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Author Details

Jonathan Sebat
University of California San Diego
2000
80
42
PMIDPaper TitleJournal TitlePublished Year
36732511Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2023
37214860A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats.bioRxiv2023
36732511Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.Nat Commun2023
37214860A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats.bioRxiv2023
35236119Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.Am J Psychiatry2022
35768728Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.Nat Genet2022
35654974A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.Nat Genet2022
36368308Genomic architecture of autism from comprehensive whole-genome sequence annotation.Cell2022
35811316Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes.Transl Psychiatry2022
36131047Rare copy number variation in posttraumatic stress disorder.Mol Psychiatry2022
35720252SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains.Cell Genom2022
35236119Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology.Am J Psychiatry2022
35768728Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.Nat Genet2022
35720252SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains.Cell Genom2022
35811316Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes.Transl Psychiatry2022
35654974A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.Nat Genet2022
36368308Genomic architecture of autism from comprehensive whole-genome sequence annotation.Cell2022
36131047Rare copy number variation in posttraumatic stress disorder.Mol Psychiatry2022
34388390Developmental and temporal characteristics of clonal sperm mosaicism.Cell2021
33727673Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling.Mol Psychiatry2021
33821956Customized de novo mutation detection for any variant calling pipeline: SynthDNM.Bioinformatics2021
34388390Developmental and temporal characteristics of clonal sperm mosaicism.Cell2021
34548630Correction: Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.Mol Psychiatry2021
34433918Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.Mol Psychiatry2021
33821956Customized de novo mutation detection for any variant calling pipeline: SynthDNM.Bioinformatics2021
33727673Autism-linked Cullin3 germline haploinsufficiency impacts cytoskeletal dynamics and cortical neurogenesis through RhoA signaling.Mol Psychiatry2021
34433918Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.Mol Psychiatry2021
34548630Correction: Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism.Mol Psychiatry2021
33219223Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.Nat Commun2020
31964429Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.Br J Psychiatry2020
31873310Autism risk in offspring can be assessed through quantification of male sperm mosaicism.Nat Med2020
33219223Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.Nat Commun2020
31873310Autism risk in offspring can be assessed through quantification of male sperm mosaicism.Nat Med2020
31964429Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.Br J Psychiatry2020
30392412Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.Am J Psychiatry2019
31748530Ranking of non-coding pathogenic variants and putative essential regions of the human genome.Nat Commun2019
31779666Common DNA sequence variation influences 3-dimensional conformation of the human genome.Genome Biol2019
31553903Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.Cell Rep2019
30392412Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.Am J Psychiatry2019
31491383Getting to the Cores of Autism.Cell2019
31279534Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.Biol Psychiatry2019
31199787Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.PLoS Comput Biol2019
31548702A framework for the investigation of rare genetic disorders in neuropsychiatry.Nat Med2019
31779666Common DNA sequence variation influences 3-dimensional conformation of the human genome.Genome Biol2019
31748530Ranking of non-coding pathogenic variants and putative essential regions of the human genome.Nat Commun2019
31553903Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.Cell Rep2019
31548702A framework for the investigation of rare genetic disorders in neuropsychiatry.Nat Med2019
31491383Getting to the Cores of Autism.Cell2019
31199787Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.PLoS Comput Biol2019
31279534Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.Biol Psychiatry2019
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Collaborators

Dheeraj Malhotra
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Shane McCarthy
Wellcome Sanger Institute
Co-authored papers 15
Alysson R Muotri
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Co-authored papers 9
Mary-Claire King
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Tom Walsh
University of Washington
Co-authored papers 8
Evan E Eichler
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Michael Gill
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Seungtai Yoon
Co-authored papers 7
Patrick F Sullivan
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Jon McClellan
University of Washington
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Joseph G Gleeson
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Balasubramanian Lakshmi
Bharathidasan University, Indian Institute of Science
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Michael J Owen
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Stephen W Scherer
The Hospital for Sick Children
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Mary Kusenda
Clinic for Cattle, University of Veterinary Medicine Hannover
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Aiden Corvin
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Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers 4
Caroline M Nievergelt
VA San Diego Healthcare System (VASDHS)
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Alex S Nord
UC Davis Center for Neuroscience.
Co-authored papers 4
Derek W Morris
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Daniel H Geschwind
University of California los angeles
Co-authored papers 4
Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
Co-authored papers 4
Eric Courchesne
University of California
Co-authored papers 4
Release 1.2