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Bernard Grandchamp

Bernard Grandchamp

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Genetics
France
2024
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Genetics and Molecular Biology
France
2024

D-Index & Metrics

Genetics

D-Index
81
Citations
21076
World Ranking
1536
National Ranking
61

Research.com Recognitions

  • 2024 - Research.com Genetics in France Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in France Leader Award

Overview

Bernard Grandchamp is affiliated with Université Paris Cité in France. Their academic profile reflects a focus on research and scholarship connected to this institution.

While information on recent papers, co-authors, publication venues, book publications, fields of study, subfields, main topics, and awards is not provided, the association with Université Paris Cité positions Bernard Grandchamp within a significant academic environment in France.

They have not been recorded as deceased and actively contribute to their field.

Best Publications

  • Lack of hepcidin gene expression and severe tissue iron overload in upstream stimulatory factor 2 (USF2) knockout mice

    Gaël Nicolas;Myriam Bennoun;Isabelle Devaux;Carole Beaumont

  • Severe iron deficiency anemia in transgenic mice expressing liver hepcidin

    Gaël Nicolas;Myriam Bennoun;Arlette Porteu;Sandrine Mativet

  • Clinical Significance of Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia

    Cavé H;van der Werff ten Bosch J;Suciu S;Guidal C

  • Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera

    Jean-Jacques Kiladjian;Bruno Cassinat;Sylvie Chevret;Pascal Turlure

  • Detection and identification of mycobacteria by amplification of mycobacterial DNA

    A. J. Hance;B. Grandchamp;V. Lévy-Frébault;D. Lecossier

  • TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome.

    Catherine Boileau;Dong Chuan Guo;Nadine Hanna;Ellen S. Regalado

  • Alternative transcription and splicing of the human porphobilinogen deaminase gene result either in tissue-specific or in housekeeping expression

    Stany Chretien;Anne Dubart;Denise Beaupain;Natacha Raich

  • Mutation in the iron responsive element of the L ferritin mRNA in a family with dominant hyperferritinaemia and cataract.

    Carole Beaumont;Patricia Leneuve;Isabelle Devaux;Jean-Yves Scoazec

  • Nephrolithiasis and Osteoporosis Associated with Hypophosphatemia Caused by Mutations in the Type 2a Sodium–Phosphate Cotransporter

    Dominique Prié;Virginie Huart;Naziha Bakouh;Gabrielle Planelles

  • Early embryonic lethality of H ferritin gene deletion in mice.

    Chrystophe Ferreira;Danièle Bucchini;Marie Elise Martin;Sonia Levi

  • 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;Bernard Grandchamp

  • 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

  • The penetrance of dominant erythropoietic protoporphyria is modulated by expression of wildtype FECH.

    Laurent Gouya;Herve Puy;Anne-Marie Robreau;Monique Bourgeois

  • Tissue-specific expression of porphobilinogen deaminase. Two isoenzymes from a single gene.

    Bernard Grandchamp;Hubert De Verneuil;Carole Beaumont;Stany Chretien

  • Familial and sporadic porphyria cutanea: two different diseases..

    H. De Verneuil;Y. Nordmann;N. Phung;B. Grandchamp

  • Contribution of a Common Single-Nucleotide Polymorphism to the Genetic Predisposition for Erythropoietic Protoporphyria

    Laurent Gouya;Caroline Martin-Schmitt;Anne-Marie Robreau;Frédéric Austerlitz

  • Clonality Analysis of Hematopoiesis in Essential Thrombocythemia: Advantages of Studying T Lymphocytes and Platelets

    Nahed El-Kassar;Gilles Hetet;Jean Brière;Bernard Grandchamp

  • NHERF1 mutations and responsiveness of renal parathyroid hormone.

    Zoubida Karim;Bénédicte Gérard;Naziha Bakouh;Rohia Alili

  • Ferritin and transferrin are both predictive of the onset of hyperglycemia in men and women over 3 years: the data from an epidemiological study on the Insulin Resistance Syndrome (DESIR) study

    Frédéric Fumeron;Franck Péan;Fatti Driss;Beverley Balkau

  • Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

    Gilles Hetet;Isabelle Devaux;Nadem Soufir;Bernard Grandchamp

Frequent Co-Authors

Carole Beaumont
Carole Beaumont Université Paris Cité
Hélène Cavé
Hélène Cavé Université Paris Cité
Céleste Lebbé
Céleste Lebbé Hôpitaux Universitaires Paris-Ouest
Nicolas Dupin
Nicolas Dupin Université Paris Cité
Armand Bensussan
Armand Bensussan Hôpital Saint-Louis
Jacques Elion
Jacques Elion Université Paris Cité
Michel Goossens
Michel Goossens Grenoble Alpes University
Sophie Vaulont
Sophie Vaulont Université Paris Cité
Pierre Wolkenstein
Pierre Wolkenstein Assistance Publique – Hôpitaux de Paris
Pavel Martásek
Pavel Martásek Charles University

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