I. Cárdenas-Reyes

The p.(Cys150Tyr) variant in CSRP3 is associated with late-onset hypertrophic cardiomyopathy in heterozygous individuals.

P. Elliott, L. Monserrat, J. Ochoa, 2020, European journal of medical genetics.

Cardiac-only Timothy Syndrome (COTS): Peripartum Cardiomyopathy and Long QT Syndrome.

R. Barriales-Villa, J. Larrañaga-Moreira, I. Cárdenas-Reyes, 2019, Revista espanola de cardiologia.

Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy

P. Elliott, L. Monserrat, P. Syrris, 2020, Heart.

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.

P. Elliott, J. Mogensen, L. Monserrat, 2018, Journal of the American College of Cardiology.

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.

P. Elliott, J. Mogensen, L. Monserrat, 2018, Journal of the American College of Cardiology.

Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction

T. Hey, P. García-Pavía, J. Rodríguez-Palomares, 2024, Circulation. Genomic and precision medicine.