Julien Thévenon

7.9k total citations
51 papers, 798 citations indexed

About

Julien Thévenon is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Julien Thévenon has authored 51 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 32 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in Julien Thévenon's work include Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Julien Thévenon is often cited by papers focused on Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). Julien Thévenon collaborates with scholars based in France, United States and Italy. Julien Thévenon's co-authors include Laurence Faivre, Patrick Callier, Alice Masurel‐Paulet, Frédéric Huet, Christel Thauvin‐Robinet, Jean‐Baptiste Rivière, Yannis Duffourd, Judith St‐Onge, Emmanuelle Escoffier and Sophie Rousseaux and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Journal of Bone and Mineral Research.

In The Last Decade

Julien Thévenon

49 papers receiving 785 citations

Peers

Julien Thévenon
Zhangyong Wei United States
Giulia Arrigo Italy
Sylvie Jaillard France
Alma Kuechler Germany
Michela Barbaro Sweden
Tiina Alitalo Finland
Maxine J. Sutcliffe United States
Sophia Kitsiou‐Tzeli Greece
Boris Keren France
Zhangyong Wei United States
Julien Thévenon
Citations per year, relative to Julien Thévenon Julien Thévenon (= 1×) peers Zhangyong Wei

Countries citing papers authored by Julien Thévenon

Since Specialization
Citations

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

Fields of papers citing papers by Julien Thévenon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julien Thévenon

This figure shows the co-authorship network connecting the top 25 collaborators of Julien Thévenon. A scholar is included among the top collaborators of Julien Thévenon 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 Julien Thévenon. Julien Thévenon 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.
2.
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
3.
Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations
4.
Assoum, Mirna, Ange‐Line Bruel, Melissa Crenshaw, et al.. (2020). NovelKIAA1033/WASHC4mutations in three patients with syndromic intellectual disability and a review of the literature. American Journal of Medical Genetics Part A. 182(4). 792–797. 10 indexed citations
5.
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
6.
Thévenon, Julien, Yannis Duffourd, Sophie Nambot, et al.. (2018). TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation. American Journal of Medical Genetics Part A. 176(12). 2813–2818. 12 indexed citations
7.
Mau‐Them, Frédéric Tran, Julien Thévenon, Thomas Guignard, et al.. (2018). LARP7 variants and further delineation of the Alazami syndrome phenotypic spectrum among primordial dwarfisms: 2 sisters. European Journal of Medical Genetics. 62(3). 161–166. 19 indexed citations
8.
Lefebvre, Mathilde, Christine Francannet, Hélène Laurichesse, et al.. (2018). Extending the ALDH18A1 clinical spectrum to severe autosomal recessive fetal cutis laxa with corpus callosum agenesis. American Journal of Medical Genetics Part A. 176(11). 2509–2512. 6 indexed citations
9.
Laviolle, Bruno, Olivier Perche, François Gueyffier, et al.. (2018). Apport de la génomique dans la médecine de demain, applications cliniques et enjeux. Therapies. 74(1). 1–8. 1 indexed citations
10.
Laviolle, Bruno, Patrice Denèfle, François Gueyffier, et al.. (2018). The contribution of genomics in the medicine of tomorrow, clinical applications and issues. Therapies. 74(1). 9–15. 3 indexed citations
11.
Lehalle, Daphné, Umut Altunoğlu, Ange‐Line Bruel, et al.. (2017). Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients. American Journal of Medical Genetics Part A. 173(12). 3136–3142. 5 indexed citations
12.
Amos, J., Linda Huang, Julien Thévenon, et al.. (2016). Autosomal recessive mutations in THOC6 cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping. Clinical Genetics. 91(1). 92–99. 16 indexed citations
13.
Kuentz, Paul, Yannis Duffourd, Judith St‐Onge, et al.. (2016). 186 Mutational spectrum in PIK3CA -Related Overgrowth Spectrum (PROS) and recommendations for molecular testing. Journal of Investigative Dermatology. 136(9). S192–S192. 1 indexed citations
14.
Thévenon, Julien, Caroline Michot, Christine Bole, et al.. (2015). RPL10 mutation segregating in a family with X‐linked syndromic Intellectual Disability. American Journal of Medical Genetics Part A. 167(8). 1908–1912. 22 indexed citations
15.
Chevrier, Véronique, Ange‐Line Bruel, Teunis J. P. van Dam, et al.. (2015). OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. Human Molecular Genetics. 25(3). 497–513. 35 indexed citations
16.
Gueneau, Lucie, Laurence Duplomb, Pierre Sarda, et al.. (2013). Congenital neutropenia with retinopathy, a new phenotype without intellectual deficiency or obesity secondary to VPS13B mutations. American Journal of Medical Genetics Part A. 164(2). 522–527. 11 indexed citations
17.
Masurel‐Paulet, Alice, Vera M. Kalscheuer, Nicolas Lebrun, et al.. (2013). Expanding the clinical phenotype of patients with a ZDHHC9 mutation. American Journal of Medical Genetics Part A. 164(3). 789–795. 28 indexed citations
18.
Magnin, Éloi, Oleg Blagosklonov, Julien Thévenon, et al.. (2013). Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation. Brain and Development. 36(8). 711–715. 6 indexed citations
19.
Rousseaux, Sophie, Jonathan Gaucher, Julien Thévenon, et al.. (2009). Spermiogenèse : l’acétylation des histones déclenche la reprogrammation du génome mâle. Gynécologie Obstétrique & Fertilité. 37(6). 519–522. 9 indexed citations
20.
Rousseaux, Sophie, A.K. Faure, Julien Thévenon, et al.. (2006). Épigénétique du spermatozoïde. Gynécologie Obstétrique & Fertilité. 34(9). 831–835. 2 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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