Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease by Buchanan, J, Blair, E, Thomson, KL, Ormondroyd, E, Watkins, H, Taylor, JC, Wordsworth, S

Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes by Ormondroyd, E, Harper , AR, Thomson, KL, Mackley, MP, Martin, J, Penkett, CJ, Salatino, S, Stark, H, Stephens, J, Watkins, H

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity by Harper, AR, Goel, A, Grace, C, Thomson, KL, Petersen, SE, Xu, X, Waring, A, Ormondroyd, E, Kramer, CM, Ho, CY, Neubauer, S, HCMR Investigators, Tadros, R, Ware, JS, Bezzina, CR, Farrall, M, Watkins, H

A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy by Harper, AR, Bowman, M, Hayesmoore, JBG, Sage, H, Salatino, S, Blair, E, Campbell, C, Currie, B, Goel, A, McGuire, K, Ormondroyd, E, Sergeant, K, Waring, A, Woodley, J, Kramer, CM, Neubauer, S, Farrall, M, Watkins, H, Thomson, KL

Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy by Walsh, R, Mazzarotto, F, Whiffin, N, Buchan, R, Midwinter, W, Wilk, A, Li, N, Felkin, L, Ingold, N, Govind, R, Ahmad, M, Mazaika, E, Allouba, M, Zhang, X, De Marvao, A, Day, SM, Ashley, E, Colan, SD, Michels, M, Pereira, AC, Jacoby, D, Ho, CY, Thomson, KL, Watkins, H, Barton, PJR, Olivotto, I, Cook, SA, Ware, JS

Reevaluating the genetic contribution of monogenic dilated cardiomyopathy by Mazzarotto, F, Tayal, U, Buchan, RJ, Midwinter, W, Wilk, A, Whiffin, N, Govind, R, Mazaika, E, de Marvao, A, Dawes, TJW, Felkin, LE, Ahmad, M, Theotokis, PI, Edwards, E, Ing, AY, Thomson, KL, Chan, LHL, Sim, D, Baksi, AJ, Pantazis, A, Roberts, AM, Watkins, H, Funke, B, O'Regan, DP, Olivotto, I, Barton, PJR, Prasad, SK, Cook, SA, Ware, JS, Walsh, R