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Jonathan Sebat

Showing results (51-60 of 100) with videos related to

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Science (New York, N.Y.)|July 27, 2004
Large-scale copy number polymorphism in the human genomeJonathan Sebat, B Lakshmi, Jennifer Troge, et al.
Molecular Psychiatry|September 22, 2021
Correction: Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autismJorge Urresti, Pan Zhang, Patricia Moran-Losada, et al.
Molecular Psychiatry|August 26, 2021
Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autismJorge Urresti, Pan Zhang, Patricia Moran-Losada, et al.
American Journal of Human Genetics|July 7, 2010
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.
Cell|August 13, 2021
Developmental and temporal characteristics of clonal sperm mosaicismXiaoxu Yang, Martin W Breuss, Xin Xu, et al.
Research Square|December 3, 2025
Determinants of pleiotropy and monotonic gene dosage responses across human traitsSayeh Kazem, Kuldeep Kumar, Guillaume Huguet, et al.
Nature|May 15, 2007
Completing the map of human genetic variation, Evan E Eichler, Deborah A Nickerson, et al.
Nature Genetics|June 2, 2022
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
Nature Genetics|June 29, 2022
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
Molecular Psychiatry|March 17, 2021
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signalingMegha Amar, Akula Bala Pramod, Nam-Kyung Yu, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
Science (New York, N.Y.)|July 27, 2004
Large-scale copy number polymorphism in the human genomeJonathan Sebat, B Lakshmi, Jennifer Troge, et al.
Molecular Psychiatry|September 22, 2021
Correction: Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autismJorge Urresti, Pan Zhang, Patricia Moran-Losada, et al.
Molecular Psychiatry|August 26, 2021
Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autismJorge Urresti, Pan Zhang, Patricia Moran-Losada, et al.
American Journal of Human Genetics|July 7, 2010
Genomic duplication and overexpression of TJP2/ZO-2 leads to altered expression of apoptosis genes in progressive nonsyndromic hearing loss DFNA51Tom Walsh, Sarah B Pierce, Danielle R Lenz, et al.
Cell|August 13, 2021
Developmental and temporal characteristics of clonal sperm mosaicismXiaoxu Yang, Martin W Breuss, Xin Xu, et al.
Research Square|December 3, 2025
Determinants of pleiotropy and monotonic gene dosage responses across human traitsSayeh Kazem, Kuldeep Kumar, Guillaume Huguet, et al.
Nature|May 15, 2007
Completing the map of human genetic variation, Evan E Eichler, Deborah A Nickerson, et al.
Nature Genetics|June 2, 2022
A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
Nature Genetics|June 29, 2022
Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sexDanny Antaki, James Guevara, Adam X Maihofer, et al.
Molecular Psychiatry|March 17, 2021
Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signalingMegha Amar, Akula Bala Pramod, Nam-Kyung Yu, et al.
Pageof 10