| Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice G Nicolas, M Bennoun, I Devaux, C Beaumont, B Grandchamp, A Kahn, ... Proceedings of the National Academy of Sciences 98 (15), 8780-8785, 2001 | 1708 | 2001 |
| Severe iron deficiency anemia in transgenic mice expressing liver hepcidin G Nicolas, M Bennoun, A Porteu, S Mativet, C Beaumont, B Grandchamp, ... Proceedings of the National Academy of Sciences 99 (7), 4596-4601, 2002 | 1240 | 2002 |
| Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia H Cavé, J van der Werff Ten Bosch, S Suciu, C Guidal, C Waterkeyn, ... New England Journal of Medicine 339 (9), 591-598, 1998 | 976 | 1998 |
| Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera JJ Kiladjian, B Cassinat, S Chevret, P Turlure, N Cambier, M Roussel, ... Blood, The Journal of the American Society of Hematology 112 (8), 3065-3072, 2008 | 692 | 2008 |
| Detection and identification of mycobacteria by amplification of mycobacterial DNA AJ Hance, B Grandchamp, V Levy‐Frebault, D Lecossier, J Rauzier, ... Molecular microbiology 3 (7), 843-849, 1989 | 467 | 1989 |
| TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome C Boileau, DC Guo, N Hanna, ES Regalado, D Detaint, L Gong, M Varret, ... Nature genetics 44 (8), 916-921, 2012 | 398 | 2012 |
| Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression. S Chretien, A Dubart, D Beaupain, N Raich, B Grandchamp, J RoSA, ... Proceedings of the National Academy of Sciences 85 (1), 6-10, 1988 | 388 | 1988 |
| Nephrolithiasis and osteoporosis associated with hypophosphatemia caused by mutations in the type 2a sodium–phosphate cotransporter D Prié, V Huart, N Bakouh, G Planelles, O Dellis, B Gérard, P Hulin, ... New England Journal of Medicine 347 (13), 983-991, 2002 | 380 | 2002 |
| Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract C Beaumont, P Leneuve, I Devaux, JY Scoazec, M Berthier, MN Loiseau, ... Nature genetics 11 (4), 444-446, 1995 | 370 | 1995 |
| Early embryonic lethality of H ferritin gene deletion in mice C Ferreira, D Bucchini, ME Martin, S Levi, P Arosio, B Grandchamp, ... Journal of Biological Chemistry 275 (5), 3021-3024, 2000 | 340 | 2000 |
| C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload SD Whatley, S Ducamp, L Gouya, B Grandchamp, C Beaumont, ... The American Journal of Human Genetics 83 (3), 408-414, 2008 | 319 | 2008 |
| The 12; 21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia S Raynaud, H Cave, M Baens, C Bastard, V Cacheux, J Grosgeorge, ... | 307 | 1996 |
| The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH L Gouya, H Puy, AM Robreau, M Bourgeois, J Lamoril, V Da Silva, ... Nature genetics 30 (1), 27-28, 2002 | 305 | 2002 |
| Tissue‐specific expression of porphobilinogen deaminase: two isoenzymes from a single gene B Grandchamp, H De Verneuil, C Beaumont, S Chretien, O Walter, ... European journal of biochemistry 162 (1), 105-110, 1987 | 272 | 1987 |
| Familial and sporadic porphyria cutanea: two different diseases H De Verneuil, Y Nordmann, N Phung, B Grandchamp, G Aitken, ... International Journal of Biochemistry 9 (12), 927-931, 1978 | 246 | 1978 |
| Clonality analysis of hematopoiesis in essential thrombocythemia: advantages of studying T lymphocytes and platelets N El-Kassar, G Hetet, J Briere, B Grandchamp Blood, The Journal of the American Society of Hematology 89 (1), 128-134, 1997 | 209 | 1997 |
| NHERF1 Mutations and Responsiveness of Renal Parathyroid Hormone Z Karim, B Gérard, N Bakouh, R Alili, C Leroy, L Beck, C Silve, ... New England Journal of Medicine 359 (11), 1128-1135, 2008 | 208 | 2008 |
| Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria L Gouya, C Martin-Schmitt, AM Robreau, F Austerlitz, V Da Silva, P Brun, ... The American Journal of Human Genetics 78 (1), 2-14, 2006 | 202 | 2006 |
| Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria RLP Lindberg, C Porcher, B Grandchamp, B Ledermann, K Bürki, ... Nature genetics 12 (2), 195-199, 1996 | 191 | 1996 |
| Ferritin and transferrin are associated with metabolic syndrome abnormalities and their change over time in a general population: Data from an Epidemiological Study on the … IS Vari, B Balkau, A Kettaneh, P André, J Tichet, F Fumeron, E Caces, ... Diabetes care 30 (7), 1795-1801, 2007 | 184 | 2007 |
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