The DOI matches its Crossref record; 254 of the 254 references it cites were found in a registry or an index.
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)
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PreambleThis international consensus statement provides the state of genetic testing for the channelopathies and cardiomyopathies.It summarizes the opinion of the international writing group members based on their own experience and on a general review of the literature with respect to the use and role of genetic testing for these potentially heritable cardiac conditions.This document focuses primarily on the state of genetic testing for the 13 distinct entities detailed and the relative diagnostic, prognostic, and therapeutic impact of the genetic test result for each entity.It does not focus on the therapeutic management of the various channelopathies and cardiomyopathies.Treatment/ management issues are only discussed for those diseases (i.e., LQTS, HCM, DCM + CCD, RCM) in which the genetic test result could potentially influence treatment considerations.
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Self-citationA molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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Self-citationPositional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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Self-citationMutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
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Self-citationCaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism
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Metadata
- Authors
- Ackerman, M. J., Priori, S. G., Willems, S., Berul, C., Brugada, R., Calkins, H., Camm, A. J., Ellinor, P. T., Gollob, M., Hamilton, R., Hershberger, R. E., Judge, D. P., Le Marec, H., McKenna, W. J., Schulze-Bahr, E., Semsarian, C., Towbin, J. A., Watkins, H., Wilde, A., Wolpert, C., & Zipes, D. P.
- Venue
- Europace
- Publisher
- Oxford University Press (OUP)
- Published
- 2011-08-01
- Volume
- 13
- Issue
- 8
- Pages
- 1077-1109
- ISSN
- 1099-5129 (ISSN-L)
- 1532-2092
- OpenAlex
- W2156109088
- Cited by
- 895
- References
- 254
- FWCI
- 40.19
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: 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). https://app.cochat.ai/papers/10.1093/europace/eur245
- The paper
- Ackerman, M. J., Priori, S. G., Willems, S., Berul, C., Brugada, R., Calkins, H., Camm, A. J., Ellinor, P. T., Gollob, M., Hamilton, R., Hershberger, R. E., Judge, D. P., Le Marec, H., McKenna, W. J., Schulze-Bahr, E., Semsarian, C., Towbin, J. A., Watkins, H., Wilde, A., . . . Zipes, D. P. (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). Europace. https://doi.org/10.1093/europace/eur245
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
