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Sean Hill

Showing results (51-60 of 105) with videos related to

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Neuroinformatics|November 22, 2015
The Resource Identification Initiative: A Cultural Shift in PublishingAnita Bandrowski, Matthew Brush, Jeffery S Grethe, et al.
Digital Health|December 30, 2025
Co-created data governance frameworks for youth mental healthcare: Values, principles, and implementation-A scoping reviewSebastian Rodriguez Duque, Eran Tal, Taite Beggs, et al.
Plos Computational Biology|July 27, 2023
The Canadian Open Neuroscience Platform-An open science framework for the neuroscience communityRachel J Harding, Patrick Bermudez, Alexander Bernier, et al.
Nature Genetics|August 24, 2004
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.
Human Mutation|May 12, 2017
Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathyTojo Nakayama, Jiang Wu, Patricia Galvin-Parton, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
American Journal of Human Genetics|May 3, 2011
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]Fowzan S Alkuraya, Xuyu Cai, Carina Emery, et al.
American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Neuroinformatics|November 22, 2015
The Resource Identification Initiative: A Cultural Shift in PublishingAnita Bandrowski, Matthew Brush, Jeffery S Grethe, et al.
Digital Health|December 30, 2025
Co-created data governance frameworks for youth mental healthcare: Values, principles, and implementation-A scoping reviewSebastian Rodriguez Duque, Eran Tal, Taite Beggs, et al.
Plos Computational Biology|July 27, 2023
The Canadian Open Neuroscience Platform-An open science framework for the neuroscience communityRachel J Harding, Patrick Bermudez, Alexander Bernier, et al.
Nature Genetics|August 24, 2004
Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndromeRussell J Ferland, Wafaa Eyaid, Randall V Collura, et al.
Human Mutation|May 12, 2017
Deficient activity of alanyl-tRNA synthetase underlies an autosomal recessive syndrome of progressive microcephaly, hypomyelination, and epileptic encephalopathyTojo Nakayama, Jiang Wu, Patricia Galvin-Parton, et al.
Annals of Neurology|May 4, 2010
Developmental and degenerative features in a complicated spastic paraplegiaM Chiara Manzini, Anna Rajab, Thomas M Maynard, et al.
Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
American Journal of Human Genetics|May 3, 2011
Human mutations in NDE1 cause extreme microcephaly with lissencephaly [corrected]Fowzan S Alkuraya, Xuyu Cai, Carina Emery, et al.
American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.
Neurology|October 1, 2013
Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humansL Benjamin Hills, Amira Masri, Kotaro Konno, et al.
Pageof 11