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 *

305 related articles for article (PubMed ID: 31337358)

  • 1. 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; 19(1):174. PubMed ID: 31337358
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sudden unexplained death in the young: epidemiology, aetiology and value of the clinically guided genetic screening.
    Anastasakis A; Papatheodorou E; Ritsatos K; Protonotarios N; Rentoumi V; Gatzoulis K; Antoniades L; Agapitos E; Koutsaftis P; Spiliopoulou C; Tousoulis D
    Europace; 2018 Mar; 20(3):472-480. PubMed ID: 28177452
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives.
    Mak CM; Mok NS; Shum HC; Siu WK; Chong YK; Lee HHC; Fong NC; Tong SF; Lee KW; Ching CK; Chen SPL; Cheung WL; Tso CB; Poon WM; Lau CL; Lo YK; Tsui PT; Shum SF; Lee KC
    Hong Kong Med J; 2019 Feb; 25(1):21-9. PubMed ID: 30670673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 18(6):888-96. PubMed ID: 26498160
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.
    Hellenthal N; Gaertner-Rommel A; Klauke B; Paluszkiewicz L; Stuhr M; Kerner T; Farr M; Püschel K; Milting H
    Europace; 2017 Nov; 19(11):1881-1890. PubMed ID: 29016939
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 254():5-11. PubMed ID: 26164358
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic screening in sudden cardiac death in the young can save future lives.
    Stattin EL; Westin IM; Cederquist K; Jonasson J; Jonsson BA; Mörner S; Norberg A; Krantz P; Wisten A
    Int J Legal Med; 2016 Jan; 130(1):59-66. PubMed ID: 26228265
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Family-based cardiac screening in relatives of victims of sudden arrhythmic death syndrome.
    McGorrian C; Constant O; Harper N; O'Donnell C; Codd M; Keelan E; Green A; O'Neill J; Galvin J; Mahon NG
    Europace; 2013 Jul; 15(7):1050-8. PubMed ID: 23382499
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Explaining sudden infant death with cardiac arrhythmias: Complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants.
    Liebrechts-Akkerman G; Liu F; van Marion R; Dinjens WNM; Kayser M
    Forensic Sci Int Genet; 2020 May; 46():102266. PubMed ID: 32145446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 69(17):2134-2145. PubMed ID: 28449774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Next generation diagnostics in inherited arrhythmia syndromes : a comparison of two approaches.
    Ware JS; John S; Roberts AM; Buchan R; Gong S; Peters NS; Robinson DO; Lucassen A; Behr ER; Cook SA
    J Cardiovasc Transl Res; 2013 Feb; 6(1):94-103. PubMed ID: 22956155
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young.
    Bagnall RD; Das K J; Duflou J; Semsarian C
    Heart Rhythm; 2014 Apr; 11(4):655-62. PubMed ID: 24440382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China.
    Zhang L; Tester DJ; Lang D; Chen Y; Zheng J; Gao R; Corliss RF; Tang S; Kyle JW; Liu C; Ackerman MJ; Makielski JC; Cheng J
    Mayo Clin Proc; 2016 Nov; 91(11):1503-1514. PubMed ID: 27707468
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Long QT molecular autopsy in sudden unexplained death in the young (1-40 years old): Lessons learnt from an eight year experience in New Zealand.
    Marcondes L; Crawford J; Earle N; Smith W; Hayes I; Morrow P; Donoghue T; Graham A; Love D; Skinner JR;
    PLoS One; 2018; 13(4):e0196078. PubMed ID: 29672598
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.
    Kumar S; Peters S; Thompson T; Morgan N; Maccicoca I; Trainer A; Zentner D; Kalman JM; Winship I; Vohra JK
    Heart Rhythm; 2013 Nov; 10(11):1653-60. PubMed ID: 23973953
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers.
    Li X; Buckton AJ; Wilkinson SL; John S; Walsh R; Novotny T; Valaskova I; Gupta M; Game L; Barton PJ; Cook SA; Ware JS
    PLoS One; 2013; 8(7):e67744. PubMed ID: 23861798
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.