Thomas Bourgeron

31.7k total citations · 4 hit papers
162 papers, 11.6k citations indexed

About

Thomas Bourgeron is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Thomas Bourgeron has authored 162 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 84 papers in Genetics, 73 papers in Cognitive Neuroscience and 65 papers in Molecular Biology. Recurrent topics in Thomas Bourgeron's work include Autism Spectrum Disorder Research (69 papers), Genetics and Neurodevelopmental Disorders (60 papers) and Genomic variations and chromosomal abnormalities (18 papers). Thomas Bourgeron is often cited by papers focused on Autism Spectrum Disorder Research (69 papers), Genetics and Neurodevelopmental Disorders (60 papers) and Genomic variations and chromosomal abnormalities (18 papers). Thomas Bourgeron collaborates with scholars based in France, United Kingdom and Germany. Thomas Bourgeron's co-authors include Pierre Rustin, Agnès Rötig, Dominique Chrétien, Arnold Münnich, Marion Leboyer, Elodie Ey, Christopher Gillberg, Antonio M. Persico, Richard Delorme and Stéphane Jamain and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Thomas Bourgeron

155 papers receiving 11.3k citations

Hit Papers

Mutations of the X-linked... 1994 2026 2004 2015 2003 1994 2015 1995 400 800 1.2k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Thomas Bourgeron 5.4k 4.9k 4.7k 1.7k 1.2k 162 11.6k
Elizabeth Berry‐Kravis 6.7k 1.2× 7.4k 1.5× 10.2k 2.2× 2.0k 1.2× 198 0.2× 345 15.8k
Richard Haas 3.6k 0.7× 2.4k 0.5× 2.0k 0.4× 888 0.5× 1.6k 1.3× 141 7.8k
Maree J. Webster 6.4k 1.2× 2.5k 0.5× 2.4k 0.5× 3.8k 2.2× 149 0.1× 160 14.1k
Antonio M. Persico 3.3k 0.6× 3.7k 0.8× 3.0k 0.6× 2.4k 1.4× 140 0.1× 166 9.0k
Walter E. Kaufmann 5.9k 1.1× 7.7k 1.6× 7.8k 1.6× 2.9k 1.7× 192 0.2× 193 16.7k
Akira Sawa 10.8k 2.0× 2.2k 0.5× 2.5k 0.5× 5.2k 3.0× 326 0.3× 325 20.4k
Peter R. Huttenlocher 1.8k 0.3× 3.4k 0.7× 1.1k 0.2× 2.1k 1.2× 801 0.7× 94 9.6k
Jacques Mallet 9.6k 1.8× 1.3k 0.3× 4.1k 0.9× 7.2k 4.2× 631 0.5× 367 18.7k
Dennis R. Grayson 6.9k 1.3× 1.6k 0.3× 3.2k 0.7× 4.1k 2.4× 138 0.1× 155 11.4k
Eden R. Martin 4.4k 0.8× 1.5k 0.3× 4.1k 0.9× 1.4k 0.8× 159 0.1× 241 11.2k

Countries citing papers authored by Thomas Bourgeron

Since Specialization
Citations

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

Fields of papers citing papers by Thomas Bourgeron

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Bourgeron

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas Bourgeron. A scholar is included among the top collaborators of Thomas Bourgeron 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 Thomas Bourgeron. Thomas Bourgeron 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.
Oakley, Bethany, Alexandra Lautarescu, Tony Charman, et al.. (2025). Data sharing in child and adolescent psychiatry research: Key challenges (and some potential solutions). Open Research Europe. 5. 93–93. 1 indexed citations
2.
Moreau, Clara, Christopher R. K. Ching, Alexandre Mathieu, et al.. (2025). Neuroimaging insights into brain mechanisms of early-onset restrictive eating disorders. Nature Mental Health. 3(7). 780–788.
3.
Nielsen, Trine Tollerup, Jakob Grove, Christina Mohr Jensen, et al.. (2025). Genetic Architecture and Risk of Childhood Maltreatment Across 5 Psychiatric Diagnoses. JAMA Psychiatry. 82(8). 790–790. 1 indexed citations
4.
Black, Melissa H., Jan K. Buitelaar, Tony Charman, et al.. (2024). Conceptual framework for data harmonisation in mental health using the International Classification of Functioning, Disability and Health: an example with the R2D2-MH consortium. SHILAP Revista de lepidopterología. 27(1). e301283–e301283. 3 indexed citations
5.
Black, Melissa H., et al.. (2023). From Symptomatology to Functioning - Applying the ICF to Autism Measures to Facilitate Neurodiversity-Affirmative Data Harmonization. Journal of Autism and Developmental Disorders. 55(1). 114–129. 6 indexed citations
6.
Loth, Eva, Jumana Ahmad, Chris Chatham, et al.. (2021). The meaning of significant mean group differences for biomarker discovery. PLoS Computational Biology. 17(11). e1009477–e1009477. 26 indexed citations
7.
Zabihi, Mariam, Dorothea L. Floris, Seyed Mostafa Kia, et al.. (2020). Fractionating autism based on neuroanatomical normative modeling. Translational Psychiatry. 10(1). 384–384. 31 indexed citations
8.
Dumas, Guillaume, Hany Goubran‐Botros, Mariette Matondo, et al.. (2020). Mass‐spectrometry analysis of the human pineal proteome during night and day and in autism. Journal of Pineal Research. 70(3). e12713–e12713. 3 indexed citations
9.
Chaumont, Fabrice de, Elodie Ey, Nicolas Torquet, et al.. (2019). Real-time analysis of the behaviour of groups of mice via a depth-sensing camera and machine learning. Nature Biomedical Engineering. 3(11). 930–942. 105 indexed citations
10.
Warrier, Varun, Roberto Toro, Hyejung Won, et al.. (2019). Social and non-social autism symptoms and trait domains are genetically dissociable. Communications Biology. 2(1). 328–328. 55 indexed citations
11.
Warrier, Varun, Roberto Toro, Bhismadev Chakrabarti, et al.. (2018). Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa. Translational Psychiatry. 8(1). 35–35. 75 indexed citations
12.
Warrier, Varun, Katrina L. Grasby, Florina Uzefovsky, et al.. (2017). Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition. Molecular Psychiatry. 23(6). 1402–1409. 100 indexed citations
13.
Kishimoto, Keiko, Jun Nomura, Jacob Ellegood, et al.. (2017). Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication. Genes to Cells. 22(5). 436–451. 7 indexed citations
14.
Traut, Nicolas, Anita Beggiato, Thomas Bourgeron, et al.. (2017). Cerebellar Volume in Autism: Literature Meta-analysis and Analysis of the Autism Brain Imaging Data Exchange Cohort. Biological Psychiatry. 83(7). 579–588. 47 indexed citations
15.
Lévy‐Leduc, Céline, et al.. (2015). Improving heritability estimation by a variable selection approach in\n sparse high dimensional linear mixed models. arXiv (Cornell University). 4 indexed citations
16.
Lefebvre, Aline, Anita Beggiato, Thomas Bourgeron, & Roberto Toro. (2015). Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation. Biological Psychiatry. 78(2). 126–134. 78 indexed citations
17.
Waltes, Regina, Eftichia Duketis, Michael Knapp, et al.. (2014). Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders. Human Genetics. 133(6). 781–792. 51 indexed citations
18.
Pinel, Philippe, Fabien Fauchereau, Antonio Moreno, et al.. (2012). Genetic Variants ofFOXP2andKIAA0319/TTRAP/THEM2Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions. Journal of Neuroscience. 32(3). 817–825. 117 indexed citations
19.
Delorme, Richard, Marie‐Odile Krebs, Nadia Chabane, et al.. (2004). Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder. Neuroreport. 15(4). 699–702. 65 indexed citations
20.
Bourgeron, Thomas, Dominique Chrétien, Shawn Doonan, et al.. (1994). Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency.. Journal of Clinical Investigation. 93(6). 2514–2518. 114 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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