Sandrine Passemard

3.5k total citations
42 papers, 1.4k citations indexed

About

Sandrine Passemard is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Sandrine Passemard has authored 42 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 21 papers in Genetics and 17 papers in Cell Biology. Recurrent topics in Sandrine Passemard's work include Microtubule and mitosis dynamics (14 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Epigenetics and DNA Methylation (5 papers). Sandrine Passemard is often cited by papers focused on Microtubule and mitosis dynamics (14 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Epigenetics and DNA Methylation (5 papers). Sandrine Passemard collaborates with scholars based in France, United Kingdom and Italy. Sandrine Passemard's co-authors include Alain Verloès, Pierre Gressèns, Angela M. Kaindl, Vincent El Ghouzzi, Olivier Cases, Jacques Callebert, Leslie Schwendimann, Tania Vitalis, John G. Parnavelas and Sophie Lebon and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Sandrine Passemard

40 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandrine Passemard France 21 710 405 396 185 168 42 1.4k
Férechté Encha‐Razavi France 21 870 1.2× 298 0.7× 529 1.3× 172 0.9× 215 1.3× 64 1.7k
Tomohide Goto Japan 18 602 0.8× 159 0.4× 165 0.4× 299 1.6× 328 2.0× 67 1.3k
Teresa M. Gunn United States 22 717 1.0× 655 1.6× 230 0.6× 53 0.3× 172 1.0× 63 1.6k
David W. Pincus United States 21 766 1.1× 431 1.1× 181 0.5× 301 1.6× 641 3.8× 51 2.0k
A. Gélot France 26 1.1k 1.5× 349 0.9× 385 1.0× 332 1.8× 465 2.8× 77 2.7k
Satoru Takahashi Japan 18 786 1.1× 368 0.9× 194 0.5× 200 1.1× 338 2.0× 50 1.6k
Francesca Galbiati Italy 21 474 0.7× 146 0.4× 145 0.4× 148 0.8× 81 0.5× 52 1.4k
Maik Dahlhoff Germany 23 589 0.8× 145 0.4× 239 0.6× 47 0.3× 105 0.6× 73 1.5k
Alex R. Paciorkowski United States 21 630 0.9× 242 0.6× 669 1.7× 28 0.2× 161 1.0× 49 1.4k
Susan Moore United Kingdom 20 873 1.2× 137 0.3× 716 1.8× 40 0.2× 121 0.7× 30 2.0k

Countries citing papers authored by Sandrine Passemard

Since Specialization
Citations

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

Fields of papers citing papers by Sandrine Passemard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandrine Passemard

This figure shows the co-authorship network connecting the top 25 collaborators of Sandrine Passemard. A scholar is included among the top collaborators of Sandrine Passemard 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 Sandrine Passemard. Sandrine Passemard 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.
Bahi‐Buisson, Nadia, et al.. (2023). Genetic Primary Microcephalies: When Centrosome Dysfunction Dictates Brain and Body Size. Cells. 12(13). 1807–1807. 10 indexed citations
2.
Passemard, Sandrine, Albert Faye, Caroline Dubertret, et al.. (2021). Covid-19 crisis impact on the next generation of physicians: a survey of 800 medical students. BMC Medical Education. 21(1). 529–529. 9 indexed citations
3.
Uwineza, Annette, Jean‐Hubert Caberg, Stéphane Wenric, et al.. (2019). VPS51 biallelic variants cause microcephaly with brain malformations: A confirmatory report. European Journal of Medical Genetics. 62(8). 103704–103704. 14 indexed citations
4.
Passemard, Sandrine, Franck Perez, Pierre Gressèns, & Vincent El Ghouzzi. (2019). Endoplasmic reticulum and Golgi stress in microcephaly. SHILAP Revista de lepidopterología. 3(12). 369–384. 26 indexed citations
5.
Bruel, Ange‐Line, Jonathan Lévy, Narcisse Elenga, et al.. (2018). INTU‐related oral‐facial‐digital syndrome type VI: A confirmatory report. Clinical Genetics. 93(6). 1205–1209. 6 indexed citations
6.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
7.
Vial, Yoann, Damien Haye, Sandrine Passemard, et al.. (2017). Phosphoglycerate dehydrogenase (PHGDH) deficiency without epilepsy mimicking primary microcephaly. American Journal of Medical Genetics Part A. 173(7). 1936–1942. 8 indexed citations
8.
Ghouzzi, Vincent El, F. Bianchi, Ivan Molineris, et al.. (2016). ZIKA virus elicits P53 activation and genotoxic stress in human neural progenitors similar to mutations involved in severe forms of genetic microcephaly and p53. Cell Death and Disease. 7(10). e2440–e2440. 101 indexed citations
9.
Harding, Brian, Séverine Drunat, Omar Soukarieh, et al.. (2016). Mutations in Citron Kinase Cause Recessive Microlissencephaly with Multinucleated Neurons. The American Journal of Human Genetics. 99(2). 511–520. 47 indexed citations
10.
Pichard, Samia, Hélène Maurey, Nuria García Segarra, et al.. (2015). Angelman syndrome and isovaleric acidemia: What is the link?. SHILAP Revista de lepidopterología. 3. 36–38. 2 indexed citations
11.
Scheidecker, Sophie, Christelle Etard, Laurence Haren, et al.. (2015). Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy. The American Journal of Human Genetics. 96(4). 666–674. 50 indexed citations
12.
Germanaud, David, Julien Lefèvre, Clara Fischer, et al.. (2014). Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification. NeuroImage. 102. 317–331. 24 indexed citations
13.
Baulny, Hélène Ogier de, Renata Kozyraki, Sandrine Passemard, et al.. (2012). How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B12 absorption?. Molecular Genetics and Metabolism. 107(1-2). 66–71. 15 indexed citations
14.
Passemard, Sandrine, Vincent El Ghouzzi, Catherine Verney, et al.. (2011). VIP blockade leads to microcephaly in mice via disruption of Mcph1-Chk1 signaling. Journal of Clinical Investigation. 121(8). 3072–3087. 22 indexed citations
15.
Manouvrier, Sylvie, Fabienne Escande, Sandrine Passemard, et al.. (2011). A familial syndromal form of omphalocele. European Journal of Medical Genetics. 54(3). 337–340. 2 indexed citations
16.
Osimani, Sara, Isabelle Husson, Sandrine Passemard, et al.. (2010). Craniosynostosis: A rare complication of pycnodysostosis. European Journal of Medical Genetics. 53(2). 89–92. 20 indexed citations
17.
Scala, Iris, Luigi Titomanlio, Ennio Del Giudice, et al.. (2010). Absence of microcephalin gene mutations in a large cohort of non‐consanguineous patients with autosomal recessive primary microcephaly. American Journal of Medical Genetics Part A. 152A(11). 2882–2885. 3 indexed citations
18.
Kaindl, Angela M., Sandrine Passemard, Pavan Kumar, et al.. (2009). Many roads lead to primary autosomal recessive microcephaly. Progress in Neurobiology. 90(3). 363–383. 140 indexed citations
19.
Tabet, Anne‐Claude, Isabelle Bailleul‐Forestier, Brigitte Benzacken, et al.. (2009). Ectodermal dysplasia‐like syndrome with mental retardation due to contiguous gene deletion: Further clinical and molecular delineation of del(2q32) syndrome. American Journal of Medical Genetics Part A. 152A(1). 111–117. 24 indexed citations
20.
Kaindl, Angela M., Sandrine Passemard, & Pierre Gressèns. (2008). Autosomal recessive primary microcephalies (MCPH). European Journal of Paediatric Neurology. 13(5). 458–458. 2 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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