Bernard Grandchamp - Concepedia

Author

Bernard Grandchamp

Also Known As

B Grandchamp, B. GRANDCHAMP, B. Grandchamp, BERNARD GRANDCHAMP, Bernard GRANDCHAMP, Bernard Grandchamp, Bernard Grandchamp (326843), G Bernard, Grandchamp Bernard, K Robinson

615

Publications

16.9K

Citations

H-Index

163

Concepts

All Affiliations

Inserm Hôpital Bichat-Claude-Bernard Université Paris Cité Assistance Publique – Hôpitaux de Paris Université Claude Bernard Lyon 1

About

Bernard Grandchamp is an author at Inserm specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	98	7.1K
2	Natural Sciences	22	26	1.8K
3	Health Sciences	4	4	1K
4	Public Health	2	2	203
5	Engineering	1	1	39

Bernard Grandchamp

189

Publications

15.9K

Citations

H-Index

Page 1

	Year	Citations
Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 ( <i>USF2</i> ) knockout mice Gaël Nicolas, Myriam Bennoun, Isabelle Devaux, Proceedings of the National Academy of Sciences	2001	1.2K
Severe iron deficiency anemia in transgenic mice expressing liver hepcidin Gaël Nicolas, Myriam Bennoun, Arlette Porteu, Proceedings of the National Academy of Sciences Usf2 Knockout MiceIron MetabolismGeneticsImmunologyPathology	2002	877
Clinical Significance of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia Hélène Cavé, Jutte van der Werff ten Bosch, Stefan Suciu, New England Journal of Medicine	1998	773
Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera Jean‐Jacques Kiladjian, Bruno Cassinat, Sylvie Chevret, Blood	2008	567
TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome Cathérine Boileau, Dong Guo, Nadine Hanna, Nature Genetics Marfan SyndromeTgfb2 MutationsPathologyCongenital Heart DefectMild Systemic Features	2012	373
Nephrolithiasis and Osteoporosis Associated with Hypophosphatemia Caused by Mutations in the Type 2a Sodium–Phosphate Cotransporter Dominique Prié, Virginie Huart, Naziha Bakouh, New England Journal of Medicine	2002	354
Detection and identification of mycobacteria by amplification of mycobacterial DNA A J Hance, Bernard Grandchamp, V. Lévy‐Frébault, Molecular Microbiology Medical MicrobiologyPulmonary TuberculosisMolecular Diagnostic TechniquesMycobacterium TuberculosisBacteriology	1989	315
Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression. Stany Chrétien, D Beaupain, Natacha Raich, Proceedings of the National Academy of Sciences GeneticsMolecular BiologyGene CharacterizationMolecular GeneticsSplicing Variant	1988	311
C-Terminal Deletions in the ALAS2 Gene Lead to Gain of Function and Cause X-linked Dominant Protoporphyria without Anemia or Iron Overload Sharon D. Whatley, Sarah Ducamp, Laurent Gouya, The American Journal of Human Genetics BiologyMedicineGeneticsPathogenesisIron Overload	2008	289
Early Embryonic Lethality of H Ferritin Gene Deletion in Mice Chrystophe Ferreira, Danièle Bucchini, Marie-Elise Martin, Journal of Biological Chemistry	2000	275

Page 1