Call for Papers! Thematic Collection on Genetic Cardiomyopathies
ABC Heart Failure & Cardiomyopathy (ABC HF) is pleased to invite Brazilian and international researchers to submit articles for the thematic collection on genetic cardiomyopathies.
The aim of this thematic collection is to gather articles that contribute to the advancement of knowledge on genetic cardiomyopathies. We are looking for introductory articles on genetic cardiomyopathies, requests for genetic testing, family cascade screening, and general aspects of genotype-phenotype correlation for review and/or viewpoint articles. We also suggest 13 genes for review articles that cover the genetic aspects related to these variants and their phenotypic manifestations. Below is the suggested list:
- What are genetic cardiomyopathies (their phenotypes)?
- When and how to investigate genetic cardiomyopathies – How to request tests – Cascade screening
- General phenotype-genotype correlation
- TTN
- ALPK3
- DSP
- MYH7
- FLNC
- BAG3
- LMNA
- PRKAG2
- MYBPC3
- GLA
- LAMP2
- Noonan-RASopathies
- Troponin complex
The final submission date is September 1, 2024.
Articles should be submitted in electronic format, according to the instructions available on the ABC HF website and through the system at: https://mc04.manuscriptcentral.com/abchf
For more information and questions, please email: abcheartfailure@cardiol.br
Thank you for your interest in contributing to this important collection.
Luis Beck da Silva Neto
Editor-in-Chief
ABC HF