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Christopher A Walsh

Showing results (91-100 of 337) with videos related to

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Elife|December 29, 2025
Biophysical basis for brain folding and misfolding patterns in ferrets and humansGary P T Choi, Chunzi Liu, Sifan Yin, et al.
Plos Genetics|July 8, 2008
Identification of neural outgrowth genes using genome-wide RNAiKatharine J Sepp, Pengyu Hong, Sofia B Lizarraga, et al.
Cell Reports|August 28, 2014
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brainXuyu Cai, Gilad D Evrony, Hillel S Lehmann, et al.
Frontiers in Genetics|January 31, 2024
Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi ArabiaManal Alaamery, Salam Massadeh, Manar Aldarwish, et al.
Rapid Communications in Mass Spectrometry : RCM|April 6, 2021
DNA Adductomics by mass tag prelabelingPoguang Wang, Elisabeth Roider, Michael E Coulter, et al.
Cell Reports|April 3, 2015
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brainXuyu Cai, Gilad D Evrony, Hillel S Lehmann, et al.
Acta Neuropathologica|November 1, 2002
Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortexAkiyoshi Kakita, Shintaro Hayashi, Francesca Moro, et al.
Nature|August 21, 2020
APP gene copy number changes reflect exogenous contaminationJunho Kim, Boxun Zhao, August Yue Huang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2002
Doublecortin is required in mice for lamination of the hippocampus but not the neocortexJoseph C Corbo, Thomas A Deuel, Jeffrey M Long, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 geneTawfeg Ben-Omran, Rehab Ali, Mariam Almureikhi, et al.
Pageof 34

Showing results (91-100 of 337) with videos related to

Sort By:
Pageof 34
Elife|December 29, 2025
Biophysical basis for brain folding and misfolding patterns in ferrets and humansGary P T Choi, Chunzi Liu, Sifan Yin, et al.
Plos Genetics|July 8, 2008
Identification of neural outgrowth genes using genome-wide RNAiKatharine J Sepp, Pengyu Hong, Sofia B Lizarraga, et al.
Cell Reports|August 28, 2014
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brainXuyu Cai, Gilad D Evrony, Hillel S Lehmann, et al.
Frontiers in Genetics|January 31, 2024
Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi ArabiaManal Alaamery, Salam Massadeh, Manar Aldarwish, et al.
Rapid Communications in Mass Spectrometry : RCM|April 6, 2021
DNA Adductomics by mass tag prelabelingPoguang Wang, Elisabeth Roider, Michael E Coulter, et al.
Cell Reports|April 3, 2015
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brainXuyu Cai, Gilad D Evrony, Hillel S Lehmann, et al.
Acta Neuropathologica|November 1, 2002
Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortexAkiyoshi Kakita, Shintaro Hayashi, Francesca Moro, et al.
Nature|August 21, 2020
APP gene copy number changes reflect exogenous contaminationJunho Kim, Boxun Zhao, August Yue Huang, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2002
Doublecortin is required in mice for lamination of the hippocampus but not the neocortexJoseph C Corbo, Thomas A Deuel, Jeffrey M Long, et al.
American Journal of Medical Genetics. Part A|October 4, 2011
Phenotypic heterogeneity in Woodhouse-Sakati syndrome: two new families with a mutation in the C2orf37 geneTawfeg Ben-Omran, Rehab Ali, Mariam Almureikhi, et al.
Pageof 34