Author

Sandra Chantot‐Bastaraud

Hôpital Armand-TrousseauORCID 0000-0001-6446-3504Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 2 Organism:human· 2 Approach:statistical model· 2 Approach:benchmark study· 1 Research Focus:differential expression· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexandra AfenjariD· 2 shared Boris KereniD· 2 shared Christèle DubourgiD· 2 shared Damien SanlavilleiD· 2 shared James Lespinasse· 2 shared Laurence Olivier FaivreiD· 2 shared Patrick EderyiD· 2 shared Abdelamdjid Benmansour· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Alexandra AfenjarORCID

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2 papers

Recent·Most cited

GenomicsbioRxivPreprintJul 17, 2020

The enrichment of breakpoints in late-replicating chromatin provides novel insights into chromoanagenesis mechanisms

Nicolas Chatron, Giuliana Giannuzzi, Pierre‐Antoine Rollat‐Farnier…·Caroline Schluth‐Bolard

The paper analyzes chromoanagenesis breakpoints in constitutional and cancer cases, finding enrichment in late-replicating chromatin and suggesting similar mechanisms for both.

14 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