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Journal Abstract Search

308 related items for PubMed ID: 34949102

  • 1. Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death.
    Neves R, Tester DJ, Simpson MA, Behr ER, Ackerman MJ, Giudicessi JR.
    Circ Genom Precis Med; 2022 Feb; 15(1):e003497. PubMed ID: 34949102
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  • 2. 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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  • 5. Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.
    Neubauer J, Lecca MR, Russo G, Bartsch C, Medeiros-Domingo A, Berger W, Haas C.
    Int J Legal Med; 2018 Jul 19; 132(4):1057-1065. PubMed ID: 29350269
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  • 6. Yield of molecular autopsy in sudden cardiac death in athletes: data from a large registry in the UK.
    Finocchiaro G, Radaelli D, Johnson D, Bhatia RT, Westaby J, D'Errico S, Papadakis M, Sharma S, Sheppard MN, Behr ER.
    Europace; 2024 Feb 01; 26(2):. PubMed ID: 38289717
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  • 7. "Concealed cardiomyopathy" as a cause of previously unexplained sudden cardiac arrest.
    Isbister JC, Nowak N, Butters A, Yeates L, Gray B, Sy RW, Ingles J, Bagnall RD, Semsarian C.
    Int J Cardiol; 2021 Feb 01; 324():96-101. PubMed ID: 32931854
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  • 8. 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 01; 9(3):259-65. PubMed ID: 27114410
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  • 11. Re-evaluation of single nucleotide variants and identification of structural variants in a cohort of 45 sudden unexplained death cases.
    Neubauer J, Wang S, Russo G, Haas C.
    Int J Legal Med; 2021 Jul 01; 135(4):1341-1349. PubMed ID: 33895855
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  • 16. Insights into sudden cardiac death: exploring the potential relevance of non-diagnostic autopsy findings.
    Raju H, Parsons S, Thompson TN, Morgan N, Zentner D, Trainer AH, James PA, Winship IM, Kalman JM, Vohra J.
    Eur Heart J; 2019 Mar 07; 40(10):831-838. PubMed ID: 30380018
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  • 17. Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome.
    Lahrouchi N, Raju H, Lodder EM, Papatheodorou E, Ware JS, Papadakis M, Tadros R, Cole D, Skinner JR, Crawford J, Love DR, Pua CJ, Soh BY, Bhalshankar JD, Govind R, Tfelt-Hansen J, Winkel BG, van der Werf C, Wijeyeratne YD, Mellor G, Till J, Cohen MC, Tome-Esteban M, Sharma S, Wilde AAM, Cook SA, Bezzina CR, Sheppard MN, Behr ER.
    J Am Coll Cardiol; 2017 May 02; 69(17):2134-2145. PubMed ID: 28449774
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  • 19. Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy.
    Hata Y, Hirono K, Yamaguchi Y, Ichida F, Oku Y, Nishida N.
    Mod Pathol; 2019 Sep 02; 32(9):1281-1290. PubMed ID: 31024045
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  • 20. Interpreting secondary cardiac disease variants in an exome cohort.
    Ng D, Johnston JJ, Teer JK, Singh LN, Peller LC, Wynter JS, Lewis KL, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG, NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program.
    Circ Cardiovasc Genet; 2013 Aug 02; 6(4):337-46. PubMed ID: 23861362
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