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Gaël Ménasché | Researchclopedia

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Gaël Ménasché

Institut des Maladies Génétiques Imagine ORCID

49

Works

4,409

Citations

26

h-index

33

i10-index

Research Topics

Autoimmune and Inflammatory Disorders Research Immune Cell Function and Interaction Cellular transport and secretion

Affiliations

Délégation Paris 52010–2019

Hôpital Necker-Enfants Malades2002–2010

Inserm2002–2025

Cancer Research Institute2006–2007

Université Paris Cité2007–2025

Top Works

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Gaël Ménasché,Élodie Pastural,et al.

2000946 citations

Mast cells and histamine

Lysosomal Storage Disorders Research

Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules

Geneviève de Saint Basile,Gaël Ménasché,et al.

2010422 citations

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

Marjorie Côte,Mickaël Ménager,et al.

2009349 citations

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

Gaël Ménasché,Chen Hsuan Ho,et al.

2003289 citations

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

Gaël Ménasché,Chen Hsuan Ho,et al.

2003285 citations

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

Mickaël Ménager,Gaël Ménasché,et al.

2007255 citations

Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis

Gaël Ménasché,Jérôme Feldmann,et al.

2005176 citations

Inherited defects in lymphocyte cytotoxic activity

Jana Pachlopnik Schmid,Marjorie Côte,et al.

2010171 citations

Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites

Claire Desnos,Jean‐Sébastien Schonn,et al.

2003164 citations