Author

Jean‐Michel Dupont

Hôpital CochinORCID 0000-0002-9680-3662Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Damien SanlavilleiD· 2 shared Abdelamdjid Benmansour· 1 shared Alain VerloèsiD· 1 shared Albert David· 1 shared Alexander HoischeniD· 1 shared Alexandra AfenjariD· 1 shared Alexandre MathieuiD· 1 shared Anne‐Claude TabetiD· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersGenetics

Damien SanlavilleORCID

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2 papers

Recent·Most cited

GeneticsbioRxivPreprintJul 15, 2020

Next generation cytogenetics: genome-imaging enables comprehensive structural variant detection for 100 constitutional chromosomal aberrations in 85 samples

Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard…·Laïla El Khattabi

This study evaluates high-resolution optical mapping for detecting chromosomal aberrations in 85 samples, achieving 100% concordance with standard tests for non-centromeric breakpoints.

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