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Jonathan Sebat

Showing results (21-30 of 100) with videos related to

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Nature Communications|November 22, 2019
Ranking of non-coding pathogenic variants and putative essential regions of the human genomeAlex Wells, David Heckerman, Ali Torkamani, et al.
Human Molecular Genetics|July 17, 2010
Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disordersXianjin Zhou, Zhiguo Nie, Amanda Roberts, et al.
Neuron|February 20, 2015
Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseasesGuan Ning Lin, Roser Corominas, Irma Lemmens, et al.
Plos Computational Biology|June 15, 2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genomeKymberleigh A Pagel, Danny Antaki, AoJie Lian, et al.
Biological Psychiatry|November 14, 2017
Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem CellsFabiele Baldino Russo, Beatriz Camille Freitas, Graciela Conceição Pignatari, et al.
The American Journal of Psychiatry|November 6, 2018
Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for SchizophreniaSarah E Bergen, Alexander Ploner, Daniel Howrigan, et al.
Bioinformatics (Oxford, England)|June 3, 2006
PROBER: oligonucleotide FISH probe design softwareNicholas Navin, Vladimir Grubor, Jim Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2007
A unified genetic theory for sporadic and inherited autismXiaoyue Zhao, Anthony Leotta, Vlad Kustanovich, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in AutismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
Cell Genomics|June 20, 2022
SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrainsMilad Mortazavi, Yangsu Ren, Shubham Saini, et al.
Pageof 10

Showing results (21-30 of 100) with videos related to

Sort By:
Pageof 10
Nature Communications|November 22, 2019
Ranking of non-coding pathogenic variants and putative essential regions of the human genomeAlex Wells, David Heckerman, Ali Torkamani, et al.
Human Molecular Genetics|July 17, 2010
Reduced NMDAR1 expression in the Sp4 hypomorphic mouse may contribute to endophenotypes of human psychiatric disordersXianjin Zhou, Zhiguo Nie, Amanda Roberts, et al.
Neuron|February 20, 2015
Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseasesGuan Ning Lin, Roser Corominas, Irma Lemmens, et al.
Plos Computational Biology|June 15, 2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genomeKymberleigh A Pagel, Danny Antaki, AoJie Lian, et al.
Biological Psychiatry|November 14, 2017
Modeling the Interplay Between Neurons and Astrocytes in Autism Using Human Induced Pluripotent Stem CellsFabiele Baldino Russo, Beatriz Camille Freitas, Graciela Conceição Pignatari, et al.
The American Journal of Psychiatry|November 6, 2018
Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for SchizophreniaSarah E Bergen, Alexander Ploner, Daniel Howrigan, et al.
Bioinformatics (Oxford, England)|June 3, 2006
PROBER: oligonucleotide FISH probe design softwareNicholas Navin, Vladimir Grubor, Jim Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 27, 2007
A unified genetic theory for sporadic and inherited autismXiaoyue Zhao, Anthony Leotta, Vlad Kustanovich, et al.
Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in AutismMilad Mortazavi, James Guevara, Joshua Diaz, et al.
Cell Genomics|June 20, 2022
SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrainsMilad Mortazavi, Yangsu Ren, Shubham Saini, et al.
Pageof 10