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Christopher A Walsh

Showing results (281-290 of 319) with videos related to

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Nature Genetics|March 3, 2017
Biallelic mutations in human DCC cause developmental split-brain syndromeSaumya S Jamuar, Klaus Schmitz-Abe, Alissa M D'Gama, et al.
Plos Genetics|May 29, 2007
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defectsWeining Lu, Fabiola Quintero-Rivera, Yanli Fan, et al.
Nature|October 1, 2020
Innovations present in the primate interneuron repertoireFenna M Krienen, Melissa Goldman, Qiangge Zhang, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
Scientific Data|November 20, 2023
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseasesMcKinzie A Garrison, Yeongjun Jang, Taejeong Bae, et al.
Neuron|August 28, 2018
Sodium Channel SCN3A (Na<sub>V</sub>1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor DevelopmentRichard S Smith, Connor J Kenny, Vijay Ganesh, et al.
Annals of Clinical and Translational Neurology|July 24, 2022
ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infectionAjay X Thomas, Nichole Link, Laurie A Robak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic featuresDiane D Shao, Rachel Straussberg, Hind Ahmed, et al.
The New England Journal of Medicine|August 21, 2014
Somatic mutations in cerebral cortical malformationsSaumya S Jamuar, Anh-Thu N Lam, Martin Kircher, et al.
Pageof 32

Showing results (281-290 of 319) with videos related to

Sort By:
Pageof 32
Nature Genetics|March 3, 2017
Biallelic mutations in human DCC cause developmental split-brain syndromeSaumya S Jamuar, Klaus Schmitz-Abe, Alissa M D'Gama, et al.
Plos Genetics|May 29, 2007
NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defectsWeining Lu, Fabiola Quintero-Rivera, Yanli Fan, et al.
Nature|October 1, 2020
Innovations present in the primate interneuron repertoireFenna M Krienen, Melissa Goldman, Qiangge Zhang, et al.
American Journal of Medical Genetics. Part A|May 18, 2021
De novo variants in TCF7L2 are associated with a syndromic neurodevelopmental disorderCaroline Dias, Rolph Pfundt, Tjitske Kleefstra, et al.
Nature Neuroscience|July 18, 2017
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorderElaine T Lim, Mohammed Uddin, Silvia De Rubeis, et al.
Scientific Data|November 20, 2023
Genomic data resources of the Brain Somatic Mosaicism Network for neuropsychiatric diseasesMcKinzie A Garrison, Yeongjun Jang, Taejeong Bae, et al.
Neuron|August 28, 2018
Sodium Channel SCN3A (Na<sub>V</sub>1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor DevelopmentRichard S Smith, Connor J Kenny, Vijay Ganesh, et al.
Annals of Clinical and Translational Neurology|July 24, 2022
ANKLE2-related microcephaly: A variable microcephaly syndrome resembling Zika infectionAjay X Thomas, Nichole Link, Laurie A Robak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 3, 2021
A recurrent, homozygous EMC10 frameshift variant is associated with a syndrome of developmental delay with variable seizures and dysmorphic featuresDiane D Shao, Rachel Straussberg, Hind Ahmed, et al.
The New England Journal of Medicine|August 21, 2014
Somatic mutations in cerebral cortical malformationsSaumya S Jamuar, Anh-Thu N Lam, Martin Kircher, et al.
Pageof 32