Stéphanie Certain

7.2k total citations · 5 hit papers
12 papers, 5.3k citations indexed

About

Stéphanie Certain is a scholar working on Hematology, Immunology and Speech and Hearing. According to data from OpenAlex, Stéphanie Certain has authored 12 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Hematology, 7 papers in Immunology and 3 papers in Speech and Hearing. Recurrent topics in Stéphanie Certain's work include Autoimmune and Inflammatory Disorders Research (7 papers), Immune Cell Function and Interaction (6 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Stéphanie Certain is often cited by papers focused on Autoimmune and Inflammatory Disorders Research (7 papers), Immune Cell Function and Interaction (6 papers) and Immunodeficiency and Autoimmune Disorders (4 papers). Stéphanie Certain collaborates with scholars based in France, United States and Switzerland. Stéphanie Certain's co-authors include Geneviève de Saint Basile, Alain Fischer, Françoise Le Deist, Jérôme Feldmann, Jean‐Laurent Casanova, Patrick Nusbaum, Fabian Gross, Salima Hacein‐Bey, Philippe Bousso and Christophe Hue and has published in prestigious journals such as Science, Cell and Nature Genetics.

In The Last Decade

Stéphanie Certain

12 papers receiving 5.1k citations

Hit Papers

Gene Therapy of Human Severe Combined Immunodeficiency (S... 1999 2026 2008 2017 2000 1999 2000 2003 2002 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, Salima Hacein‐Bey et al. Science profile →
  2. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis
    1999 904 citations Susan E. Stepp, Rémi Dufourcq-Lagelouse et al. Science 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, Isabelle Callebaut et al. Cell profile →
  5. 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
Stéphanie Certain France 10 2.5k 2.2k 1.9k 1.5k 957 12 5.3k
Özden Sanal Türkiye 38 2.5k 1.0× 2.6k 1.2× 699 0.4× 929 0.6× 605 0.6× 165 5.8k
I L Weissman United States 37 1.8k 0.7× 3.4k 1.6× 1.1k 0.6× 733 0.5× 625 0.7× 61 6.4k
Anne Galy France 45 3.3k 1.3× 2.7k 1.3× 939 0.5× 1.6k 1.1× 214 0.2× 155 6.6k
Christine Kinnon United Kingdom 39 3.4k 1.4× 3.0k 1.4× 889 0.5× 2.9k 2.0× 333 0.3× 117 7.2k
Stacie M. Anderson United States 39 3.8k 1.5× 2.3k 1.1× 1.3k 0.7× 1.3k 0.9× 1.2k 1.3× 83 9.8k
İlhan Tezcan Türkiye 29 1.3k 0.5× 2.1k 1.0× 522 0.3× 796 0.5× 374 0.4× 210 4.2k
Sylvain Latour France 47 1.8k 0.8× 5.7k 2.6× 1.2k 0.7× 698 0.5× 624 0.7× 99 7.7k
Gay M. Crooks United States 42 2.8k 1.1× 1.3k 0.6× 1.0k 0.6× 1.1k 0.8× 180 0.2× 118 5.4k
Robert E. Donahue United States 46 3.9k 1.6× 1.9k 0.9× 2.0k 1.1× 3.5k 2.4× 504 0.5× 177 7.8k
Silvia Giliani Italy 35 1.6k 0.7× 3.1k 1.4× 627 0.3× 968 0.7× 222 0.2× 135 5.6k

Countries citing papers authored by Stéphanie Certain

Since Specialization
Citations

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

Fields of papers citing papers by Stéphanie Certain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphanie Certain

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphanie Certain. A scholar is included among the top collaborators of Stéphanie Certain 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 Stéphanie Certain. Stéphanie Certain is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Stepp, Susan E., Rémi Dufourcq-Lagelouse, Françoise Le Deist, et al.. (2015). Pillars Article: Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis. Science. 1999. 286: 1957–1959. The Journal of Immunology. 194(11). 5044–5046. 6 indexed citations
2.
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 →
3.
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
4.
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 →
5.
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 →
6.
Certain, Stéphanie, Franck J. Barrat, Élodie Pastural, et al.. (2000). Protein truncation test of LYST reveals heterogenous mutations in patients with Chediak-Higashi syndrome.. Blood. 95(3). 979–83. 66 indexed citations
7.
Cavazzana, Marina, Salima Hacein‐Bey, Geneviève de Saint Basile, et al.. (2000). Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease. Science. 288(5466). 669–672. 1819 indexed citations breakdown →
8.
Stepp, Susan E., Rémi Dufourcq-Lagelouse, Françoise Le Deist, et al.. (1999). Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis. Science. 286(5446). 1957–1959. 904 indexed citations breakdown →
9.
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
10.
Barrat, Franck J., D. Depétris, Stéphanie Certain, Marie‐Geneviève Mattéi, & Geneviève de Saint Basile. (1997). Localization of the Rab Escort Protein-2 (REP2) and Inositol 1,4,5-Trisphosphate 3-Kinase (ITPKB) Genes to Mouse Chromosome 1 byin SituHybridization and Precision of the Syntenic Regions between Mouse and Human 1q42–q44. Genomics. 43(1). 111–113. 4 indexed citations
11.
Santo, James P. Di, Stéphanie Certain, Alain Fischer, Geneviève de Saint Basile, & Alice Dautry‐Varsat. (1994). Interleukin‐2 (IL‐2) receptor γ chain mutations in X‐linked severe combined immunodeficiency disease result in the loss of high‐affinity IL‐2 receptor binding. European Journal of Immunology. 24(2). 475–479. 58 indexed citations
12.
Santo, James P. Di, Stéphanie Certain, Anne E. Wilson, et al.. (1994). The murine interleukin‐2 receptor γ chain gene: Organization, chromosomal localization and expression in the adult thymus. European Journal of Immunology. 24(12). 3014–3018. 19 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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