Correction to: Nature Genetics https://doi.org/10.1038/s41588-020-0695-1, published online 28 September 2020.
In the version of this article originally published, author Hongyu Zhao was not included in the author list. The error has been corrected in the HTML and PDF versions of the article.
Author information
These authors contributed equally: Sheng Chih Jin, Sara A. Lewis, Somayeh Bakhtiari, Xue Zeng.
These authors jointly supervised this work: Qinghe Xing, Changlian Zhu, Kaya Bilguvar, Sergio Padilla-Lopez, Richard P. Lifton, Jozef Gecz, Alastair H. MacLennan, Michael C. Kruer.
Authors and Affiliations
Department of Genetics, Yale University School of Medicine, New Haven, CT, USA
Sheng Chih Jin, Xue Zeng, Michael C. Sierant, Junhui Zhang, Amar H. Sheth, Kaya Bilguvar & Richard P. Lifton
Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA
Sheng Chih Jin, Xue Zeng, Michael C. Sierant & Richard P. Lifton
Department of Genetics, Washington University School of Medicine, St Louis, MO, USA
Sheng Chih Jin
Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children’s Hospital, Phoenix, AZ, USA
Sara A. Lewis, Somayeh Bakhtiari, Sheetal Shetty, Sandra M. Nordlie, Aureliane Elie, Bethany Y. Norton, Brandon S. Guida, Helen Magee, James Liu, Jennifer Heim, Sergio Padilla-Lopez & Michael C. Kruer
Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine–Phoenix, Phoenix, AZ, USA
Sara A. Lewis, Somayeh Bakhtiari, Sheetal Shetty, Sandra M. Nordlie, Aureliane Elie, Bethany Y. Norton, Brandon S. Guida, Helen Magee, James Liu, Sergio Padilla-Lopez & Michael C. Kruer
Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia
Mark A. Corbett, Clare L. van Eyk, Jesia G. Berry, Kelly Harper, Dani L. Webber, Mahalia S. B. Frank, Jozef Gecz & Alastair H. MacLennan
Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, London, UK
Shozeb Haider
Molecular Brain Sciences, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada
Stephen Pastore & John B. Vincent
One CP Place, Plano, TX, USA
Janice Brunstrom-Hernandez
Division of Paediatric Neurology, Iaso Children’s Hospital, Athens, Greece
Antigone Papavasileiou
Department of Pediatrics, Monash University, Melbourne, Victoria, Australia
Michael C. Fahey
Henan Key Laboratory of Child Genetics and Metabolism, Rehabilitation Department, Children’s Hospital of Zhengzhou University, Zhengzhou, China
Chongchen Zhou & Qing Shang
Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA
Boyang Li & Hongyu Zhao
Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China
Lei Xia, Yiran Xu, Dengna Zhu, Bohao Zhang, Xiaoyang Wang & Changlian Zhu
Yale Center for Genome Analysis, Yale University, New Haven, CT, USA
James R. Knight, Christopher Castaldi, Irina R. Tikhonova, Francesc López-Giráldez, Shrikant M. Mane & Kaya Bilguvar
Department of Genetics, Pitié-Salpêtrière Hospital, APHP.Sorbonne Université, Paris, France
Boris Keren & Julien Buratti
UF de Génétique Clinique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, APHP.Sorbonne Université, Hôpital Armand Trousseau, Paris, France
Sandra Whalen
Sorbonne Université, APHP, Service de Neurologie Pédiatrique et Centre de Référence Neurogénétique, Hôpital Armand Trousseau, Paris, France
Diane Doummar
GeneDx, Gaithersburg, MD, USA
Megan Cho, Kyle Retterer & Francisca Millan
Institute of Biomedical Science and Children’s Hospital, and Key Laboratory of Reproduction Regulation of the National Population and Family Planning Commission (NPFPC), Shanghai Institute of Planned Parenthood Research (SIPPR), IRD, Fudan University, Shanghai, China
Yangong Wang & Qinghe Xing
Departments of Pediatrics & Neurology, University of Texas Southwestern and Children’s Medical Center of Dallas, Dallas, TX, USA
Jeff L. Waugh
Departments of Genetics & Genomics and Neurology, Boston Children’s Hospital, Boston, MA, USA
Lance Rodan
Division of Neurogenetics and Hugo W. Moser Research Institute, Kennedy Krieger Institute, Baltimore, MD, USA
Julie S. Cohen & Ali Fatemi
Medical Genetics, Department of Pediatrics, MassGeneral Hospital for Children, Boston, MA, USA
Angela E. Lin
Departments of Pediatrics and Neurology, University of New Mexico, Albuquerque, NM, USA
John P. Phillips
Division of Pediatric Neurology, Gillette Children’s Hospital, St Paul, MN, USA
Timothy Feyma
Department of Paediatric Neurology, Women’s & Children’s Hospital, Adelaide, South Australia, Australia
Suzanna C. MacLennan
Departments of Molecular & Cellular Biology and Neuroscience, University of Arizona, Tucson, AZ, USA
Spencer Vaughan & Daniela C. Zarnescu
Murdoch Children’s Research Institute and University of Melbourne Department of Paediatrics, Royal Children’s Hospital, Melbourne, Victoria, Australia
Kylie E. Crompton, Susan M. Reid, Dinah S. Reddihough & David J. Amor
Rehabilitation Department, Children’s Hospital of Zhengzhou University/Henan Children’s Hospital, Zhengzhou, China
Chao Gao
Cerebral Palsy Alliance Research Institute, University of Sydney, Sydney, New South Wales, Australia
Iona Novak, Nadia Badawi, Yana A. Wilson & Sarah J. McIntyre
Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden
Xiaoyang Wang & Changlian Zhu
Department of Biostatistics & Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA
Qiongshi Lu
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Correspondence to Michael C. Kruer.
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Jin, S.C., Lewis, S.A., Bakhtiari, S. et al. Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy. Nat Genet 53, 412 (2021). https://doi.org/10.1038/s41588-021-00780-8
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DOI: https://doi.org/10.1038/s41588-021-00780-8
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