1. Targeted next-generation sequencing detects novel gene–phenotype associations and expands the mutational spectrum in cardiomyopathies
   Cinzia Forleo et al, 2017, PLOS ONE CrossRef
2. Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy
   Irene Mademont-Soler et al, 2017, PLOS ONE CrossRef
3. No Effect of the p.Arg230His Variant Of The VCL Protein on the Course of the Hypertrophic Cardiomyopathy In Russian Family Carrying The p.Gln1233Ter Pathogenic Variant In The MYBPC3 Gene
   E. V. Filatova et al, 2023, Kardiologiia CrossRef
4. Finding the candidate sequence variants for diagnosis of hypertrophic cardiomyopathy in East Slovak patients
   Michaela Zigova et al, 2018, Journal of Clinical Laboratory Analysis CrossRef
5. Mechanisms of pathogenicity in the hypertrophic cardiomyopathy-associated TPM1 variant S215L
   Saiti S Halder et al, 2023, PNAS Nexus CrossRef
6. Compact SchCas9 Recognizes the Simple NNGR PAM
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7. Next generation sequencing applications for cardiovascular disease
   Samira Kalayinia et al, 2018, Annals of Medicine CrossRef
8. Genetic analysis of patients with hypertrophic cardiomyopathy
   E. V Dementyeva et al, 2020, Genes & Cells CrossRef
9. Identification of LAMP2 mutations in early-onset hypertrophic cardiomyopathy by targeted exome sequencing
   Inkyu Gill et al, 2018, Journal of Genetic Medicine CrossRef
10. Identification of key genes for hypertrophic cardiomyopathy using integrated network analysis of differential lncRNA and gene expression
    Jing Cao et al, 2022, Frontiers in Cardiovascular Medicine CrossRef
11. Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy
    Thuy Vy Nguyen et al, 2021, Circulation Journal CrossRef
12. Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy
    Judith Montag et al, 2017, Journal of Muscle Research and Cell Motility CrossRef
13. Targeted exome analysis of Russian patients with hypertrophic cardiomyopathy
    Elena V. Filatova et al, 2021, Molecular Genetics & Genomic Medicine CrossRef
14. Pruebas genéticas en la miocardiopatía hipertrófica: beneficios, limitaciones y aplicaciones en la práctica clínica
    I. Gómez Arraiz et al, 2018, Medicina de Familia. SEMERGEN CrossRef
15. Mutations in MYBPC3 and MYH7 in Association with Brugada Type 1 ECG Pattern: Overlap between Brugada Syndrome and Hypertrophic Cardiomyopathy?
    Marianna Farnè et al, 2021, Cardiogenetics CrossRef
16. Bioplatforms in liquid biopsy: advances in the techniques for isolation, characterization and clinical applications
    Ushma Jaykamal Shah et al, 2022, Biotechnology and Genetic Engineering Reviews CrossRef
17. High-Resolution Cryo-EM Structure of the Cardiac Actomyosin Complex
    Cristina Risi et al, 2021, Structure CrossRef
18. Combining whole exome sequencing with in silico analysis and clinical data to identify candidate variants in pediatric left ventricular noncompaction
    John Collyer et al, 2022, International Journal of Cardiology CrossRef
19. The role of the M-band myomesin proteins in muscle integrity and cardiac disease
    Ekaterina P. Lamber et al, 2022, Journal of Biomedical Science CrossRef