S Blanchard

920 total citations
8 papers, 710 citations indexed

About

S Blanchard is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, S Blanchard has authored 8 papers receiving a total of 710 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 2 papers in Sensory Systems and 2 papers in Genetics. Recurrent topics in S Blanchard's work include Hearing, Cochlea, Tinnitus, Genetics (2 papers), RNA regulation and disease (2 papers) and Biomarkers in Disease Mechanisms (2 papers). S Blanchard is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (2 papers), RNA regulation and disease (2 papers) and Biomarkers in Disease Mechanisms (2 papers). S Blanchard collaborates with scholars based in France, Italy and Germany. S Blanchard's co-authors include Christine Petit, Claude Moraine, Renaud Legouis, Jacqueline Levilliers, Ignacio del Castillo, Jeremy Kirk, Jean‐Pierre Hardelin, Pierre-Marc Bouloux, Martine Cohen‐Salmon and Didier Négre and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Cell Death and Differentiation.

In The Last Decade

S Blanchard

8 papers receiving 703 citations

Peers

S Blanchard
Barbara K. Lee United States
Jason Treadaway United States
Cinzia G. Scarpini United Kingdom
José L. Estrada United States
Paul Carmillo United States
Tatiana V. Cohen United States
Barbara K. Lee United States
S Blanchard
Citations per year, relative to S Blanchard S Blanchard (= 1×) peers Barbara K. Lee

Countries citing papers authored by S Blanchard

Since Specialization
Citations

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

Fields of papers citing papers by S Blanchard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S Blanchard

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

All Works

8 of 8 papers shown
1.
Cunin, Pierre, Céline Beauvillain, Charline Miot, et al.. (2016). Clusterin facilitates apoptotic cell clearance and prevents apoptotic cell-induced autoimmune responses. Cell Death and Disease. 7(5). e2215–e2215. 88 indexed citations
2.
Jacquier, Arnaud, et al.. (2009). Astrocytic protection of spinal motor neurons but not cortical neurons against loss of Als2/alsin function. Human Molecular Genetics. 18(12). 2127–2139. 15 indexed citations
3.
Jaillon, Sébastien, Pascale Jeannin, Isabelle Frémaux, et al.. (2008). Endogenous PTX3 translocates at the membrane of late apoptotic human neutrophils and is involved in their engulfment by macrophages. Cell Death and Differentiation. 16(3). 465–474. 67 indexed citations
4.
Négre, Didier, Philippe Mangeot, Ghislaine Duisit, et al.. (2000). Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells. Gene Therapy. 7(19). 1613–1623. 172 indexed citations
5.
Zwaenepoel, Ingrid, Elisabeth Verpy, S Blanchard, et al.. (2000). Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis. Human Mutation. 17(1). 34–41. 33 indexed citations
6.
Marlin, Sandrine, S Blanchard, Rima Slim, et al.. (1999). Townes-Brocks syndrome: Detection of aSALL1 mutation hot spot and evidence for a position effect in one patient. Human Mutation. 14(5). 377–386. 49 indexed citations
7.
Weil, Dominique, G Lévy, Iman Sahly, et al.. (1996). Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.. Proceedings of the National Academy of Sciences. 93(8). 3232–3237. 138 indexed citations
8.
Hardelin, Jean‐Pierre, Jacqueline Levilliers, Ignacio del Castillo, et al.. (1992). X chromosome-linked Kallmann syndrome: stop mutations validate the candidate gene.. Proceedings of the National Academy of Sciences. 89(17). 8190–8194. 148 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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