, Serradas P, Passa P, Demenais F, Froguel P.

Diabetes Metab. 1997 Apr;23(2):137-42.PMID: 9137902 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians.

Hani EH, Clément K, Velho G, Vionnet N, Hager J, Philippi A, Dina C, Inoue H, Permutt MA, Basdevant A, North M, Demenais F, Guy-Grand B, Froguel P.

Diabetes. 1997 Apr;46(4):688-94.PMID: 9075812 [PubMed - indexed for MEDLINE]Related articles

Indication for genetic linkage of the phosphoenolpyruvate carboxykinase (PCK1) gene region on chromosome 20q to non-insulin-dependent diabetes mellitus.

Hani EH, Zouali H, Philippi A, Beaudoin JC, Vionnet N, Passa P, Demenais F, Froguel P.

Diabetes Metab. 1996 Dec;22(6):451-4.PMID: 8985654 [PubMed - indexed for MEDLINE]Related articles

Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.

Velho G, Byrne MM, Clément K, Sturis J, Pueyo ME, Blanché H, Vionnet N, Fiet J, Passa P, Robert JJ, Polonsky KS, Froguel P.

Diabetes. 1996 Apr;45(4):478-87.PMID: 8603770 [PubMed - indexed for MEDLINE]Related articles

Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.

Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N.

Diabetes. 1995 Oct;44(10):1243-7.PMID: 7556965 [PubMed - indexed for MEDLINE]Related articles

Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptor.

Gremlich S, Porret A, Hani EH, Cherif D, Vionnet N, Froguel P, Thorens B.

Diabetes. 1995 Oct;44(10):1202-8.PMID: 7556958 [PubMed - indexed for MEDLINE]Related articles

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

Genetics of non-insulin-dependent diabetes mellitus: from genes to the disease.

Froguel P, Vionnet N.

Adv Nephrol Necker Hosp. 1995;24:157-63. Review. No abstract available. PMID: 7572407 [PubMed - indexed for MEDLINE]Related articles

Insulin secretory abnormalities in subjects with hyperglycemia due to glucokinase mutations.

Byrne MM, Sturis J, Clément K, Vionnet N, Pueyo ME, Stoffel M, Takeda J, Passa P, Cohen D, Bell GI, et al.

J Clin Invest. 1994 Mar;93(3):1120-30.PMID: 8132752 [PubMed - indexed for MEDLINE]Related articlesFree article

Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.

Vaxillaire M, Vionnet N, Vigouroux C, Sun F, Espinosa R 3rd, Lebeau MM, Stoffel M, Lehto M, Beckmann JS, Detheux M, et al.

Diabetes. 1994 Mar;43(3):389-95.PMID: 7508874 [PubMed - indexed for MEDLINE]Related articles

Prevalence of mitochondrial gene mutations in families with diabetes mellitus.

Vionnet N, Passa P, Froguel P.

Lancet. 1993 Dec 4;342(8884):1429-30. No abstract available. PMID: 7901716 [PubMed - indexed for MEDLINE]Related articles

Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.

Zouali H, Vaxillaire M, Lesage S, Sun F, Velho G, Vionnet N, Chiu K, Passa P, Permutt A, Demenais F, et al.

Diabetes. 1993 Sep;42(9):1238-45.PMID: 8349034 [PubMed - indexed for MEDLINE]Related articles

Identification of glucokinase mutations in subjects with gestational diabetes mellitus.

Stoffel M, Bell KL, Blackburn CL, Powell KL, Seo TS, Takeda J, Vionnet N, Xiang KS, Gidh-Jain M, Pilkis SJ, et al.

Diabetes. 1993 Jun;42(6):937-40.PMID: 8495817 [PubMed - indexed for MEDLINE]Related articles

Identification of a simple tandem repeat DNA polymorphism in the human glycogen synthase gene and linkage to five markers on chromosome 19q.

Vionnet N, Bell GI.

Diabetes. 1993 Jun;42(6):930-2.PMID: 8495815 [PubMed - indexed for MEDLINE]Related articles

Mutations of the human glucokinase gene and diabetes mellitus.

Bell GI, Froguel P, Nishi S, Pilkis SJ, Stoffel M, Takeda J, Vionnet N, Yasuda K.

Trends Endocrinol Metab. 1993 Apr;4(3):86-90.PMID: 18407139 [PubMed - in process]Related articles

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.

Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, Lesage S, Stoffel M, Takeda J, Passa P, et al.

N Engl J Med. 1993 Mar 11;328(10):697-702.PMID: 8433729 [PubMed - indexed for MEDLINE]Related articlesFree article

Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships.

Gidh-Jain M, Takeda J, Xu LZ, Lange AJ, Vionnet N, Stoffel M, Froguel P, Velho G, Sun F, Cohen D, et al.

Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):1932-6.PMID: 8446612 [PubMed - indexed for MEDLINE]Related articlesFree article

[Genetics of non-insulin-dependent diabetes mellitus: the end of the nightmare?]

Froguel P, Vionnet N, Cohen D, Passa P.

Pathol Biol (Paris). 1992 Dec;40(10):977-9. Review. French. No abstract available. PMID: 1299811 [PubMed - indexed for MEDLINE]Related articles

Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.

Stoffel M, Froguel P, Takeda J, Zouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S, et al.

Proc Natl Acad Sci U S A. 1992 Aug 15;89(16):7698-702. Erratum in: Proc Natl Acad Sci U S A 1992 Nov 1;89(21):10562. PMID: 1502186 [PubMed - indexed for MEDLINE]Related articlesFree article

Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus.

Vionnet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, Lesage S, Velho G, Iris F, Passa P, et al.

Nature. 1992 Apr 23;356(6371):721-2.PMID: 1570017 [PubMed - indexed for MEDLINE]Related articles

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus.

Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, et al.

Nature. 1992 Mar 12;356(6365):162-4. Erratum in: Nature 1992 Jun 18;357(6379):607. PMID: 1545870 [PubMed - indexed for MEDLINE]Related articles

Two TaqI RFLPs at the GLUT2 locus in French Caucasian population.

Froguel P, Vionnet N, Lesage S, Velho G, Cohen D.

Nucleic Acids Res. 1991 Oct 25;19(20):5799. No abstract available. PMID: 1682886 [PubMed - indexed for MEDLINE]Related articlesFree article