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Prediction of mortality from 12-lead electrocardiogram voltage data using a deep neural network.
Raghunath S, Ulloa Cerna AE, Jing L, vanMaanen DP, Stough J, Hartzel DN, Leader JB, Kirchner HL, Stumpe MC, Hafez A, Nemani A, Carbonati T, Johnson KW, Young K, Good CW, Pfeifer JM, Patel AA, Delisle BP, Alsaid A, Beer D, Haggerty CM, Fornwalt BK. Raghunath S, et al. Among authors: delisle bp. Nat Med. 2020 Jun;26(6):886-891. doi: 10.1038/s41591-020-0870-z. Epub 2020 May 11. Nat Med. 2020. PMID: 32393799
Feeding Behavior Modifies the Circadian Variation in RR and QT intervals by Distinct Mechanisms in Mice.
Ono M, Burgess DE, Johnson SR, Elayi CS, Esser KA, Seward TS, Boychuk CR, Carreño AP, Stalcup RA, Prabhat A, Schroder EA, Delisle BP. Ono M, et al. Among authors: delisle bp. bioRxiv [Preprint]. 2024 Apr 20:2023.11.02.565372. doi: 10.1101/2023.11.02.565372. bioRxiv. 2024. Update in: Am J Physiol Regul Integr Comp Physiol. 2024 Jul 1;327(1):R109-R121. doi: 10.1152/ajpregu.00025.2024 PMID: 37961515 Free PMC article. Updated. Preprint.
New role for cardiomyocyte Bmal1 in the regulation of sex-specific heart transcriptomes.
Zhang X, Procopio SB, Ding H, Semel MG, Schroder EA, Seward TS, Du P, Wu K, Johnson SR, Prabhat A, Schneider DJ, Stumpf IG, Rozmus ER, Huo Z, Delisle BP, Esser KA. Zhang X, et al. Among authors: delisle bp. bioRxiv [Preprint]. 2024 Apr 21:2024.04.18.590181. doi: 10.1101/2024.04.18.590181. bioRxiv. 2024. PMID: 38659967 Free PMC article. Preprint.
Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Haggerty CM, James CA, Calkins H, Tichnell C, Leader JB, Hartzel DN, Nevius CD, Pendergrass SA, Person TN, Schwartz M, Ritchie MD, Carey DJ, Ledbetter DH, Williams MS, Dewey FE, Lopez A, Penn J, Overton JD, Reid JG, Lebo M, Mason-Suares H, Austin-Tse C, Rehm HL, Delisle BP, Makowski DJ, Mehra VC, Murray MF, Fornwalt BK. Haggerty CM, et al. Among authors: delisle bp. Genet Med. 2017 Nov;19(11):1245-1252. doi: 10.1038/gim.2017.40. Epub 2017 May 4. Genet Med. 2017. PMID: 28471438 Free PMC article.
Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the KCNH2-Encoded Kv11.1 Channel.
Smith JL, Tester DJ, Hall AR, Burgess DE, Hsu CC, Elayi SC, Anderson CL, January CT, Luo JZ, Hartzel DN, Mirshahi UL, Murray MF, Mirshahi T, Ackerman MJ, Delisle BP. Smith JL, et al. Among authors: delisle bp. Circ Arrhythm Electrophysiol. 2018 May;11(5):e005859. doi: 10.1161/CIRCEP.117.005859. Circ Arrhythm Electrophysiol. 2018. PMID: 29752375 Free PMC article.
88 results