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Jonathan Sebat

Showing results (81-90 of 100) with videos related to

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Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Science (New York, N.Y.)|April 21, 2018
Paternally inherited cis-regulatory structural variants are associated with autismWilliam M Brandler, Danny Antaki, Madhusudan Gujral, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
The Lancet. Psychiatry|June 29, 2025
The Psychiatric Genomics Consortium: discoveries and directionsArpana Agrawal, Cynthia M Bulik, Dawit Shawel Abebe, et al.
Journal of Medical Genetics|July 24, 2017
<i>FOXP1</i>-related intellectual disability syndrome: a recognisable entityIlse Meerschaut, Daniel Rochefort, Nicole Revençu, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Cell Genomics|March 27, 2024
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Nature Genetics|February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
Pageof 10

Showing results (81-90 of 100) with videos related to

Sort By:
Pageof 10
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Science (New York, N.Y.)|April 21, 2018
Paternally inherited cis-regulatory structural variants are associated with autismWilliam M Brandler, Danny Antaki, Madhusudan Gujral, et al.
JAMA Psychiatry|January 18, 2013
Implication of a rare deletion at distal 16p11.2 in schizophreniaSaurav Guha, Elliott Rees, Ariel Darvasi, et al.
The Lancet. Psychiatry|June 29, 2025
The Psychiatric Genomics Consortium: discoveries and directionsArpana Agrawal, Cynthia M Bulik, Dawit Shawel Abebe, et al.
Journal of Medical Genetics|July 24, 2017
<i>FOXP1</i>-related intellectual disability syndrome: a recognisable entityIlse Meerschaut, Daniel Rochefort, Nicole Revençu, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Cell Genomics|March 27, 2024
A revamped rat reference genome improves the discovery of genetic diversity in laboratory ratsTristan V de Jong, Yanchao Pan, Pasi Rastas, et al.
Medrxiv : the Preprint Server for Health Sciences|May 7, 2026
Combinatorial effects of gene dosage, polygenic background and environment on complex traitsMolly F Sacks, Marieke Klein, Tim B Bigdeli, et al.
Nature|February 5, 2011
Mapping copy number variation by population-scale genome sequencingRyan E Mills, Klaudia Walter, Chip Stewart, et al.
Nature Genetics|February 16, 2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delaySanthosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, et al.
Pageof 10