Geneviève de Saint Basile

31.2k total citations · 6 hit papers
226 papers, 17.0k citations indexed

About

Geneviève de Saint Basile is a scholar working on Immunology, Hematology and Molecular Biology. According to data from OpenAlex, Geneviève de Saint Basile has authored 226 papers receiving a total of 17.0k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Immunology, 86 papers in Hematology and 44 papers in Molecular Biology. Recurrent topics in Geneviève de Saint Basile's work include Immune Cell Function and Interaction (85 papers), Immunodeficiency and Autoimmune Disorders (77 papers) and Autoimmune and Inflammatory Disorders Research (76 papers). Geneviève de Saint Basile is often cited by papers focused on Immune Cell Function and Interaction (85 papers), Immunodeficiency and Autoimmune Disorders (77 papers) and Autoimmune and Inflammatory Disorders Research (76 papers). Geneviève de Saint Basile collaborates with scholars based in France, United States and Italy. Geneviève de Saint Basile's co-authors include Alain Fischer, Françoise Le Deist, Stéphanie Certain, Gaël Ménasché, Marina Cavazzana, Jérôme Feldmann, Jean‐Laurent Casanova, James P. Di Santo, Salima Hacein‐Bey and Philippe Bousso and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Geneviève de Saint Basile

220 papers receiving 16.5k citations

Hit Papers

Gene Therapy of Human Severe Combined Immunodeficiency (S... 1993 2026 2004 2015 2000 1999 2000 2003 1993 500 1000 1.5k
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. Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease
    2000 1.8k citations Marina Cavazzana, Geneviève de Saint Basile et al. profile →
  2. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis
    1999 904 citations Rémi Dufourcq-Lagelouse, Françoise Le Deist et al. profile →
  3. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
    2000 708 citations Gaël Ménasché, Élodie Pastural et al. Nature Genetics profile →
  4. Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)
    2003 684 citations Jérôme Feldmann, Graça Raposo et al. profile →
  5. CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM
    1993 556 citations Alain Fischer, Geneviève de Saint Basile et al. profile →
  6. 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, Stéphanie Certain et al. profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Geneviève de Saint Basile France 66 9.7k 5.5k 4.9k 3.3k 2.6k 226 17.0k
Françoise Le Deist France 73 10.6k 1.1× 4.4k 0.8× 5.9k 1.2× 4.0k 1.2× 2.6k 1.0× 226 19.4k
Luigi D. Notarangelo United States 70 11.6k 1.2× 2.1k 0.4× 4.1k 0.8× 4.5k 1.4× 1.3k 0.5× 371 18.2k
Leonard D. Shultz United States 92 14.0k 1.4× 4.8k 0.9× 10.5k 2.1× 5.4k 1.6× 1.6k 0.6× 452 32.2k
Jordan S. Orange United States 74 14.1k 1.5× 2.1k 0.4× 3.2k 0.7× 2.9k 0.9× 1.4k 0.5× 322 19.8k
Robert Winchester United States 68 14.6k 1.5× 3.1k 0.6× 3.3k 0.7× 1.9k 0.6× 912 0.3× 209 28.3k
Smith Rjh Sweden 68 9.3k 1.0× 2.6k 0.5× 8.5k 1.7× 3.2k 1.0× 896 0.3× 723 20.5k
David A. Williams United States 74 5.5k 0.6× 3.6k 0.7× 11.0k 2.2× 4.7k 1.4× 606 0.2× 338 21.2k
R. Keith Humphries Canada 85 4.7k 0.5× 7.5k 1.3× 13.0k 2.6× 3.2k 1.0× 873 0.3× 314 21.5k
David H. Sachs United States 87 14.1k 1.4× 4.3k 0.8× 6.9k 1.4× 6.9k 2.1× 593 0.2× 697 32.0k
Jennifer M. Puck United States 73 13.4k 1.4× 2.2k 0.4× 4.8k 1.0× 5.8k 1.8× 1.4k 0.5× 245 19.3k

Countries citing papers authored by Geneviève de Saint Basile

Since Specialization
Citations

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

Fields of papers citing papers by Geneviève de Saint Basile

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Geneviève de Saint Basile. 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 Geneviève de Saint Basile. The network helps show where Geneviève de Saint Basile may publish in the future.

Co-authorship network of co-authors of Geneviève de Saint Basile

This figure shows the co-authorship network connecting the top 25 collaborators of Geneviève de Saint Basile. A scholar is included among the top collaborators of Geneviève de Saint Basile 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 Geneviève de Saint Basile. Geneviève de Saint Basile 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.
Blouin, Cédric M., Christine Gaillet, Stéphanie Solier, et al.. (2022). Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling. Angewandte Chemie. 134(32). 1 indexed citations
3.
Blouin, Cédric M., Christine Gaillet, Stéphanie Solier, et al.. (2022). Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling. Angewandte Chemie International Edition. 61(32). e202205231–e202205231. 6 indexed citations
4.
Cagnard, Nicolas, Marine Gil, Fernando E. Sepulveda, et al.. (2018). Tetratricopeptide repeat domain 7A is a nuclear factor that modulates transcription and chromatin structure. Cell Discovery. 4(1). 61–61. 11 indexed citations
5.
Walzer, Thierry, et al.. (2017). Late‐onset hemophagocytic lymphohistiocytosis with neurological presentation. Clinical Case Reports. 5(11). 1743–1749. 1 indexed citations
6.
Durand, Amandine, Fernando E. Sepulveda, Julie Rivière, et al.. (2017). Gene transfer into hematopoietic stem cells reduces HLH manifestations in a murine model of Munc13-4 deficiency. Blood Advances. 1(27). 2781–2789. 21 indexed citations
7.
Maschalidi, Sophia, Fernando E. Sepulveda, Alexandrine Garrigue, Alain Fischer, & Geneviève de Saint Basile. (2016). Therapeutic effect of JAK1/2 blockade on the manifestations of hemophagocytic lymphohistiocytosis in mice. Blood. 128(1). 60–71. 143 indexed citations
8.
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
9.
Mahlaoui, Nizar, Isabelle Pellier, Cyril Mignot, et al.. (2012). Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndrome. Blood. 121(9). 1510–1516. 48 indexed citations
10.
Sepulveda, Fernando E., Franck Debeurme, Gaël Ménasché, et al.. (2012). Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11. Blood. 121(4). 595–603. 49 indexed citations
11.
Yenicesu, İdil, Geneviève de Saint Basile, Hamdi Cihan Emeksiz, & Buket Dalgıç. (2012). Familial Hemophagocytic Lymphohistiocytosis with A665 G Perforin Gene Mutation: A Case Report. SHILAP Revista de lepidopterología. 29(3). 265–269. 1 indexed citations
12.
Markert, M. Louise, José Gonçalo Marques, Bénédicte Neven, et al.. (2010). First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases. Blood. 117(2). 688–696. 73 indexed citations
13.
Pivôt-Pajot, Christophe, Frédérique Varoqueaux, Geneviève de Saint Basile, & Sylvain Bourgoin. (2008). Munc13-4 Regulates Granule Secretion in Human Neutrophils. The Journal of Immunology. 180(10). 6786–6797. 54 indexed citations
14.
Schmid, Jana Pachlopnik, Chen‐Hsuan Ho, James S. Diana, et al.. (2008). A Griscelli syndrome type 2 murine model of hemophagocytic lymphohistiocytosis (HLH). European Journal of Immunology. 38(11). 3219–3225. 49 indexed citations
15.
Basile, Geneviève de Saint, et al.. (2007). L’articolo 20 del Nuovo Codice di Deontologia Medica: “rispetto dei diritti della persona”. 33. 1 indexed citations
16.
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
17.
Bourc’his, Déborah, Pierre Miniou, Marc Jeanpierre, et al.. (1999). Abnormal methylation does not prevent X inactivation in ICF patients. Cytogenetic and Genome Research. 84(3-4). 245–252. 32 indexed citations
18.
Pastural, Élodie, Franck J. Barrat, Rémi Dufourcq-Lagelouse, et al.. (1997). Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene. Nature Genetics. 16(3). 289–292. 328 indexed citations
19.
Basile, Geneviève de Saint, Nathalie Lambert, Klaus Schwarz, et al.. (1996). Isolated X-linked thrombocytopenia in two unrelated families is associated with point mutations in the Wiskott-Aldrich syndrome protein gene. The Journal of Pediatrics. 129(1). 56–62. 33 indexed citations
20.
Milili, Michèle, Françoise Le Deist, Geneviève de Saint Basile, et al.. (1993). Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.. Journal of Clinical Investigation. 91(4). 1616–1629. 28 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.

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