Familial Hypertrophic Cardiomyopathy Latest Advances

Identification of novel genetic variants in hypertrophic cardiomyopathy.

Journal: Cardiology in the young

Published: October 20, 2025

Uncovering genetic architecture of the heart via genetic association studies of unsupervised deep learning derived endophenotypes.

Journal: bioRxiv : the preprint server for biology

Published: September 26, 2025

Survival, clinical, and genetic findings in paediatric cardiomyopathy: a five-year prospective study from Brazil.

Journal: Cardiology in the young

Published: September 25, 2025

Danon disease: From genetic origins and molecular defects to therapeutic advances.

Journal: Disease-a-month : DM

Published: September 17, 2025

Genetic, Clinical, and Sociodemographic Profile of Individuals with Diagnosis or Family History of Hypertrophic Cardiomyopathy: Insights from a Prospective Cohort.

Journal: Genes

Published: August 31, 2025

Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate Effect Variants.

Journal: Circulation

Published: August 29, 2025

Novel Cardiac Troponin-I Missense Variant (c.593C>T) Is Associated With Familial Hypertrophic Cardiomyopathy in Golden Retrievers.

Journal: Circulation. Genomic and precision medicine

Published: August 22, 2025

Discovering Genetic Variants in Hypertrophic Cardiomyopathy With Multiple Machine Learning Techniques.

Journal: IEEE transactions on computational biology and bioinformatics

Published: August 14, 2025

Clinical manifestations, genetic profiles, and sudden cardiac arrest in pediatric hypertrophic cardiomyopathy: Challenges of risk prediction for initial sudden cardiac arrest presentations.

Journal: Heart rhythm O2

Published: July 30, 2025

Reconsidering the causal role of cardiovascular risk factors in genotype-negative hypertrophic cardiomyopathy: The importance of polygenic inheritance and genetic architecture.

Journal: International journal of cardiology

Published: July 09, 2025

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic non-obstructive hypertrophic cardiomyopathy.

Journal: Journal of applied physiology (Bethesda, Md. : 1985)

Published: June 30, 2025

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic nonobstructive hypertrophic cardiomyopathy.

Journal: Journal of applied physiology (Bethesda, Md. : 1985)

Published: June 30, 2025

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Identification of novel genetic variants in hypertrophic cardiomyopathy.

Identification of novel genetic variants in hypertrophic cardiomyopathy.

Uncovering genetic architecture of the heart via genetic association studies of unsupervised deep learning derived endophenotypes.

Uncovering genetic architecture of the heart via genetic association studies of unsupervised deep learning derived endophenotypes.

Survival, clinical, and genetic findings in paediatric cardiomyopathy: a five-year prospective study from Brazil.

Survival, clinical, and genetic findings in paediatric cardiomyopathy: a five-year prospective study from Brazil.

Danon disease: From genetic origins and molecular defects to therapeutic advances.

Danon disease: From genetic origins and molecular defects to therapeutic advances.

Genetic, Clinical, and Sociodemographic Profile of Individuals with Diagnosis or Family History of Hypertrophic Cardiomyopathy: Insights from a Prospective Cohort.

Genetic, Clinical, and Sociodemographic Profile of Individuals with Diagnosis or Family History of Hypertrophic Cardiomyopathy: Insights from a Prospective Cohort.

Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate Effect Variants.

Redefining the Genetic Architecture of Hypertrophic Cardiomyopathy: Role of Intermediate Effect Variants.

Novel Cardiac Troponin-I Missense Variant (c.593C>T) Is Associated With Familial Hypertrophic Cardiomyopathy in Golden Retrievers.

Novel Cardiac Troponin-I Missense Variant (c.593C>T) Is Associated With Familial Hypertrophic Cardiomyopathy in Golden Retrievers.

Discovering Genetic Variants in Hypertrophic Cardiomyopathy With Multiple Machine Learning Techniques.

Discovering Genetic Variants in Hypertrophic Cardiomyopathy With Multiple Machine Learning Techniques.

Clinical manifestations, genetic profiles, and sudden cardiac arrest in pediatric hypertrophic cardiomyopathy: Challenges of risk prediction for initial sudden cardiac arrest presentations.

Clinical manifestations, genetic profiles, and sudden cardiac arrest in pediatric hypertrophic cardiomyopathy: Challenges of risk prediction for initial sudden cardiac arrest presentations.

Reconsidering the causal role of cardiovascular risk factors in genotype-negative hypertrophic cardiomyopathy: The importance of polygenic inheritance and genetic architecture.

Reconsidering the causal role of cardiovascular risk factors in genotype-negative hypertrophic cardiomyopathy: The importance of polygenic inheritance and genetic architecture.

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic non-obstructive hypertrophic cardiomyopathy.

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic non-obstructive hypertrophic cardiomyopathy.

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic nonobstructive hypertrophic cardiomyopathy.

Heterozygous MYH7 R403Q mutation impairs left atrial mitochondrial function in a Yucatan mini-pig model of genetic nonobstructive hypertrophic cardiomyopathy.