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Assessing the association between genetic and phenotypic features of dilated cardiomyopathy and outcome in patients with coronary artery disease.
Jones RE, Hammersley DJ, Zheng S, McGurk KA, de Marvao A, Theotokis PI, Owen R, Tayal U, Rea G, Hatipoglu S, Buchan RJ, Mach L, Curran L, Lota AS, Simard F, Reddy RK, Talukder S, Yoon WY, Vazir A, Pennell DJ, O'Regan DP, Baksi AJ, Halliday BP, Ware JS, Prasad SK. Jones RE, et al. Among authors: mcgurk ka. Eur J Heart Fail. 2024 Jan;26(1):46-55. doi: 10.1002/ejhf.3033. Epub 2023 Oct 5. Eur J Heart Fail. 2024. PMID: 37702310
The use of missing values in proteomic data-independent acquisition mass spectrometry to enable disease activity discrimination.
McGurk KA, Dagliati A, Chiasserini D, Lee D, Plant D, Baricevic-Jones I, Kelsall J, Eineman R, Reed R, Geary B, Unwin RD, Nicolaou A, Keavney BD, Barton A, Whetton AD, Geifman N. McGurk KA, et al. Bioinformatics. 2020 Apr 1;36(7):2217-2223. doi: 10.1093/bioinformatics/btz898. Bioinformatics. 2020. PMID: 31790148 Free PMC article.
The Open Science of Atrial Fibrillation.
Keavney BD, McGurk KA. Keavney BD, et al. Among authors: mcgurk ka. Circ Res. 2020 Jan 17;126(2):210-211. doi: 10.1161/CIRCRESAHA.119.316357. Epub 2020 Jan 16. Circ Res. 2020. PMID: 31944917 No abstract available.
Heritability of haemodynamics in the ascending aorta.
McGurk KA, Owen B, Watson WD, Nethononda RM, Cordell HJ, Farrall M, Rider OJ, Watkins H, Revell A, Keavney BD. McGurk KA, et al. Sci Rep. 2020 Sep 1;10(1):14356. doi: 10.1038/s41598-020-71354-7. Sci Rep. 2020. PMID: 32873833 Free PMC article.
Genotype-Phenotype Taxonomy of Hypertrophic Cardiomyopathy.
Curran L, de Marvao A, Inglese P, McGurk KA, Schiratti PR, Clement A, Zheng SL, Li S, Pua CJ, Shah M, Jafari M, Theotokis P, Buchan RJ, Jurgens SJ, Raphael CE, Baksi AJ, Pantazis A, Halliday BP, Pennell DJ, Bai W, Chin CWL, Tadros R, Bezzina CR, Watkins H, Cook SA, Prasad SK, Ware JS, O'Regan DP. Curran L, et al. Among authors: mcgurk ka. Circ Genom Precis Med. 2023 Dec;16(6):e004200. doi: 10.1161/CIRCGEN.123.004200. Epub 2023 Nov 28. Circ Genom Precis Med. 2023. PMID: 38014537 Free PMC article.
The penetrance of rare variants in cardiomyopathy-associated genes: A cross-sectional approach to estimating penetrance for secondary findings.
McGurk KA, Zhang X, Theotokis P, Thomson K, Harper A, Buchan RJ, Mazaika E, Ormondroyd E, Wright WT, Macaya D, Pua CJ, Funke B, MacArthur DG, Prasad SK, Cook SA, Allouba M, Aguib Y, Yacoub MH, O'Regan DP, Barton PJR, Watkins H, Bottolo L, Ware JS. McGurk KA, et al. Am J Hum Genet. 2023 Sep 7;110(9):1482-1495. doi: 10.1016/j.ajhg.2023.08.003. Epub 2023 Aug 30. Am J Hum Genet. 2023. PMID: 37652022 Free PMC article.
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