Gaël Ménasché

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Gaël Ménasché, Élodie Pastural, Jérôme Feldmann et al. · Nature Genetics · 2000 · 940 citations

Mendelian Disorder, Autoimmune Disease, Disease Mechanism +10

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 · 346 citations · Full text

Immunology, Pathology, Cell Death +18

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

Melanophilin Defect, Genetics, Pathology +18

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

Melanophilin Defect, Genetics, Pathology +18

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

Mickaël Ménager, Gaël Ménasché, Maryse Romao et al. · Nature Immunology · 2007 · 255 citations

Protein Secretion, Signal Transduction, Cell Signaling +9