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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Author

Listed:
  • Tianyun Wang

    (University of Washington)

  • Kendra Hoekzema

    (University of Washington)

  • Davide Vecchio

    (Rare Disease and Medical Genetics, Academic Department of Pediatrics, Bambino Gesù Children’s Hospital
    Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital)

  • Huidan Wu

    (Central South University)

  • Arvis Sulovari

    (University of Washington)

  • Bradley P. Coe

    (University of Washington)

  • Madelyn A. Gillentine

    (University of Washington)

  • Amy B. Wilfert

    (University of Washington)

  • Luis A. Perez-Jurado

    (Women’s and Children’s Hospital
    South Australian Health and Medical Research Institute
    Genetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER)

  • Malin Kvarnung

    (Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet
    Karolinska University Hospital)

  • Yoeri Sleyp

    (Centre for Human Genetics, KU Leuven and Leuven Autism Research (LAuRes))

  • Rachel K. Earl

    (University of Washington)

  • Jill A. Rosenfeld

    (Department of Molecular & Human Genetics, Baylor College of Medicine
    Baylor Genetics)

  • Madeleine R. Geisheker

    (University of Washington)

  • Lin Han

    (Central South University)

  • Bing Du

    (Central South University)

  • Chris Barnett

    (Women’s and Children’s Hospital
    the University of Adelaide)

  • Elizabeth Thompson

    (Women’s and Children’s Hospital)

  • Marie Shaw

    (the University of Adelaide)

  • Renee Carroll

    (the University of Adelaide)

  • Kathryn Friend

    (Genetics and Molecular Pathology, SA Pathology)

  • Rachael Catford

    (Genetics and Molecular Pathology, SA Pathology)

  • Elizabeth E. Palmer

    (Hunter New England Health Service
    University of New South Wales)

  • Xiaobing Zou

    (Sun Yat-Sen University, Guangzhou)

  • Jianjun Ou

    (Central South University)

  • Honghui Li

    (Liuzhou Maternity and Child Healthcare Hospital)

  • Hui Guo

    (Central South University)

  • Jennifer Gerdts

    (University of Washington)

  • Emanuela Avola

    (Oasi Research Institute-IRCCS)

  • Giuseppe Calabrese

    (Oasi Research Institute-IRCCS)

  • Maurizio Elia

    (Oasi Research Institute-IRCCS)

  • Donatella Greco

    (Oasi Research Institute-IRCCS)

  • Anna Lindstrand

    (Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet
    Karolinska University Hospital)

  • Ann Nordgren

    (Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet
    Karolinska University Hospital)

  • Britt-Marie Anderlid

    (Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet
    Karolinska University Hospital)

  • Geert Vandeweyer

    (University of Antwerp)

  • Anke Dijck

    (University of Antwerp)

  • Nathalie Aa

    (University of Antwerp)

  • Brooke McKenna

    (Emory University)

  • Miroslava Hancarova

    (Charles University 2nd Faculty of Medicine and University Hospital Motol)

  • Sarka Bendova

    (Charles University 2nd Faculty of Medicine and University Hospital Motol)

  • Marketa Havlovicova

    (Charles University 2nd Faculty of Medicine and University Hospital Motol)

  • Giovanni Malerba

    (University of Verona)

  • Bernardo Dalla Bernardina

    (Child Neuropsychiatry Unit, AOUI)

  • Pierandrea Muglia

    (UCB Pharma)

  • Arie Haeringen

    (Leiden University Medical Center (LUMC))

  • Mariette J. V. Hoffer

    (Leiden University Medical Center (LUMC))

  • Barbara Franke

    (Radboud University Medical Center
    Radboud University Medical Center)

  • Gerarda Cappuccio

    (Federico II University
    Telethon Institute of Genetics and Medicine, Pozzuoli)

  • Martin Delatycki

    (Murdoch Children’s Research Institute)

  • Paul J. Lockhart

    (Murdoch Children’s Research Institute
    University of Melbourne)

  • Melanie A. Manning

    (Stanford University
    Stanford University)

  • Pengfei Liu

    (Department of Molecular & Human Genetics, Baylor College of Medicine
    Baylor Genetics)

  • Ingrid E. Scheffer

    (Murdoch Children’s Research Institute
    University of Melbourne, Royal Children’s Hospital
    University of Melbourne, Austin Health
    The Florey Institute of Neuroscience and Mental Health)

  • Nicola Brunetti-Pierri

    (Federico II University
    Telethon Institute of Genetics and Medicine, Pozzuoli)

  • Nanda Rommelse

    (Radboud University Medical Center
    Karakter Child and Adolescent Psychiatry Center)

  • David G. Amaral

    (University of California, Davis)

  • Gijs W. E. Santen

    (Leiden University Medical Center (LUMC))

  • Elisabetta Trabetti

    (University of Verona)

  • Zdeněk Sedláček

    (Charles University 2nd Faculty of Medicine and University Hospital Motol)

  • Jacob J. Michaelson

    (University of Iowa Carver College of Medicine)

  • Karen Pierce

    (University of California San Diego)

  • Eric Courchesne

    (University of California San Diego)

  • R. Frank Kooy

    (University of Antwerp)

  • Magnus Nordenskjöld

    (Department of Molecular Medicine and Surgery, Center for Molecular Medicine, Karolinska Institutet
    Karolinska University Hospital)

  • Corrado Romano

    (Oasi Research Institute-IRCCS)

  • Hilde Peeters

    (Centre for Human Genetics, KU Leuven and Leuven Autism Research (LAuRes))

  • Raphael A. Bernier

    (University of Washington)

  • Jozef Gecz

    (South Australian Health and Medical Research Institute
    the University of Adelaide
    Genetics and Molecular Pathology, SA Pathology)

  • Kun Xia

    (Central South University
    CAS Center for Excellence in Brain Science and Intelligences Technology (CEBSIT), Chinese Academy of Sciences)

  • Evan E. Eichler

    (University of Washington
    University of Washington)

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Suggested Citation

  • Tianyun Wang & Kendra Hoekzema & Davide Vecchio & Huidan Wu & Arvis Sulovari & Bradley P. Coe & Madelyn A. Gillentine & Amy B. Wilfert & Luis A. Perez-Jurado & Malin Kvarnung & Yoeri Sleyp & Rachel K., 2020. "Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders," Nature Communications, Nature, vol. 11(1), pages 1-1, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19289-5
    DOI: 10.1038/s41467-020-19289-5
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    Cited by:

    1. Jie Zhang & Gongcheng Hu & Yuli Lu & Huawei Ren & Yin Huang & Yulin Wen & Binrui Ji & Diyang Wang & Haidong Wang & Huisheng Liu & Ning Ma & Lingling Zhang & Guangjin Pan & Yibo Qu & Hua Wang & Wei Zha, 2024. "CTCF mutation at R567 causes developmental disorders via 3D genome rearrangement and abnormal neurodevelopment," Nature Communications, Nature, vol. 15(1), pages 1-21, December.
    2. Yudong Gao & Daichi Shonai & Matthew Trn & Jieqing Zhao & Erik J. Soderblom & S. Alexandra Garcia-Moreno & Charles A. Gersbach & William C. Wetsel & Geraldine Dawson & Dmitry Velmeshev & Yong-hui Jian, 2024. "Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions," Nature Communications, Nature, vol. 15(1), pages 1-18, December.
    3. Hyoseon Oh & Suho Lee & Yusang Oh & Seongbin Kim & Young Seo Kim & Yeji Yang & Woochul Choi & Ye-Eun Yoo & Heejin Cho & Seungjoon Lee & Esther Yang & Wuhyun Koh & Woojin Won & Ryunhee Kim & C. Justin , 2023. "Kv7/KCNQ potassium channels in cortical hyperexcitability and juvenile seizure-related death in Ank2-mutant mice," Nature Communications, Nature, vol. 14(1), pages 1-20, December.

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