Gene diagnostics for cardiovascular diseases-Reference-Cited by-同舟云学术

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Gene diagnostics for cardiovascular diseases

Published:2023-08-30 Issue:5 Volume:17 Page:300-349
ISSN:2731-7129
Container-title:Die Kardiologie
language:de
Short-container-title:Kardiologie

Author:

Schulze-Bahr E.,Klaassen S.,Gerull B.,von Kodolitsch Y.,Landmesser U.,Rieß O.,Meder B.,Schunkert H.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

https://link.springer.com/content/pdf/10.1007/s12181-023-00622-3.pdf

Reference315 articles.

1. Aalberts JJ, Thio CH, Schuurman AG et al (2012) Diagnostic yield in adults screened at the Marfan outpatient clinic using the 1996 and 2010 Ghent nosologies. Am J Med Genet A 158A:982–988

2. Abdullah-Koolmees H, van Keulen AM, Nijenhuis M et al (2020) Pharmacogenetics guidelines: overview and comparison of the DPWG, CPIC, CPNDS, and RNPGx guidelines. Front Pharmacol 11:595219

3. Ackerman MJ, Priori SG, Willems S et al (2011) HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the heart rhythm society (HRS) and the European heart rhythm association (EHRA). Heart Rhythm 8:1308–1339

4. Adler A, Novelli V, Amin AS et al (2020) An international, multicentered, evidence-based reappraisal of genes reported to cause congenital long QT syndrome. Circulation 141:418–428

5. Ahamed H, Balegadde AV, Menon S et al (2020) Phenotypic expression and clinical outcomes in a South Asian PRKAG2 cardiomyopathy cohort. Sci Rep 10:20610

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