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Showing results (721-730 of 915) with videos related to

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Molecular Psychiatry|May 13, 2022
Genome-wide tandem repeat expansions contribute to schizophrenia riskBahareh A Mojarad, Worrawat Engchuan, Brett Trost, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports|November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic VariantsVickie Kwan, Durga Praveen Meka, Sean H White, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
Nature Genetics|June 18, 2002
Mutations in SUFU predispose to medulloblastomaMichael D Taylor, Ling Liu, Corey Raffel, et al.
Nature Neuroscience|March 27, 2019
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neuronsKirill Zaslavsky, Wen-Bo Zhang, Fraser P McCready, et al.
Acta Neuropathologica|February 24, 2012
Subgroup-specific alternative splicing in medulloblastomaAdrian M Dubuc, A Sorana Morrissy, Nanne K Kloosterhof, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2014
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genesAbdul Noor, Anath C Lionel, Sarah Cohen-Woods, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Pageof 92

Showing results (721-730 of 915) with videos related to

Sort By:
Pageof 92
Molecular Psychiatry|May 13, 2022
Genome-wide tandem repeat expansions contribute to schizophrenia riskBahareh A Mojarad, Worrawat Engchuan, Brett Trost, et al.
Nature Genetics|November 23, 2006
Genome assembly comparison identifies structural variants in the human genomeRazi Khaja, Junjun Zhang, Jeffrey R MacDonald, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
Cell Reports|November 10, 2016
DIXDC1 Phosphorylation and Control of Dendritic Morphology Are Impaired by Rare Genetic VariantsVickie Kwan, Durga Praveen Meka, Sean H White, et al.
European Journal of Human Genetics : EJHG|February 18, 2018
Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testingGregory Costain, Rebekah Jobling, Susan Walker, et al.
Nature Genetics|June 18, 2002
Mutations in SUFU predispose to medulloblastomaMichael D Taylor, Ling Liu, Corey Raffel, et al.
Nature Neuroscience|March 27, 2019
SHANK2 mutations associated with autism spectrum disorder cause hyperconnectivity of human neuronsKirill Zaslavsky, Wen-Bo Zhang, Fraser P McCready, et al.
Acta Neuropathologica|February 24, 2012
Subgroup-specific alternative splicing in medulloblastomaAdrian M Dubuc, A Sorana Morrissy, Nanne K Kloosterhof, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 5, 2014
Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genesAbdul Noor, Anath C Lionel, Sarah Cohen-Woods, et al.
Human Mutation|August 20, 2015
Diagnostic interpretation of array data using public databases and internet sourcesNicole de Leeuw, Trijnie Dijkhuizen, Jayne Y Hehir-Kwa, et al.
Pageof 92