Martin Chevarin

792 total citations
14 papers, 125 citations indexed

About

Martin Chevarin is a scholar working on Genetics, Molecular Biology and Infectious Diseases. According to data from OpenAlex, Martin Chevarin has authored 14 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 1 paper in Infectious Diseases. Recurrent topics in Martin Chevarin's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Martin Chevarin is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Martin Chevarin collaborates with scholars based in France, United States and United Kingdom. Martin Chevarin's co-authors include Laurence Faivre, Yannis Duffourd, Antonio Vitobello, Christophe Philippe, Christel Thauvin‐Robinet, Arthur Sorlin, Sébastien Moutton, Sophie Nambot, Ange‐Line Bruel and Mirna Assoum and has published in prestigious journals such as Biochemical and Biophysical Research Communications, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Martin Chevarin

14 papers receiving 125 citations

Peers

Martin Chevarin

GENET

CCM

Jessica Sebastian United States

Sophie Nambot France

Hatip Aydın Türkiye

Gwenaël Nadeau France

Catrina M. Loucks Canada

Leonhard Wachutka Germany

Joe Brown United States

Nirmal Vadgama United Kingdom

Matthew Edwards United States

Christel Thauvin France

Jessica Sebastian United States

Martin Chevarin

92 ×1.3

GENET

64 ×1.0

11 ×0.6

8 ×0.6

CCM

9 ×0.7

Citations per year, relative to Martin Chevarin Martin Chevarin (= 1×) peers Jessica Sebastian

Countries citing papers authored by Martin Chevarin

Since Specialization

Citations

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

Fields of papers citing papers by Martin Chevarin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Chevarin

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

All Works

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14 of 14 papers shown

Vitobello, Antonio, Bekim Sadiković, Juliette Albuisson, et al.. (2025). Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype. American Journal of Medical Genetics Part A. 197(7). e64043–e64043. 1 indexed citations

Chevarin, Martin, Juliette Piard, Quentin Thomas, et al.. (2024). Allelic heterogeneity in a patient with postzygotic MTOR ‐related hypomelanosis of Ito with neurodevelopmental abnormalities. Clinical Genetics. 105(5). 581–583. 2 indexed citations

Chevarin, Martin, Antonio Vitobello, Cyril Fournier, et al.. (2022). A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort. European Journal of Human Genetics. 31(7). 761–768. 6 indexed citations

Rocco, Federico Di, Aurore Garde, C. Mottolèse, et al.. (2022). Surgical management of Chiari malformation type 1 associated to MCAP syndrome and study of cerebellar and adjacent tissues for PIK3CA mosaicism. European Journal of Medical Genetics. 66(2). 104678–104678. 2 indexed citations

Valot, Stéphane, Anne Vincent, Yannis Duffourd, et al.. (2022). Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study. Pathogens. 11(8). 938–938. 6 indexed citations

Chevarin, Martin, et al.. (2022). Detection of the novel allele, HLA‐A*32:165, in a French individual by next‐generation sequencing. HLA. 100(6). 631–632. 1 indexed citations

Theiler, Martin, Lisa Weibel, Stéphanie Christen‐Zaech, et al.. (2021). Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations. Journal of the European Academy of Dermatology and Venereology. 35(10). 2085–2090. 4 indexed citations

Mau‐Them, Frédéric Tran, Yannis Duffourd, Antonio Vitobello, et al.. (2021). Interest of exome sequencing trio‐like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases. Molecular Genetics & Genomic Medicine. 9(12). e1836–e1836. 4 indexed citations

Delplancq, Geoffroy, Antonio Vitobello, Sophie Nambot, et al.. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 129–135. 15 indexed citations

10.

Chevarin, Martin, S. Hadj‐Rabia, Stéphanie Leclerc‐Mercier, et al.. (2020). Neutralization of HSF1 in cells from PIK3CA-related overgrowth spectrum patients blocks abnormal proliferation. Biochemical and Biophysical Research Communications. 530(3). 520–526. 7 indexed citations

11.

Bruel, Ange‐Line, Sophie Nambot, Antonio Vitobello, et al.. (2019). Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing. European Journal of Human Genetics. 27(10). 1519–1531. 39 indexed citations

12.

Lecoquierre, François, Yannis Duffourd, Antonio Vitobello, et al.. (2019). Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants. Genetics in Medicine. 21(11). 2504–2511. 20 indexed citations

13.

Kuentz, Paul, Virginie Carmignac, Arthur Sorlin, et al.. (2019). First prenatal PI3K-AKT-mTOR pathway related overgrowth spectrum cohort: Phenotypic and molecular characterization. European Journal of Obstetrics & Gynecology and Reproductive Biology. 234. e169–e169. 1 indexed citations

14.

Moutton, Sébastien, Ange‐Line Bruel, Mirna Assoum, et al.. (2018). Truncating variants of the DLG4 gene are responsible for intellectual disability with marfanoid features. Clinical Genetics. 93(6). 1172–1178. 17 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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