| Clinical spectrum associated with hepatocyte nuclear factor-1β mutations C Bellanné-Chantelot, D Chauveau, JF Gautier, D Dubois-Laforgue, ... Annals of internal medicine 140 (7), 510-517, 2004 | 442 | 2004 |
| Maternally inherited diabetes and deafness: a multicenter study PJ Guillausseau, P Massin, D Dubois-LaForgue, J Timsit, M Virally, H Gin, ... Annals of internal medicine 134 (9_Part_1), 721-728, 2001 | 390 | 2001 |
| Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5 C Bellanné-Chantelot, S Clauin, D Chauveau, P Collin, M Daumont, ... Diabetes 54 (11), 3126-3132, 2005 | 325 | 2005 |
| Acceleration of type 1 diabetes mellitus in proinsulin 2–deficient NOD mice K Thébault-Baumont, D Dubois-Laforgue, P Krief, JP Briand, P Halbout, ... The Journal of clinical investigation 111 (6), 851-857, 2003 | 273 | 2003 |
| The Type and the Position of HNF1A Mutation Modulate Age at Diagnosis of Diabetes in Patients with Maturity-Onset Diabetes of the Young (MODY)-3 C Bellanné-Chantelot, C Carette, JP Riveline, R Valéro, JF Gautier, ... Diabetes 57 (2), 503-508, 2008 | 253 | 2008 |
| Vitamin D receptor gene polymorphisms are associated with obesity in type 2 diabetic subjects with early age of onset WZ Ye, AF Reis, D Dubois-Laforgue, C Bellanne-Chantelot, J Timsit, ... European journal of endocrinology 145 (2), 181-186, 2001 | 240 | 2001 |
| Conventional and neo-antigenic peptides presented by β cells are targeted by circulating naïve CD8+ T cells in type 1 diabetic and healthy donors S Gonzalez-Duque, ME Azoury, ML Colli, G Afonso, JV Turatsinze, L Nigi, ... Cell metabolism 28 (6), 946-960. e6, 2018 | 184 | 2018 |
| Recognition of a subregion of human proinsulin by class I-restricted T cells in type 1 diabetic patients A Toma, S Haddouk, JP Briand, L Camoin, H Gahery, F Connan, ... Proceedings of the National Academy of Sciences 102 (30), 10581-10586, 2005 | 147 | 2005 |
| Diabetes, associated clinical spectrum, long-term prognosis, and genotype/phenotype correlations in 201 adult patients with hepatocyte nuclear factor 1B (HNF1B) molecular defects D Dubois-Laforgue, E Cornu, C Saint-Martin, J Coste, ... Diabetes Care 40 (11), 1436-1443, 2017 | 136 | 2017 |
| Factors associated with preterm delivery in women with type 1 diabetes: a cohort study J Lepercq, J Coste, A Theau, D Dubois-Laforgue, J Timsit Diabetes care 27 (12), 2824-2828, 2004 | 122 | 2004 |
| Clinical Characteristics and Diagnostic Criteria of Maturity-Onset Diabetes Of The Young (MODY) due to Molecular Anomalies of the HNF1A Gene C Bellanné-Chantelot, DJ Lévy, C Carette, C Saint-Martin, JP Riveline, ... The Journal of Clinical Endocrinology & Metabolism 96 (8), E1346-E1351, 2011 | 113 | 2011 |
| Heterogeneity of fetal growth in type 1 diabetic pregnancy J Lepercq, P Taupin, D Dubois-Laforgue, L Duranteau, N Lahlou, ... Diabetes and Metabolism 27 (3), 339-346, 2001 | 99 | 2001 |
| The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes M Laloi-Michelin, T Meas, C Ambonville, C Bellanné-Chantelot, S Beaufils, ... The Journal of Clinical Endocrinology & Metabolism 94 (8), 3025-3030, 2009 | 98 | 2009 |
| PTPN22 R620W functional variant in type 1 diabetes and autoimmunity related traits C Chelala, S Duchatelet, ML Joffret, R Bergholdt, D Dubois-Laforgue, ... Diabetes 56 (2), 522-526, 2007 | 95 | 2007 |
| Association of a variant in exon 31 of the sulfonylurea receptor 1 (SUR1) gene with type 2 diabetes mellitus in French Caucasians AF Reis, WZ Ye, D Dubois-Laforgue, C Bellanné-Chantelot, J Timsit, ... Human genetics 107, 138-144, 2000 | 93 | 2000 |
| The N363S polymorphism in the glucocorticoid receptor gene is associated with overweight in subjects with type 2 diabetes mellitus R Roussel, AF Reis, D Dubois‐Laforgue, C Bellanné‐Chantelot, J Timsit, ... Clinical endocrinology 59 (2), 237-241, 2003 | 92 | 2003 |
| Diagnosis and management of maturity-onset diabetes of the young J Timsit, C Bellanné-Chantelot, D Dubois-Laforgue, G Velho Treatments in endocrinology 4, 9-18, 2005 | 82 | 2005 |
| Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD) PJ Guillausseau, D Dubois-Laforgue, P Massin, M Laloi-Michelin, ... Diabetes & metabolism 30 (2), 181-186, 2004 | 82 | 2004 |
| A common stromal cell–derived factor-1 chemokine gene variant is associated with the early onset of type 1 diabetes D Dubois-Laforgue, H Hendel, S Caillat-Zucman, JF Zagury, C Winkler, ... Diabetes 50 (5), 1211-1213, 2001 | 75 | 2001 |
| Searching for maturity-onset diabetes of the young (MODY): when and what for? J Timsit, C Saint-Martin, D Dubois-Laforgue, C Bellanné-Chantelot Canadian journal of diabetes 40 (5), 455-461, 2016 | 73 | 2016 |
