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Christopher A Walsh

Showing results (221-230 of 337) with videos related to

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Nature Genetics|October 5, 2010
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architectureTimothy W Yu, Ganeshwaran H Mochida, David J Tischfield, et al.
Biorxiv : the Preprint Server for Biology|March 17, 2025
Recurrent patterns of widespread neuronal genomic damage shared by major neurodegenerative disordersZinan Zhou, Lovelace J Luquette, Guanlan Dong, et al.
Nature Neuroscience|August 29, 2023
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Schizophrenia Research|October 13, 2025
Corrigendum to "The burden of early onset psychosis: Diagnostic complexity, high comorbidity, and poor functioning in patients and their relatives" [Schizophr. Res. Volume 285, November 2025, Pages 165-174]Josephine Mollon, Nuria Lanzagorta, Samuel R Mathias, et al.
Neurology. Genetics|December 27, 2023
Somatic Mosaicism in <i>PIK3CA</i> Variant Correlates With Stereoelectroencephalography-Derived ElectrophysiologyH Westley Phillips, Alissa M D'Gama, Yilan Wang, et al.
Human Molecular Genetics|June 24, 2005
The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle proteinNatalay Kouprina, Adam Pavlicek, N Keith Collins, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.
Cell Reports|December 28, 2017
Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical DysplasiasAlissa M D'Gama, Mollie B Woodworth, Amer A Hossain, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 14, 2018
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic featuresRaida Khalil, Connor Kenny, R Sean Hill, et al.
Cell Genomics|July 17, 2024
Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.
Pageof 34

Showing results (221-230 of 337) with videos related to

Sort By:
Pageof 34
Nature Genetics|October 5, 2010
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architectureTimothy W Yu, Ganeshwaran H Mochida, David J Tischfield, et al.
Biorxiv : the Preprint Server for Biology|March 17, 2025
Recurrent patterns of widespread neuronal genomic damage shared by major neurodegenerative disordersZinan Zhou, Lovelace J Luquette, Guanlan Dong, et al.
Nature Neuroscience|August 29, 2023
Author Correction: The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencingRachel E Rodin, Yanmei Dou, Minseok Kwon, et al.
Schizophrenia Research|October 13, 2025
Corrigendum to "The burden of early onset psychosis: Diagnostic complexity, high comorbidity, and poor functioning in patients and their relatives" [Schizophr. Res. Volume 285, November 2025, Pages 165-174]Josephine Mollon, Nuria Lanzagorta, Samuel R Mathias, et al.
Neurology. Genetics|December 27, 2023
Somatic Mosaicism in <i>PIK3CA</i> Variant Correlates With Stereoelectroencephalography-Derived ElectrophysiologyH Westley Phillips, Alissa M D'Gama, Yilan Wang, et al.
Human Molecular Genetics|June 24, 2005
The microcephaly ASPM gene is expressed in proliferating tissues and encodes for a mitotic spindle proteinNatalay Kouprina, Adam Pavlicek, N Keith Collins, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Rare variation in noncoding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.
Cell Reports|December 28, 2017
Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical DysplasiasAlissa M D'Gama, Mollie B Woodworth, Amer A Hossain, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 14, 2018
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic featuresRaida Khalil, Connor Kenny, R Sean Hill, et al.
Cell Genomics|July 17, 2024
Rare variation in non-coding regions with evolutionary signatures contributes to autism spectrum disorder riskTaehwan Shin, Janet H T Song, Michael Kosicki, et al.
Pageof 34