Nicolas Chatron

2.2k total citations
44 papers, 263 citations indexed

About

Nicolas Chatron is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Nicolas Chatron has authored 44 papers receiving a total of 263 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Genetics, 17 papers in Molecular Biology and 7 papers in Psychiatry and Mental health. Recurrent topics in Nicolas Chatron's work include Genetics and Neurodevelopmental Disorders (15 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). Nicolas Chatron is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Genomics and Rare Diseases (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). Nicolas Chatron collaborates with scholars based in France, Italy and United States. Nicolas Chatron's co-authors include Damien Sanlaville, Gaëtan Lesca, Audrey Labalme, Vincent des Portes, Patrick Edery, Christine Vinciguerra, Dorothée Ville, Maryline Carneiro, Caroline Schluth‐Bolard and Massimiliano Rossi and has published in prestigious journals such as Brain, Annals of Neurology and Molecular Biology and Evolution.

In The Last Decade

Nicolas Chatron

38 papers receiving 262 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicolas Chatron France 10 129 123 37 30 29 44 263
Elisa Rahikkala Finland 9 163 1.3× 81 0.7× 37 1.0× 18 0.6× 12 0.4× 38 269
Daniel Amsallem France 10 173 1.3× 222 1.8× 25 0.7× 29 1.0× 18 0.6× 21 335
Eve Õiglane‐Shlik Estonia 10 177 1.4× 185 1.5× 39 1.1× 76 2.5× 9 0.3× 17 320
Angelika Köhler Germany 10 222 1.7× 134 1.1× 36 1.0× 34 1.1× 9 0.3× 12 321
Seema Kapoor India 11 157 1.2× 62 0.5× 38 1.0× 37 1.2× 17 0.6× 40 283
Taghreed Shuaib Saudi Arabia 9 133 1.0× 74 0.6× 45 1.2× 14 0.5× 4 0.1× 13 243
Antonella Lettieri Italy 12 165 1.3× 75 0.6× 41 1.1× 29 1.0× 31 1.1× 23 345
Michèle Mathieu‐Dramard France 9 200 1.6× 170 1.4× 18 0.5× 44 1.5× 12 0.4× 15 363
Audrey Putoux France 11 236 1.8× 215 1.7× 36 1.0× 72 2.4× 5 0.2× 32 369
Marcos Delgado United Kingdom 3 135 1.0× 104 0.8× 19 0.5× 5 0.2× 21 0.7× 5 363

Countries citing papers authored by Nicolas Chatron

Since Specialization
Citations

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

Fields of papers citing papers by Nicolas Chatron

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicolas Chatron

This figure shows the co-authorship network connecting the top 25 collaborators of Nicolas Chatron. A scholar is included among the top collaborators of Nicolas Chatron 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 Nicolas Chatron. Nicolas Chatron 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
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Chatron, Nicolas, et al.. (2025). Advocating a specific risk calculation of trisomy 18 in case of low maternal serum markers during screening for fetal Down syndrome. Journal of Gynecology Obstetrics and Human Reproduction. 54(3). 102915–102915.
4.
Heurck, Roxane Van, Eva Hammar, Dorothée Ville, et al.. (2025). Comprehensive genetic diagnosis and therapeutic perspectives in 155 children with developmental and epileptic encephalopathy. European Journal of Paediatric Neurology. 56. 97–103.
5.
Chatron, Nicolas, C. Zawadzki, Anne Lienhart, et al.. (2024). Whole F8 gene sequencing identified pathogenic structural variants in the remaining unsolved patients with severe hemophilia A. Journal of Thrombosis and Haemostasis. 22(6). 1616–1626. 3 indexed citations
6.
Chaussenot, Annabelle, Xavier Ayrignac, Nicolas Chatron, et al.. (2024). Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European Journal of Human Genetics. 32(7). 876–878. 2 indexed citations
7.
Tusseau, Maud, Mélanie Eyries, Nicolas Chatron, et al.. (2024). Genome sequencing identify chromosome 9 inversions disrupting ENG in 2 unrelated HHT families. European Journal of Medical Genetics. 68. 104919–104919. 3 indexed citations
8.
Quēlin, Chloé, Laurent Pasquier, Philippe Loget, et al.. (2023). PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect. European Journal of Medical Genetics. 66(11). 104852–104852.
9.
Rocco, Federico Di, Massimiliano Rossi, Alexandru Szathmári, et al.. (2023). Clinical interest of molecular study in cases of isolated midline craniosynostosis. European Journal of Human Genetics. 31(6). 621–628. 7 indexed citations
10.
Chatron, Nicolas, et al.. (2023). Whole F9 gene sequencing identified deep intronic variations in genetically unresolved hemophilia B patients. Journal of Thrombosis and Haemostasis. 21(4). 828–837. 5 indexed citations
11.
Ragnarsson, Lotten, Zihan Zhang, Åsa Andersson, et al.. (2023). GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms. Epilepsia. 64(12). 3377–3388. 5 indexed citations
12.
Chatron, Nicolas, Audrey Labalme, Yavuz Şahin, et al.. (2023). GRM7-related disorder: five additional patients from three independent families and review of the literature. European Journal of Medical Genetics. 67. 104893–104893. 2 indexed citations
13.
Larasati, Yonika Arum, Gonzalo P. Solis, Alexey Koval, et al.. (2023). Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. Cells. 12(20). 2469–2469. 7 indexed citations
14.
Arzimanoglou, Alexis, et al.. (2022). STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes. European Journal of Medical Genetics. 65(12). 104636–104636. 3 indexed citations
15.
McTague, Amy, Andreas Brunklaus, Giulia Barcia, et al.. (2022). Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologists. European Journal of Medical Genetics. 65(7). 104531–104531. 3 indexed citations
16.
Lesca, Gaëtan, Dorothée Ville, Anne‐Lise Poulat, et al.. (2022). CNTNAP1-encephalopathy: Six novel patients surviving the neonatal period. European Journal of Paediatric Neurology. 37. 98–104. 5 indexed citations
17.
Janin, Alexandre, Nicolas Chatron, Luc Dauchet, et al.. (2020). PCSK9 post-transcriptional regulation: Role of a 3′UTR microRNA-binding site variant in linkage disequilibrium with c.1420G. Atherosclerosis. 314. 63–70. 10 indexed citations
18.
Poisson, Alice, Nicolas Chatron, Audrey Labalme, et al.. (2020). Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report. BMC Medical Genetics. 21(1). 10–10. 10 indexed citations
19.
Mazzola, Laure, Karen Oliver, Audrey Labalme, et al.. (2020). Progressive Myoclonus Epilepsy Caused by a Homozygous Splicing Variant of SLC7A6OS. Annals of Neurology. 89(2). 402–407. 2 indexed citations
20.
Poulat, Anne‐Lise, Nicolas Chatron, Audrey Labalme, et al.. (2019). Asparagine synthetase deficiency: A novel case with an unusual molecular mechanism. Molecular Genetics and Metabolism Reports. 21. 100509–100509. 6 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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