Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect-Reference-Cited by-同舟云学术

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Published:2021-01-25 Issue:2 Volume:53 Page:128-134
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Tadros Rafik^ORCID,Francis Catherine,Xu Xiao,Vermeer Alexa M. C.,Harper Andrew R.^ORCID,Huurman Roy^ORCID,Kelu Bisabu Ken^ORCID,Walsh Roddy^ORCID,Hoorntje Edgar T.,te Rijdt Wouter P.,Buchan Rachel J.^ORCID,van Velzen Hannah G.,van Slegtenhorst Marjon A.,Vermeulen Jentien M.,Offerhaus Joost Allard,Bai Wenjia^ORCID,de Marvao Antonio,Lahrouchi Najim^ORCID,Beekman Leander,Karper Jacco C.,Veldink Jan H.^ORCID,Kayvanpour Elham,Pantazis Antonis,Baksi A. John,Whiffin Nicola^ORCID,Mazzarotto Francesco^ORCID,Sloane Geraldine,Suzuki Hideaki^ORCID,Schneider-Luftman Deborah,Elliott Paul^ORCID,Richard Pascale,Ader Flavie^ORCID,Villard Eric,Lichtner Peter,Meitinger Thomas^ORCID,Tanck Michael W. T.^ORCID,van Tintelen J. Peter^ORCID,Thain Andrew,McCarty David,Hegele Robert A.^ORCID,Roberts Jason D.,Amyot Julie,Dubé Marie-Pierre^ORCID,Cadrin-Tourigny Julia,Giraldeau Geneviève,L’Allier Philippe L.,Garceau Patrick,Tardif Jean-Claude,Boekholdt S. Matthijs,Lumbers R. Thomas^ORCID,Asselbergs Folkert W.^ORCID,Barton Paul J. R.^ORCID,Cook Stuart A.,Prasad Sanjay K.,O’Regan Declan P.^ORCID,van der Velden Jolanda^ORCID,Verweij Karin J. H.^ORCID,Talajic Mario,Lettre Guillaume,Pinto Yigal M.^ORCID,Meder Benjamin,Charron Philippe^ORCID,de Boer Rudolf A.^ORCID,Christiaans Imke,Michels Michelle,Wilde Arthur A. M.,Watkins Hugh^ORCID,Matthews Paul M.^ORCID,Ware James S.^ORCID,Bezzina Connie R.^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/s41588-020-00762-2.pdf

Reference46 articles.

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2. Walsh, R. et al. Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy. Genome Med. 11, 5 (2019).

3. Elliott, P. M. et al. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC). Eur. Heart J. 35, 2733–2779 (2014).

4. Yang, J. et al. Common SNPs explain a large proportion of the heritability for human height. Nat. Genet. 42, 565–569 (2010).

5. Yang, J. et al. Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Nat. Genet. 47, 1114–1120 (2015).

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