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Page 1
The Open Science of Atrial Fibrillation.
Keavney BD, McGurk KA. Keavney BD, et al. 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. Among authors: keavney bd. Sci Rep. 2020 Sep 1;10(1):14356. doi: 10.1038/s41598-020-71354-7. Sci Rep. 2020. PMID: 32873833 Free PMC article.
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. Among authors: keavney bd. Bioinformatics. 2020 Apr 1;36(7):2217-2223. doi: 10.1093/bioinformatics/btz898. Bioinformatics. 2020. PMID: 31790148 Free PMC article.
Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes.
Córdova-Palomera A, Tcheandjieu C, Fries JA, Varma P, Chen VS, Fiterau M, Xiao K, Tejeda H, Keavney BD, Cordell HJ, Tanigawa Y, Venkataraman G, Rivas MA, Ré C, Ashley E, Priest JR. Córdova-Palomera A, et al. Among authors: keavney bd. Circ Genom Precis Med. 2020 Dec;13(6):e003014. doi: 10.1161/CIRCGEN.120.003014. Epub 2020 Oct 30. Circ Genom Precis Med. 2020. PMID: 33125279 Free article.
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams SG, Keavney BD, Thiruvahindrapuram B, Scherer SW, Bassett AS. Reuter MS, et al. Among authors: keavney bd. Circ Genom Precis Med. 2021 Aug;14(4):e003410. doi: 10.1161/CIRCGEN.121.003410. Epub 2021 Jul 30. Circ Genom Precis Med. 2021. PMID: 34328347 Free PMC article. Clinical Trial.
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, Devriendt K, Gewillig M, Brook JD, Setchfield KJ, Bu'Lock FA, O'Sullivan J, Stuart G, Bezzina CR, Mulder BJM, Postma AV, Bentham JR, Baron M, Bhaskar SS, Black GC, Newman WG, Hentges KE, Lathrop GM, Santibanez-Koref M, Keavney BD. Page DJ, et al. Among authors: keavney bd. Circ Res. 2019 Feb 15;124(4):553-563. doi: 10.1161/CIRCRESAHA.118.313250. Circ Res. 2019. PMID: 30582441 Free PMC article.
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