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Page 1
Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias.
Weng LC, Khurshid S, Hall AW, Nauffal V, Morrill VN, Sun YV, Rämö JT, Beer D, Lee S, Nadkarni G, Johnson R, Andreasen L, Clayton A, Pullinger CR, Yoneda ZT, Friedman DJ, Hyman MC, Judy RL, Skanes AC, Orland KM, Jordà P, Treu TM, Oetjens MT, Subbiah R, Hartmann JP, May HT, Kane JP, Issa TZ, Nafissi NA, Leong-Sit P, Dubé MP, Roselli C, Choi SH; FinnGen, Million Veteran Program, Regeneron Genetics Center; Tardif JC, Khan HR, Knight S, Svendsen JH, Walker B, Karlsson Linnér R, Gaziano JM, Tadros R, Fatkin D, Rader DJ, Shah SH, Roden DM, Marcus GM, Loos RJF, Damrauer SM, Haggerty CM, Cho K, Palotie A, Olesen MS, Eckhardt LL, Roberts JD, Cutler MJ, Shoemaker MB, Wilson PWF, Ellinor PT, Lubitz SA. Weng LC, et al. Among authors: eckhardt ll. Circ Genom Precis Med. 2024 Jun;17(3):e004320. doi: 10.1161/CIRCGEN.123.004320. Epub 2024 May 28. Circ Genom Precis Med. 2024. PMID: 38804128
Progress toward the prevention and treatment of atrial fibrillation: A summary of the Heart Rhythm Society Research Forum on the Treatment and Prevention of Atrial Fibrillation, Washington, DC, December 9-10, 2013.
Van Wagoner DR, Piccini JP, Albert CM, Anderson ME, Benjamin EJ, Brundel B, Califf RM, Calkins H, Chen PS, Chiamvimonvat N, Darbar D, Eckhardt LL, Ellinor PT, Exner DV, Fogel RI, Gillis AM, Healey J, Hohnloser SH, Kamel H, Lathrop DA, Lip GY, Mehra R, Narayan SM, Olgin J, Packer D, Peters NS, Roden DM, Ross HM, Sheldon R, Wehrens XH. Van Wagoner DR, et al. Among authors: eckhardt ll. Heart Rhythm. 2015 Jan;12(1):e5-e29. doi: 10.1016/j.hrthm.2014.11.011. Epub 2014 Nov 18. Heart Rhythm. 2015. PMID: 25460864 Free PMC article. No abstract available.
Flecainide treats a novel KCNJ2 mutation associated with Andersen-Tawil syndrome.
Van Ert HA, McCune EC, Orland KM, Maginot KR, Von Bergen NH, January CT, Eckhardt LL. Van Ert HA, et al. Among authors: eckhardt ll. HeartRhythm Case Rep. 2016 Dec 9;3(2):151-154. doi: 10.1016/j.hrcr.2016.11.009. eCollection 2017 Feb. HeartRhythm Case Rep. 2016. PMID: 28491792 Free PMC article. No abstract available.
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia.
Ng K, Titus EW, Lieve KV, Roston TM, Mazzanti A, Deiter FH, Denjoy I, Ingles J, Till J, Robyns T, Connors SP, Steinberg C, Abrams DJ, Pang B, Scheinman MM, Bos JM, Duffett SA, van der Werf C, Maltret A, Green MS, Rutberg J, Balaji S, Cadrin-Tourigny J, Orland KM, Knight LM, Brateng C, Wu J, Tang AS, Skanes AC, Manlucu J, Healey JS, January CT, Krahn AD, Collins KK, Maginot KR, Fischbach P, Etheridge SP, Eckhardt LL, Hamilton RM, Ackerman MJ, Noguer FRI, Semsarian C, Jura N, Leenhardt A, Gollob MH, Priori SG, Sanatani S, Wilde AAM, Deo RC, Roberts JD. Ng K, et al. Among authors: eckhardt ll. Circulation. 2020 Sep 8;142(10):932-947. doi: 10.1161/CIRCULATIONAHA.120.045723. Epub 2020 Jul 22. Circulation. 2020. PMID: 32693635 Free PMC article. Clinical Trial.
Long QT Syndrome KCNH2 Variant Induces hERG1a/1b Subunit Imbalance in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes.
Feng L, Zhang J, Lee C, Kim G, Liu F, Petersen AJ, Lim E, Anderson CL, Orland KM, Robertson GA, Eckhardt LL, January CT, Kamp TJ. Feng L, et al. Among authors: eckhardt ll. Circ Arrhythm Electrophysiol. 2021 Apr;14(4):e009343. doi: 10.1161/CIRCEP.120.009343. Epub 2021 Mar 17. Circ Arrhythm Electrophysiol. 2021. PMID: 33729832 Free PMC article.
Management of Congenital Long-QT Syndrome: Commentary From the Experts.
Kaufman ES, Eckhardt LL, Ackerman MJ, Aziz PF, Behr ER, Cerrone M, Chung MK, Cutler MJ, Etheridge SP, Krahn AD, Lubitz SA, Perez MV, Priori SG, Roberts JD, Roden DM, Schulze-Bahr E, Schwartz PJ, Shimizu W, Shoemaker MB, Sy RW, Towbin JA, Viskin S, A M Wilde A, Zareba W. Kaufman ES, et al. Among authors: eckhardt ll. Circ Arrhythm Electrophysiol. 2021 Jul;14(7):e009726. doi: 10.1161/CIRCEP.120.009726. Epub 2021 Jul 9. Circ Arrhythm Electrophysiol. 2021. PMID: 34238011 Free PMC article. Review.
Clinical and Functional Characterization of Ryanodine Receptor 2 Variants Implicated in Calcium-Release Deficiency Syndrome.
Roston TM, Wei J, Guo W, Li Y, Zhong X, Wang R, Estillore JP, Peltenburg PJ, Noguer FRI, Till J, Eckhardt LL, Orland KM, Hamilton R, LaPage MJ, Krahn AD, Tadros R, Vinocur JM, Kallas D, Franciosi S, Roberts JD, Wilde AAM, Jensen HK, Sanatani S, Chen SRW. Roston TM, et al. Among authors: eckhardt ll. JAMA Cardiol. 2022 Jan 1;7(1):84-92. doi: 10.1001/jamacardio.2021.4458. JAMA Cardiol. 2022. PMID: 34730774 Free PMC article.
Elucidation of ALG10B as a Novel Long-QT Syndrome-Susceptibility Gene.
Zhou W, Ye D, Tester DJ, Bains S, Giudicessi JR, Haglund-Turnquist CM, Orland KM, January CT, Eckhardt LL, Maginot KR, Ackerman MJ. Zhou W, et al. Among authors: eckhardt ll. Circ Genom Precis Med. 2023 Apr;16(2):e003726. doi: 10.1161/CIRCGEN.122.003726. Epub 2023 Feb 22. Circ Genom Precis Med. 2023. PMID: 37071726 Free PMC article.
Clinical Management of Brugada Syndrome: Commentary From the Experts.
Cutler MJ, Eckhardt LL, Kaufman ES, Arbelo E, Behr ER, Brugada P, Cerrone M, Crotti L, deAsmundis C, Gollob MH, Horie M, Huang DT, Krahn AD, London B, Lubitz SA, Mackall JA, Nademanee K, Perez MV, Probst V, Roden DM, Sacher F, Sarquella-Brugada G, Scheinman MM, Shimizu W, Shoemaker B, Sy RW, Watanabe A, Wilde AAM. Cutler MJ, et al. Among authors: eckhardt ll. Circ Arrhythm Electrophysiol. 2024 Jan;17(1):e012072. doi: 10.1161/CIRCEP.123.012072. Epub 2023 Dec 15. Circ Arrhythm Electrophysiol. 2024. PMID: 38099441 Review.
66 results