Showing results 1 to 20 of 29
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Issue Date | Title | Author(s) |
1-Jan-2019 | A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy | Horvat, C; Johnson, R; Lam, L; Munro, J; Mazzarotto, F, et al |
22-May-2018 | A genetic etiology for alcohol-induced cardiac toxicity | Ware, JS; Amor-Salamanca, A; Tayal, U; Govind, R; Serrano, I, et al |
Apr-2015 | Anthropometric and genetic determinants of cardiac morphology and function | Cook, Stuart; O'Regan, Declan; de Marvao, Antonio; , et al |
28-Jun-2019 | Association between titin truncating variants and life-threatening cardiac arrhythmias in patients with dilated cardiomyopathy and implantable defibrillator | Corden, B; Jarman, J; Whiffin, N; Tayal, U; Buchan, R, et al |
23-Dec-2015 | Cardiac regeneration: epicardial mediated repair | Kennedy-Lydon, T; Rosenthal, N; |
25-Jan-2018 | CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretation | Whiffin, N; Walsh, R; Govind, R; Edwards, M; Ahmad, M, et al |
27-May-2020 | Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals | Whiffin, N; Karczewski, KJ; Zhang, X; Chothani, S; Smith, MJ, et al |
11-Jan-2017 | Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes | Walsh, R; Buchan, R; Wilk, A; John, S; Felkin, L, et al |
1-Sep-2019 | Efficacy of dexrazoxane in preventing anthracycline cardiotoxicity in breast cancer | Macedo, AVS; Hajjar, LA; Lyon, AR; Nascimento, BR; Putzu, A, et al |
15-Mar-2017 | Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy | Esslinger, U; Garnier, S; Korniat, A; Proust, C; Kararigas, G, et al |
11-Feb-2020 | Global longitudinal strain and cardiac events in patients with immune checkpoint inhibitor-related myocarditis | Awadalla, M; Mahmood, SS; Groarke, JD; Hassan, MZO; Nohria, A, et al |
1-Jul-2017 | Hypoxia-mediated regulation of the secretory properties of mitral valve interstitial cells | Salhiyyah, K; Sarathchandra, P; Latif, N; Yacoub, MH; Chester, AH, et al |
14-Sep-2017 | Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy | Heinig, M; Adriaens, ME; Schafer, S; Van Deutekom, HWM; Lodder, EM, et al |
31-Aug-2021 | New variant with a previously unrecognized mechanism of pathogenicity in hypertrophic cardiomyopathy | Aguib, Y; Allouba, M; Walsh, R; Ibrahim, AM; Halawa, S, et al |
31-Oct-2017 | Phenotype and clinical outcomes of titin cardiomyopathy | Tayal, U; Newsome, S; Buchan, R; Whiffin, N; Halliday, B, et al |
29-Jan-2019 | Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: The case of hypertrophic cardiomyopathy | Walsh, R; Mazzarotto, F; Whiffin, N; Buchan, R; Midwinter, W, et al |
4-Feb-2020 | Re-evaluating the genetic contribution of monogenic dilated cardiomyopathy | Mazzarotto, F; Tayal, U; Buchan, RJ; Midwinter, W; Wilk, A, et al |
6-Apr-2016 | Recovery of cardiac function in cardiomyopathy due to titin truncation | Felkin, LE; Walsh, R; Ware, JS; Yacoub, MH; Birks, EJ, et al |
26-Jan-2021 | Systematic large-scale assessment of the genetic architecture of left ventricular non-compaction reveals diverse aetiologies | Mazzarotto, F; Hawley, MH; Beltrami, M; Beekman, L; De Marvao, A, et al |
1-May-2017 | T2 mapping by cardiovasular magnetic resonance in acute and recovered myocarditis: potential role in clinical surveillance | Lota, A; Wassall, R; Scott, A; Wage, R; Smith, G, et al |