| Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies MF Ortiz-Genga, S Cuenca, M Dal Ferro, E Zorio, R Salgado-Aranda, ... Journal of the American College of Cardiology 68 (22), 2440-2451, 2016 | 415 | 2016 |
| Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations F Domínguez, S Cuenca, Z Bilińska, R Toro, E Villard, R Barriales-Villa, ... Journal of the American College of Cardiology 72 (20), 2471-2481, 2018 | 108 | 2018 |
| Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene MM Akhtar, M Lorenzini, M Cicerchia, JP Ochoa, TM Hey, ... Circulation: Heart Failure 13 (10), e006832, 2020 | 93 | 2020 |
| Association of genetic variants with outcomes in patients with nonischemic dilated cardiomyopathy L Escobar-Lopez, JP Ochoa, JG Mirelis, MÁ Espinosa, M Navarro, ... Journal of the American College of Cardiology 78 (17), 1682-1699, 2021 | 73 | 2021 |
| Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy JP Ochoa, M Sabater-Molina, JM García-Pinilla, J Mogensen, ... Journal of the American College of Cardiology 72 (20), 2457-2467, 2018 | 73 | 2018 |
| Ambulatory blood pressure is associated with polymorphic variation in P2X receptor genes J Palomino-Doza, TJ Rahman, PJ Avery, BM Mayosi, M Farrall, H Watkins, ... Hypertension 52 (5), 980-985, 2008 | 68 | 2008 |
| An homozygous mutation in KCNK3 is associated with an aggressive form of hereditary pulmonary arterial hypertension P Navas Tejedor, J Tenorio Castaño, J Palomino Doza, P Arias Lajara, ... Clinical Genetics 91 (3), 453-457, 2017 | 63 | 2017 |
| Molecular analysis of BMPR2, TBX4, and KCNK3 and genotype-phenotype correlations in Spanish patients and families with idiopathic and hereditary pulmonary arterial hypertension P Navas, J Tenorio, CA Quezada, E Barrios, G Gordo, P Arias, ... Revista Española de Cardiología (English Edition) 69 (11), 1011-1019, 2016 | 60 | 2016 |
| Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis A Lopez-Sainz, F Dominguez, LR Lopes, JP Ochoa, R Barriales-Villa, ... Journal of the American College of Cardiology 76 (2), 186-197, 2020 | 59 | 2020 |
| Clinical risk prediction in patients with left ventricular myocardial noncompaction G Casas, J Limeres, G Oristrell, L Gutierrez-Garcia, D Andreini, ... Journal of the American College of Cardiology 78 (7), 643-662, 2021 | 49 | 2021 |
| Palbociclib and ribociclib in breast cancer: consensus workshop on the management of concomitant medication M Bellet, F Ahmad, R Villanueva, C Valdivia, J Palomino-Doza, A Ruiz, ... Therapeutic Advances in Medical Oncology 11, 1758835919833867, 2019 | 47 | 2019 |
| Association of left ventricular systolic dysfunction among carriers of truncating variants in filamin C with frequent ventricular arrhythmia and end-stage heart failure MM Akhtar, M Lorenzini, M Pavlou, JP Ochoa, C O’mahony, ... JAMA cardiology 6 (8), 891-901, 2021 | 45 | 2021 |
| Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13 125 controls C Mamasoula, RR Prentice, T Pierscionek, F Pangilinan, JL Mills, ... Circulation: Cardiovascular Genetics 6 (4), 347-353, 2013 | 45 | 2013 |
| A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot JA Goodship, D Hall, A Topf, C Mamasoula, H Griffin, TJ Rahman, E Glen, ... Circulation: Cardiovascular Genetics 5 (3), 287-292, 2012 | 43 | 2012 |
| Calmodulin 2 mutation N98S is associated with unexplained cardiac arrest in infants due to low clinical penetrance electrical disorders J Jiménez-Jáimez, J Palomino Doza, Á Ortega, R Macías-Ruiz, F Perin, ... PLoS One 11 (4), e0153851, 2016 | 42 | 2016 |
| Alteraciones del equilibrio ácido-base JMP de Paula, SF Hidalgo, EM Toranzo, JP Doza, JFP de Paula Diálisis y Trasplante 33 (1), 25-34, 2012 | 39 | 2012 |
| Natural History of MYH7-Related Dilated Cardiomyopathy F De Frutos, JP Ochoa, M Navarro-Peñalver, A Baas, JV Bjerre, E Zorio, ... Journal of the American College of Cardiology 80 (15), 1447-1461, 2022 | 35 | 2022 |
| Mutations in TRIM63 cause an autosomal-recessive form of hypertrophic cardiomyopathy J Salazar-Mendiguchía, JP Ochoa, J Palomino-Doza, F Domínguez, ... Heart 106 (17), 1342-1348, 2020 | 30 | 2020 |
| Variable expressivity of a founder mutation in the EIF2AK4 gene in hereditary pulmonary veno-occlusive disease and its impact on survival PN Tejedor, JP Doza, JAT Castaño, ABE Valls, JJR Reguero, AM Meñaca, ... Revista Española de Cardiología (English Edition) 71 (2), 86-94, 2018 | 28 | 2018 |
| Clinical risk score to predict pathogenic genotypes in patients with dilated cardiomyopathy L Escobar-Lopez, JP Ochoa, A Royuela, JAJ Verdonschot, M Dal Ferro, ... Journal of the American College of Cardiology 80 (12), 1115-1126, 2022 | 27 | 2022 |
Lorenzo MonserratHealth in CodeVerified email at healthincode.com
