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Cell|March 20, 2012
CNVs: harbingers of a rare variant revolution in psychiatric geneticsDheeraj Malhotra, Jonathan SebatHuman 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.Nature Genetics|September 5, 2007
Major changes in our DNA lead to major changes in our thinkingJonathan SebatNature Methods|July 4, 2012
forestSV: structural variant discovery through statistical learningJacob J Michaelson, Jonathan SebatAnnual Review of Medicine|January 15, 2015
From de novo mutations to personalized therapeutic interventions in autismWilliam M Brandler, Jonathan SebatBMC Genomics|February 1, 2020
The effects of common structural variants on 3D chromatin structureOmar Shanta, Amina Noor, , et al.Journal of Child Neurology|September 23, 2015
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription ProfilesMary Kusenda, Vladimir Vacic, Dheeraj Malhotra, et al.Bioinformatics (Oxford, England)|January 5, 2018
SV2: accurate structural variation genotyping and de novo mutation detection from whole genomesDanny Antaki, William M Brandler, Jonathan SebatNucleic Acids Research|May 14, 2025
Cell type- and factor-specific nonsense-mediated RNA decayKun Tan, Jonathan Sebat, Miles F WilkinsonStem Cell Reports|February 21, 2017
Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of PsychosisJulia Tcw, Claudia M B Carvalho, Bo Yuan, et al.Pageof 12