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Journal Abstract Search

584 related items for PubMed ID: 27114410

  • 1. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH, Tester DJ, Will ML, Ackerman MJ.
    Circ Cardiovasc Genet; 2016 Jun; 9(3):259-65. PubMed ID: 27114410
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  • 2. Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
    Tester DJ, Medeiros-Domingo A, Will ML, Haglund CM, Ackerman MJ.
    Mayo Clin Proc; 2012 Jun; 87(6):524-39. PubMed ID: 22677073
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  • 5. 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
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  • 6. Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.
    Sutphin BS, Boczek NJ, Barajas-Martínez H, Hu D, Ye D, Tester DJ, Antzelevitch C, Ackerman MJ.
    Congenit Heart Dis; 2016 Dec; 11(6):683-692. PubMed ID: 27218670
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  • 7. Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case Series.
    Shanks GW, Tester DJ, Ackerman JP, Simpson MA, Behr ER, White SM, Ackerman MJ.
    Circulation; 2018 Jun 19; 137(25):2705-2715. PubMed ID: 29915097
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  • 8. Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.
    Nunn LM, Lopes LR, Syrris P, Murphy C, Plagnol V, Firman E, Dalageorgou C, Zorio E, Domingo D, Murday V, Findlay I, Duncan A, Carr-White G, Robert L, Bueser T, Langman C, Fynn SP, Goddard M, White A, Bundgaard H, Ferrero-Miliani L, Wheeldon N, Suvarna SK, O'Beirne A, Lowe MD, McKenna WJ, Elliott PM, Lambiase PD.
    Europace; 2016 Jun 19; 18(6):888-96. PubMed ID: 26498160
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  • 9. Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy.
    Raju H, Ware JS, Skinner JR, Hedley PL, Arno G, Love DR, van der Werf C, Tfelt-Hansen J, Winkel BG, Cohen MC, Li X, John S, Sharma S, Jeffery S, Wilde AAM, Christiansen M, Sheppard MN, Behr ER.
    BMC Cardiovasc Disord; 2019 Jul 23; 19(1):174. PubMed ID: 31337358
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  • 12. Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths.
    Farrugia A, Keyser C, Hollard C, Raul JS, Muller J, Ludes B.
    Forensic Sci Int; 2015 Sep 23; 254():5-11. PubMed ID: 26164358
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  • 15. Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young.
    Tester DJ, Ackerman JP, Giudicessi JR, Ackerman NC, Cerrone M, Delmar M, Ackerman MJ.
    JACC Clin Electrophysiol; 2019 Jan 23; 5(1):120-127. PubMed ID: 30678776
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  • 16. Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases.
    Tester DJ, Spoon DB, Valdivia HH, Makielski JC, Ackerman MJ.
    Mayo Clin Proc; 2004 Nov 23; 79(11):1380-4. PubMed ID: 15544015
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  • 17. Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case series.
    Narula N, Tester DJ, Paulmichl A, Maleszewski JJ, Ackerman MJ.
    Pediatr Cardiol; 2015 Apr 23; 36(4):768-78. PubMed ID: 25500949
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  • 18. Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
    Neubauer J, Haas C, Bartsch C, Medeiros-Domingo A, Berger W.
    Int J Legal Med; 2016 Jul 23; 130(4):1011-1021. PubMed ID: 26846766
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  • 20. The role of molecular autopsy in unexplained sudden cardiac death.
    Tester DJ, Ackerman MJ.
    Curr Opin Cardiol; 2006 May 23; 21(3):166-72. PubMed ID: 16601452
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