| Dietary fructooligosaccharides and potential benefits on health M Sabater-Molina, E Larqué, F Torrella, S Zamora Journal of physiology and biochemistry 65, 315-328, 2009 | 412 | 2009 |
| Biological significance of dietary polyamines E Larqué, M Sabater-Molina, S Zamora Nutrition 23 (1), 87-95, 2007 | 369 | 2007 |
| Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy G Luxán, JC Casanova, B Martínez-Poveda, B Prados, G D'amato, ... Nature medicine 19 (2), 193-201, 2013 | 346 | 2013 |
| Genetics of hypertrophic cardiomyopathy: A review of current state M Sabater‐Molina, I Pérez‐Sánchez, JP Hernández del Rincón, ... Clinical genetics 93 (1), 3-14, 2018 | 196 | 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 |
| 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 |
| Filamin C variants are associated with a distinctive clinical and immunohistochemical arrhythmogenic cardiomyopathy phenotype CL Hall, MM Akhtar, M Sabater-Molina, M Futema, A Asimaki, ... International journal of cardiology 307, 101-108, 2020 | 70 | 2020 |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls R Walsh, N Lahrouchi, R Tadros, F Kyndt, C Glinge, PG Postema, ... Genetics in medicine 23 (1), 47-58, 2021 | 65 | 2021 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 64 | 2022 |
| 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 |
| Effects of dietary polyamines at physiologic doses in early-weaned piglets M Sabater-Molina, E Larqué, F Torrella, J Plaza, T Lozano, A Muñoz, ... Nutrition 25 (9), 940-946, 2009 | 58 | 2009 |
| Polymorphisms in ACE, ACE2, AGTR1 genes and severity of COVID-19 disease M Sabater Molina, E Nicolás Rocamora, AI Bendicho, EG Vázquez, ... PloS one 17 (2), e0263140, 2022 | 56 | 2022 |
| 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 |
| A gene variant in the transcription factor 7-like 2 (TCF7L2) is associated with an increased risk of gestational diabetes mellitus A Pagán, M Sabater-Molina, J Olza, MT Prieto-Sánchez, ... European Journal of Obstetrics & Gynecology and Reproductive Biology 180, 77-82, 2014 | 45 | 2014 |
| Polyamines in human breast milk for preterm and term infants J Plaza-Zamora, M Sabater-Molina, M Rodríguez-Palmero, M Rivero, ... British journal of nutrition 110 (3), 524-528, 2013 | 45 | 2013 |
| 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 |
| A novel founder mutation in MYBPC3: phenotypic comparison with the most prevalent MYBPC3 mutation in Spain M Sabater-Molina, D Saura, EGM Sáez, J González-Carrillo, L Polo, ... Revista Española de Cardiología (English Edition) 70 (2), 105-114, 2017 | 33 | 2017 |
| Factors influencing the phenotypic expression of hypertrophic cardiomyopathy in genetic carriers I Pérez-Sánchez, AJ Romero-Puche, EGM Sáez, M Sabater-Molina, ... Revista Española de Cardiología (English Edition) 71 (3), 146-154, 2018 | 31 | 2018 |
| Protein haploinsufficiency drivers identify MYBPC3 variants that cause hypertrophic cardiomyopathy C Suay-Corredera, MR Pricolo, E Herrero-Galán, D Velázquez-Carreras, ... Journal of Biological Chemistry 297 (1), 2021 | 28 | 2021 |
| RNA sequencing-based transcriptome profiling of cardiac tissue implicates novel putative disease mechanisms in FLNC-associated arrhythmogenic cardiomyopathy CL Hall, P Gurha, M Sabater-Molina, A Asimaki, M Futema, RC Lovering, ... International journal of cardiology 302, 124-130, 2020 | 28 | 2020 |
