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Jonathan Sebat

Showing results (41-50 of 100) with videos related to

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Human Mutation|April 27, 2018
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypesChristopher M Grochowski, Shen Gu, Bo Yuan, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 23, 2020
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort studyClaire Foley, Elizabeth A Heron, Denise Harold, et al.
American Journal of Human Genetics|January 9, 2008
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMaricela Alarcón, Brett S Abrahams, Jennifer L Stone, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Reduced transcript expression of genes affected by inherited and de novo CNVs in autismAlex S Nord, Wendy Roeb, Diane E Dickel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
Gene dosage architecture across complex traitsSayeh Kazem, Kuldeep Kumar, Martineau Jean-Louis, et al.
Translational Psychiatry|July 10, 2022
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genesHiroki Kimura, Masahiro Nakatochi, Branko Aleksic, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
NPJ Schizophrenia|March 18, 2016
Characterization of molecular and cellular phenotypes associated with a heterozygous <i>CNTNAP2</i> deletion using patient-derived hiPSC neural cellsInkyu S Lee, Claudia M B Carvalho, Panagiotis Douvaras, et al.
Biological Psychiatry|October 31, 2009
Genomewide association study of movement-related adverse antipsychotic effectsKarolina Aberg, Daniel E Adkins, József Bukszár, et al.
Cell Reports|September 26, 2019
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial DevelopmentYuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, et al.
Pageof 10

Showing results (41-50 of 100) with videos related to

Sort By:
Pageof 10
Human Mutation|April 27, 2018
Marker chromosome genomic structure and temporal origin implicate a chromoanasynthesis event in a family with pleiotropic psychiatric phenotypesChristopher M Grochowski, Shen Gu, Bo Yuan, et al.
The British Journal of Psychiatry : the Journal of Mental Science|January 23, 2020
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort studyClaire Foley, Elizabeth A Heron, Denise Harold, et al.
American Journal of Human Genetics|January 9, 2008
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility geneMaricela Alarcón, Brett S Abrahams, Jennifer L Stone, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Reduced transcript expression of genes affected by inherited and de novo CNVs in autismAlex S Nord, Wendy Roeb, Diane E Dickel, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
Gene dosage architecture across complex traitsSayeh Kazem, Kuldeep Kumar, Martineau Jean-Louis, et al.
Translational Psychiatry|July 10, 2022
Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genesHiroki Kimura, Masahiro Nakatochi, Branko Aleksic, et al.
Genome Research|September 17, 2003
Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variationRobert Lucito, John Healy, Joan Alexander, et al.
NPJ Schizophrenia|March 18, 2016
Characterization of molecular and cellular phenotypes associated with a heterozygous <i>CNTNAP2</i> deletion using patient-derived hiPSC neural cellsInkyu S Lee, Claudia M B Carvalho, Panagiotis Douvaras, et al.
Biological Psychiatry|October 31, 2009
Genomewide association study of movement-related adverse antipsychotic effectsKarolina Aberg, Daniel E Adkins, József Bukszár, et al.
Cell Reports|September 26, 2019
Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial DevelopmentYuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, et al.
Pageof 10