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Christopher A Walsh

Showing results (141-150 of 337) with videos related to

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European Journal of Medical Genetics|March 4, 2017
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophyShenela Lakhani, Ryan Doan, Mariam Almureikhi, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
Brain : a Journal of Neurology|February 3, 2026
ARX mutation-associated interneuron defects provide insights into mechanisms underlying developmental epilepsiesYoungshin Lim, Shyam K Akula, Abigail K Myers, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Autism-Associated Genes and Neighboring lncRNAs Converge on Key Gene Regulatory NetworksRebecca E Andersen, Maya Talukdar, Tyler Sakamoto, et al.
Science (New York, N.Y.)|March 19, 2021
Landmarks of human embryonic development inscribed in somatic mutationsSara Bizzotto, Yanmei Dou, Javier Ganz, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
BRN1/2 Function in Neocortical Size Determination and MicrocephalySoraia Barão, Yijun Xu, José P Llongueras, et al.
Nature Neuroscience|January 12, 2021
Large mosaic copy number variations confer autism riskMaxwell A Sherman, Rachel E Rodin, Giulio Genovese, et al.
Nature Communications|October 7, 2022
Prevalence and mechanisms of somatic deletions in single human neurons during normal aging and in DNA repair disordersJunho Kim, August Yue Huang, Shelby L Johnson, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohortCecilia Mellado, Annapurna Poduri, Danielle Gleason, et al.
Neuron|January 9, 2015
Cell lineage analysis in human brain using endogenous retroelementsGilad D Evrony, Eunjung Lee, Bhaven K Mehta, et al.
Pageof 34

Showing results (141-150 of 337) with videos related to

Sort By:
Pageof 34
European Journal of Medical Genetics|March 4, 2017
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophyShenela Lakhani, Ryan Doan, Mariam Almureikhi, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
Brain : a Journal of Neurology|February 3, 2026
ARX mutation-associated interneuron defects provide insights into mechanisms underlying developmental epilepsiesYoungshin Lim, Shyam K Akula, Abigail K Myers, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Autism-Associated Genes and Neighboring lncRNAs Converge on Key Gene Regulatory NetworksRebecca E Andersen, Maya Talukdar, Tyler Sakamoto, et al.
Science (New York, N.Y.)|March 19, 2021
Landmarks of human embryonic development inscribed in somatic mutationsSara Bizzotto, Yanmei Dou, Javier Ganz, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
BRN1/2 Function in Neocortical Size Determination and MicrocephalySoraia Barão, Yijun Xu, José P Llongueras, et al.
Nature Neuroscience|January 12, 2021
Large mosaic copy number variations confer autism riskMaxwell A Sherman, Rachel E Rodin, Giulio Genovese, et al.
Nature Communications|October 7, 2022
Prevalence and mechanisms of somatic deletions in single human neurons during normal aging and in DNA repair disordersJunho Kim, August Yue Huang, Shelby L Johnson, et al.
American Journal of Medical Genetics. Part A|October 16, 2010
Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohortCecilia Mellado, Annapurna Poduri, Danielle Gleason, et al.
Neuron|January 9, 2015
Cell lineage analysis in human brain using endogenous retroelementsGilad D Evrony, Eunjung Lee, Bhaven K Mehta, et al.
Pageof 34