Author

Vincent Gâtinois

Centre Hospitalier Universitaire de MontpellierORCID 0000-0003-0480-6709Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Chantal MissirianiD· 2 shared Charles CouttoniD· 2 shared Lucile Pinson· 2 shared Olivier PichoniD· 2 shared Véronique SatreiD· 2 shared Abdelamdjid Benmansour· 1 shared Alain VerloèsiD· 1 shared Albert David· 1 shared

Activity by Year

2017-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Chantal MissirianORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicineJournal of Medical GeneticsPeer-reviewedSep 22, 2022

Exome sequencing as a first-tier test for copy number variant detection : retrospective evaluation and prospective screening in 2418 cases.

Quentin Testard, Xavier Vanhoye, Kévin Yauy…·Julien Thévenon

This paper evaluates exome sequencing as an alternative to chromosomal microarray for detecting copy number variants in rare disorders, showing improved diagnostic yield in prospective cases.

47 citationstop 1%

humanwhole-exome sequencing

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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

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