362 related articles for article (PubMed ID: 24561134)
1. Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome.
Weeke P; Mosley JD; Hanna D; Delaney JT; Shaffer C; Wells QS; Van Driest S; Karnes JH; Ingram C; Guo Y; Shyr Y; Norris K; Kannankeril PJ; Ramirez AH; Smith JD; Mardis ER; Nickerson D; George AL; Roden DM
J Am Coll Cardiol; 2014 Apr; 63(14):1430-7. PubMed ID: 24561134
[TBL] [Abstract][Full Text] [Related]
2. A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.
Kääb S; Crawford DC; Sinner MF; Behr ER; Kannankeril PJ; Wilde AA; Bezzina CR; Schulze-Bahr E; Guicheney P; Bishopric NH; Myerburg RJ; Schott JJ; Pfeufer A; Beckmann BM; Martens E; Zhang T; Stallmeyer B; Zumhagen S; Denjoy I; Bardai A; Van Gelder IC; Jamshidi Y; Dalageorgou C; Marshall V; Jeffery S; Shakir S; Camm AJ; Steinbeck G; Perz S; Lichtner P; Meitinger T; Peters A; Wichmann HE; Ingram C; Bradford Y; Carter S; Norris K; Ritchie MD; George AL; Roden DM
Circ Cardiovasc Genet; 2012 Feb; 5(1):91-9. PubMed ID: 22100668
[TBL] [Abstract][Full Text] [Related]
3. Novel rare variants in congenital cardiac arrhythmia genes are frequent in drug-induced torsades de pointes.
Ramirez AH; Shaffer CM; Delaney JT; Sexton DP; Levy SE; Rieder MJ; Nickerson DA; George AL; Roden DM
Pharmacogenomics J; 2013 Aug; 13(4):325-9. PubMed ID: 22584458
[TBL] [Abstract][Full Text] [Related]
4. Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.
Yang P; Kanki H; Drolet B; Yang T; Wei J; Viswanathan PC; Hohnloser SH; Shimizu W; Schwartz PJ; Stanton M; Murray KT; Norris K; George AL; Roden DM
Circulation; 2002 Apr; 105(16):1943-8. PubMed ID: 11997281
[TBL] [Abstract][Full Text] [Related]
5. The genetics of drug-induced QT prolongation: evaluating the evidence for pharmacodynamic variants.
Lopez-Medina AI; Chahal CAA; Luzum JA
Pharmacogenomics; 2022 Jun; 23(9):543-557. PubMed ID: 35698903
[TBL] [Abstract][Full Text] [Related]
6. Drug-induced long QT syndrome and exome sequencing: Chinese shadows link past and future.
Crotti L; Schwartz PJ
J Am Coll Cardiol; 2014 Apr; 63(14):1438-40. PubMed ID: 24561140
[No Abstract] [Full Text] [Related]
7. Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients.
Paulussen AD; Gilissen RA; Armstrong M; Doevendans PA; Verhasselt P; Smeets HJ; Schulze-Bahr E; Haverkamp W; Breithardt G; Cohen N; Aerssens J
J Mol Med (Berl); 2004 Mar; 82(3):182-8. PubMed ID: 14760488
[TBL] [Abstract][Full Text] [Related]
8. Latent genetic backgrounds and molecular pathogenesis in drug-induced long-QT syndrome.
Itoh H; Sakaguchi T; Ding WG; Watanabe E; Watanabe I; Nishio Y; Makiyama T; Ohno S; Akao M; Higashi Y; Zenda N; Kubota T; Mori C; Okajima K; Haruna T; Miyamoto A; Kawamura M; Ishida K; Nagaoka I; Oka Y; Nakazawa Y; Yao T; Jo H; Sugimoto Y; Ashihara T; Hayashi H; Ito M; Imoto K; Matsuura H; Horie M
Circ Arrhythm Electrophysiol; 2009 Oct; 2(5):511-23. PubMed ID: 19843919
[TBL] [Abstract][Full Text] [Related]
9. Epidemiology of symptomatic drug-induced long QT syndrome and Torsade de Pointes in Germany.
Sarganas G; Garbe E; Klimpel A; Hering RC; Bronder E; Haverkamp W
Europace; 2014 Jan; 16(1):101-8. PubMed ID: 23833046
[TBL] [Abstract][Full Text] [Related]
10. Predicting the Unpredictable: Drug-Induced QT Prolongation and Torsades de Pointes.
Schwartz PJ; Woosley RL
J Am Coll Cardiol; 2016 Apr; 67(13):1639-1650. PubMed ID: 27150690
[TBL] [Abstract][Full Text] [Related]
11. Relationship between genetic variants in myocardial sodium and potassium channel genes and QT interval duration in diabetics: the Diabetes Heart Study.
Lehtinen AB; Daniel KR; Shah SA; Nelson MR; Ziegler JT; Freedman BI; Carr JJ; Herrington DM; Langefeld CD; Bowden DW
Ann Noninvasive Electrocardiol; 2009 Jan; 14(1):72-9. PubMed ID: 19149796
[TBL] [Abstract][Full Text] [Related]
12. [Genetic background predisposing the drug-induced long QT syndrome].
Horie M
Nihon Yakurigaku Zasshi; 2003 Jun; 121(6):401-7. PubMed ID: 12835534
[TBL] [Abstract][Full Text] [Related]
13. [Long-QT caused by drugs and torsade de pointes: a genetic basis?].
Schwartz PJ
Cardiologia; 1999 Dec; 44 Suppl 1(Pt 1):277-9. PubMed ID: 12497921
[No Abstract] [Full Text] [Related]
14. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
Vincent GM
Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
[TBL] [Abstract][Full Text] [Related]
15. Hypokalemia-induced long QT syndrome with an underlying novel missense mutation in S4-S5 linker of KCNQ1.
Kubota T; Shimizu W; Kamakura S; Horie M
J Cardiovasc Electrophysiol; 2000 Sep; 11(9):1048-54. PubMed ID: 11021476
[TBL] [Abstract][Full Text] [Related]
16. Molecular predictors of drug-induced prolongation of the QT interval.
Dilaveris PE
Curr Med Chem Cardiovasc Hematol Agents; 2005 Apr; 3(2):105-18. PubMed ID: 15853698
[TBL] [Abstract][Full Text] [Related]
17. Drug-induced QT-interval prolongation and recurrent torsade de pointes in a child with heterotaxy syndrome and KCNE1 D85N polymorphism.
Lin L; Horigome H; Nishigami N; Ohno S; Horie M; Sumazaki R
J Electrocardiol; 2012; 45(6):770-3. PubMed ID: 22999324
[TBL] [Abstract][Full Text] [Related]
18. Genetics of acquired long QT syndrome.
Roden DM; Viswanathan PC
J Clin Invest; 2005 Aug; 115(8):2025-32. PubMed ID: 16075043
[TBL] [Abstract][Full Text] [Related]
19. [KCNQ1, KCNH2, KCNE1 and KCNE2 potassium channels gene variants in sudden manhood death syndrome].
Zhao QH; Liu C; Lu LW; Lü GL; Liu H; Tang SB; Quan L; Cheng JD
Fa Yi Xue Za Zhi; 2012 Oct; 28(5):337-41, 346. PubMed ID: 23213782
[TBL] [Abstract][Full Text] [Related]
20. Atrioventricular block-induced Torsades de Pointes with clinical and molecular backgrounds similar to congenital long QT syndrome.
Oka Y; Itoh H; Ding WG; Shimizu W; Makiyama T; Ohno S; Nishio Y; Sakaguchi T; Miyamoto A; Kawamura M; Matsuura H; Horie M
Circ J; 2010 Nov; 74(12):2562-71. PubMed ID: 20975234
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]