Browsing by Sponsor/Funder Fondation Leducq

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:  
Showing results 1 to 20 of 29  next >
Issue DateTitleAuthor(s)
1-Jan-2019A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyHorvat, C; Johnson, R; Lam, L; Munro, J; Mazzarotto, F, et al
22-May-2018A genetic etiology for alcohol-induced cardiac toxicityWare, JS; Amor-Salamanca, A; Tayal, U; Govind, R; Serrano, I, et al
Apr-2015Anthropometric and genetic determinants of cardiac morphology and functionCook, Stuart; O'Regan, Declan; de Marvao, Antonio; , et al
28-Jun-2019Association between titin truncating variants and life-threatening cardiac arrhythmias in patients with dilated cardiomyopathy and implantable defibrillatorCorden, B; Jarman, J; Whiffin, N; Tayal, U; Buchan, R, et al
23-Dec-2015Cardiac regeneration: epicardial mediated repairKennedy-Lydon, T; Rosenthal, N;
25-Jan-2018CardioClassifier: disease- and gene-specific computational decision support for clinical genome interpretationWhiffin, N; Walsh, R; Govind, R; Edwards, M; Ahmad, M, et al
27-May-2020Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individualsWhiffin, N; Karczewski, KJ; Zhang, X; Chothani, S; Smith, MJ, et al
11-Jan-2017Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genesWalsh, R; Buchan, R; Wilk, A; John, S; Felkin, L, et al
1-Sep-2019Efficacy of dexrazoxane in preventing anthracycline cardiotoxicity in breast cancerMacedo, AVS; Hajjar, LA; Lyon, AR; Nascimento, BR; Putzu, A, et al
15-Mar-2017Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathyEsslinger, U; Garnier, S; Korniat, A; Proust, C; Kararigas, G, et al
11-Feb-2020Global longitudinal strain and cardiac events in patients with immune checkpoint inhibitor-related myocarditisAwadalla, M; Mahmood, SS; Groarke, JD; Hassan, MZO; Nohria, A, et al
1-Jul-2017Hypoxia-mediated regulation of the secretory properties of mitral valve interstitial cellsSalhiyyah, K; Sarathchandra, P; Latif, N; Yacoub, MH; Chester, AH, et al
14-Sep-2017Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyHeinig, M; Adriaens, ME; Schafer, S; Van Deutekom, HWM; Lodder, EM, et al
31-Aug-2021New variant with a previously unrecognized mechanism of pathogenicity in hypertrophic cardiomyopathyAguib, Y; Allouba, M; Walsh, R; Ibrahim, AM; Halawa, S, et al
31-Oct-2017Phenotype and clinical outcomes of titin cardiomyopathyTayal, U; Newsome, S; Buchan, R; Whiffin, N; Halliday, B, et al
29-Jan-2019Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: The case of hypertrophic cardiomyopathyWalsh, R; Mazzarotto, F; Whiffin, N; Buchan, R; Midwinter, W, et al
4-Feb-2020Re-evaluating the genetic contribution of monogenic dilated cardiomyopathyMazzarotto, F; Tayal, U; Buchan, RJ; Midwinter, W; Wilk, A, et al
6-Apr-2016Recovery of cardiac function in cardiomyopathy due to titin truncationFelkin, LE; Walsh, R; Ware, JS; Yacoub, MH; Birks, EJ, et al
26-Jan-2021Systematic large-scale assessment of the genetic architecture of left ventricular non-compaction reveals diverse aetiologiesMazzarotto, F; Hawley, MH; Beltrami, M; Beekman, L; De Marvao, A, et al
1-May-2017T2 mapping by cardiovasular magnetic resonance in acute and recovered myocarditis: potential role in clinical surveillanceLota, A; Wassall, R; Scott, A; Wage, R; Smith, G, et al