These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 20400777)

  • 1. Common variants in cardiac ion channel genes are associated with sudden cardiac death.
    Albert CM; MacRae CA; Chasman DI; VanDenburgh M; Buring JE; Manson JE; Cook NR; Newton-Cheh C
    Circ Arrhythm Electrophysiol; 2010 Jun; 3(3):222-9. PubMed ID: 20400777
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cardiac sodium channel gene variants and sudden cardiac death in women.
    Albert CM; Nam EG; Rimm EB; Jin HW; Hajjar RJ; Hunter DJ; MacRae CA; Ellinor PT
    Circulation; 2008 Jan; 117(1):16-23. PubMed ID: 18071069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population.
    Gouas L; Nicaud V; Berthet M; Forhan A; Tiret L; Balkau B; Guicheney P;
    Eur J Hum Genet; 2005 Nov; 13(11):1213-22. PubMed ID: 16132053
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Common variants at ten loci influence QT interval duration in the QTGEN Study.
    Newton-Cheh C; Eijgelsheim M; Rice KM; de Bakker PI; Yin X; Estrada K; Bis JC; Marciante K; Rivadeneira F; Noseworthy PA; Sotoodehnia N; Smith NL; Rotter JI; Kors JA; Witteman JC; Hofman A; Heckbert SR; O'Donnell CJ; Uitterlinden AG; Psaty BM; Lumley T; Larson MG; Stricker BH
    Nat Genet; 2009 Apr; 41(4):399-406. PubMed ID: 19305408
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long QT and Brugada syndrome gene mutations in New Zealand.
    Chung SK; MacCormick JM; McCulley CH; Crawford J; Eddy CA; Mitchell EA; Shelling AN; French JK; Skinner JR; Rees MI
    Heart Rhythm; 2007 Oct; 4(10):1306-14. PubMed ID: 17905336
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Allelic dropout in long QT syndrome genetic testing: a possible mechanism underlying false-negative results.
    Tester DJ; Cronk LB; Carr JL; Schulz V; Salisbury BA; Judson RS; Ackerman MJ
    Heart Rhythm; 2006 Jul; 3(7):815-21. PubMed ID: 16818214
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic variants of potassium voltage-gated channel genes (KCNQ1, KCNH2, and KCNE1) affected the risk of atrial fibrillation in elderly patients.
    Li L; Shen C; Yao Z; Liang J; Huang C
    Genet Test Mol Biomarkers; 2015 Jul; 19(7):359-65. PubMed ID: 26066992
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic mutation in Korean patients of sudden cardiac arrest as a surrogating marker of idiopathic ventricular arrhythmia.
    Son MK; Ki CS; Park SJ; Huh J; Kim JS; On YK
    J Korean Med Sci; 2013 Jul; 28(7):1021-6. PubMed ID: 23853484
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias.
    Bush WS; Crawford DC; Alexander C; George AL; Roden DM; Ritchie MD
    Pharmacogenomics; 2009 Jun; 10(6):1043-53. PubMed ID: 19530973
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C; Zhao Q; Su T; Tang S; Lv G; Liu H; Quan L; Cheng J
    Forensic Sci Int; 2013 Sep; 231(1-3):82-7. PubMed ID: 23890619
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation screening in KCNQ1, HERG, KCNE1, KCNE2 and SCN5A genes in a long QT syndrome family.
    Koo SH; Teo WS; Ching CK; Chan SH; Lee EJ
    Ann Acad Med Singap; 2007 Jun; 36(6):394-8. PubMed ID: 17597962
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Cardiac ion channel gene mutations in sudden infant death syndrome.
    Otagiri T; Kijima K; Osawa M; Ishii K; Makita N; Matoba R; Umetsu K; Hayasaka K
    Pediatr Res; 2008 Nov; 64(5):482-7. PubMed ID: 18596570
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.
    Winkel BG; Larsen MK; Berge KE; Leren TP; Nissen PH; Olesen MS; Hollegaard MV; Jespersen T; Yuan L; Nielsen N; Haunsø S; Svendsen JH; Wang Y; Kristensen IB; Jensen HK; Tfelt-Hansen J; Banner J
    J Cardiovasc Electrophysiol; 2012 Oct; 23(10):1092-8. PubMed ID: 22882672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance.
    Barc J; Briec F; Schmitt S; Kyndt F; Le Cunff M; Baron E; Vieyres C; Sacher F; Redon R; Le Caignec C; Le Marec H; Probst V; Schott JJ
    J Am Coll Cardiol; 2011 Jan; 57(1):40-7. PubMed ID: 21185499
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of ion channel gene variants in patients with long QT syndrome.
    Ernesto C; Cruz FE; Lima FS; Coutinho JL; Silva R; Urményi TP; Carvalho AC; Rondinelli E
    Arq Bras Cardiol; 2011 Mar; 96(3):172-8. PubMed ID: 21308345
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Associations between common ion channel single nucleotide polymorphisms and sudden cardiac death in adults: A MOOSE-compliant meta-analysis.
    Liu X; Shi J; Xiao P
    Medicine (Baltimore); 2018 Sep; 97(38):e12428. PubMed ID: 30235722
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
    Kapplinger JD; Tester DJ; Salisbury BA; Carr JL; Harris-Kerr C; Pollevick GD; Wilde AA; Ackerman MJ
    Heart Rhythm; 2009 Sep; 6(9):1297-303. PubMed ID: 19716085
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D; Shah KR; Um SY; Eng LS; Zhou B; Lin Y; Mitchell AA; Nicaj L; Prinz M; McDonald TV; Sampson BA; Tang Y
    Forensic Sci Int; 2014 Apr; 237():90-9. PubMed ID: 24631775
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.