Jérôme Feldmann

4.6k total citations · 3 hit papers
22 papers, 3.5k citations indexed

About

Jérôme Feldmann is a scholar working on Immunology, Hematology and Molecular Biology. According to data from OpenAlex, Jérôme Feldmann has authored 22 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Immunology, 9 papers in Hematology and 8 papers in Molecular Biology. Recurrent topics in Jérôme Feldmann's work include Autoimmune and Inflammatory Disorders Research (9 papers), Immune Cell Function and Interaction (6 papers) and HIV Research and Treatment (5 papers). Jérôme Feldmann is often cited by papers focused on Autoimmune and Inflammatory Disorders Research (9 papers), Immune Cell Function and Interaction (6 papers) and HIV Research and Treatment (5 papers). Jérôme Feldmann collaborates with scholars based in France, United States and Türkiye. Jérôme Feldmann's co-authors include Geneviève de Saint Basile, Alain Fischer, Stéphanie Certain, Gaël Ménasché, Françoise Le Deist, Fügen Ersoy, Nico Wulffraat, Élodie Pastural, Pierre Quartier and Diana W. Bianchi and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Jérôme Feldmann

22 papers receiving 3.4k citations

Hit Papers

Mutations in RAB27A cause Griscelli syndrome associated w... 2000 2026 2008 2017 2000 2003 2002 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
    2000 708 citations Gaël Ménasché, Élodie Pastural et al. Nature Genetics profile →
  2. Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
    2003 684 citations Jérôme Feldmann, Isabelle Callebaut et al. Cell profile →
  3. Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes
    2002 544 citations Jérôme Feldmann, Anne‐Marie Prieur et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jérôme Feldmann France 18 1.8k 1.4k 1.2k 755 684 22 3.5k
HD Ochs United States 30 2.0k 1.1× 916 0.7× 875 0.8× 312 0.4× 231 0.3× 63 3.9k
Dennis E. Hourcade United States 34 2.3k 1.3× 878 0.6× 737 0.6× 134 0.2× 296 0.4× 74 3.8k
Sylvain Latour France 47 5.7k 3.1× 1.2k 0.9× 1.8k 1.6× 213 0.3× 624 0.9× 99 7.7k
Jean‐Michel Heard France 26 1.9k 1.0× 193 0.1× 1.4k 1.2× 359 0.5× 585 0.9× 52 4.5k
Özden Sanal Türkiye 38 2.6k 1.4× 699 0.5× 2.5k 2.1× 604 0.8× 605 0.9× 165 5.8k
John P. Atkinson United States 20 2.3k 1.2× 512 0.4× 447 0.4× 74 0.1× 262 0.4× 23 3.1k
Anthony R. French United States 33 4.3k 2.3× 594 0.4× 696 0.6× 143 0.2× 200 0.3× 66 5.5k
Fügen Ersoy Türkiye 21 1.0k 0.5× 515 0.4× 551 0.5× 572 0.8× 256 0.4× 47 2.2k
Francine Jotereau France 45 4.3k 2.3× 288 0.2× 2.0k 1.7× 261 0.3× 283 0.4× 109 5.9k
Hector Molina United States 36 3.6k 1.9× 718 0.5× 647 0.6× 49 0.1× 229 0.3× 51 4.8k

Countries citing papers authored by Jérôme Feldmann

Since Specialization
Citations

This map shows the geographic impact of Jérôme Feldmann'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 Jérôme Feldmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jérôme Feldmann more than expected).

Fields of papers citing papers by Jérôme Feldmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jérôme Feldmann. 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 Jérôme Feldmann. The network helps show where Jérôme Feldmann may publish in the future.

Co-authorship network of co-authors of Jérôme Feldmann

This figure shows the co-authorship network connecting the top 25 collaborators of Jérôme Feldmann. A scholar is included among the top collaborators of Jérôme Feldmann 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 Jérôme Feldmann. Jérôme Feldmann 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.
Casartelli, Nicoletta, Marion Sourisseau, Jérôme Feldmann, et al.. (2010). Tetherin Restricts Productive HIV-1 Cell-to-Cell Transmission. PLoS Pathogens. 6(6). e1000955–e1000955. 130 indexed citations
2.
Feldmann, Jérôme & Olivier Schwartz. (2010). HIV-1 Virological Synapse: Live Imaging of Transmission. Viruses. 2(8). 1666–1680. 35 indexed citations
3.
Leligdowicz, Aleksandra, Jérôme Feldmann, Assan Jaye, et al.. (2009). Direct Relationship between Virus Load and Systemic Immune Activation in HIV‐2 Infection. The Journal of Infectious Diseases. 201(1). 114–122. 44 indexed citations
4.
Rudnicka, Dominika, Jérôme Feldmann, Françoise Porrot, et al.. (2009). Simultaneous Cell-to-Cell Transmission of Human Immunodeficiency Virus to Multiple Targets through Polysynapses. Journal of Virology. 83(12). 6234–6246. 191 indexed citations
5.
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
6.
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
7.
Ménasché, Gaël, Özden Sanal, Jérôme Feldmann, et al.. (2005). Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1). Journal of Clinical Investigation. 115(4). 1100–1100. 1 indexed citations
8.
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
9.
10.
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
11.
Feldmann, Jérôme, Isabelle Callebaut, Graça Raposo, et al.. (2003). Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3). Cell. 115(4). 461–473. 684 indexed citations breakdown →
12.
Ménasché, Gaël, Jérôme Feldmann, Anne Houdusse, et al.. (2003). Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients. Blood. 101(7). 2736–2742. 73 indexed citations
13.
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. 197 indexed citations
14.
Bidère, Nicolas, Marie Briet, Antoine Dürrbach, et al.. (2002). Selective Inhibition of Dipeptidyl Peptidase I, Not Caspases, Prevents the Partial Processing of Procaspase-3 in CD3-activated Human CD8+ T Lymphocytes. Journal of Biological Chemistry. 277(35). 32339–32347. 22 indexed citations
15.
Feldmann, Jérôme, Françoise Le Deist, O Marie, et al.. (2002). Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis. British Journal of Haematology. 117(4). 965–972. 113 indexed citations
16.
Feldmann, Jérôme, Anne‐Marie Prieur, Pierre Quartier, et al.. (2002). Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes. The American Journal of Human Genetics. 71(1). 198–203. 544 indexed citations breakdown →
17.
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 →
18.
Dufourcq-Lagelouse, Rémi, Élodie Pastural, Franck J. Barrat, et al.. (1999). Genetic basis of hemophagocytic lymphohistiocytosis syndrome (Review).. International Journal of Molecular Medicine. 4(2). 127–33. 44 indexed citations
19.
Barrat, Franck J., Françoise Le Deist, Malika Benkerrou, et al.. (1999). Defective CTLA-4 cycling pathway in Chediak–Higashi syndrome: A possible mechanism for deregulation of T lymphocyte activation. Proceedings of the National Academy of Sciences. 96(15). 8645–8650. 55 indexed citations
20.
Feldmann, Jérôme, et al.. (1968). Tomato bushy stunt virus on Tomato crops in Argentina.. ˜The œPlant disease reporter. 52(9). 676–677. 7 indexed citations

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by HD Ochs Breakdown of academic impact, for papers by Dennis E. Hourcade Breakdown of academic impact, for papers by Sylvain Latour Breakdown of academic impact, for papers by Jean‐Michel Heard Breakdown of academic impact, for papers by Özden Sanal Breakdown of academic impact, for papers by John P. Atkinson Breakdown of academic impact, for papers by Anthony R. French Breakdown of academic impact, for papers by Fügen Ersoy Breakdown of academic impact, for papers by Francine Jotereau Breakdown of academic impact, for papers by Hector Molina
Rankless by CCL
2026