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| Atlas of the clinical genetics of human dilated cardiomyopathy J Haas, KS Frese, B Peil, W Kloos, A Keller, R Nietsch, Z Feng, S Müller, ... European heart journal 36 (18), 1123-1135, 2015 | 661 | 2015 |
| Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nature Communications, 2015 | 482 | 2015 |
| Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing LR Lopes, A Zekavati, P Syrris, M Hubank, C Giambartolomei, ... Journal of medical genetics 50 (4), 228-239, 2013 | 349 | 2013 |
| A systematic review and meta-analysis of genotype–phenotype associations in patients with hypertrophic cardiomyopathy caused by sarcomeric protein mutations LR Lopes, MS Rahman, PM Elliott Heart 99 (24), 1800-1811, 2013 | 280 | 2013 |
| Dilated cardiomyopathy and arrhythmogenic left ventricular cardiomyopathy: a comprehensive genotype-imaging phenotype study JB Augusto, R Eiros, E Nakou, S Moura-Ferreira, TA Treibel, G Captur, ... European Heart Journal-Cardiovascular Imaging 21 (3), 326-336, 2020 | 226 | 2020 |
| Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy LR Lopes, P Syrris, OP Guttmann, C O'Mahony, HC Tang, C Dalageorgou, ... Heart 101 (4), 294-301, 2015 | 205 | 2015 |
| Penetrance of hypertrophic cardiomyopathy in sarcomere protein mutation carriers M Lorenzini, G Norrish, E Field, JP Ochoa, M Cicerchia, MM Akhtar, ... Journal of the American College of Cardiology 76 (5), 550-559, 2020 | 201 | 2020 |
| 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 | 182 | 2020 |
| 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 | 180 | 2018 |
| Abnormal cardiac formation in hypertrophic cardiomyopathy: fractal analysis of trabeculae and preclinical gene expression G Captur, LR Lopes, V Patel, C Li, P Bassett, P Syrris, DM Sado, ... Circulation: Cardiovascular Genetics 7 (3), 241-248, 2014 | 133 | 2014 |
| Diagnosis and risk stratification in hypertrophic cardiomyopathy using machine learning wall thickness measurement: a comparison with human test-retest performance JB Augusto, RH Davies, AN Bhuva, KD Knott, A Seraphim, M Alfarih, ... The Lancet Digital Health 3 (1), e20-e28, 2021 | 132 | 2021 |
| Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy G Captur, LR Lopes, TJ Mohun, V Patel, C Li, P Bassett, G Finocchiaro, ... Circulation: Cardiovascular Imaging 7 (6), 863-871, 2014 | 119 | 2014 |
| Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator A Protonotarios, R Bariani, C Cappelletto, M Pavlou, A García-García, ... European heart journal 43 (32), 3053-3067, 2022 | 111 | 2022 |
| 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 | 109 | 2018 |
| Proteomic analysis of the myocardium in hypertrophic obstructive cardiomyopathy CJ Coats, WE Heywood, A Virasami, N Ashrafi, P Syrris, C Dos Remedios, ... Circulation: Genomic and Precision Medicine 11 (12), e001974, 2018 | 103 | 2018 |
| Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing. N LM, L LR, S P Europace, 2015 | 100 | 2015 |
| 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 | 97 | 2020 |
| Precision measurement of cardiac structure and function in cardiovascular magnetic resonance using machine learning RH Davies, JB Augusto, A Bhuva, H Xue, TA Treibel, Y Ye, RK Hughes, ... Journal of Cardiovascular Magnetic Resonance 24 (1), 16, 2022 | 96 | 2022 |
| Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy LR Lopes, S Garcia-Hernández, M Lorenzini, M Futema, O Chumakova, ... European heart journal 42 (32), 3063-3073, 2021 | 96 | 2021 |
