Author

Cortlandt Myers

Nationwide Children's HospitalORCID 0000-0002-2995-3222Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 1 Organism:mouse· 1 Organism:zebrafish· 1

Frequent Co-Authors

Ange‐Line BrueliD· 1 shared Anne O’Donnell‐LuriaiD· 1 shared Annie GodwiniD· 1 shared Antonio NovelliiD· 1 shared Claudia CiaccioiD· 1 shared Cyril F. BourgeoisiD· 1 shared Daniel C. KoboldtiD· 1 shared Dennis BartholomewiD· 1 shared

Activity by Year

2023-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

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1 paper

Recent·Most cited

Monoallelic de novo variants in DDX17 cause a novel neurodevelopmental disorder

Eleanor G. Seaby, Annie Godwin, Valentine Clerc, Géraldine Meyer-Dilhet, Xavier Grand, Tia Fletcher, Laloé Monteiro, Valério Carelli, Flavia Palombo, Marco Seri, Giulia Olivucci, Mina Grippa, Claudia Ciaccio, Stefano D’Arrigo, Maria Rosaria Iascone, , Sarah Ennis

The paper identifies de novo monoallelic DDX17 variants in 11 patients with neurodevelopmental disorders and shows DDX17 dysfunction causes neuronal migration and axon outgrowth defects in multiple models.

medRxiv · Oct 11, 2023 · PreprintGenetic & Genomic Medicine