Correction to: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (Nature Genetics, (2019), 51, 3, (481-493), 10.1038/s41588-018-0321-7)

dc.contributor.authorShrine N.
dc.contributor.authorGuyatt A.L.
dc.contributor.authorErzurumluoglu A.M.
dc.contributor.authorJackson V.E.
dc.contributor.authorHobbs B.D.
dc.contributor.authorMelbourne C.A.
dc.contributor.authorBatini C.
dc.contributor.authorFawcett K.A.
dc.contributor.authorSong K.
dc.contributor.authorSakornsakolpat P.
dc.contributor.authorLi X.
dc.contributor.authorBoxall R.
dc.contributor.authorReeve N.F.
dc.contributor.authorObeidat M.
dc.contributor.authorZhao J.H.
dc.contributor.authorWielscher M.
dc.contributor.authorWeiss S.
dc.contributor.authorKentistou K.A.
dc.contributor.authorCook J.P.
dc.contributor.authorSun B.B.
dc.contributor.authorZhou J.
dc.contributor.authorHui J.
dc.contributor.authorKarrasch S.
dc.contributor.authorImboden M.
dc.contributor.authorHarris S.E.
dc.contributor.authorMarten J.
dc.contributor.authorEnroth S.
dc.contributor.authorKerr S.M.
dc.contributor.authorSurakka I.
dc.contributor.authorVitart V.
dc.contributor.authorLehtimäki T.
dc.contributor.authorAllen R.J.
dc.contributor.authorBakke P.S.
dc.contributor.authorBeaty T.H.
dc.contributor.authorBleecker E.R.
dc.contributor.authorBossé Y.
dc.contributor.authorBrandsma C.A.
dc.contributor.authorChen Z.
dc.contributor.authorCrapo J.D.
dc.contributor.authorDanesh J.
dc.contributor.authorDeMeo D.L.
dc.contributor.authorDudbridge F.
dc.contributor.authorEwert R.
dc.contributor.authorGieger C.
dc.contributor.authorGulsvik A.
dc.contributor.authorHansell A.L.
dc.contributor.authorHao K.
dc.contributor.authorHoffman J.D.
dc.contributor.authorHokanson J.E.
dc.contributor.authorHomuth G.
dc.contributor.authorJoshi P.K.
dc.contributor.authorJoubert P.
dc.contributor.authorLangenberg C.
dc.contributor.authorLi X.
dc.contributor.authorLi L.
dc.contributor.authorLin K.
dc.contributor.authorLind L.
dc.contributor.authorLocantore N.
dc.contributor.authorLuan J.
dc.contributor.authorMahajan A.
dc.contributor.authorMaranville J.C.
dc.contributor.authorMurray A.
dc.contributor.authorNickle D.C.
dc.contributor.authorPacker R.
dc.contributor.authorParker M.M.
dc.contributor.authorPaynton M.L.
dc.contributor.authorPorteous D.J.
dc.contributor.authorProkopenko D.
dc.contributor.authorQiao D.
dc.contributor.authorRawal R.
dc.contributor.authorRunz H.
dc.contributor.authorSayers I.
dc.contributor.authorSin D.D.
dc.contributor.authorSmith B.H.
dc.contributor.authorArtigas M.S.
dc.contributor.authorSparrow D.
dc.contributor.authorTal-Singer R.
dc.contributor.authorTimmers P.R.H.J.
dc.contributor.authorVan den Berge M.
dc.contributor.authorWhittaker J.C.
dc.contributor.authorWoodruff P.G.
dc.contributor.authorYerges-Armstrong L.M.
dc.contributor.authorTroyanskaya O.G.
dc.contributor.authorRaitakari O.T.
dc.contributor.authorKähönen M.
dc.contributor.authorPolašek O.
dc.contributor.authorGyllensten U.
dc.contributor.authorRudan I.
dc.contributor.authorDeary I.J.
dc.contributor.authorProbst-Hensch N.M.
dc.contributor.authorSchulz H.
dc.contributor.authorJames A.L.
dc.contributor.authorWilson J.F.
dc.contributor.authorStubbe B.
dc.contributor.authorZeggini E.
dc.contributor.authorJarvelin M.R.
dc.contributor.authorWareham N.
dc.contributor.authorSilverman E.K.
dc.contributor.authorHayward C.
dc.contributor.authorMorris A.P.
dc.contributor.correspondenceShrine N.
dc.contributor.otherMahidol University
dc.date.accessioned2024-05-15T18:24:49Z
dc.date.available2024-05-15T18:24:49Z
dc.date.issued2024-01-01
dc.description.abstractCorrection to: Nature Geneticshttps://doi.org/10.1038/s41588-018-0321-7, published online 25 February 2019. In the version of the article initially published, unconsented individuals were erroneously included in SPIROMICS consortium results. The analysis has now been repeated with the unconsented individuals removed. The change in the results does not affect the conclusions in the paper. The corrections required to the paper are as follows: In the third paragraph of the “Association with FEV1/FVC and COPD in multiple ancestries” section: “(n = 6,979 cases and 3,915 controls)”, should be “(n = 6,964 cases and 3,904 controls)” and “P = 2.87 × 10–75” should be “P = 2.21 × 10–75”. In the fourth paragraph of the “Association with FEV1/FVC and COPD in multiple ancestries” section: “4.73 (95% CI: [3.79, 5.90]), P = 3.00 × 10−43”, should be “4.71 (95% CI: [3.77, 5.87]), P = 7.24 × 10−43”. In the Fig. 3b table, the SPIROMICS row: “1.54, 1.38, 1.72, 4.47 × 10–14, 988, 537”, should be “1.55, 1.39, 1.74, 6.80 × 10–14, 973, 526”; and the Meta-analysis row: “1.55, 1.48, 1.62, 1.48 × 10–75, 6,979, 3,915”, should be “1.55, 1.48, 1.62, 2.21 × 10–75, 6,964, 3,904”. In the final paragraph of the Discussion: “The 279-variant GRS we constructed was associated with a 4.73-fold increased relative risk…”, should be “The 279-variant GRS we constructed was associated with a 4.71-fold increased relative risk…” In the fifth paragraph of the “Effect of genetic risk score on COPD susceptibility in multiple ancestries” section in the Methods: “SPIROMICS (988 cases, 537 controls)”, should be “SPIROMICS (973 cases, 526 controls)”. In the third paragraph of the “Association with FEV1/FVC and COPD in multiple ancestries” section: “(n = 6,979 cases and 3,915 controls)”, should be “(n = 6,964 cases and 3,904 controls)” and “P = 2.87 × 10–75” should be “P = 2.21 × 10–75”. In the fourth paragraph of the “Association with FEV1/FVC and COPD in multiple ancestries” section: “4.73 (95% CI: [3.79, 5.90]), P = 3.00 × 10−43”, should be “4.71 (95% CI: [3.77, 5.87]), P = 7.24 × 10−43”. In the Fig. 3b table, the SPIROMICS row: “1.54, 1.38, 1.72, 4.47 × 10–14, 988, 537”, should be “1.55, 1.39, 1.74, 6.80 × 10–14, 973, 526”; and the Meta-analysis row: “1.55, 1.48, 1.62, 1.48 × 10–75, 6,979, 3,915”, should be “1.55, 1.48, 1.62, 2.21 × 10–75, 6,964, 3,904”. In the final paragraph of the Discussion: “The 279-variant GRS we constructed was associated with a 4.73-fold increased relative risk…”, should be “The 279-variant GRS we constructed was associated with a 4.71-fold increased relative risk…” In the fifth paragraph of the “Effect of genetic risk score on COPD susceptibility in multiple ancestries” section in the Methods: “SPIROMICS (988 cases, 537 controls)”, should be “SPIROMICS (973 cases, 526 controls)”. The correction is due to 26 unconsented SPIROMICS samples being originally included in the analysis. The analyses that previously included these samples have been rerun with data from these 26 samples removed. Supplementary Information accompanies the online version of this amendment and includes: Updated Supplementary Text and Figures wherein we have changed: On page 23 (description of SPIROMICS cohort) the number of COPD cases has been changed from 988 to 973 and controls from 537 to 526. Supplementary Figure 9 – the forest plots have been updated for the new results for association with 279 variants after reanalysis of SPIROMICS. Supplementary Table 20 – the demographics for SPIROMICS have been updated. Supplementary Table 21 – the results rows for the SPIROMICS and “Meta-analysis of 5 European-ancestry study groups” have been updated. Supplementary Table 22 – The “Meta-analysis of 5 European cohorts” columns have been updated after SPIROMICS reanalysis. Updated Supplementary Tables wherein we have changed: Supplementary Table 29 – columns X–Z (“Meta-analysis of 5 external European-ancestry COPD cohorts (Cases = 6,964; Controls = 3,904)”) after reanalysis of SPIROMICS data. Updated Supplementary Text and Figures wherein we have changed: On page 23 (description of SPIROMICS cohort) the number of COPD cases has been changed from 988 to 973 and controls from 537 to 526. Supplementary Figure 9 – the forest plots have been updated for the new results for association with 279 variants after reanalysis of SPIROMICS. Supplementary Table 20 – the demographics for SPIROMICS have been updated. Supplementary Table 21 – the results rows for the SPIROMICS and “Meta-analysis of 5 European-ancestry study groups” have been updated. Supplementary Table 22 – The “Meta-analysis of 5 European cohorts” columns have been updated after SPIROMICS reanalysis. Updated Supplementary Tables wherein we have changed: Supplementary Table 29 – columns X–Z (“Meta-analysis of 5 external European-ancestry COPD cohorts (Cases = 6,964; Controls = 3,904)”) after reanalysis of SPIROMICS data.
dc.identifier.citationNature Genetics (2024)
dc.identifier.doi10.1038/s41588-024-01752-4
dc.identifier.eissn15461718
dc.identifier.issn10614036
dc.identifier.pmid38641645
dc.identifier.scopus2-s2.0-85192394658
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/98339
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.titleCorrection to: New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries (Nature Genetics, (2019), 51, 3, (481-493), 10.1038/s41588-018-0321-7)
dc.typeErratum
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85192394658&origin=inward
oaire.citation.titleNature Genetics
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationGossamer Bio
oairecerif.author.affiliationMRC Centre for Environment and Health
oairecerif.author.affiliationUniversity of Dundee School of Medicine
oairecerif.author.affiliationCollege of Health and Life Sciences
oairecerif.author.affiliationSchool of Engineering and Applied Science
oairecerif.author.affiliationDepartment of Public Health and Primary Care
oairecerif.author.affiliationFimlab Laboratoriot Oy
oairecerif.author.affiliationEdinburgh Medical School
oairecerif.author.affiliationVA Boston Healthcare System
oairecerif.author.affiliationSimons Foundation
oairecerif.author.affiliationCentro de Investigación Biomédica En Red de Salud Mental
oairecerif.author.affiliationTerveyden ja Hyvinvoinnin Laitos
oairecerif.author.affiliationNational Jewish Health
oairecerif.author.affiliationThe Wellcome Centre for Human Genetics
oairecerif.author.affiliationGlaxoSmithKline, USA
oairecerif.author.affiliationUniversity of Western Australia, School of Medicine and Pharmacology
oairecerif.author.affiliationSchool of Medicine, University of Split
oairecerif.author.affiliationCentre for Heart Lung Innovation
oairecerif.author.affiliationInstitut Universitaire de Cardiologie et de pneumologie de Québec - Université Laval
oairecerif.author.affiliationUniversity of Leicester
oairecerif.author.affiliationUniversité Laval
oairecerif.author.affiliationThe University of Western Australia
oairecerif.author.affiliationUniversitetet i Bergen
oairecerif.author.affiliationUniversity of Colorado Anschutz Medical Campus
oairecerif.author.affiliationWalter and Eliza Hall Institute of Medical Research
oairecerif.author.affiliationThe University of Edinburgh
oairecerif.author.affiliationUniversity of Melbourne
oairecerif.author.affiliationSir Charles Gairdner Hospital
oairecerif.author.affiliationTurun Yliopistollinen Keskussairaala
oairecerif.author.affiliationHelmholtz Center Munich German Research Center for Environmental Health
oairecerif.author.affiliationUniversity of California, San Francisco
oairecerif.author.affiliationUniversität Basel
oairecerif.author.affiliationSwiss Tropical and Public Health Institute Swiss TPH
oairecerif.author.affiliationUniversitat Autònoma de Barcelona
oairecerif.author.affiliationSt Mary's Hospital
oairecerif.author.affiliationUniversitätsmedizin Greifswald
oairecerif.author.affiliationClinical Trial Service Unit and Epidemiological Studies Unit
oairecerif.author.affiliationUniversity of Arizona College of Medicine – Tucson
oairecerif.author.affiliationUniversity of Liverpool
oairecerif.author.affiliationGlaxoSmithKline plc.
oairecerif.author.affiliationAddenbrooke's Hospital
oairecerif.author.affiliationBrigham and Women's Hospital
oairecerif.author.affiliationOulu University Hospital
oairecerif.author.affiliationUniversity of Nottingham
oairecerif.author.affiliationFaculty of Medicine
oairecerif.author.affiliationIcahn School of Medicine at Mount Sinai
oairecerif.author.affiliationOulun Yliopisto
oairecerif.author.affiliationMRC Human Genetics Unit
oairecerif.author.affiliationHospital Universitari Vall d'Hebron
oairecerif.author.affiliationLääketieteellinen Tiedekunta
oairecerif.author.affiliationUniversity of Aberdeen School of Medicine, Medical Sciences and Nutrition
oairecerif.author.affiliationUniversity of Edinburgh, College of Medicine and Veterinary Medicine
oairecerif.author.affiliationThe University of British Columbia
oairecerif.author.affiliationMRC Epidemiology Unit
oairecerif.author.affiliationUniversity Hospital of Tampere
oairecerif.author.affiliationMerck & Co., Inc.
oairecerif.author.affiliationBoston University Chobanian & Avedisian School of Medicine
oairecerif.author.affiliationJohns Hopkins Bloomberg School of Public Health
oairecerif.author.affiliationUniversitair Medisch Centrum Groningen
oairecerif.author.affiliationWellcome Sanger Institute
oairecerif.author.affiliationPeking University Health Science Center
oairecerif.author.affiliationUppsala Universitet
oairecerif.author.affiliationPrinceton University
oairecerif.author.affiliationHelsingin Yliopisto
oairecerif.author.affiliationUniversity of Oxford Medical Sciences Division
oairecerif.author.affiliationUniversity of Münster
oairecerif.author.affiliationKlinikum der Universität München
oairecerif.author.affiliationMember of the German Center for Lung Research (DZL)

Files

Collections