Author

Hanane El Kenz

Université Libre de Bruxelles

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

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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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 Claudine Giroux‐Lathuile· 1 shared Guy Laiguillon· 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

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1 shared paperGenetic & Genomic Medicine

Bérengère KoehlORCID

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1 paper

Recent·Most cited

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, Thankam Nair, Lucy Yang, Guy Laiguillon, Sophie Anselme-Martin, Claudine Giroux‐Lathuile, Hanane El Kenz, Olivier Hermine, Narla Mohandas, Jean‐Pierre Cartron, Yves Colin, Olivier Detante, Caroline Le Van Kim, , Thierry Peyrard

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

medRxiv · May 13, 2022 · PreprintGenetic & Genomic Medicine