Genetic variants associated with cardiac hypertrophy-related sudden cardiac death and cardiovascular outcomes in a Finnish population
We identified rare deleterious variants associated with LVH in SCD subjects. Several of the identified rare variants associated with cardiovascular endpoints including heart failure, cardiomyopathies, cardiac arrest and hypertension in general population.
Authors
- Katri Pylkäs (ORCID: https://orcid.org/0000-0002-2449-0521)
- Heikki V. Huikuri (ORCID: https://orcid.org/0000-0001-8800-963X)
- Juhani Junttila (ORCID: https://orcid.org/0000-0002-8896-1281)
- Sini Skarp (ORCID: https://orcid.org/0000-0003-2336-4221)
- Lauri T. A. Holmström (ORCID: https://orcid.org/0000-0002-6166-5589)
- Risto Kerkelä (ORCID: https://orcid.org/0000-0001-7194-9326)
- Lasse Pakanen (ORCID: https://orcid.org/0000-0002-3494-7652)
- Samu Saarimäki (ORCID: https://orcid.org/0000-0002-2054-3657)
- Anne Doedens
Institutions
- Oulu University Hospital (FI)
- Oulu University of Applied Sciences (FI)
- University of Oulu (FI)
Publication Details
- Journal
- Heart
- Published
- 2024-10-03
- DOI
- https://doi.org/10.1136/heartjnl-2024-324623
- Citations
- 3
- Primary Topic
- Cardiomyopathy and Myosin Studies
- Type
- article
- Field-Weighted Citation Impact
- 1.21
Funders
- Academy of Finland
- Jane ja Aatos Erkon Säätiö
- Orionin Tutkimussäätiö