Author

Alexis Beauchamp-Châtel

Institut universitaire en santé mentale de Montréal

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ana Isabel SilvaiD· 1 shared Bogdan DraganskiiD· 1 shared Carrie E. BeardeniD· 1 shared Charles-Olivier MartiniD· 1 shared Clara A. MoreauiD· 1 shared Claudia ModenatoiD· 1 shared Danilo BzdokiD· 1 shared David C. GlahniD· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperNeuroscience

Ana Isabel SilvaORCID

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1 paper

Recent·Most cited

Using rare genetic mutations to revisit structural brain asymmetry

Jakub Kopál, Kuldeep Kumar, Kimia Shafighi, Karin Saltoun, Claudia Modenato, Clara A. Moreau, Guillaume Huguet, Martineau Jean‐Louis, Charles-Olivier Martin, Zohra Saci, Nadine Younis, Elise A. Douard, Khadijé Jizi, Alexis Beauchamp-Châtel, Leila Kushan, , Danilo Bzdok

The paper investigates how rare genetic mutations affect brain asymmetry by analyzing CNVs in a cohort of individuals and linking genetic alterations to brain structure and function.

Nature Communications · Mar 26, 2024Peer-reviewedNeuroscience