Publications by authors named "Jonathan Sebat"

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Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopal, Jonathan Sebat

bioRxiv· November 2025

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Determinants of pleiotropy and monotonic gene dosage responses across human traits.
Sayeh Kazem, Kuldeep Kumar, Guillaume Huguet, Josephine Mollon, Thomas Renne, Jonathan Sebat

Res Sq· November 2025

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Mirror effect of genomic deletions and duplications on cognitive ability across the human cerebral cortex.
Kuldeep Kumar, Sayeh Kazem, Guillaume Huguet, Worrawat Engchuan, Jakub Kopal, Jonathan Sebat

Res Sq· November 2025

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Long-Read Genome Sequencing in Clinical Psychiatry: Haploinsufficiency in a Hospitalized Adolescent With Autism, Intellectual Disability, and Behavioral Decompensation.
Milad Mortazavi, Sergey Batalov, Jerica Lenberg, Corrine Blucher, Aisha Omorodion, Jonathan Sebat

Am J Psychiatry· August 2025

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The Psychiatric Genomics Consortium: discoveries and directions.
Arpana Agrawal, Cynthia M Bulik, Dawit Shawel Abebe, Ole A Andreassen, Elizabeth G Atkinson, Jonathan Sebat

Lancet Psychiatry· August 2025

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Long Read Genome Sequencing Elucidates Diverse Functional Consequences of Structural and Repeat Variation in Autism.
Milad Mortazavi, James Guevara, Joshua Diaz, Stephen Tran, Helyaneh Ziaei Jam, Jonathan Sebat

medRxiv· July 2025

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Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects.
Worrawat Engchuan, Omar Shanta, Kuldeep Kumar, Jeffrey R MacDonald, Bhooma Thiruvahindrapuram, Jonathan Sebat

medRxiv· July 2025

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A cross-disorder analysis of CNVs finds novel loci and dose-dependent relationships of genes to psychiatric traits.
Omar Shanta, Marieke Klein, Molly Sacks, Jeffrey R MacDonald, Adam Maihofer, Jonathan Sebat

medRxiv· July 2025

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Cell type- and factor-specific nonsense-mediated RNA decay.
Kun Tan, Jonathan Sebat, Miles F Wilkinson

Nucleic Acids Res· May 2025

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Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications.
Ruben C Gur, Carrie E Bearden, Sebastien Jacquemont, Ann Swillen, Therese van Amelsvoort, Jonathan Sebat

Mol Psychiatry· February 2025

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Gene dosage architecture across complex traits.
Sayeh Kazem, Kuldeep Kumar, Martineau Jean-Louis, Guillaume Huguet, Thomas Renne, Jonathan Sebat

medRxiv· February 2025

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Integrative genetic analysis: cornerstone of precision psychiatry.
Jacob Vorstman, Jonathan Sebat, Vincent-Raphaël Bourque, Sébastien Jacquemont

Mol Psychiatry· January 2025

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Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
Guillaume Huguet, Thomas Renne, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Jonathan Sebat

Cell Genom· December 2024

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A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats.
Tristan V de Jong, Yanchao Pan, Pasi Rastas, Daniel Munro, Monika Tutaj, Jonathan Sebat

Cell Genom· April 2024

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Effects of genetically predicted posttraumatic stress disorder on autoimmune phenotypes.
Adam X Maihofer, Andrew Ratanatharathorn, Sian M J Hemmings, Karen H Costenbader, Vasiliki Michopoulos, Jonathan Sebat

Transl Psychiatry· April 2024

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Neurocognitive Profiles of 22q11.2 and 16p11.2 Deletions and Duplications.
Ruben Gur, Carrie Bearden, Sébastien Jacquemont, Khadije Jizi, Therese Amelsvoort van, Jonathan Sebat

Res Sq· December 2023

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A revamped rat reference genome improves the discovery of genetic diversity in laboratory rats.
Tristan V de Jong, Yanchao Pan, Pasi Rastas, Daniel Munro, Monika Tutaj, Jonathan Sebat

bioRxiv· September 2023

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Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent and disruptions.
Eduardo A Maury, Maxwell A Sherman, Giulio Genovese, Thomas G Gilgenast, Tushar Kamath, Jonathan Sebat

Cell Genom· August 2023

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Control-independent mosaic single nucleotide variant detection with DeepMosaic.
Xiaoxu Yang, Xin Xu, Martin W Breuss, Danny Antaki, Laurel L Ball, Jonathan L Sebat

Nat Biotechnol· June 2023

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Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Roser Corominas, Xinping Yang, Guan Ning Lin, Shuli Kang, Yun Shen, Jonathan Sebat

Nat Commun· February 2023

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Rare copy number variation in posttraumatic stress disorder.
Adam X Maihofer, Worrawat Engchuan, Guillaume Huguet, Marieke Klein, Jeffrey R MacDonald, Jonathan Sebat

Mol Psychiatry· December 2022

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Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
Daniel J Weiner, Emi Ling, Serkan Erdin, Derek J C Tai, Rachita Yadav, Jonathan Sebat

Nat Genet· November 2022

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Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Brett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, Worrawat Engchuan, Edward J Higginbotham, Jonathan Sebat

Cell· November 2022

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Publisher Correction: A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.
Danny Antaki, James Guevara, Adam X Maihofer, Marieke Klein, Madhusudan Gujral, Jonathan Sebat

Nat Genet· August 2022

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Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes.
Hiroki Kimura, Masahiro Nakatochi, Branko Aleksic, James Guevara, Miho Toyama, Jonathan Sebat

Transl Psychiatry· July 2022

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