Author

Odelia Chorin

Sheba Medical CenterORCID 0000-0001-8968-0732Unclaimed 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:Drosophila· 2 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Annick Raas‐RothschildiD· 2 shared Boris KereniD· 2 shared Carrie Costin· 2 shared Jill Anne RosenfeldiD· 2 shared Maria Rosaria IasconeiD· 2 shared Aidin ForoutaniD· 1 shared Alden Yen-Wen Huang· 1 shared Alice S. BrooksiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Annick Raas‐RothschildORCID

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2 papers

Recent·Most cited

A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene

María del Rocío Pérez Baca, Eva Jacobs, Lies Vantomme, Pontus Leblanc, Elke Bogaert, Annelies Dheedene, Laurenz De Cock, Sadegheh Haghshenas, Aidin Foroutan, Michael A. Levy, Jennifer Kerkhof, Haley McConkey, Chun‐An Chen, Nurit Assia Batzir, Xia Wang, , Dorothea Wand

This paper identifies loss-of-function variants in ZFHX3 as a cause of syndromic intellectual disability and describes its role in chromatin remodeling and DNA methylation.

The American Journal of Human Genetics · Feb 26, 2024Peer-reviewedGenetic & Genomic Medicine

Loss of function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

Yue Huang, Kristy L. Jay, Alden Yen-Wen Huang, Jijun Wan, Sharayu V. Jangam, Odelia Chorin, Annick Raas‐Rothschild, Ortal Barel, Milena Mariani, Maria Rosaria Iascone, Han Xue, Undiagnosed Diseases Network, Jing Yang Huang, Cyril Mignot, Boris Keren, , Julián A. Martínez-Agosto

The paper identifies de novo RBBP5 variants in individuals with neurodevelopmental disorders and shows they cause loss of function through structural and Drosophila model analyses.

bioRxiv · Feb 6, 2024 · PreprintGenetics