The genetic architecture of hypertrophic cardiomyopathy by Harper, AR

Critical evaluation of the efficacy and tolerability of azilsartan by Cuculi F, Harper AR, De Caterina AR

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Corrigendum by De Caterina AR, Harper AR, Cuculi F

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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

Genome-wide analysis of left ventricular maximum wall thickness in the UK biobank cohort reveals a shared genetic background with hypertrophic cardiomyopathy by Aung, N, Lopes, LR, van Duijvenboden, S, Harper, AR, Goel, A, Grace, C, Ho, CY, Weintraub, WS, Kramer, CM, Neubauer, S, Watkins, H, Petersen, SE, Munroe, PB

Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance st... by Raman, B, Smillie, RW, Mahmod, M, Chan, K, Ariga, R, Nikolaidou, C, Ormondroyd, E, Thomson, K, Harper, AR, Tan, G, Lewandowski, AJ, Rodriguez Bajo, F, Wicks, EC, Casadei, B, Watkins, H, Neubauer, S

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

Distinct subgroups in hypertrophic cardiomyopathy in the NHLBI HCM Registry by Neubauer, S, Kolm, P, Ho, CY, Kwong, RY, Desai, MY, Dolman, SF, Appelbaum, E, Desvigne-Nickens, P, Dimarco, JP, Friedrich, MG, Geller, N, Harper, AR, Jarolim, P, Jerosch-Herold, M, Kim, DY, Maron, MS, Schulz-Menger, J, Piechnik, SK, Thomson, K, Zhang, C, Watkins, H, Weintraub, WS, Kramer, CM

Human genetics uncovers MAP3K15 as an obesity-independent therapeutic target for diabetes by Nag, A, Dhindsa, RS, Mitchell, J, Vasavda, C, Harper, AR, Vitsios, D, Ahnmark, A, Bilican, B, Madeyski-Bengtson, K, Zarrouki, B, Zoghbi, AW, Wang, Q, Smith, KR, Alegre-Díaz, J, Kuri-Morales, P, Berumen, J, Tapia-Conyer, R, Emberson, J, Torres, JM, Collins, R, Smith, DM, Challis, B, Paul, DS, Bohlooly-Y, M, Snowden, M, Baker, D, Fritsche-Danielson, R, Pangalos, MN, Petrovski, S

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect by Tadros, R, Francis, C, Xu, X, Vermeer, AMC, Harper, AR, Huurman, R, Kelu Bisabu, K, Walsh, R, Hoorntje, ET, Te Rijdt, WP, Buchan, RJ, van Velzen, HG, van Slegtenhorst, MA, Vermeulen, JM, Offerhaus, JA, Bai, W, de Marvao, A, Lahrouchi, N, Beekman, L, Karper, JC, Veldink, JH, Kayvanpour, E, Pantazis, A, Baksi, AJ, Whiffin, N, Mazzarotto, F, Sloane, G, Suzuki, H, Schneider-Luftman, D, Elliott, P, Richard, P, Ader, F, Villard, E, Lichtner, P, Meitinger, T, Tanck, MWT, van Tintelen, JP, Thain, A, McCarty, D, Hegele, RA, Roberts, JD, Amyot, J, Dubé, M-P, Cadrin-Tourigny, J, Giraldeau, G, L'Allier, PL, Garceau, P, Tardif, J-C, Boekholdt, SM, Lumbers, RT, Watkins, H