Stéphane Jamain

25.1k citations
72 papers · 4.4k · 1 hit paper · h-index 29

Impact in

Papers in

    • Bipolar Disorder and Treatment 26
    • Schizophrenia research and treatment 7
    • Genetics and Neurodevelopmental Disorders 19
    • Genetic Associations and Epidemiology 7

Stéphane Jamain

71 papers receiving 4.3k citations

Stéphane Jamain's Hit Papers

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism 2003 · 1.3k citations
1.3k0+7+15Years since publication4008001.2k

Peers

Stéphane Jamain
Comparison fields: 5 of 119
  • Biological Psychiatry 448
  • Cognitive Neuroscience 1.5k
  • Psychiatry and Mental health 1.0k
  • Genetics 1.8k
  • Cellular and Molecular Neuroscience 962
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Citations per field
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Citations per year

Countries citing papers authored by Stéphane Jamain

Since Specialization
Citations

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

Fields of papers citing papers by Stéphane Jamain

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Stéphane Jamain, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stéphane Jamain Line = papers co-authored together Stéphane Jamain links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
Hit paper breakdown →
20031316
2 2008425
3 2004423
4 2002230
5 2013188
6 2011141
7 2012103
8 201298
9 201789
10 201378
11 201276
12 201475
13 200968
14 201565
15 201161
16 201459
17 201550
18 201350
19 201544
20 201043

About Stéphane Jamain

Stéphane Jamain is a scholar working on Psychiatry and Mental health, Genetics, Molecular Biology, Biological Psychiatry and Cellular and Molecular Neuroscience, having authored 72 papers that have together received 4.4k indexed citations. Recurring topics across this work include Bipolar Disorder and Treatment (26 papers), Genetics and Neurodevelopmental Disorders (19 papers), Tryptophan and brain disorders (12 papers), Autism Spectrum Disorder Research (8 papers), Adolescent and Pediatric Healthcare (7 papers), Genetic Associations and Epidemiology (7 papers), Schizophrenia research and treatment (7 papers) and Receptor Mechanisms and Signaling (6 papers). The work is most often cited by research in Biological Psychiatry (448 citations), Cognitive Neuroscience (1.5k citations), Psychiatry and Mental health (1.0k citations), Genetics (1.8k citations) and Cellular and Molecular Neuroscience (962 citations). Stéphane Jamain has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Marion Leboyer, Thomas Bourgeron, Nils Brose, Frédérique Varoqueaux, Hélène Quach, Catalina Betancur, Bruno Giros, Christopher Gillberg, Maria Råstam and Henrik Söderström. Their work appears in journals such as Molecular Psychiatry, Scientific Reports, Genes Brain & Behavior, Translational Psychiatry and The World Journal of Biological Psychiatry.

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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