Dorothée Ville

5.0k total citations
56 papers, 1.2k citations indexed

About

Dorothée Ville is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Dorothée Ville has authored 56 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 19 papers in Molecular Biology and 18 papers in Psychiatry and Mental health. Recurrent topics in Dorothée Ville's work include Genetics and Neurodevelopmental Disorders (19 papers), Epilepsy research and treatment (18 papers) and Genomics and Rare Diseases (12 papers). Dorothée Ville is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Epilepsy research and treatment (18 papers) and Genomics and Rare Diseases (12 papers). Dorothée Ville collaborates with scholars based in France, United States and Switzerland. Dorothée Ville's co-authors include Catherine Chiron, Olivier Dulac, Anna Kamińska, Vincent des Portes, Gaëtan Lesca, Nadia Bahi‐Buisson, Damien Sanlaville, O Enjolras, Mathieu Milh and Alexis Arzimanoglou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Brain and Neurology.

In The Last Decade

Dorothée Ville

54 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dorothée Ville France 20 559 367 355 230 172 56 1.2k
Francesco Nicita Italy 23 343 0.6× 288 0.8× 412 1.2× 188 0.8× 244 1.4× 94 1.3k
Jiro Ono Japan 21 244 0.4× 200 0.5× 332 0.9× 294 1.3× 131 0.8× 57 1.1k
Nathalie Dorison France 16 187 0.3× 281 0.8× 293 0.8× 163 0.7× 154 0.9× 30 741
M. Di Capua Italy 20 200 0.4× 406 1.1× 454 1.3× 377 1.6× 310 1.8× 53 1.3k
Zaid Afawi Israel 17 441 0.8× 449 1.2× 442 1.2× 90 0.4× 266 1.5× 27 1.1k
Adam L. Numis United States 14 222 0.4× 355 1.0× 213 0.6× 245 1.1× 156 0.9× 34 853
Marina Trivisano Italy 25 644 1.2× 875 2.4× 460 1.3× 406 1.8× 307 1.8× 104 1.7k
Xiu‐Yu Shi China 15 234 0.4× 369 1.0× 283 0.8× 143 0.6× 219 1.3× 57 731
Lucio Parmeggiani Italy 18 255 0.5× 641 1.7× 241 0.7× 321 1.4× 274 1.6× 44 1.0k
Amy McTague United Kingdom 16 653 1.2× 640 1.7× 344 1.0× 275 1.2× 223 1.3× 32 1.2k

Countries citing papers authored by Dorothée Ville

Since Specialization
Citations

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

Fields of papers citing papers by Dorothée Ville

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dorothée Ville

This figure shows the co-authorship network connecting the top 25 collaborators of Dorothée Ville. A scholar is included among the top collaborators of Dorothée Ville 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 Dorothée Ville. Dorothée Ville 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.
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.
2.
3.
Massoud, Mona, Marine Butin, Yahia Mekki, et al.. (2023). Predicting Outcome of Congenital Cytomegalovirus Infection by Differentiating and Revisiting Severe versus Mild Prenatal Imaging Features. Fetal Diagnosis and Therapy. 50(3). 143–157. 4 indexed citations
4.
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
5.
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
6.
Ville, Dorothée, et al.. (2022). Use of mTOR inhibitors (rapalogs) for the treatment of skin changes in tuberous sclerosis complex. Archives de Pédiatrie. 29(5). 5S20–5S24. 3 indexed citations
7.
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
8.
Schaeffer, Mickaël, Claude Cancés, Jacques Motté, et al.. (2017). Efficacy of a ketogenic diet in resistant myoclono-astatic epilepsy: A French multicenter retrospective study. Epilepsy Research. 131. 64–69. 17 indexed citations
9.
Alfaiz, Ali Abdullah, Verena Müller, Nadia Boutry‐Kryza, et al.. (2015). West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1. European Journal of Human Genetics. 24(7). 1001–1008. 13 indexed citations
10.
Boutry‐Kryza, Nadia, Audrey Labalme, Dorothée Ville, et al.. (2014). Molecular characterization of a cohort of 73 patients with infantile spasms syndrome. European Journal of Medical Genetics. 58(2). 51–58. 51 indexed citations
11.
Ville, Dorothée, et al.. (2013). Pre- and postnatal imaging of early cerebral damage in Sturge-Weber syndrome. Pediatric Radiology. 43(11). 1536–1539. 11 indexed citations
12.
Rossi, Massimiliano, Audrey Labalme, Marie‐Pierre Cordier, et al.. (2012). Mosaic 18q21.2 deletions including the TCF4 gene: A clinical report. American Journal of Medical Genetics Part A. 158A(12). 3174–3181. 10 indexed citations
13.
Verloès, Alain, D. Héron, Thierry Billette de Villemeur, et al.. (2012). Stratégie d’exploration d’une déficience intellectuelle inexpliquée. Archives de Pédiatrie. 19(2). 194–207. 6 indexed citations
14.
Mignot, Cyril, Marie‐Laure Moutard, Oriane Trouillard, et al.. (2011). STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients. Epilepsia. 52(10). 1820–1827. 76 indexed citations
15.
Bussy, Gérald, et al.. (2008). Déficiences intellectuelles liées au chromosome X. MTP. Médecine thérapeutique pédiatrie. 11(4). 218–223. 1 indexed citations
16.
Ville, Dorothée, et al.. (2008). Pericallosal lipoma associated with Pai syndrome: prenatal imaging findings. Ultrasound in Obstetrics and Gynecology. 32(5). 708–710. 15 indexed citations
17.
Pintaudi, Maria, Monika Eisermann, Dorothée Ville, et al.. (2007). Can fever treat epileptic encephalopathies?. Epilepsy Research. 77(1). 44–61. 5 indexed citations
18.
Eisermann, Monika, Dorothée Ville, Christine Soufflet, et al.. (2006). Cryptogenic Late‐onset Epileptic Spasms: An Overlooked Syndrome of Early Childhood?. Epilepsia. 47(6). 1035–1042. 46 indexed citations
19.
Bahi‐Buisson, Nadia, Dorothée Ville, Monika Eisermann, et al.. (2005). L'épilepsie dans les aberrations chromosomiques. Archives de Pédiatrie. 12(4). 449–458. 13 indexed citations
20.
Ville, Dorothée, O Enjolras, Catherine Chiron, & Olivier Dulac. (2002). Prophylactic antiepileptic treatment in Sturge–Weber disease. Seizure. 11(3). 145–150. 70 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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