Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Sheng Chih Jin^#^{1

2

3}, Sara A Lewis^#^{4

5}, Somayeh Bakhtiari^#^{4

5}, Xue Zeng^#^{1

2}, Michael C Sierant^{1

2}, Sheetal Shetty^{4

5}, Sandra M Nordlie^{4

5}, Aureliane Elie^{4

5}, Mark A Corbett⁶, Bethany Y Norton^{4

5}, Clare L van Eyk⁶, Shozeb Haider⁷, Brandon S Guida^{4

5}, Helen Magee^{4

5}, James Liu^{4

5}, Stephen Pastore⁸, John B Vincent⁸, Janice Brunstrom-Hernandez⁹, Antigone Papavasileiou¹⁰, Michael C Fahey¹¹, Jesia G Berry⁶, Kelly Harper⁶, Chongchen Zhou¹², Junhui Zhang¹, Boyang Li¹³, Hongyu Zhao¹³, Jennifer Heim⁴, Dani L Webber⁶, Mahalia S B Frank⁶, Lei Xia¹⁴, Yiran Xu¹⁴, Dengna Zhu¹⁴, Bohao Zhang¹⁴, Amar H Sheth¹, James R Knight¹⁵, Christopher Castaldi¹⁵, Irina R Tikhonova¹⁵, Francesc López-Giráldez¹⁵, Boris Keren¹⁶, Sandra Whalen¹⁷, Julien Buratti¹⁶, Diane Doummar¹⁸, Megan Cho¹⁹, Kyle Retterer¹⁹, Francisca Millan¹⁹, Yangong Wang²⁰, Jeff L Waugh²¹, Lance Rodan²², Julie S Cohen²³, Ali Fatemi²³, Angela E Lin²⁴, John P Phillips²⁵, Timothy Feyma²⁶, Suzanna C MacLennan²⁷, Spencer Vaughan²⁸, Kylie E Crompton²⁹, Susan M Reid²⁹, Dinah S Reddihough²⁹, Qing Shang¹², Chao Gao³⁰, Iona Novak³¹, Nadia Badawi³¹, Yana A Wilson³¹, Sarah J McIntyre³¹, Shrikant M Mane¹⁵, Xiaoyang Wang^{14

32}, David J Amor²⁹, Daniela C Zarnescu²⁸, Qiongshi Lu³³, Qinghe Xing²⁰, Changlian Zhu^{14

32}, Kaya Bilguvar^{1

15}, Sergio Padilla-Lopez^{4

5}, Richard P Lifton^{1

2}, Jozef Gecz⁶, Alastair H MacLennan⁶, Michael C Kruer^{34

35}

Affiliations

¹ Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
² Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA.
³ Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
⁴ Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
⁵ Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
⁶ Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
⁷ Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, London, UK.
⁸ Molecular Brain Sciences, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
⁹ One CP Place, Plano, TX, USA.
¹⁰ Division of Paediatric Neurology, Iaso Children's Hospital, Athens, Greece.
¹¹ Department of Pediatrics, Monash University, Melbourne, Victoria, Australia.
¹² Henan Key Laboratory of Child Genetics and Metabolism, Rehabilitation Department, Children's Hospital of Zhengzhou University, Zhengzhou, China.
¹³ Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA.
¹⁴ Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
¹⁵ Yale Center for Genome Analysis, Yale University, New Haven, CT, USA.
¹⁶ Department of Genetics, Pitié-Salpêtrière Hospital, APHP.Sorbonne Université, Paris, France.
¹⁷ UF de Génétique Clinique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, APHP.Sorbonne Université, Hôpital Armand Trousseau, Paris, France.
¹⁸ Sorbonne Université, APHP, Service de Neurologie Pédiatrique et Centre de Référence Neurogénétique, Hôpital Armand Trousseau, Paris, France.
¹⁹ GeneDx, Gaithersburg, MD, USA.
²⁰ 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.
²¹ Departments of Pediatrics & Neurology, University of Texas Southwestern and Children's Medical Center of Dallas, Dallas, TX, USA.
²² Departments of Genetics & Genomics and Neurology, Boston Children's Hospital, Boston, MA, USA.
²³ Division of Neurogenetics and Hugo W. Moser Research Institute, Kennedy Krieger Institute, Baltimore, MD, USA.
²⁴ Medical Genetics, Department of Pediatrics, MassGeneral Hospital for Children, Boston, MA, USA.
²⁵ Departments of Pediatrics and Neurology, University of New Mexico, Albuquerque, NM, USA.
²⁶ Division of Pediatric Neurology, Gillette Children's Hospital, St Paul, MN, USA.
²⁷ Department of Paediatric Neurology, Women's & Children's Hospital, Adelaide, South Australia, Australia.
²⁸ Departments of Molecular & Cellular Biology and Neuroscience, University of Arizona, Tucson, AZ, USA.
²⁹ Murdoch Children's Research Institute and University of Melbourne Department of Paediatrics, Royal Children's Hospital, Melbourne, Victoria, Australia.
³⁰ Rehabilitation Department, Children's Hospital of Zhengzhou University/Henan Children's Hospital, Zhengzhou, China.
³¹ Cerebral Palsy Alliance Research Institute, University of Sydney, Sydney, New South Wales, Australia.
³² Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
³³ Department of Biostatistics & Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA.
³⁴ Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA. kruerm@email.arizona.edu.
³⁵ Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA. kruerm@email.arizona.edu.

^# Contributed equally.

PMID: 33432185
DOI: 10.1038/s41588-021-00780-8

Published Erratum

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Sheng Chih Jin et al. Nat Genet. 2021 Mar.

. 2021 Mar;53(3):412.

doi: 10.1038/s41588-021-00780-8.

Authors

Affiliations

¹ Department of Genetics, Yale University School of Medicine, New Haven, CT, USA.
² Laboratory of Human Genetics and Genomics, Rockefeller University, New York, NY, USA.
³ Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
⁴ Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
⁵ Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
⁶ Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
⁷ Department of Pharmaceutical and Biological Chemistry, UCL School of Pharmacy, London, UK.
⁸ Molecular Brain Sciences, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
⁹ One CP Place, Plano, TX, USA.
¹⁰ Division of Paediatric Neurology, Iaso Children's Hospital, Athens, Greece.
¹¹ Department of Pediatrics, Monash University, Melbourne, Victoria, Australia.
¹² Henan Key Laboratory of Child Genetics and Metabolism, Rehabilitation Department, Children's Hospital of Zhengzhou University, Zhengzhou, China.
¹³ Department of Biostatistics, Yale School of Public Health, New Haven, CT, USA.
¹⁴ Henan Key Laboratory of Child Brain Injury, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
¹⁵ Yale Center for Genome Analysis, Yale University, New Haven, CT, USA.
¹⁶ Department of Genetics, Pitié-Salpêtrière Hospital, APHP.Sorbonne Université, Paris, France.
¹⁷ UF de Génétique Clinique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, APHP.Sorbonne Université, Hôpital Armand Trousseau, Paris, France.
¹⁸ Sorbonne Université, APHP, Service de Neurologie Pédiatrique et Centre de Référence Neurogénétique, Hôpital Armand Trousseau, Paris, France.
¹⁹ GeneDx, Gaithersburg, MD, USA.
²⁰ 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.
²¹ Departments of Pediatrics & Neurology, University of Texas Southwestern and Children's Medical Center of Dallas, Dallas, TX, USA.
²² Departments of Genetics & Genomics and Neurology, Boston Children's Hospital, Boston, MA, USA.
²³ Division of Neurogenetics and Hugo W. Moser Research Institute, Kennedy Krieger Institute, Baltimore, MD, USA.
²⁴ Medical Genetics, Department of Pediatrics, MassGeneral Hospital for Children, Boston, MA, USA.
²⁵ Departments of Pediatrics and Neurology, University of New Mexico, Albuquerque, NM, USA.
²⁶ Division of Pediatric Neurology, Gillette Children's Hospital, St Paul, MN, USA.
²⁷ Department of Paediatric Neurology, Women's & Children's Hospital, Adelaide, South Australia, Australia.
²⁸ Departments of Molecular & Cellular Biology and Neuroscience, University of Arizona, Tucson, AZ, USA.
²⁹ Murdoch Children's Research Institute and University of Melbourne Department of Paediatrics, Royal Children's Hospital, Melbourne, Victoria, Australia.
³⁰ Rehabilitation Department, Children's Hospital of Zhengzhou University/Henan Children's Hospital, Zhengzhou, China.
³¹ Cerebral Palsy Alliance Research Institute, University of Sydney, Sydney, New South Wales, Australia.
³² Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
³³ Department of Biostatistics & Medical Informatics, University of Wisconsin-Madison, Madison, WI, USA.
³⁴ Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA. kruerm@email.arizona.edu.
³⁵ Departments of Child Health, Neurology, and Cellular & Molecular Medicine, and Program in Genetics, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA. kruerm@email.arizona.edu.

^# Contributed equally.

PMID: 33432185
DOI: 10.1038/s41588-021-00780-8

No abstract available

PubMed Disclaimer

Erratum for

Mutations disrupting neuritogenesis genes confer risk for cerebral palsy.
Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu J, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou C, Zhang J, Li B, Zhao H, Heim J, Webber DL, Frank MSB, Xia L, Xu Y, Zhu D, Zhang B, Sheth AH, Knight JR, Castaldi C, Tikhonova IR, López-Giráldez F, Keren B, Whalen S, Buratti J, Doummar D, Cho M, Retterer K, Millan F, Wang Y, Waugh JL, Rodan L, Cohen JS, Fatemi A, Lin AE, Phillips JP, Feyma T, MacLennan SC, Vaughan S, Crompton KE, Reid SM, Reddihough DS, Shang Q, Gao C, Novak I, Badawi N, Wilson YA, McIntyre SJ, Mane SM, Wang X, Amor DJ, Zarnescu DC, Lu Q, Xing Q, Zhu C, Bilguvar K, Padilla-Lopez S, Lifton RP, Gecz J, MacLennan AH, Kruer MC. Jin SC, et al. Nat Genet. 2020 Oct;52(10):1046-1056. doi: 10.1038/s41588-020-0695-1. Epub 2020 Sep 28. Nat Genet. 2020. PMID: 32989326 Free PMC article.

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Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Affiliations

Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

Authors

Affiliations

Erratum for

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