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2. Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy
   Sathiya N. Manivannan et al, 2020, PLOS Genetics CrossRef
3. When Paying Attention Pays Back: Missense Mutation c.1006G>A p. (Val336Ile) in PRKAG2 Gene Causing Left Ventricular Hypertrophy and Conduction Abnormalities in a Caucasian Patient: Case Report and Literature Review
   Emanuele Micaglio et al, 2024, International Journal of Molecular Sciences CrossRef
4. A Bayesian Analysis to Determine the Prevalence of Barth Syndrome in the Pediatric Population
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5. Clinical Interpretation of Sequence Variants
   Junyu Zhang et al, 2020, Current Protocols in Human Genetics CrossRef
6. Presence of Hypertrophic Cardiomyopathy Related Gene Mutations and Clinical Manifestations in Vietnamese Patients With Hypertrophic Cardiomyopathy
   Minh Thu Tran Vu et al, 2019, Circulation Journal CrossRef
7. Heart rate variability as predictive factor for sudden cardiac death
   Francesco Sessa et al, 2018, Aging CrossRef
8. Progress of Genetics in Inherited Cardiomyopathies-Induced Heart Failure
   Baoli Zhang et al, 2018, Heart Genomics CrossRef