Marcos N. Cicerchia
A Coruna, GA, Spain
Last Updated: 09/26/2026
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Found 11 publications
Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients.
Journal: Frontiers in cardiovascular medicine
Published: July 06, 2023
Cardiac myosin binding protein-C variants in paediatric-onset hypertrophic cardiomyopathy: natural history and clinical outcomes.
Journal: Journal of medical genetics
Published: February 10, 2021
Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene.
Journal: Circulation. Heart failure
Published: September 23, 2020
The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.
Journal: European journal of medical genetics
Published: May 25, 2020
Prognostic implications of pathogenic truncating variants in the TTN gene.
Journal: International journal of cardiology
Published: April 08, 2020
Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers.
Journal: Journal of the American College of Cardiology
Published: April 02, 2020
Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy.
Journal: Heart (British Cardiac Society)
Published: March 18, 2020
Clinical utility of genetic testing in patients with dilated cardiomyopathy.
Journal: Medicina clinica
Published: February 10, 2020
Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives.
Journal: Circulation
Published: April 23, 2019
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
Journal: Journal of the American College of Cardiology
Published: June 07, 2018
Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.
Journal: Journal of the American College of Cardiology
Published: February 25, 2018
Showing 1-11 of 11
Last Updated: 09/26/2026