Gaël Ménasché

4.4k total citations · 1 hit paper
37 papers, 3.2k citations indexed

About

Gaël Ménasché is a scholar working on Immunology, Hematology and Cell Biology. According to data from OpenAlex, Gaël Ménasché has authored 37 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Immunology, 14 papers in Hematology and 14 papers in Cell Biology. Recurrent topics in Gaël Ménasché's work include Autoimmune and Inflammatory Disorders Research (14 papers), Immune Cell Function and Interaction (12 papers) and Cellular transport and secretion (10 papers). Gaël Ménasché is often cited by papers focused on Autoimmune and Inflammatory Disorders Research (14 papers), Immune Cell Function and Interaction (12 papers) and Cellular transport and secretion (10 papers). Gaël Ménasché collaborates with scholars based in France, United States and Hong Kong. Gaël Ménasché's co-authors include Geneviève de Saint Basile, Alain Fischer, Jérôme Feldmann, Fügen Ersoy, Françoise Le Deist, Élodie Pastural, Diana W. Bianchi, Stéphanie Certain, Nico Wulffraat and Sophie Dupuis and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Nature Genetics.

In The Last Decade

Gaël Ménasché

36 papers receiving 3.2k citations

Hit Papers

Mutations in RAB27A cause Griscelli syndrome associated w... 2000 2026 2008 2017 2000 200 400 600

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Gaël Ménasché France 24 1.7k 1.2k 974 900 539 37 3.2k
Fügen Ersoy Türkiye 21 1.0k 0.6× 515 0.4× 572 0.6× 551 0.6× 256 0.5× 47 2.2k
Sarah Booth United Kingdom 18 1.8k 1.1× 298 0.3× 433 0.4× 937 1.0× 90 0.2× 26 3.1k
Ute Koch Switzerland 33 2.1k 1.2× 400 0.3× 320 0.3× 2.8k 3.2× 200 0.4× 70 5.1k
Jean‐Michel Heard France 26 1.9k 1.1× 193 0.2× 359 0.4× 1.4k 1.6× 585 1.1× 52 4.5k
Lindsay Hewlett United Kingdom 18 668 0.4× 407 0.3× 738 0.8× 950 1.1× 33 0.1× 20 2.1k
Nobuo Sakaguchi Japan 37 2.7k 1.6× 400 0.3× 207 0.2× 1.9k 2.2× 245 0.5× 119 4.7k
Silvia Parolini Italy 32 4.4k 2.6× 624 0.5× 137 0.1× 484 0.5× 157 0.3× 62 5.2k
Ulrich Pannicke Germany 26 1.9k 1.1× 233 0.2× 318 0.3× 2.5k 2.8× 163 0.3× 40 4.5k
Konrad Krzewski United States 27 1.4k 0.8× 156 0.1× 230 0.2× 522 0.6× 104 0.2× 43 2.0k
Emily M. Mace United States 34 2.3k 1.3× 334 0.3× 161 0.2× 583 0.6× 207 0.4× 103 3.1k

Countries citing papers authored by Gaël Ménasché

Since Specialization
Citations

This map shows the geographic impact of Gaël Ménasché's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gaël Ménasché with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gaël Ménasché more than expected).

Fields of papers citing papers by Gaël Ménasché

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gaël Ménasché. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gaël Ménasché. The network helps show where Gaël Ménasché may publish in the future.

Co-authorship network of co-authors of Gaël Ménasché

This figure shows the co-authorship network connecting the top 25 collaborators of Gaël Ménasché. A scholar is included among the top collaborators of Gaël Ménasché based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Gaël Ménasché. Gaël Ménasché is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kurowska, Mathieu, Mirjana Weimershaus, François‐Xavier Mauvais, et al.. (2025). Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migration. Science Advances. 11(42). eadx7672–eadx7672.
2.
Blank, Ulrich, et al.. (2025). LRO biogenesis and function: what can we learn from mast cells?. Frontiers in Cell and Developmental Biology. 13. 1613677–1613677. 1 indexed citations
3.
Menche, Constantin, Mathieu Kurowska, Despina Moshous, et al.. (2023). Actin dynamics regulation by TTC7A/PI4KIIIα limits DNA damage and cell death under confinement. Journal of Allergy and Clinical Immunology. 152(4). 949–960. 4 indexed citations
4.
Vibhushan, Shamila, Despoina Koumantou, Gaël Ménasché, et al.. (2022). Insulin-regulated aminopeptidase contributes to setting the intensity of FcR-mediated inflammation. Frontiers in Immunology. 13. 1029759–1029759. 2 indexed citations
5.
Kurowska, Mathieu, Shamila Vibhushan, Jian‐Dong Huang, et al.. (2022). Rab44 regulates murine mast cell–driven anaphylaxis through kinesin-1–dependent secretory granule translocation. Journal of Allergy and Clinical Immunology. 150(3). 676–689. 10 indexed citations
6.
Ménasché, Gaël, et al.. (2021). Cytoskeletal Transport, Reorganization, and Fusion Regulation in Mast Cell-Stimulus Secretion Coupling. Frontiers in Cell and Developmental Biology. 9. 652077–652077. 24 indexed citations
7.
Belabed, Meriem, François‐Xavier Mauvais, Sophia Maschalidi, et al.. (2020). Kinesin-1 regulates antigen cross-presentation through the scission of tubulations from early endosomes in dendritic cells. Nature Communications. 11(1). 1817–1817. 19 indexed citations
8.
Madera‐Salcedo, Iris K., Luca Danelli, Neeraj Tiwari, et al.. (2018). Tomosyn functions as a PKCδ-regulated fusion clamp in mast cell degranulation. Science Signaling. 11(537). 16 indexed citations
9.
Sepulveda, Fernando E., Xavier Heiligenstein, Nicolas Goudin, et al.. (2014). LYST Controls the Biogenesis of the Endosomal Compartment Required for Secretory Lysosome Function. Traffic. 16(2). 191–203. 49 indexed citations
10.
Basile, Geneviève de Saint, Gaël Ménasché, & Sylvain Latour. (2011). Inherited defects causing hemophagocytic lymphohistiocytic syndrome. Annals of the New York Academy of Sciences. 1246(1). 64–76. 21 indexed citations
11.
Basile, Geneviève de Saint, Gaël Ménasché, & Alain Fischer. (2010). Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules. Nature reviews. Immunology. 10(8). 568–579. 324 indexed citations
12.
Schmid, Jana Pachlopnik, Marjorie Côte, Mickaël Ménager, et al.. (2010). Inherited defects in lymphocyte cytotoxic activity. Immunological Reviews. 235(1). 10–23. 116 indexed citations
13.
Côte, Marjorie, Mickaël Ménager, Nizar Mahlaoui, et al.. (2009). Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells. Journal of Clinical Investigation. 119(12). 3765–3773. 247 indexed citations
14.
Ménasché, Gaël, et al.. (2007). RIAM Links the ADAP/SKAP-55 Signaling Module to Rap1, Facilitating T-Cell-Receptor-Mediated Integrin Activation. Molecular and Cellular Biology. 27(11). 4070–4081. 93 indexed citations
15.
Ménager, Mickaël, Gaël Ménasché, Maryse Romao, et al.. (2007). Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4. Nature Immunology. 8(3). 257–267. 207 indexed citations
16.
Ménasché, Gaël, Mickaël Ménager, Françoise Le Deist, Alain Fischer, & Geneviève de Saint Basile. (2006). Défaut d’exocytose des granules lytiques. médecine/sciences. 22(8-9). 733–738. 8 indexed citations
17.
Ménasché, Gaël, Jérôme Feldmann, Alain Fischer, & Geneviève de Saint Basile. (2005). Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis. Immunological Reviews. 203(1). 165–179. 124 indexed citations
18.
Bizário, João C. S., Jérôme Feldmann, Fabíola Attié de Castro, et al.. (2004). Griscelli Syndrome: Characterization of a New Mutation and Rescue of T-Cytotoxic Activity by Retroviral Transfer of RAB27A Gene. Journal of Clinical Immunology. 24(4). 397–410. 41 indexed citations
19.
Ménasché, Gaël, Özden Sanal, Jérôme Feldmann, et al.. (2003). Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). Journal of Clinical Investigation. 112(3). 450–456. 214 indexed citations
20.
Ménasché, Gaël, Élodie Pastural, Jérôme Feldmann, et al.. (2000). Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome. Nature Genetics. 25(2). 173–176. 708 indexed citations breakdown →

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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