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366 results

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Page 1
Unsupervised deep learning of electrocardiograms enables scalable human disease profiling.
Friedman SF, Khurshid S, Venn RA, Wang X, Diamant N, Di Achille P, Weng LC, Choi SH, Reeder C, Pirruccello JP, Singh P, Lau ES, Philippakis A, Anderson CD, Maddah M, Batra P, Ellinor PT, Ho JE, Lubitz SA. Friedman SF, et al. Among authors: lubitz sa. NPJ Digit Med. 2025 Jan 12;8(1):23. doi: 10.1038/s41746-024-01418-9. NPJ Digit Med. 2025. PMID: 39799251 Free PMC article.
The impact of common and rare genetic variants on bradyarrhythmia development.
Weng LC, Rämö JT, Jurgens SJ, Khurshid S, Chaffin M, Hall AW, Morrill VN, Wang X, Nauffal V, Sun YV, Beer D, Lee S, Nadkarni GN, Duong T, Wang B, Czuba T, Austin TR, Yoneda ZT, Friedman DJ, Clayton A, Hyman MC, Judy RL, Skanes AC, Orland KM, Treu TM, Oetjens MT, Alonso A, Soliman EZ, Lin H, Lunetta KL, van der Pals J, Issa TZ, Nafissi NA, May HT, Leong-Sit P, Roselli C, Choi SH; FinnGen; Million Veteran Program; Regeneron Genetics Center; Khan HR, Knight S, Karlsson Linnér R, Bezzina CR, Ripatti S, Heckbert SR, Gaziano JM, Loos RJF, Psaty BM, Smith JG, Benjamin EJ, Arking DE, Rader DJ, Shah SH, Roden DM, Damrauer SM, Eckhardt LL, Roberts JD, Cutler MJ, Shoemaker MB, Haggerty CM, Cho K, Palotie A, Wilson PWF, Ellinor PT, Lubitz SA. Weng LC, et al. Among authors: lubitz sa. Nat Genet. 2025 Jan 2. doi: 10.1038/s41588-024-01978-2. Online ahead of print. Nat Genet. 2025. PMID: 39747593
Natural Language Processing to Adjudicate Heart Failure Hospitalizations in Global Clinical Trials.
Marti-Castellote PM, Reeder C, Claggett BL, Singh P, Lau ES, Khurshid S, Batra P, Lubitz SA, Maddah M, Vardeny O, Lewis EF, Pfeffer MA, Jhund PS, Desai AS, McMurray JJV, Ellinor PT, Ho JE, Solomon SD, Cunningham JW. Marti-Castellote PM, et al. Among authors: lubitz sa. Circ Heart Fail. 2024 Nov 16. doi: 10.1161/CIRCHEARTFAILURE.124.012514. Online ahead of print. Circ Heart Fail. 2024. PMID: 39549261 Free article.
Clinical Characteristics and Outcomes in Patients With Atrial Fibrillation and Pathogenic TTN Variants.
Virk ZM, El-Harasis MA, Yoneda ZT, Anderson KC, Sun L, Quintana JA, Murphy BS, Laws JL, Davogustto GE, O'Neill MJ, Varghese BT, Crawford DM, Williams HL, Shabani M, Pelphrey CJ, Grauherr DD, Tomasek K, Su YR, Lancaster MC, Wells QS, Dendy JM, Saavedra P, Estrada JC, Richardson TD, Shen ST, Kanagasundram AN, Montgomery JA, Ellis CR, Crossley GH, Tandri H, Kannankeril PJ, Lubitz SA, Stevenson WG, Ye F, Ellinor PT, Stevenson LW, Roden DM, Shoemaker MB. Virk ZM, et al. Among authors: lubitz sa. JACC Clin Electrophysiol. 2024 Nov;10(11):2445-2457. doi: 10.1016/j.jacep.2024.07.029. Epub 2024 Oct 23. JACC Clin Electrophysiol. 2024. PMID: 39453294 Free article.
Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height.
Hawkes G, Beaumont RN, Li Z, Mandla R, Li X, Albert CM, Arnett DK, Ashley-Koch AE, Ashrani AA, Barnes KC, Boerwinkle E, Brody JA, Carson AP, Chami N, Chen YI, Chung MK, Curran JE, Darbar D, Ellinor PT, Fornage M, Gordeuk VR, Guo X, He J, Hwu CM, Kalyani RR, Kaplan R, Kardia SLR, Kooperberg C, Loos RJF, Lubitz SA, Minster RL, Naseri T, Viali S, Mitchell BD, Murabito JM, Palmer ND, Psaty BM, Redline S, Shoemaker MB, Silverman EK, Telen MJ, Weiss ST, Yanek LR, Zhou H; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Liu CT, North KE, Justice AE, Locke JM, Owens N, Murray A, Patel K, Frayling TM, Wright CF, Wood AR, Lin X, Manning A, Weedon MN. Hawkes G, et al. Among authors: lubitz sa. Nat Commun. 2024 Oct 3;15(1):8549. doi: 10.1038/s41467-024-52579-w. Nat Commun. 2024. PMID: 39362880 Free PMC article.
Atrial Fibrillation Burden on a 14-Day ECG Monitor: Findings From the GUARD-AF Trial Screening Arm.
Singer DE, Atlas SJ, Go AS, Lubitz SA, McManus DD, Dolor RJ, Chatterjee R, Rothberg MB, Rushlow DR, Crosson LA, Aronson RS, Mills D, Patlakh M, Gallup D, O'Brien EC, Lopes RD. Singer DE, et al. Among authors: lubitz sa. JACC Clin Electrophysiol. 2024 Sep 1:S2405-500X(24)00756-4. doi: 10.1016/j.jacep.2024.08.010. Online ahead of print. JACC Clin Electrophysiol. 2024. PMID: 39297839 Free article.
Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes.
El-Harasis MA, Yoneda ZT, Anderson KC, Ye F, Quintana JA, Martinez-Parachini JR, Jackson GG, Varghese BT, Crawford DM, Sun L, Williams HL, O'Neill MJ, Davogustto GE, Laws JL, Murphy BS, Tomasek K, Su YR, McQuillen E, Metz E, Smith C, Stubbs D, Grauherr DD, Wells QS, Michaud GF, Saavedra P, Carlos Estrada J, Richardson TD, Shen ST, Kanagasundram AN, Montgomery JA, Tandri H, Ellis CR, Crossley GH, Kannankeril PJ, Stevenson LW, Stevenson WG, Lubitz SA, Ellinor PT, Roden DM, Shoemaker MB. El-Harasis MA, et al. Among authors: lubitz sa. JACC Clin Electrophysiol. 2024 Nov;10(11):2359-2370. doi: 10.1016/j.jacep.2024.06.035. Epub 2024 Sep 4. JACC Clin Electrophysiol. 2024. PMID: 39243256 Free article.
Effect of Screening for Undiagnosed Atrial Fibrillation on Stroke Prevention.
Lopes RD, Atlas SJ, Go AS, Lubitz SA, McManus DD, Dolor RJ, Chatterjee R, Rothberg MB, Rushlow DR, Crosson LA, Aronson RS, Patlakh M, Gallup D, Mills DJ, O'Brien EC, Singer DE. Lopes RD, et al. Among authors: lubitz sa. J Am Coll Cardiol. 2024 Nov 19;84(21):2073-2084. doi: 10.1016/j.jacc.2024.08.019. Epub 2024 Sep 1. J Am Coll Cardiol. 2024. PMID: 39230544 Clinical Trial.
Rare coding variant analysis for human diseases across biobanks and ancestries.
Jurgens SJ, Wang X, Choi SH, Weng LC, Koyama S, Pirruccello JP, Nguyen T, Smadbeck P, Jang D, Chaffin M, Walsh R, Roselli C, Elliott AL, Wijdeveld LFJM, Biddinger KJ, Kany S, Rämö JT, Natarajan P, Aragam KG, Flannick J, Burtt NP, Bezzina CR, Lubitz SA, Lunetta KL, Ellinor PT. Jurgens SJ, et al. Among authors: lubitz sa. Nat Genet. 2024 Sep;56(9):1811-1820. doi: 10.1038/s41588-024-01894-5. Epub 2024 Aug 29. Nat Genet. 2024. PMID: 39210047
366 results