Jesia G Berry

6PUBLICATIONS
37CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesChild and adolescent development
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Publications (6)

|Sep 17, 2021
Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing.

C L van Eyk, D L Webber, A E Minoche

|Jan 12, 2021
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari

|Dec 14, 2020
Cerebral palsy with autism and ADHD: time to pay attention.

Jozef Gecz, Jesia G Berry

|Sep 29, 2020
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.

Sheng Chih Jin, Sara A Lewis, Somayeh Bakhtiari

|Jun 17, 2020
Definition and diagnosis of cerebral palsy in genetic studies: a systematic review.

Ryan Pham, Ben W Mol, Jozef Gecz

|Nov 09, 2019
Targeted resequencing identifies genes with recurrent variation in cerebral palsy.

C L van Eyk, M A Corbett, M S B Frank

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