Kévin Cassinari

445 total citations
18 papers, 150 citations indexed

About

Kévin Cassinari is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Kévin Cassinari has authored 18 papers receiving a total of 150 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Kévin Cassinari's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (3 papers). Kévin Cassinari is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cancer Genomics and Diagnostics (3 papers). Kévin Cassinari collaborates with scholars based in France, United States and Netherlands. Kévin Cassinari's co-authors include Pascal Chambon, Thierry Frébourg, Gaël Nicolas, Anne Rovelet‐Lecrux, Olivier Quenez, Annie Laquerrière, Ludivine Beaussire, Dominique Campion, Claude Houdayer and Pascale Saugier-Véber and has published in prestigious journals such as Scientific Reports, Clinical Chemistry and Movement Disorders.

In The Last Decade

Kévin Cassinari

16 papers receiving 148 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kévin Cassinari France 9 56 34 25 22 22 18 150
Narayan Chandra Saha Bangladesh 6 55 1.0× 30 0.9× 17 0.7× 2 0.1× 14 0.6× 34 192
Christopher Markosian United States 9 55 1.0× 6 0.2× 23 0.9× 12 0.5× 6 0.3× 26 183
Eduardo de Paula Estephan Brazil 9 38 0.7× 23 0.7× 28 1.1× 9 0.4× 6 0.3× 19 219
Sarah Groves United Kingdom 4 250 4.5× 55 1.6× 12 0.5× 6 0.3× 29 1.3× 8 334
Stacey Hume Canada 10 108 1.9× 68 2.0× 6 0.2× 3 0.1× 8 0.4× 19 207
Khalid Hundallah Saudi Arabia 7 88 1.6× 48 1.4× 24 1.0× 3 0.1× 15 0.7× 21 165
Anita Chhabra United States 4 55 1.0× 19 0.6× 13 0.5× 2 0.1× 22 1.0× 9 161
Daniel A. Michelson United States 9 60 1.1× 18 0.5× 21 0.8× 5 0.2× 14 0.6× 11 237
Bettina Thomas Germany 12 79 1.4× 40 1.2× 10 0.4× 4 0.2× 12 0.5× 16 274
Jessica Camacho Spain 7 55 1.0× 8 0.2× 10 0.4× 3 0.1× 30 1.4× 14 156

Countries citing papers authored by Kévin Cassinari

Since Specialization
Citations

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

Fields of papers citing papers by Kévin Cassinari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kévin Cassinari

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

All Works

18 of 18 papers shown
1.
Rovelet‐Lecrux, Anne, Olivier Quenez, Kévin Cassinari, et al.. (2024). Upstream open reading frame-introducing variants in patients with primary familial brain calcification. European Journal of Human Genetics. 32(7). 779–785. 2 indexed citations
2.
Lecoquierre, François, Kévin Cassinari, Nathalie Drouot, et al.. (2024). Assessment of parental mosaicism rates in neurodevelopmental disorders caused by apparent de novo pathogenic variants using deep sequencing. Scientific Reports. 14(1). 5289–5289. 2 indexed citations
3.
Rovelet‐Lecrux, Anne, Kévin Cassinari, Elise Brischoux‐Boucher, et al.. (2022). uORF‐introducing variants in the 5′UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome. Human Mutation. 43(9). 1239–1248. 9 indexed citations
4.
Blanluet, Maud, Sandra Chantot‐Bastaraud, Pascal Chambon, et al.. (2021). Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings. American Journal of Medical Genetics Part A. 185(10). 3057–3061. 1 indexed citations
5.
Hureaux, Marguerite, Sandra Chantot‐Bastaraud, Kévin Cassinari, et al.. (2021). When a maternal heterozygous mutation of the CYP24A1 gene leads to infantile hypercalcemia through a maternal uniparental disomy of chromosome 20. Molecular Cytogenetics. 14(1). 23–23. 4 indexed citations
6.
Marguet, Florent, Myriam Vézain, Pascale Marcorelles, et al.. (2021). Neuropathological hallmarks of fetal hydrocephalus linked to CCDC88C pathogenic variants. Acta Neuropathologica Communications. 9(1). 104–104. 15 indexed citations
7.
Grangeon, Lou, Kévin Cassinari, Stéphane Rousseau, et al.. (2021). Early-Onset Cerebral Amyloid Angiopathy and Alzheimer Disease Related to an APP Locus Triplication. Neurology Genetics. 7(5). e609–e609. 20 indexed citations
8.
Cassinari, Kévin, Élodie Alessandri-Gradt, Pascal Chambon, et al.. (2020). Assessment of Multiplex Digital Droplet RT-PCR as a Diagnostic Tool for SARS-CoV-2 Detection in Nasopharyngeal Swabs and Saliva Samples. Clinical Chemistry. 67(5). 736–741. 30 indexed citations
9.
Fontanilles, Maxime, Florent Marguet, Philippe Ruminy, et al.. (2020). Simultaneous detection of EGFR amplification and EGFRvIII variant using digital PCR-based method in glioblastoma. Acta Neuropathologica Communications. 8(1). 52–52. 9 indexed citations
10.
Cassinari, Kévin, Anne Rovelet‐Lecrux, Olivier Quenez, et al.. (2020). Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element. Movement Disorders. 35(8). 1336–1345. 9 indexed citations
11.
Wang, Qing, Julie Leclerc, Gaëlle Bougeard, et al.. (2020). Characterisation of heterozygous PMS2 variants in French patients with Lynch syndrome. Journal of Medical Genetics. 57(7). 487–499. 8 indexed citations
12.
Lecoquierre, François, Kévin Cassinari, Pascal Chambon, et al.. (2019). Patients with 10q22.3q23.1 recurrent deletion syndrome are at risk for juvenile polyposis. European Journal of Medical Genetics. 63(4). 103773–103773. 3 indexed citations
13.
Quenez, Olivier, Annie Laquerrière, Florent Marguet, et al.. (2019). Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer’s Disease. Journal of Alzheimer s Disease. 68(3). 1243–1255. 17 indexed citations
14.
Cassinari, Kévin, Olivier Quenez, Géraldine Joly‐Hélas, et al.. (2019). A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations. Clinical Chemistry. 65(9). 1153–1160. 11 indexed citations
15.
Cassinari, Kévin, et al.. (2018). 2009-2017 report on the attractiveness of laboratory medicine among young doctors. Annales de biologie clinique. 76(2). 125–130. 1 indexed citations
16.
Cassinari, Kévin, François Lecoquierre, Jean‐Christophe Théry, et al.. (2017). Cost-effectiveness evaluation of pre-counseling telephone interviews before face-to-face genetic counseling in cancer genetics. Familial Cancer. 17(3). 451–457. 2 indexed citations
17.
Cassinari, Kévin. (2017). La réforme du troisième cycle des études de médecine. Morphologie. 101(335). 266–266.
18.
Faivre, Jean, Mikaël Agopiantz, Kévin Cassinari, et al.. (2015). Évaluation nationale de l’enseignement théorique du troisième cycle des études médicales en France. La Revue de Médecine Interne. 36(9). 579–587. 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.

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