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All papers authored by Jonathan Sebat

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2021 Jorge Urresti, Pan Zhang, Patricia Moran-Losada, Nam-Kyung Yu, Priscilla D. Negraes, Cleber A. Trujillo, Danny Antaki, Megha Amar

ORCID

ORCID

, Akula Bala Pramod, Jolene Diedrich, Leon Tejwani, Sarah Romero, Jonathan Sebat

ORCID

, John R. Yates Iii

ORCID

and 2 other authors

Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism

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2020 Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez

ORCID

, Kymberleigh A. Pagel, Guan Ning Lin

ORCID

, Hyun-Jun Nam, Matthew Mort, David N. Cooper

ORCID

, Jonathan Sebat

ORCID

, Lilia M. Iakoucheva

ORCID

, Sean D. Mooney, Predrag Radivojac

ORCID

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2

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2019 Martin W. Breuss, Danny Antaki, Renee D. George, Morgan Kleiber, Kiely N. James, Laurel L. Ball, Oanh Hong, Ileena Mitra, Xiaoxu Yang

ORCID

, Sara A. Wirth, Jing Gu, Camila A. B. Garcia, Madhusudan Gujral, William M. Brandler, Damir Musaev and 15 other authors

Autism risk in offspring can be assessed through quantification of male sperm mosaicism

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Alex Wells

ORCID

, David Heckerman

ORCID

, Ali Torkamani

ORCID

, Li Yin

ORCID

, Jonathan Sebat

ORCID

, Bing Ren

ORCID

, Amalio Telenti, Julia di Iulio

ORCID

Ranking of non-coding pathogenic variants and putative essential regions of the human genome

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Stephan J. Sanders, Mustafa Sahin

ORCID

, Joseph Hostyk

ORCID

, Audrey Thurm, Sebastien Jacquemont, Paul Avillach

ORCID

, Elise Douard, Christa L. Martin, Meera E. Modi, Andres Moreno-De-Luca

ORCID

, Armin Raznahan, Alan Anticevic, Ricardo Dolmetsch, Guoping Feng

ORCID

, Daniel H. Geschwind

ORCID

and 11 other authors

A framework for the investigation of rare genetic disorders in neuropsychiatry

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2016 Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Peter A. Holmans, Dalila Pinto

ORCID

, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Zhouzhi Wang, Karin V. Fuentes Fajarado and 258 other authors

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

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2015 Mary Kusenda, Vladimir Vacic, Dheeraj Malhotra, Linda Rodgers, Kevin Pavon, Jennifer Meth, Ravinesh A. Kumar, Susan L. Christian, Hilde Peeters, Shawn S. Cho, Anjene Addington, Judith L. Rapoport, Jonathan Sebat

ORCID

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles

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William M. Brandler, Jonathan Sebat

ORCID

From De Novo Mutations to Personalized Therapeutic Interventions in Autism

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Guan Ning Lin, Roser Corominas, Irma Lemmens, Xinping Yang, Jan Tavernier, David E. Hill, Marc Vidal, Jonathan Sebat

ORCID

, Lilia M. Iakoucheva

Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases

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2014 Roser Corominas, Xinping Yang, Guan Ning Lin, Shuli Kang, Yun Shen, Lila Ghamsari, Martin Broly, Maria Rodriguez, Stanley Tam, Shelly A. Trigg, Shelly A. Wanamaker, Changyu Fan, Song Yi, Murat Tasan, Irma Lemmens and 16 other authors

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

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2013 Caitlin Rippey, Tom Walsh, Suleyman Gulsuner, Matt Brodsky, Alex S. Nord

ORCID

, Molly Gasperini, Sarah Pierce, Cailyn Spurrell, Bradley P. Coe, Niklas Krumm, Ming K. Lee, Jonathan Sebat

ORCID

, Jon M. McClellan, Mary-Claire King

Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia

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Jennifer Gladys Mulle, Ann E. Pulver, John M. McGrath, John A. McGrath, Paula S. Wolyniec, Anne F. Dodd, David J. Cutler, Jonathan Sebat

ORCID

, Dheeraj Malhotra, Gerald Nestadt, Donald F. Conrad, Matthew Hurles, Chris P. Barnes, Masashi Ikeda, Nakao Iwata and 21 other authors

Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia

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E. Rees, D. Ivanov

ORCID

, M. Ikeda, P. K. Magnusson, D. Morris, J. A. Rosenfeld, A. Lee, J. M. Kane, A. K. Malhotra, M. Rietschel, M. M. Nöthen, L. Priebe, J. Strohmaier, D. M. Ruderfer, J. L. Moran and 31 other authors

Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia

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2012 Jacob J. Michaelson, Yujian Shi, Madhusudan Gujral, Hancheng Zheng, Dheeraj Malhotra, Xin Jin

ORCID

, Minghan Jian, Guangming Liu, Douglas Greer, Abhishek Bhandari, Wenting Wu, Roser Corominas, Áine Peoples, Amnon Koren, Athurva Gore and 13 other authors

Whole-Genome Sequencing in Autism Identifies Hot Spots for De Novo Germline Mutation

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Amnon Koren, Paz Polak, James Nemesh, Jacob J. Michaelson, Jonathan Sebat

ORCID

, Shamil R. Sunyaev, Steven A. McCarroll

Differential Relationship of DNA Replication Timing to Different Forms of Human Mutation and Variation

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Jacob J. Michaelson, Jonathan Sebat

ORCID

forestSV: structural variant discovery through statistical learning

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Dheeraj Malhotra, Jonathan Sebat

ORCID

Fish heads and human disease

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Dheeraj Malhotra, Jonathan Sebat

ORCID

CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

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2011 Dheeraj Malhotra, Shane McCarthy, Jacob J. Michaelson, Vladimir Vacic, Katherine E. Burdick, Seungtai Yoon, Sven Cichon, Aiden Corvin, Sydney Gary, Elliot S. Gershon, Michael Gill, Maria Karayiorgou, John R. Kelsoe, Olga Krastoshevsky, Verena Krause and 11 other authors

High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia

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Mamoru Kato, Seungtai Yoon, Naoya Hosono, Anthony Leotta, Jonathan Sebat

ORCID

, Tatsuhiko Tsunoda, Michael Q. Zhang, B. J. Andrews

Inferring Haplotypes of Copy Number Variations From High-Throughput Data With Uncertainty

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