Roddy Walsh
Roddy Walsh
Amsterdam UMC
Verified email at - Homepage
Cited by
Cited by
Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples
R Walsh, KL Thomson, JS Ware, BH Funke, J Woodley, KJ McGuire, ...
Genetics in Medicine 19 (2), 192-203, 2017
Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease
AM Roberts, JS Ware, DS Herman, S Schafer, J Baksi, AG Bick, ...
Science translational medicine 7 (270), 270ra6-270ra6, 2015
Using high-resolution variant frequencies to empower clinical genome interpretation
N Whiffin, E Minikel, R Walsh, AH O’Donnell-Luria, K Karczewski, AY Ing, ...
Genetics in Medicine 19 (10), 1151-1158, 2017
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
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
Titin-truncating variants affect heart function in disease cohorts and the general population
S Schafer, A De Marvao, E Adami, LR Fiedler, B Ng, E Khin, ...
Nature genetics 49 (1), 46-53, 2017
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
Genetic variants associated with cancer therapy–induced cardiomyopathy
P Garcia-Pavia, Y Kim, MA Restrepo-Cordoba, IG Lunde, H Wakimoto, ...
Circulation 140 (1), 31-41, 2019
Genetic etiology for alcohol-induced cardiac toxicity
JS Ware, A Amor-Salamanca, U Tayal, R Govind, I Serrano, ...
Journal of the American College of Cardiology 71 (20), 2293-2302, 2018
Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes
R Walsh, R Buchan, A Wilk, S John, LE Felkin, KL Thomson, TH Chiaw, ...
European heart journal 38 (46), 3461-3468, 2017
Reevaluating the genetic contribution of monogenic dilated cardiomyopathy
F Mazzarotto, U Tayal, RJ Buchan, W Midwinter, A Wilk, N Whiffin, ...
Circulation 141 (5), 387-398, 2020
Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect
R Tadros, C Francis, X Xu, AMC Vermeer, AR Harper, R Huurman, ...
Nature genetics 53 (2), 128-134, 2021
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathy
R Walsh, F Mazzarotto, N Whiffin, R Buchan, W Midwinter, A Wilk, N Li, ...
Genome medicine 11, 1-18, 2019
Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations
F Domínguez, S Cuenca, Z Bilińska, R Toro, E Villard, R Barriales-Villa, ...
Journal of the American College of Cardiology 72 (20), 2471-2481, 2018
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ...
Circulation 142 (4), 324-338, 2020
Phenotype and clinical outcomes of titin cardiomyopathy
U Tayal, S Newsome, R Buchan, N Whiffin, B Halliday, A Lota, A Roberts, ...
Journal of the American College of Cardiology 70 (18), 2264-2274, 2017
Complex roads from genotype to phenotype in dilated cardiomyopathy: scientific update from the Working Group of Myocardial Function of the European Society of Cardiology
A Bondue, E Arbustini, A Bianco, M Ciccarelli, D Dawson, M De Rosa, ...
Cardiovascular Research 114 (10), 1287-1303, 2018
Development of a comprehensive sequencing assay for inherited cardiac condition genes
CJ Pua, J Bhalshankar, K Miao, R Walsh, S John, SQ Lim, K Chow, ...
Journal of cardiovascular translational research 9, 3-11, 2016
CardioClassifier: disease-and gene-specific computational decision support for clinical genome interpretation
N Whiffin, R Walsh, R Govind, M Edwards, M Ahmad, X Zhang, U Tayal, ...
Genetics in Medicine 20 (10), 1246-1254, 2018
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies
F Mazzarotto, MH Hawley, M Beltrami, L Beekman, A De Marvao, ...
Genetics in Medicine 23 (5), 856-864, 2021
The system can't perform the operation now. Try again later.
Articles 1–20