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Paul J Barton
Paul J Barton
Verified email at imperial.ac.uk - Homepage
Title
Cited by
Cited by
Year
Truncations of titin causing dilated cardiomyopathy
DS Herman, L Lam, MRG Taylor, L Wang, P Teekakirikul, ...
New England Journal of Medicine 366 (7), 619-628, 2012
14212012
Alterations in sarcoplasmic reticulum gene expression in human heart failure. A possible mechanism for alterations in systolic and diastolic properties of the failing myocardium.
M Arai, NR Alpert, DH MacLennan, P Barton, M Periasamy
Circulation research 72 (2), 463-469, 1993
6311993
Developmental regulation of myosin gene expression in mouse cardiac muscle.
GE Lyons, S Schiaffino, D Sassoon, P Barton, M Buckingham
The Journal of cell biology 111 (6), 2427-2436, 1990
4981990
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
4442015
The translational landscape of the human heart
S van Heesch, F Witte, V Schneider-Lunitz, JF Schulz, E Adami, AB Faber, ...
Cell 178 (1), 242-260. e29, 2019
4412019
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
4132017
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy
E Villard, C Perret, F Gary, C Proust, G Dilanian, C Hengstenberg, ...
European heart journal 32 (9), 1065-1076, 2011
3672011
Troponin I gene expression during human cardiac development and in end-stage heart failure.
S Sasse, NJ Brand, P Kyprianou, GK Dhoot, R Wade, M Arai, ...
Circulation research 72 (5), 932-938, 1993
3211993
Localization of human immunoglobulin kappa light chain variable region genes to the short arm of chromosome 2 by in situ hybridization.
S Malcolm, P Barton, C Murphy, MA Ferguson-Smith, DL Bentley, ...
Proceedings of the National Academy of Sciences 79 (16), 4957-4961, 1982
3111982
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
2892017
Hyperubiquitination of proteins in dilated cardiomyopathy
J Weekes, K Morrison, A Mullen, R Wait, P Barton, MJ Dunn
Proteomics 3 (2), 208-216, 2003
2672003
Molecular cloning of human cardiac troponin I using polymerase chain reaction
WJ Vallins, NJ Brand, N Dabhade, G Butler-Browne, MH Yacoub, ...
FEBS letters 270 (1-2), 57-61, 1990
2551990
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
2372019
The myosin alkali light chain proteins and their genes.
PJ Barton, ME Buckingham
Biochemical Journal 231 (2), 249, 1985
2371985
Direct intramyocardial but not intracoronary injection of bone marrow cells induces ventricular arrhythmias in a rat chronic ischemic heart failure model
S Fukushima, A Varela-Carver, SR Coppen, K Yamahara, LE Felkin, ...
Circulation 115 (17), 2254-2261, 2007
2352007
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
2342018
A conserved family of genes related to the testis determining gene, SRY.
P Denny, S Swift, N Brand, N Dabhade, P Barton, A Ashworth
Nucleic Acids Research 20 (11), 2887, 1992
2131992
RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing
H Maatz, M Jens, M Liss, S Schafer, M Heinig, M Kirchner, E Adami, ...
The Journal of clinical investigation 124 (8), 3419-3430, 2014
2112014
Expression of homeobox genes Msx‐1 (Hox‐7) and Msx‐2 (Hox‐8) during cardiac development in the chick
PS Chan‐Thomas, RP Thompson, B Robert, MH Yacoub, PJR Barton
Developmental dynamics 197 (3), 203-216, 1993
2091993
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
AK Arndt, S Schafer, JD Drenckhahn, MK Sabeh, ER Plovie, A Caliebe, ...
The American Journal of Human Genetics 93 (1), 67-77, 2013
2012013
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