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Journal Abstract Search

443 related items for PubMed ID: 25691686

  • 1. Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
    Jabbari J, Olesen MS, Yuan L, Nielsen JB, Liang B, Macri V, Christophersen IE, Nielsen N, Sajadieh A, Ellinor PT, Grunnet M, Haunsø S, Holst AG, Svendsen JH, Jespersen T.
    Circ Cardiovasc Genet; 2015 Feb; 8(1):64-73. PubMed ID: 25691686
    [Abstract] [Full Text] [Related]

  • 2. SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation.
    Savio-Galimberti E, Weeke P, Muhammad R, Blair M, Ansari S, Short L, Atack TC, Kor K, Vanoye CG, Olesen MS, LuCamp, Yang T, George AL, Roden DM, Darbar D.
    Cardiovasc Res; 2014 Nov 01; 104(2):355-63. PubMed ID: 25053638
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  • 3. Common SCN10A variants modulate PR interval and heart rate response during atrial fibrillation.
    Delaney JT, Muhammad R, Shi Y, Schildcrout JS, Blair M, Short L, Roden DM, Darbar D.
    Europace; 2014 Apr 01; 16(4):485-90. PubMed ID: 24072447
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  • 4. Common Coding Variants in SCN10A Are Associated With the Nav1.8 Late Current and Cardiac Conduction.
    Macri V, Brody JA, Arking DE, Hucker WJ, Yin X, Lin H, Mills RW, Sinner MF, Lubitz SA, Liu CT, Morrison AC, Alonso A, Li N, Fedorov VV, Janssen PM, Bis JC, Heckbert SR, Dolmatova EV, Lumley T, Sitlani CM, Cupples LA, Pulit SL, Newton-Cheh C, Barnard J, Smith JD, Van Wagoner DR, Chung MK, Vlahakes GJ, O'Donnell CJ, Rotter JI, Margulies KB, Morley MP, Cappola TP, Benjamin EJ, Muzny D, Gibbs RA, Jackson RD, Magnani JW, Herndon CN, Rich SS, Psaty BM, Milan DJ, Boerwinkle E, Mohler PJ, Sotoodehnia N, Ellinor PT.
    Circ Genom Precis Med; 2018 May 01; 11(5):e001663. PubMed ID: 29752399
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  • 5. Association of SCN10A Polymorphisms with the Recurrence of Atrial Fibrillation after Catheter Ablation in a Chinese Han Population.
    Wu H, Xu J, Chen S, Zhou G, Qi B, Wei Y, Hu E, Tang D, Chen G, Li H, Zhao L, Shi Y, Liu S.
    Sci Rep; 2017 Mar 10; 7():44003. PubMed ID: 28281580
    [Abstract] [Full Text] [Related]

  • 6. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
    Behr ER, Savio-Galimberti E, Barc J, Holst AG, Petropoulou E, Prins BP, Jabbari J, Torchio M, Berthet M, Mizusawa Y, Yang T, Nannenberg EA, Dagradi F, Weeke P, Bastiaenan R, Ackerman MJ, Haunso S, Leenhardt A, Kääb S, Probst V, Redon R, Sharma S, Wilde A, Tfelt-Hansen J, Schwartz P, Roden DM, Bezzina CR, Olesen M, Darbar D, Guicheney P, Crotti L, UK10K Consortium, Jamshidi Y.
    Cardiovasc Res; 2015 Jun 01; 106(3):520-9. PubMed ID: 25691538
    [Abstract] [Full Text] [Related]

  • 7. Variant Intronic Enhancer Controls SCN10A-short Expression and Heart Conduction.
    Man JCK, Bosada FM, Scholman KT, Offerhaus JA, Walsh R, van Duijvenboden K, van Eif VWW, Bezzina CR, Verkerk AO, Boukens BJ, Barnett P, Christoffels VM.
    Circulation; 2021 Jul 20; 144(3):229-242. PubMed ID: 33910361
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  • 14. High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.
    Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH.
    Circ Cardiovasc Genet; 2012 Aug 01; 5(4):450-9. PubMed ID: 22685113
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  • 15. The rs6771157 C/G polymorphism in SCN10A is associated with the risk of atrial fibrillation in a Chinese Han population.
    Fang Z, Jiang Y, Wang Y, Lin Y, Liu Y, Zhao L, Xu Y, Toorabally MB, He S, Zhang F.
    Sci Rep; 2016 Oct 11; 6():35212. PubMed ID: 27725708
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  • 18. Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis.
    Roostaei T, Sadaghiani S, Park MT, Mashhadi R, Nazeri A, Noshad S, Salehi MJ, Naghibzadeh M, Moghadasi AN, Owji M, Doosti R, Taheri AP, Rad AS, Azimi A, Chakravarty MM, Voineskos AN, Nazeri A, Sahraian MA.
    Neurology; 2016 Feb 02; 86(5):410-7. PubMed ID: 26740675
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  • 19. A SCN10A SNP biases human pain sensitivity.
    Duan G, Han C, Wang Q, Guo S, Zhang Y, Ying Y, Huang P, Zhang L, Macala L, Shah P, Zhang M, Li N, Dib-Hajj SD, Waxman SG, Zhang X.
    Mol Pain; 2016 Feb 02; 12():. PubMed ID: 27590072
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