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David Skuse

Showing results (121-130 of 132) with videos related to

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Biological Psychiatry|August 23, 2020
Atypical Neurogenesis in Induced Pluripotent Stem Cells From Autistic IndividualsDwaipayan Adhya, Vivek Swarup, Roland Nagy, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorderSarah Curran, Patrick Bolton, Kinga Rozsnyai, et al.
Nature Genetics|March 22, 2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationElise B Robinson, Beate St Pourcain, Verneri Anttila, et al.
World Psychiatry : Official Journal of the World Psychiatric Association (WPA)|January 12, 2021
An organization- and category-level comparison of diagnostic requirements for mental disorders in ICD-11 and DSM-5Michael B First, Wolfgang Gaebel, Mario Maj, et al.
Nature Genetics|May 16, 2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disordersDaniel J Weiner, Emilie M Wigdor, Stephan Ripke, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 1, 2018
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplicationsKate Wolfe, Andrew McQuillin, Viola Alesi, et al.
Science (New York, N.Y.)|March 17, 2007
Strong association of de novo copy number mutations with autismJonathan Sebat, B Lakshmi, Dheeraj Malhotra, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Pageof 14

Showing results (121-130 of 132) with videos related to

Sort By:
Pageof 14
Biological Psychiatry|August 23, 2020
Atypical Neurogenesis in Induced Pluripotent Stem Cells From Autistic IndividualsDwaipayan Adhya, Vivek Swarup, Roland Nagy, et al.
Translational Psychiatry|March 7, 2019
Correction: Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
Translational Psychiatry|January 22, 2019
Psychiatric disorders in children with 16p11.2 deletion and duplicationMaria Niarchou, Samuel J R A Chawner, Joanne L Doherty, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorderSarah Curran, Patrick Bolton, Kinga Rozsnyai, et al.
Nature Genetics|March 22, 2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationElise B Robinson, Beate St Pourcain, Verneri Anttila, et al.
World Psychiatry : Official Journal of the World Psychiatric Association (WPA)|January 12, 2021
An organization- and category-level comparison of diagnostic requirements for mental disorders in ICD-11 and DSM-5Michael B First, Wolfgang Gaebel, Mario Maj, et al.
Nature Genetics|May 16, 2017
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disordersDaniel J Weiner, Emilie M Wigdor, Stephan Ripke, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 1, 2018
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplicationsKate Wolfe, Andrew McQuillin, Viola Alesi, et al.
Science (New York, N.Y.)|March 17, 2007
Strong association of de novo copy number mutations with autismJonathan Sebat, B Lakshmi, Dheeraj Malhotra, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Pageof 14