Associated Papers
Identification of recurrent MYH7 variant hypertrophic cardiomyopathy patients in Korea: a case series.
Ryu SW et al.
Cardiovascular Diagnosis and Therapy, 2025
41509624 (PubMed )
Supplement: cdt-15-06-1174-supplementary.pdf
Hypertrophic Cardiomyopathy: The Impact of Age at Diagnosis of the Proband on Genetic Yield, Clinical Presentation, Outcomes, and Yield of Family Screening.
Silajdzija E et al.
Journal of the American Heart Association, 2025
41195766 (PubMed )
Supplement: JAH3-14-e043711-s001.pdf
Age-Dependent Role of Genetics and Renal Function for Atrial Fibrillation Development in Hypertrophic Cardiomyopathy.
Chung H et al.
Korean Circulation Journal, 2025
40736383 (PubMed )
Supplement: kcj-55-1001-s006.xls › kcj-55-1001-s006
Hypertrophic Cardiomyopathy: Genetic Foundations, Outcomes, Interconnections, and Their Modifiers.
Glavaški M et al.
Medicina (kaunas, Lithuania), 2023
Stochastic allelic expression as trigger for contractile imbalance in hypertrophic cardiomyopathy.
Montag J et al.
Biophysical Reviews, 2020
Altered force generation and cell-to-cell contractile imbalance in hypertrophic cardiomyopathy.
Kraft T et al.
Pflugers Archiv : European Journal of Physiology, 2019
Cardiomyopathies and Related Changes in Contractility of Human Heart Muscle.
Vikhorev PG et al.
International Journal of Molecular Sciences, 2018
Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy.
Montag J et al.
Frontiers in Physiology, 2018
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Montag J et al.
Journal of Muscle Research and Cell Motility, 2017
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