| Year |
Citation |
Score |
| 2002 |
Reis AF, Hani EH, Beressi N, Robert JJ, Bresson JL, Froguel P, Velho G. Allelic variation in exon 18 of the sulfonylurea receptor 1 (SUR1) gene, insulin secretion and insulin sensitivity in nondiabetic relatives of type 2 diabetic subjects. Diabetes & Metabolism. 28: 209-15. PMID 12149601 |
0.475 |
|
| 2001 |
Hani EH, Dupont S, Durand E, Dina C, Gallina S, Gantz I, Froguel P. Naturally occurring mutations in the melanocortin receptor 3 gene are not associated with type 2 diabetes mellitus in French Caucasians. The Journal of Clinical Endocrinology and Metabolism. 86: 2895-8. PMID 11397906 DOI: 10.1210/Jcem.86.6.7589 |
0.74 |
|
| 2001 |
Dupont S, Hani EH, Cras-Méneur C, De Matos F, Lobbens S, Lecoeur C, Vaxillaire M, Scharfmann R, Froguel P. No evidence for linkage or for diabetes-associated mutations in the activin type 2B receptor gene (ACVR2B) in French patients with mature-onset diabetes of the young or type 2 diabetes. Diabetes. 50: 1219-21. PMID 11334431 DOI: 10.2337/Diabetes.50.5.1219 |
0.728 |
|
| 2000 |
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. 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. American Journal of Human Genetics. 67: 1470-80. PMID 11067779 DOI: 10.1086/316887 |
0.718 |
|
| 2000 |
Abderrahmani A, Chèvre JC, Otabe S, Chikri M, Hani EH, Vaxillaire M, Hinokio Y, Horikawa Y, Bell GI, Froguel P. Genetic variation in the hepatocyte nuclear factor-3beta gene (HNF3B) does not contribute to maturity-onset diabetes of the young in French Caucasians. Diabetes. 49: 306-8. PMID 10868949 DOI: 10.2337/Diabetes.49.2.306 |
0.715 |
|
| 2000 |
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. The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetes. Nature Genetics. 24: 291-5. PMID 10700186 DOI: 10.1038/73523 |
0.732 |
|
| 1999 |
Dupont S, Dina C, Hani EH, Froguel P. Absence of replication in the French population of the association between beta 2/NEUROD-A45T polymorphism and type 1 diabetes. Diabetes & Metabolism. 25: 516-7. PMID 10633878 |
0.51 |
|
| 1999 |
Hani EH, Stoffers DA, Chèvre JC, Durand E, Stanojevic V, Dina C, Habener JF, Froguel P. Defective mutations in the insulin promoter factor-1 (IPF-1) gene in late-onset type 2 diabetes mellitus. The Journal of Clinical Investigation. 104: R41-8. PMID 10545531 DOI: 10.1172/Jci7469 |
0.678 |
|
| 1998 |
Hani EH, Boutin P, Durand E, Inoue H, Permutt MA, Velho G, Froguel P. Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in Caucasians. Diabetologia. 41: 1511-5. PMID 9867219 DOI: 10.1007/S001250051098 |
0.63 |
|
| 1998 |
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. Mutation screening in 18 Caucasian families suggest the existence of other MODY genes. Diabetologia. 41: 1017-23. PMID 9754819 DOI: 10.1007/S001250051025 |
0.61 |
|
| 1998 |
Chèvre JC, Hani EH, Stoffers DA, Habener JF, Froguel P. Insulin promoter factor 1 gene is not a major cause of maturity-onset diabetes of the young in French Caucasians. Diabetes. 47: 843-4. PMID 9588460 DOI: 10.2337/Diabetes.47.5.843 |
0.546 |
|
| 1998 |
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. A missense mutation in hepatocyte nuclear factor-4 alpha, resulting in a reduced transactivation activity, in human late-onset non-insulin-dependent diabetes mellitus. The Journal of Clinical Investigation. 101: 521-6. PMID 9449683 DOI: 10.1172/Jci1403 |
0.655 |
|
| 1997 |
Boutin P, Chèvre JC, Hani EH, Gomis R, Pardini VC, Guillausseau PJ, Vaxillaire M, Velho G, Froguel P. An automated fluorescent single-strand conformation polymorphism technique for screening mutations in the hepatocyte nuclear factor-1alpha gene (maturity-onset diabetes of the young). Diabetes. 46: 2108-9. PMID 9392505 DOI: 10.2337/Diab.46.12.2108 |
0.584 |
|
| 1997 |
Boutin P, Hani EH, Vasseur F, Roche C, Bailleul B, Hager J, Froguel P. Automated fluorescence-based screening for mutation by SSCP: use of universal M13 dye primers for labeling and detection. Biotechniques. 23: 358-62. PMID 9298196 DOI: 10.2144/97233Bm01 |
0.405 |
|
| 1997 |
Zouali H, Hani EH, Philippi A, Vionnet N, Beckmann JS, Demenais F, Froguel P. A susceptibility locus for early-onset non-insulin dependent (type 2) diabetes mellitus maps to chromosome 20q, proximal to the phosphoenolpyruvate carboxykinase gene. Human Molecular Genetics. 6: 1401-8. PMID 9285775 DOI: 10.1093/Hmg/6.9.1401 |
0.667 |
|
| 1997 |
Hani EH, Hager J, Philippi A, Demenais F, Froguel P, Vionnet N. Mapping NIDDM susceptibility loci in French families: studies with markers in the region of NIDDM1 on chromosome 2q. Diabetes. 46: 1225-6. PMID 9200659 DOI: 10.2337/Diab.46.7.1225 |
0.521 |
|
| 1997 |
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. Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs. Diabetes. 46: 1062-8. PMID 9166680 DOI: 10.2337/Diab.46.6.1062 |
0.675 |
|
| 1997 |
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. Genetic studies of the sulfonylurea receptor gene locus in NIDDM and in morbid obesity among French Caucasians. Diabetes. 46: 688-94. PMID 9075812 DOI: 10.2337/Diab.46.4.688 |
0.501 |
|
| 1996 |
Hani EH, Zouali H, Philippi A, Beaudoin JC, Vionnet N, Passa P, Demenais F, Froguel P. Indication for genetic linkage of the phosphoenolpyruvate carboxykinase (PCK1) gene region on chromosome 20q to non-insulin-dependent diabetes mellitus. Diabetes & Metabolism. 22: 451-4. PMID 8985654 |
0.55 |
|
| 1995 |
Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N. Rapid publication: Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM Diabetes. 44: 1243-1247. PMID 7556965 DOI: 10.2337/Diab.44.10.1243 |
0.735 |
|
| 1995 |
Gremlich S, Porret A, Hani EH, Cherif D, Vionnet N, Froguel P, Thorens B. Cloning, functional expression, and chromosomal localization of the human pancreatic islet glucose-dependent insulinotropic polypeptide receptor. Diabetes. 44: 1202-8. PMID 7556958 DOI: 10.2337/Diab.44.10.1202 |
0.475 |
|
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