Author

Anne‐Claude Tabet

Centre National de la Recherche ScientifiqueORCID 0000-0003-2910-7744Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:gene regulatory network inference· 2 Assay:whole-genome sequencing· 2 Approach:benchmark study· 1 Research Focus:cell-cell communication· 1 Research Focus:clustering· 1 Research Focus:database / resource· 1

Frequent Co-Authors

Richard DelormeiD· 3 shared Thomas BourgeroniD· 3 shared Alexandre MathieuiD· 2 shared Frédérique Amsellem· 2 shared James Lespinasse· 2 shared Jonathan LévyiD· 2 shared Julien BurattiiD· 2 shared Roberto ToroiD· 2 shared

Activity by Year

2017-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Richard DelormeORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintNov 24, 2025

LEAP-InovAND a multiscale resource to explore genetics, brain imaging and clinical data in autism

Mathis Fleury, Zakaria Mougin, Claire S. Leblond…·Thomas Bourgeron

The paper introduces a multiscale resource integrating genetics, brain imaging, and clinical data from autistic individuals and their relatives to explore genetic and neurobiological patterns in autism.

2 citations

humanwhole-genome sequencing

𝕏 PostBluesky

Genetic & Genomic Medicinenpj Genomic MedicinePeer-reviewedNov 4, 2021

A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder

Livia Oliveira Loureiro, Jennifer Howe, Miriam S. Reuter…·Stephen W. Scherer

The paper identifies a recurrent SHANK3 frameshift variant in Autism Spectrum Disorder, showing de novo mutations and variable expressivity.

24 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GeneticsbioRxivPreprintMar 18, 2017

A framework to identify modifier genes in patients with Phelan-McDermid syndrome

Anne‐Claude Tabet, Thomas Rolland, Marie Ducloy…·Thomas Bourgeron

This study identifies modifier genes in Phelan-McDermid syndrome patients by analyzing 22q13 rearrangements and their association with clinical features.

1 citation

humanstatistical model

𝕏 PostBluesky