Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.

التفاصيل البيبلوغرافية
العنوان: Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia.
المؤلفون: Doust C; Department of Psychology, University of Edinburgh, Edinburgh, UK., Fontanillas P; 23andMe, Inc., Sunnyvale, CA, USA., Eising E; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands., Gordon SD; Genetic Epidemiology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia., Wang Z; School of Psychology, Shaanxi Normal University and Shaanxi Key Research Center of Child Mental and Behavioral Health, Xi'an, China., Alagöz G; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands., Molz B; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands., Pourcain BS; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands.; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK., Francks C; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Marioni RE; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK., Zhao J; School of Psychology, Shaanxi Normal University and Shaanxi Key Research Center of Child Mental and Behavioral Health, Xi'an, China., Paracchini S; School of Medicine, University of St Andrews, St Andrews, UK., Talcott JB; Institute of Health and Neurodevelopment, Aston University, Birmingham, UK., Monaco AP; Office of the President, Tufts University, Medford, MA, USA., Stein JF; Department of Physiology, Anatomy and Genetics, Oxford University, Oxford, UK., Gruen JR; Departments of Pediatrics and Genetics, Yale Medical School, New Haven, CT, USA., Olson RK; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA., Willcutt EG; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA., DeFries JC; Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA.; Institute for Behavioral Genetics, University of Colorado, Boulder, CO, USA., Pennington BF; Department of Psychology, University of Denver, Denver, CO, USA., Smith SD; Department of Neurological Sciences, College of Medicine, University of Nebraska Medical Center, Omaha, NE, USA., Wright MJ; Queensland Brain Institute, University of Queensland, Brisbane, Queensland, Australia., Martin NG; Genetic Epidemiology Laboratory, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia., Auton A, Bates TC; Department of Psychology, University of Edinburgh, Edinburgh, UK., Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, the Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherlands., Luciano M; Department of Psychology, University of Edinburgh, Edinburgh, UK. michelle.luciano@ed.ac.uk.
مؤلفون مشاركون: 23andMe Research Team, Quantitative Trait Working Group of the GenLang Consortium
المصدر: Nature genetics [Nat Genet] 2023 Mar; Vol. 55 (3), pp. 520.
نوع المنشور: Published Erratum
اللغة: English
بيانات الدورية: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: PubMed not MEDLINE; MEDLINE
أسماء مطبوعة: Original Publication: New York, NY : Nature Pub. Co., c1992-
التعليقات: Erratum for: Nat Genet. 2022 Nov;54(11):1621-1629. (PMID: 36266505)
معلومات مُعتمدة: UL1 TR001863 United States TR NCATS NIH HHS; 61807023 National Natural Science Foundation of China (National Science Foundation of China); 389891 Department of Health | National Health and Medical Research Council (NHMRC); 797/17290 Waterloo Foundation (TWF)
فهرسة مساهمة: Investigator: S Aslibekyan; A Auton; E Babalola; RK Bell; J Bielenberg; K Bryc; E Bullis; D Coker; GC Partida; D Dhamija; S Das; SL Elson; T Filshtein; K Fletez-Brant; W Freyman; PM Gandhi; K Heilbron; B Hicks; DA Hinds; EM Jewett; Y Jiang; K Kukar; KH Lin; M Lowe; J McCreight; MH McIntyre; SJ Micheletti; ME Moreno; JL Mountain; P Nandakumar; ES Noblin; J O'Connell; AA Petrakovitz; GD Poznik; M Schumacher; AJ Shastri; JF Shelton; J Shi; S Shringarpure; V Tran; JY Tung; X Wang; W Wang; CH Weldon; P Wilton; A Hernandez; C Wong; CT Tchakouté; F Abbondanza; AG Allegrini; TFM Andlauer; CL Barr; M Bernard; K Blokland; M Bonte; DI Boomsma; T Bourgeron; D Brandeis; M Carreiras; F Ceroni; V Csépe; PS Dale; PF de Jong; JF Démonet; EL de Zeeuw; Y Feng; MJ Franken; M Gerritse; A Gialluisi; SL Guger; ME Hayiou-Thomas; J Hernández-Cabrera; JJ Hottenga; C Hulme; PR Jansen; J Kere; EN Kerr; T Koomar; K Landerl; GT Leonard; Z Liao; MW Lovett; H Lyytinen; A Martinelli; U Maurer; JJ Michaelson; N Mirza-Schreiber; K Moll; AT Morgan; B Müller-Myhsok; DF Newbury; MM Nöthen; T Paus; Z Pausova; CE Pennell; RJ Plomin; KM Price; F Ramus; S Reilly; L Richer; K Rimfeld; G Schulte-Körne; CY Shapland; NH Simpson; MJ Snowling; JF Stein; LJ Strug; H Tiemeier; JB Tomblin; DT Truong; E van Bergen; MP van der Schroeff; M Van Donkelaar; E Verhoef; CA Wang; KE Watkins; AJO Whitehouse; KG Wigg; M Wilkinson; G Zhu
تواريخ الأحداث: Date Created: 20230224 Latest Revision: 20230324
رمز التحديث: 20230324
مُعرف محوري في PubMed: PMC10011121
DOI: 10.1038/s41588-023-01336-8
PMID: 36823321
قاعدة البيانات: MEDLINE
الوصف
تدمد:1546-1718
DOI:10.1038/s41588-023-01336-8