Oriane Trouillard

2.7k total citations
20 papers, 490 citations indexed

About

Oriane Trouillard is a scholar working on Genetics, Neurology and Psychiatry and Mental health. According to data from OpenAlex, Oriane Trouillard has authored 20 papers receiving a total of 490 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Neurology and 6 papers in Psychiatry and Mental health. Recurrent topics in Oriane Trouillard's work include Epilepsy research and treatment (6 papers), Genomics and Rare Diseases (5 papers) and Neurological disorders and treatments (5 papers). Oriane Trouillard is often cited by papers focused on Epilepsy research and treatment (6 papers), Genomics and Rare Diseases (5 papers) and Neurological disorders and treatments (5 papers). Oriane Trouillard collaborates with scholars based in France, Germany and Norway. Oriane Trouillard's co-authors include Christel Depienne, Eric Leguern, Isabelle Gourfinkel‐An, Stéphanie Baulac, Charlotte Dravet, Cécile Saint‐Martin, Rima Nabbout, Michel Baulac, Aurélie Méneret and Emmanuel Roze and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Oriane Trouillard

19 papers receiving 484 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oriane Trouillard France 10 249 232 182 111 77 20 490
A.-E. Lehesjoki Finland 12 133 0.5× 310 1.3× 241 1.3× 128 1.2× 91 1.2× 16 610
Stefania Bigoni Italy 14 82 0.3× 255 1.1× 190 1.0× 105 0.9× 65 0.8× 33 520
Sara Baldassari France 14 291 1.2× 437 1.9× 435 2.4× 157 1.4× 67 0.9× 27 859
Delphine Héron France 11 60 0.2× 157 0.7× 201 1.1× 138 1.2× 63 0.8× 27 421
Pierre Cacciagli France 15 104 0.4× 391 1.7× 410 2.3× 100 0.9× 20 0.3× 25 739
Liri Jin China 11 151 0.6× 60 0.3× 141 0.8× 140 1.3× 73 0.9× 34 391
Katsuhisa Uruno United States 9 209 0.8× 225 1.0× 281 1.5× 373 3.4× 21 0.3× 11 671
Liwen Wu China 7 94 0.4× 227 1.0× 179 1.0× 77 0.7× 23 0.3× 14 420
Greta Gillies Australia 9 114 0.5× 216 0.9× 302 1.7× 56 0.5× 18 0.2× 13 481
Christopher M. LaCoursiere United States 6 142 0.6× 324 1.4× 315 1.7× 93 0.8× 15 0.2× 7 584

Countries citing papers authored by Oriane Trouillard

Since Specialization
Citations

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

Fields of papers citing papers by Oriane Trouillard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oriane Trouillard

This figure shows the co-authorship network connecting the top 25 collaborators of Oriane Trouillard. A scholar is included among the top collaborators of Oriane Trouillard 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 Oriane Trouillard. Oriane Trouillard 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.
Wirth, Thomas, Emmanuel Roze, Oriane Trouillard, et al.. (2024). Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia. Movement Disorders. 39(5). 897–905. 1 indexed citations
2.
Trouillard, Oriane, P. Dupaigne, Mohamed Doulazmi, et al.. (2023). Congenital mirror movements are associated with defective polymerisation of RAD51. Journal of Medical Genetics. 60(11). 1116–1126. 1 indexed citations
3.
Gras, Domitille, et al.. (2023). Mirror Movements Due To a TUBB3 Variant. Pediatric Neurology. 148. 142–144. 1 indexed citations
4.
Moretti, Raffaella, Lionel Arnaud, Delphine Bouteiller, et al.. (2021). SCN1A-related epilepsy with recessive inheritance: Two further families. European Journal of Paediatric Neurology. 33. 121–124. 4 indexed citations
5.
Welniarz, Quentin, Marie‐Pierre Morel, Cécile Galléa, et al.. (2017). Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline. Scientific Reports. 7(1). 410–410. 27 indexed citations
6.
Trouillard, Oriane, Jeanette Koht, Thorsten Gerstner, et al.. (2016). Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature. SHILAP Revista de lepidopterología. 6. 424–424. 3 indexed citations
7.
Trouillard, Oriane, Jeanette Koht, Thorsten Gerstner, et al.. (2016). Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature. Tremor and Other Hyperkinetic Movements. 6(0). 424–424. 5 indexed citations
8.
Méneret, Aurélie, Oriane Trouillard, Vanessa Brochard, & Emmanuel Roze. (2015). Congenital mirror movements caused by a mutation in the DCC gene. Developmental Medicine & Child Neurology. 57(8). 776–776. 14 indexed citations
9.
Méneret, Aurélie, Quentin Welniarz, Oriane Trouillard, & Emmanuel Roze. (2015). Congenital mirror movements: from piano player to opera singer.. PubMed. 84(8). 860–860. 11 indexed citations
10.
Méneret, Aurélie, et al.. (2014). Congenital mirror movements. Neurology. 82(22). 1999–2002. 1 indexed citations
11.
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
12.
Couarch, Philippe, Santiago Vernia, Isabelle Gourfinkel‐An, et al.. (2011). Lafora progressive myoclonus epilepsy: NHLRC1 mutations affect glycogen metabolism. Journal of Molecular Medicine. 89(9). 915–925. 19 indexed citations
13.
Piard, Juliette, Christel Depienne, Boris Keren, et al.. (2011). Intragenic deletion of UBE3A gene in 2 sisters with Angelman syndrome detected by MLPA. American Journal of Medical Genetics Part A. 155(12). 3170–3173. 5 indexed citations
14.
Depienne, Christel, Oriane Trouillard, Isabelle Gourfinkel‐An, et al.. (2010). Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome. Journal of Medical Genetics. 47(6). 404–410. 117 indexed citations
15.
Vahedi, Katayoun, Christel Depienne, Florence Riant, et al.. (2009). Elicited repetitive daily blindness. Neurology. 72(13). 1178–1183. 66 indexed citations
16.
Nabbout, Rima, Christel Depienne, Mathilde Chipaux, et al.. (2009). CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy. Epilepsy Research. 87(1). 25–30. 3 indexed citations
17.
Depienne, Christel, Delphine Héron, Catalina Betancur, et al.. (2009). Autism, language delay and mental retardation in a patient with 7q11 duplication. BMJ Case Reports. 2009. bcr0520091911–bcr0520091911. 5 indexed citations
18.
Chabrol, E, Isabelle Gourfinkel‐An, Ingrid E. Scheffer, et al.. (2007). Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy. Epilepsy Research. 76(1). 41–48. 19 indexed citations
19.
Chabrol, E, Isabelle Gourfinkel‐An, Oriane Trouillard, et al.. (2007). Two Novel Epilepsy-Linked Mutations Leading to a Loss of Function of LGI1. Archives of Neurology. 64(2). 217–217. 36 indexed citations
20.
Depienne, Christel, Alexis Arzimanoglou, Oriane Trouillard, et al.. (2006). Parental mosaicism can cause recurrent transmission ofSCN1A mutations associated with severe myoclonic epilepsy of infancy. Human Mutation. 27(4). 389–389. 76 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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