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Christopher A Walsh

Showing results (231-240 of 319) with videos related to

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Epilepsia|June 14, 2012
Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancyAnnapurna Poduri, Sameer S Chopra, Edward G Neilan, et al.
Cell|November 27, 2012
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiationYawei J Yang, Andrew E Baltus, Rebecca S Mathew, et al.
Science (New York, N.Y.)|February 18, 2014
Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterningByoung-Il Bae, Ian Tietjen, Kutay D Atabay, et al.
Cell|July 1, 2026
Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disordersZinan Zhou, Lovelace J Luquette, Guanlan Dong, et al.
Nature Communications|June 10, 2022
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorderElaine T Lim, Yingleong Chan, Pepper Dawes, et al.
Neurology|April 3, 2015
Loss of PCLO function underlies pontocerebellar hypoplasia type IIIMustafa Y Ahmed, Barry A Chioza, Anna Rajab, et al.
Science (New York, N.Y.)|October 10, 2024
Somatic mosaicism in schizophrenia brains reveals prenatal mutational processesEduardo A Maury, Attila Jones, Vladimir Seplyarskiy, et al.
Annals of Neurology|February 11, 2026
Diverse Genetic Etiologies of Unilateral PolymicrogyriaAbbe Lai, Jennifer E Neil, Shyam K Akula, et al.
American Journal of Human Genetics|November 2, 2010
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic systemEfrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Cell Reports|July 29, 2014
CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasisM Chiara Manzini, Lan Xiong, Ranad Shaheen, et al.
Pageof 32

Showing results (231-240 of 319) with videos related to

Sort By:
Pageof 32
Epilepsia|June 14, 2012
Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancyAnnapurna Poduri, Sameer S Chopra, Edward G Neilan, et al.
Cell|November 27, 2012
Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiationYawei J Yang, Andrew E Baltus, Rebecca S Mathew, et al.
Science (New York, N.Y.)|February 18, 2014
Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterningByoung-Il Bae, Ian Tietjen, Kutay D Atabay, et al.
Cell|July 1, 2026
Recurrent patterns of TOP1-mediated neuronal genomic damage shared by major neurodegenerative disordersZinan Zhou, Lovelace J Luquette, Guanlan Dong, et al.
Nature Communications|June 10, 2022
Orgo-Seq integrates single-cell and bulk transcriptomic data to identify cell type specific-driver genes associated with autism spectrum disorderElaine T Lim, Yingleong Chan, Pepper Dawes, et al.
Neurology|April 3, 2015
Loss of PCLO function underlies pontocerebellar hypoplasia type IIIMustafa Y Ahmed, Barry A Chioza, Anna Rajab, et al.
Science (New York, N.Y.)|October 10, 2024
Somatic mosaicism in schizophrenia brains reveals prenatal mutational processesEduardo A Maury, Attila Jones, Vladimir Seplyarskiy, et al.
Annals of Neurology|February 11, 2026
Diverse Genetic Etiologies of Unilateral PolymicrogyriaAbbe Lai, Jennifer E Neil, Shyam K Akula, et al.
American Journal of Human Genetics|November 2, 2010
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic systemEfrat Birk, Adi Har-Zahav, Chiara M Manzini, et al.
Cell Reports|July 29, 2014
CC2D1A regulates human intellectual and social function as well as NF-κB signaling homeostasisM Chiara Manzini, Lan Xiong, Ranad Shaheen, et al.
Pageof 32