Author

Claudine Giroux‐Lathuile

Établissement Français du Sang

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

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Bérengère KoehliD· 1 shared Caroline Le Van KimiD· 1 shared Cédric VrignaudiD· 1 shared Guy Laiguillon· 1 shared Hanane El Kenz· 1 shared Jean‐Pierre CartroniD· 1 shared Lucy YangiD· 1 shared Mahmoud MikdariD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenetic & Genomic Medicine

Bérengère KoehlORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 13, 2022

Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype

Bérengère Koehl, Cédric Vrignaud, Mahmoud Mikdar…·Thierry Peyrard

The paper identifies CTL2 deficiency in humans causing hearing loss, arterial aneurysms, and epilepsy, while showing normal platelet function and erythropoiesis.

DOI 10.1101/2022.05.13.22273920

humanDNA methylation

𝕏 PostBluesky