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Page 1
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data sets.
Butters A, Thomson K, Harrington F, Henden N, McGuire K, Byrne AB, Bryen S, McGurk KA, Leask M, Ackerman MJ, Atherton J, Bos JM, Caleshu C, Day SM, Dunn K, Hayes I, Juang J, McGaughran J, Nowak N, Parikh VN, Ronan A, Semsarian C, Tardiff JC, Tiemensma M, Merriman TR, Ware JS, Skinner JR, MacArthur DG, Siggs OM, Bagnall RD, Ingles J. Butters A, et al. Among authors: mcgurk ka. Eur Heart J. 2025 Mar 5:ehaf001. doi: 10.1093/eurheartj/ehaf001. Online ahead of print. Eur Heart J. 2025. PMID: 40038847 No abstract available.
Artificial intelligence-enhanced electrocardiography for the identification of a sex-related cardiovascular risk continuum: a retrospective cohort study.
Sau A, Sieliwonczyk E, Patlatzoglou K, Pastika L, McGurk KA, Ribeiro AH, Ribeiro ALP, Ho JE, Peters NS, Ware JS, Tayal U, Kramer DB, Waks JW, Ng FS. Sau A, et al. Among authors: mcgurk ka. Lancet Digit Health. 2025 Mar;7(3):e184-e194. doi: 10.1016/j.landig.2024.12.003. Lancet Digit Health. 2025. PMID: 40015763 Free article.
Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy.
Tadros R, Zheng SL, Grace C, Jordà P, Francis C, West DM, Jurgens SJ, Thomson KL, Harper AR, Ormondroyd E, Xu X, Theotokis PI, Buchan RJ, McGurk KA, Mazzarotto F, Boschi B, Pelo E, Lee M, Noseda M, Varnava A, Vermeer AMC, Walsh R, Amin AS, van Slegtenhorst MA, Roslin NM, Strug LJ, Salvi E, Lanzani C, de Marvao A; Hypergenes InterOmics Collaborators; Roberts JD, Tremblay-Gravel M, Giraldeau G, Cadrin-Tourigny J, L'Allier PL, Garceau P, Talajic M, Gagliano Taliun SA, Pinto YM, Rakowski H, Pantazis A, Bai W, Baksi J, Halliday BP, Prasad SK, Barton PJR, O'Regan DP, Cook SA, de Boer RA, Christiaans I, Michels M, Kramer CM, Ho CY, Neubauer S; HCMR Investigators; Matthews PM, Wilde AAM, Tardif JC, Olivotto I, Adler A, Goel A, Ware JS, Bezzina CR, Watkins H. Tadros R, et al. Among authors: mcgurk ka. Nat Genet. 2025 Mar;57(3):530-538. doi: 10.1038/s41588-025-02087-4. Epub 2025 Feb 18. Nat Genet. 2025. PMID: 39966646 Free PMC article.
Evaluation of polygenic scores for hypertrophic cardiomyopathy in the general population and across clinical settings.
Zheng SL, Jurgens SJ, McGurk KA, Xu X, Grace C, Theotokis PI, Buchan RJ, Francis C, de Marvao A, Curran L, Bai W, Pua CJ, Tang HC, Jorda P, van Slegtenhorst MA, Verhagen JMA, Harper AR, Ormondroyd E, Chin CWL; HCM GWAS Collaborators; Pantazis A, Baksi J, Halliday BP, Matthews P, Pinto YM, Walsh R, Amin AS, Wilde AAM, Cook SA, Prasad SK, Barton PJR, O'Regan DP, Lumbers RT, Goel A, Tadros R, Michels M, Watkins H, Bezzina CR, Ware JS. Zheng SL, et al. Among authors: mcgurk ka. Nat Genet. 2025 Mar;57(3):563-571. doi: 10.1038/s41588-025-02094-5. Epub 2025 Feb 18. Nat Genet. 2025. PMID: 39966645 Free PMC article.
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy.
Zheng SL, Henry A, Cannie D, Lee M, Miller D, McGurk KA, Bond I, Xu X, Issa H, Francis C, De Marvao A, Theotokis PI, Buchan RJ, Speed D, Abner E, Adams L, Aragam KG, Ärnlöv J, Raja AA, Backman JD, Baksi J, Barton PJR, Biddinger KJ, Boersma E, Brandimarto J, Brunak S, Bundgaard H, Carey DJ, Charron P, Cook JP, Cook SA, Denaxas S, Deleuze JF, Doney AS, Elliott P, Erikstrup C, Esko T, Farber-Eger EH, Finan C, Garnier S, Ghouse J, Giedraitis V, Guðbjartsson DF, Haggerty CM, Halliday BP, Helgadottir A, Hemingway H, Hillege HL, Kardys I, Lind L, Lindgren CM, Lowery BD, Manisty C, Margulies KB, Moon JC, Mordi IR, Morley MP, Morris AD, Morris AP, Morton L, Noursadeghi M, Ostrowski SR, Owens AT, Palmer CNA, Pantazis A, Pedersen OBV, Prasad SK, Shekhar A, Smelser DT, Srinivasan S, Stefansson K, Sveinbjörnsson G, Syrris P, Tammesoo ML, Tayal U, Teder-Laving M, Thorgeirsson G, Thorsteinsdottir U, Tragante V, Trégouët DA, Treibel TA, Ullum H, Valdes AM, van Setten J, van Vugt M, Veluchamy A, Verschuren WMM, Villard E, Yang Y; COVIDsortium; DBDS Genomic Consortium; Estonian Biobank Research Team; HERMES Consortium; Asselbergs FW, Cappola TP, Dube MP, Dunn ME, Ellinor PT, Hingorani AD, La… See abstract for full author list ➔ Zheng SL, et al. Among authors: mcgurk ka. Nat Genet. 2024 Dec;56(12):2646-2658. doi: 10.1038/s41588-024-01952-y. Epub 2024 Nov 21. Nat Genet. 2024. PMID: 39572783 Free PMC article.
Genetic and phenotypic architecture of human myocardial trabeculation.
McGurk KA, Qiao M, Zheng SL, Sau A, Henry A, Ribeiro ALP, Ribeiro AH, Ng FS, Lumbers RT, Bai W, Ware JS, O'Regan DP. McGurk KA, et al. Nat Cardiovasc Res. 2024 Dec;3(12):1503-1515. doi: 10.1038/s44161-024-00564-3. Epub 2024 Nov 20. Nat Cardiovasc Res. 2024. PMID: 39567769 Free PMC article.
Prognostic Significance and Associations of Neural Network-Derived Electrocardiographic Features.
Sau A, Ribeiro AH, McGurk KA, Pastika L, Bajaj N, Gurnani M, Sieliwonczyk E, Patlatzoglou K, Ardissino M, Chen JY, Wu H, Shi X, Hnatkova K, Zheng SL, Britton A, Shipley M, Andršová I, Novotný T, Sabino EC, Giatti L, Barreto SM, Waks JW, Kramer DB, Mandic D, Peters NS, O'Regan DP, Malik M, Ware JS, Ribeiro ALP, Ng FS. Sau A, et al. Among authors: mcgurk ka. Circ Cardiovasc Qual Outcomes. 2024 Dec;17(12):e010602. doi: 10.1161/CIRCOUTCOMES.123.010602. Epub 2024 Nov 14. Circ Cardiovasc Qual Outcomes. 2024. PMID: 39540287 Free PMC article.
38 results