Phenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population.

HomeCirculation: Genomic and Precision MedicineAhead of PrintPhenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population Open AccessResearch ArticlePDF/EPUBAboutView PDFSections ToolsAdd to favoritesDownload citationsTrack citationsPermissions ShareShare onFacebookTwitterLinked InMendeleyReddit Jump toOpen AccessResearch ArticlePDF/EPUBPhenotype of ASDs Associated With 4p16 Risk Locus and Novel Genome-Wide Associations of ASD Patients in the Finnish Population Valtteri Muroke, Mikko Jalanko, Sanni Ruotsalainen, Markus Perola, Emmi Helle and Juha Sinisalo Valtteri MurokeValtteri Muroke Correspondence to: Valtteri Muroke, MD, HUS Heart and Lung Center, Helsinki University Hospital, Meilahti Tower Hospital, PL 340, 00029 HUS, Helsinki, Finland. Email E-mail Address: [email protected] https://orcid.org/0000-0003-0972-3873 Department of Cardiology, Helsinki University Hospital, University of Helsinki, Finland. (V.M., M.J., J.S.) Search for more papers by this author , Mikko JalankoMikko Jalanko https://orcid.org/0000-0001-5409-3300 Department of Cardiology, Helsinki University Hospital, University of Helsinki, Finland. (V.M., M.J., J.S.) Search for more papers by this author , Sanni RuotsalainenSanni Ruotsalainen Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Finland. (S.R.) Search for more papers by this author , Markus PerolaMarkus Perola https://orcid.org/0000-0003-4842-1667 Finnish Institute for Health and Welfare, Helsinki, Finland (M.P.). Search for more papers by this author , Emmi HelleEmmi Helle Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, Finland. (E.H.) New Children’s Hospital, Pediatric Research Center, Helsinki University Hospital and University of Helsinki, Finland (E.H.). Search for more papers by this author and Juha SinisaloJuha Sinisalo https://orcid.org/0000-0002-0169-5137 Department of Cardiology, Helsinki University Hospital, University of Helsinki, Finland. (V.M., M.J., J.S.) Search for more papers by this author Originally published14 Aug 2023https://doi.org/10.1161/CIRCGEN.123.004070Circulation: Genomic and Precision Medicine. 2023;0:e004070FootnotesFor Sources of Funding and Disclosures, see page XXX.Correspondence to: Valtteri Muroke, MD, HUS Heart and Lung Center, Helsinki University Hospital, Meilahti Tower Hospital, PL 340, 00029 HUS, Helsinki, Finland. Email valtteri.muroke@helsinki.fi eLetters(0)eLetters should relate to an article recently published in the journal and are not a forum for providing unpublished data. Comments are reviewed for appropriate use of tone and language. Comments are not peer-reviewed. Acceptable comments are posted to the journal website only. Comments are not published in an issue and are not indexed in PubMed. Comments should be no longer than 500 words and will only be posted online. References are limited to 10. Authors of the article cited in the comment will be invited to reply, as appropriate.Comments and feedback on AHA/ASA Scientific Statements and Guidelines should be directed to the AHA/ASA Manuscript Oversight Committee via its Correspondence page.Sign In to Submit a Response to This Article Previous Back to top Next FiguresReferencesRelatedDetails Advertisement Article InformationMetrics © 2023 The Authors. Circulation: Genomic and Precision Medicine is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.https://doi.org/10.1161/CIRCGEN.123.004070PMID: 37577800 Originally publishedAugust 14, 2023 Keywordsgenome-wide association studyforamen ovalecongenital heart defectquantitative trait locimutationsPDF download Advertisement SubjectsCongenital Heart DiseaseGenetic, Association Studies