| New perspectives on the prevalence of hypertrophic cardiomyopathy C Semsarian, J Ingles, MS Maron, BJ Maron Journal of the American College of Cardiology 65 (12), 1249-1254, 2015 | 1435 | 2015 |
| 2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC) E Arbelo, A Protonotarios, JR Gimeno, E Arbustini, R Barriales-Villa, ... European heart journal 44 (37), 3503-3626, 2023 | 1102 | 2023 |
| 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy JA Towbin, WJ McKenna, DJ Abrams, MJ Ackerman, H Calkins, ... Heart rhythm 16 (11), e301-e372, 2019 | 932 | 2019 |
| A prospective study of sudden cardiac death among children and young adults RD Bagnall, RG Weintraub, J Ingles, J Duflou, L Yeates, L Lam, AM Davis, ... New England Journal of Medicine 374 (25), 2441-2452, 2016 | 865 | 2016 |
| Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling J Ingles, A Doolan, C Chiu, J Seidman, C Seidman, C Semsarian Journal of medical genetics 42 (10), e59-e59, 2005 | 459 | 2005 |
| Evaluating the clinical validity of hypertrophic cardiomyopathy genes J Ingles, J Goldstein, C Thaxton, C Caleshu, EW Corty, SB Crowley, ... Circulation: Genomic and Precision Medicine 12 (2), e002460, 2019 | 394 | 2019 |
| Evidence-based assessment of genes in dilated cardiomyopathy E Jordan, L Peterson, T Ai, B Asatryan, L Bronicki, E Brown, R Celeghin, ... Circulation 144 (1), 7-19, 2021 | 372 | 2021 |
| Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen’s Inherited Cardiomyopathy … MA Kelly, C Caleshu, A Morales, J Buchan, Z Wolf, SM Harrison, S Cook, ... Genetics in Medicine 20 (3), 351-359, 2018 | 365 | 2018 |
| Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives C Semsarian, J Ingles, AAM Wilde European heart journal 36 (21), 1290-1296, 2015 | 344 | 2015 |
| 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families MK Stiles, AAM Wilde, DJ Abrams, MJ Ackerman, CM Albert, ER Behr, ... Journal of arrhythmia 37 (3), 481-534, 2021 | 284 | 2021 |
| Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis C Chiu, RD Bagnall, J Ingles, L Yeates, M Kennerson, JA Donald, ... Journal of the American College of Cardiology 55 (11), 1127-1135, 2010 | 226 | 2010 |
| Nonfamilial hypertrophic cardiomyopathy: prevalence, natural history, and clinical implications J Ingles, C Burns, RD Bagnall, L Lam, L Yeates, T Sarina, R Puranik, ... Circulation: Cardiovascular Genetics 10 (2), e001620, 2017 | 217 | 2017 |
| A validated model for sudden cardiac death risk prediction in pediatric hypertrophic cardiomyopathy A Miron, M Lafreniere-Roula, CP Steve Fan, KR Armstrong, A Dragulescu, ... Circulation 142 (3), 217-229, 2020 | 188 | 2020 |
| Whole genome sequencing improves outcomes of genetic testing in patients with hypertrophic cardiomyopathy RD Bagnall, J Ingles, ME Dinger, MJ Cowley, SB Ross, AE Minoche, S Lal, ... Journal of the American College of Cardiology 72 (4), 419-429, 2018 | 187 | 2018 |
| A cost-effectiveness model of genetic testing for the evaluation of families with hypertrophic cardiomyopathy J Ingles, J McGaughran, PA Scuffham, J Atherton, C Semsarian Heart 98 (8), 625-630, 2012 | 169 | 2012 |
| Hypertrophic cardiomyopathy with left ventricular systolic dysfunction: insights from the SHaRe registry P Marstrand, L Han, SM Day, I Olivotto, EA Ashley, M Michels, AC Pereira, ... Circulation 141 (17), 1371-1383, 2020 | 163 | 2020 |
| Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy J Ingles, T Sarina, L Yeates, L Hunt, I Macciocca, L McCormack, I Winship, ... Genetics in Medicine 15 (12), 972-977, 2013 | 145 | 2013 |
| Recommendations for clinical interpretation of variants found in non-coding regions of the genome JM Ellingford, JW Ahn, RD Bagnall, D Baralle, S Barton, C Campbell, ... Genome medicine 14 (1), 73, 2022 | 141 | 2022 |
| Regional Variation in RBM20 Causes a Highly Penetrant Arrhythmogenic Cardiomyopathy VN Parikh, C Caleshu, C Reuter, LC Lazzeroni, J Ingles, J Garcia, ... Circulation: Heart Failure 12 (3), e005371, 2019 | 128 | 2019 |
| Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy J Ingles, JM Lind, P Phongsavan, C Semsarian Genetics in Medicine 10 (2), 117-120, 2008 | 128 | 2008 |
Richard BagnallCentenary Institute | University of SydneyE-mailová adresa ověřena na: centenary.org.au