Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)

23andMe Research Team; Quantitative Trait Working Group of the GenLang Consortium

doi:10.1038/s41588-023-01336-8

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)

23andMe Research Team
, Quantitative Trait Working Group of the GenLang Consortium

University of Edinburgh
23andMe Inc.
Max Planck Institute for Psycholinguistics
Queensland Institute of Medical Research
Shaanxi Normal University
Vrije Universiteit Amsterdam
University of St Andrews
King's College London
Max Planck Institute of Psychiatry
Technical University of Munich
Krembil Research Institute
University of Toronto
Maastricht University
Netherlands Twin Register
Amsterdam UMC
Institut Pasteur Paris
Université Paris Cité
University of Zurich
Heidelberg University
BCBL – Basque Center on Cognition, Brain and Language
Ikerbasque Basque Foundation for Science
University of the Basque Country
University of Bologna
Oxford Brookes University
Research Centre for Natural Sciences
University of Pannonia
University of New Mexico
University of Amsterdam
University of Lausanne
Erasmus University Rotterdam
IRCCS Istituto Neurologico Mediterraneo Neuromed - Pozzilli (IS)
University of York
University of La Laguna
University of Oxford
VU University Medical Center
Karolinska Institutet
University of Helsinki
University of Iowa
University of Graz
BioTechMed-Graz
Cognitive Neuroscience Neurology and Neurosurgery
University of Jyväskylä
Chinese University of Hong Kong
Helmholtz Zentrum München - German Research Center for Environmental Health
Ludwig Maximilian University of Munich
Murdoch Children's Research Institute
Department of Audiology and Speech Pathology
Royal Children's Hospital Melbourne
University of Liverpool
University of Bonn
University of Montreal
University of Newcastle
Hunter Medical Research Institute, Australia
Hunter New England Health
Laboratoire de Sciences Cognitives et Psycholinguistique
Menzies Health Institute Queensland
Université du Québec à Chicoutimi
University of Bristol
Harvard University
Yale University
Telethon Kids Institute
Radboud University Nijmegen
Aston University
Tufts University
University of Colorado Boulder
University of Denver
University of Nebraska Medical Center
University of Queensland

Research output: Contribution to journal › Comment/debate

Abstract

In the version of this article originally published, a paragraph was omitted in the Methods section, reading “Genomic control. Top SNPs are reported from the more conservative GWAS results adjusted for genomic control (Fig. 1, Extended Data Figs. 1–4, and Supplementary Tables 1, 2, 9 and 10), whereas downstream analyses (including gene-set analysis, enrichment and heritability partitioning, genetic correlations, polygenic prediction, candidate gene replication) are based on GWAS results without genomic control.” The paragraph has now been included in the HTML and PDF versions of the article.

Original language	English
Pages (from-to)	520
Number of pages	1
Journal	Nature Genetics
Volume	55
Issue number	3
DOIs	https://doi.org/10.1038/s41588-023-01336-8
Publication status	Published - Mar 2023
Externally published	Yes

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10.1038/s41588-023-01336-8

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@article{aaa18d4a09b64f5dbbc19ccb2cc748eb,

title = "Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)",

abstract = "In the version of this article originally published, a paragraph was omitted in the Methods section, reading “Genomic control. Top SNPs are reported from the more conservative GWAS results adjusted for genomic control (Fig. 1, Extended Data Figs. 1–4, and Supplementary Tables 1, 2, 9 and 10), whereas downstream analyses (including gene-set analysis, enrichment and heritability partitioning, genetic correlations, polygenic prediction, candidate gene replication) are based on GWAS results without genomic control.” The paragraph has now been included in the HTML and PDF versions of the article.",

author = "\{23andMe Research Team\} and \{Quantitative Trait Working Group of the GenLang Consortium\} and Catherine Doust and Pierre Fontanillas and Else Eising and Gordon, \{Scott D.\} and Zhengjun Wang and G{\"o}kberk Alag{\"o}z and Barbara Molz and Stella Aslibekyan and Adam Auton and Elizabeth Babalola and Bell, \{Robert K.\} and Jessica Bielenberg and Katarzyna Bryc and Emily Bullis and Daniella Coker and Partida, \{Gabriel Cuellar\} and Devika Dhamija and Sayantan Das and Elson, \{Sarah L.\} and Teresa Filshtein and Kipper Fletez-Brant and Will Freyman and Gandhi, \{Pooja M.\} and Karl Heilbron and Barry Hicks and Hinds, \{David A.\} and Jewett, \{Ethan M.\} and Yunxuan Jiang and Katelyn Kukar and Lin, \{Keng Han\} and Maya Lowe and Jey McCreight and McIntyre, \{Matthew H.\} and Micheletti, \{Steven J.\} and Moreno, \{Meghan E.\} and Mountain, \{Joanna L.\} and Priyanka Nandakumar and Noblin, \{Elizabeth S.\} and Jared O{\textquoteright}Connell and Petrakovitz, \{Aaron A.\} and Poznik, \{G. David\} and Morgan Schumacher and Shastri, \{Anjali J.\} and Shelton, \{Janie F.\} and Jingchunzi Shi and Suyash Shringarpure and Vinh Tran and Tung, \{Joyce Y.\} and Xin Wang and Hottenga, \{Jouke Jan\}",

note = "Publisher Copyright: {\textcopyright} 2023, The Author(s).",

year = "2023",

month = mar,

doi = "10.1038/s41588-023-01336-8",

language = "English",

volume = "55",

pages = "520",

journal = "Nature Genetics",

issn = "1061-4036",

publisher = "Nature Research",

number = "3",

}

TY - JOUR

T1 - Author Correction

T2 - Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)

AU - 23andMe Research Team

AU - Quantitative Trait Working Group of the GenLang Consortium

AU - Doust, Catherine

AU - Fontanillas, Pierre

AU - Eising, Else

AU - Gordon, Scott D.

AU - Wang, Zhengjun

AU - Alagöz, Gökberk

AU - Molz, Barbara

AU - Aslibekyan, Stella

AU - Auton, Adam

AU - Babalola, Elizabeth

AU - Bell, Robert K.

AU - Bielenberg, Jessica

AU - Bryc, Katarzyna

AU - Bullis, Emily

AU - Coker, Daniella

AU - Partida, Gabriel Cuellar

AU - Dhamija, Devika

AU - Das, Sayantan

AU - Elson, Sarah L.

AU - Filshtein, Teresa

AU - Fletez-Brant, Kipper

AU - Freyman, Will

AU - Gandhi, Pooja M.

AU - Heilbron, Karl

AU - Hicks, Barry

AU - Hinds, David A.

AU - Jewett, Ethan M.

AU - Jiang, Yunxuan

AU - Kukar, Katelyn

AU - Lin, Keng Han

AU - Lowe, Maya

AU - McCreight, Jey

AU - McIntyre, Matthew H.

AU - Micheletti, Steven J.

AU - Moreno, Meghan E.

AU - Mountain, Joanna L.

AU - Nandakumar, Priyanka

AU - Noblin, Elizabeth S.

AU - O’Connell, Jared

AU - Petrakovitz, Aaron A.

AU - Poznik, G. David

AU - Schumacher, Morgan

AU - Shastri, Anjali J.

AU - Shelton, Janie F.

AU - Shi, Jingchunzi

AU - Shringarpure, Suyash

AU - Tran, Vinh

AU - Tung, Joyce Y.

AU - Wang, Xin

AU - Hottenga, Jouke Jan

PY - 2023/3

Y1 - 2023/3

N2 - In the version of this article originally published, a paragraph was omitted in the Methods section, reading “Genomic control. Top SNPs are reported from the more conservative GWAS results adjusted for genomic control (Fig. 1, Extended Data Figs. 1–4, and Supplementary Tables 1, 2, 9 and 10), whereas downstream analyses (including gene-set analysis, enrichment and heritability partitioning, genetic correlations, polygenic prediction, candidate gene replication) are based on GWAS results without genomic control.” The paragraph has now been included in the HTML and PDF versions of the article.

AB - In the version of this article originally published, a paragraph was omitted in the Methods section, reading “Genomic control. Top SNPs are reported from the more conservative GWAS results adjusted for genomic control (Fig. 1, Extended Data Figs. 1–4, and Supplementary Tables 1, 2, 9 and 10), whereas downstream analyses (including gene-set analysis, enrichment and heritability partitioning, genetic correlations, polygenic prediction, candidate gene replication) are based on GWAS results without genomic control.” The paragraph has now been included in the HTML and PDF versions of the article.

UR - https://www.scopus.com/pages/publications/85166290570

U2 - 10.1038/s41588-023-01336-8

DO - 10.1038/s41588-023-01336-8

M3 - Comment/debate

AN - SCOPUS:85166290570

SN - 1061-4036

VL - 55

SP - 520

JO - Nature Genetics

JF - Nature Genetics

IS - 3

ER -

Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia (Nature Genetics, (2022), 54, 11, (1621-1629), 10.1038/s41588-022-01192-y)

Abstract

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