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

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

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

Research output: Contribution to journal › Erratum / corrigendum / retractions › Academic

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
Article number	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 - 1 Mar 2023

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10.1038/s41588-023-01336-8Licence: CC BY

1 Article

Discovery of 42 genome-wide significant loci associated with dyslexia
23andMe Research team, Quantitative Trait Working Group of the GenLang Consortium & Luciano, M., 1 Nov 2022, In: Nature Genetics. 54, 11, p. 1621-1629 9 p.
Research output: Contribution to journal › Article › Academic › peer-review

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Cite this

@article{f2be3f5d7bc44391a35f0b630891b946,

title = "Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia",

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 = "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 Milene Bonte and {23andMe Research team} and {Quantitative Trait Working Group of the GenLang Consortium}",

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

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TY - JOUR

T1 - Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

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 - Bonte, Milene

AU - 23andMe Research team

AU - Quantitative Trait Working Group of the GenLang Consortium

PY - 2023/3/1

Y1 - 2023/3/1

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.

U2 - 10.1038/s41588-023-01336-8

DO - 10.1038/s41588-023-01336-8

M3 - Erratum / corrigendum / retractions

C2 - 36823321

SN - 1061-4036

VL - 55

JO - Nature Genetics

JF - Nature Genetics

IS - 3

M1 - 520

ER -