Browse by Author "Ortiz Genga, Martín"

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy

2015- Monserrat Iglesias, Lorenzo; Ortiz Genga, Martín

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

2023- Lopes, L.R.; Losi, M.-A.; Sheikh, N.; Laroche, C.; Charron, P.; [et al.]

Atlas of the clinical genetics of human dilated cardiomyopathy

2015- Monserrat Iglesias, Lorenzo; Crespo Leiro, Marisa; Ortiz Genga, Martín; García Giustiniani, Daniel

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

2011- Monserrat Iglesias, Lorenzo; López, Begoña; González, Arantxa; Hermida Prieto, Manuel; Barriales Villa, Roberto; [et al.]

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain

2011- Monserrat Iglesias, Lorenzo; Nuñez Fernandez, Lucia; García Estévez, Daniel Apolinar; Barriales Villa, Roberto; Ortiz Genga, Martín; [et al.]

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype

2014- Monserrat Iglesias, Lorenzo; Ortiz Genga, Martín

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

2022- Wilde, A.A.M.; Semsarian, C.; Márquez, M.F.; Sepehri Shamloo, A.; Ackerman, M.J.; [et al.]

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

2022- Wilde, A.A.M.; Semsarian, C.; Márquez, M.F.; Shamloo, A.S.; Ackerman, M.J.; [et al.]

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

2022- Wilde, A.A.M.; Semsarian, C.; Márquez, M.F.; Sepehri Shamloo, A.; Ackerman, M.J.; [et al.]

Genética, muerte súbita y deporte

2011- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín

Genetics of cardiomyopathies: novel perspectives with next generation sequencing

2015- Monserrat Iglesias, Lorenzo; Castro Beiras, Alfonso; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel [et al.]

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course

2015- Monserrat Iglesias, Lorenzo; Fernández Fernández, Xusto; Barriales Villa, Roberto; Ortiz Genga, Martín

iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic Cardiomyopathy

2023- Escribá, R.; Larrañaga Moreira, José María; Richaud-Patin, Y.; Pourchet, L.; Lazis, I.; [et al.]

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain

2015- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel; Rodriguez García, Isabel [et al.]

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain.

2012- Barriales Villa, Roberto; Ortiz Genga, Martín

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave

2014- Monserrat Iglesias, Lorenzo; Barriales Villa, Roberto; Ortiz Genga, Martín; García Giustiniani, Daniel

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy

2011- Monserrat Iglesias, Lorenzo; Crespo Leiro, Marisa; Castro Beiras, Alfonso; Barriales Villa, Roberto; Ortiz Genga, Martín; [et al.]

RUNA digital repository

Browse by Author "Ortiz Genga, Martín"

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy ﻿

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry ﻿

Atlas of the clinical genetics of human dilated cardiomyopathy ﻿

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy ﻿

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain ﻿

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype ﻿

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases ﻿

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases ﻿

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases ﻿

Genética, muerte súbita y deporte ﻿

Genetics of cardiomyopathies: novel perspectives with next generation sequencing ﻿

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course ﻿

iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic Cardiomyopathy ﻿

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain ﻿

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain. ﻿

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave ﻿

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy ﻿

A mutation in the Z-line Cypher/ZASP protein is associated with arrhythmogenic right ventricular cardiomyopathy

Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

Atlas of the clinical genetics of human dilated cardiomyopathy

Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy

Clinical and functional consequences associated to a PKP2 founder mutation in north-west Spain

Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

Genética, muerte súbita y deporte

Genetics of cardiomyopathies: novel perspectives with next generation sequencing

High prevalence of N271I founder mutation in TNNT2 gene detected by NGS in a galician cohort cause hypertrophic cardiomyopathy associated with a benign course

iPSC-Based Modeling of Variable Clinical Presentation in Hypertrophic Cardiomyopathy

Phenotype and prognostic correlations of the converter region mutations affecting the beta myosin heavy chain

Phenotype-genotype correlation in patients with mutations in the beta-myosin converter domain.

Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave

Yield of genetic testing in patients with familial vs. non-familial idiopathic dilated cardiomyopathy