Concepedia

Gaël Ménasché

GM

Statistics

Publications

26

Citations

3.5K

H-Index

22

Active since

2000

Affiliations

Inserm(Current)

Hôpital Necker-Enfants Malades

Université Paris Cité

Assistance Publique – Hôpitaux de Paris

Institut des Maladies Génétiques Imagine

Gaël Ménasché is an author at Inserm specializing in life sciences, genetics, and cell biology.

ORCID

Publications per year

2000–2022

26

Publications

26

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Gaël Ménasché, Élodie Pastural, Jérôme Feldmann et al. · Nature Genetics · 2000 · 952 citations

, , +7

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

Marjorie Côte, Mickaël Ménager, Agathe Burgess et al. · Journal of Clinical Investigation · 2009 · 349 citations · Full text

, , +13

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Gaël Ménasché, Chen Hsuan Ho, Özden Sanal et al. · Journal of Clinical Investigation · 2003 · 289 citations · Full text

, , +17

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Gaël Ménasché, Chen Hsuan Ho, Özden Sanal et al. · Journal of Clinical Investigation · 2003 · 285 citations · Full text

, , +17

Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4

Mickaël Ménager, Gaël Ménasché, Maryse Romao et al. · Nature Immunology · 2007 · 256 citations

, , +12

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