260 related articles for article (PubMed ID: 34379075)
1. Genomic Autopsy of Sudden Deaths in Young Individuals.
Webster G; Puckelwartz MJ; Pesce LL; Dellefave-Castillo LM; Vanoye CG; Potet F; Page P; Kearns SD; Pottinger T; White S; Arunkumar P; Olson R; Kofman A; Ibrahim N; Ing A; Brew C; Yap KL; Kadri S; George AL; McNally EM
JAMA Cardiol; 2021 Nov; 6(11):1247-1256. PubMed ID: 34379075
[TBL] [Abstract][Full Text] [Related]
2. Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two-year prospective study in a large medical examiner's office with an in-house molecular genetics laboratory and genetic counseling services.
Williams N; Manderski E; Stewart S; Bao R; Tang Y
J Genet Couns; 2020 Apr; 29(2):293-302. PubMed ID: 31436011
[TBL] [Abstract][Full Text] [Related]
3. Postmortem genetic testing in sudden unexplained death: A public health laboratory experience.
Rohrer CT; Lager AM; Brooks EG; Horner VL
J Forensic Sci; 2023 Nov; 68(6):2065-2075. PubMed ID: 37614113
[TBL] [Abstract][Full Text] [Related]
4. Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young.
Methner DN; Scherer SE; Welch K; Walkiewicz M; Eng CM; Belmont JW; Powell MC; Korchina V; Doddapaneni HV; Muzny DM; Gibbs RA; Wolf DA; Sanchez LA; Kahn R
Genome Res; 2016 Sep; 26(9):1170-7. PubMed ID: 27435932
[TBL] [Abstract][Full Text] [Related]
5. Genetic Variants Associated With Unexplained Sudden Cardiac Death in Adult White and African American Individuals.
Guo L; Torii S; Fernandez R; Braumann RE; Fuller DT; Paek KH; Gadhoke NV; Maloney KA; Harris K; Mayhew CM; Zarpak R; Stevens LM; Gaynor BJ; Jinnouchi H; Sakamoto A; Sato Y; Mori H; Kutyna MD; Lee PJ; Weinstein LM; Collado-Rivera CJ; Ali BB; Atmakuri DR; Dhingra R; Finn ELB; Bell MW; Lynch M; Cornelissen A; Kuntz SH; Park JH; Kutys R; Park JE; Wang L; Hong SN; Gupta A; Hall JL; Kolodgie FD; Romero ME; Jeng LJB; Mitchell BD; Surve D; Fowler DR; Hong CC; Virmani R; Finn AV
JAMA Cardiol; 2021 Sep; 6(9):1013-1022. PubMed ID: 34076677
[TBL] [Abstract][Full Text] [Related]
6. 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
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
Tester DJ; Ackerman MJ
J Am Coll Cardiol; 2007 Jan; 49(2):240-6. PubMed ID: 17222736
[TBL] [Abstract][Full Text] [Related]
9. The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Puckelwartz MJ; Pesce LL; Hernandez EJ; Webster G; Dellefave-Castillo LM; Russell MW; Geisler SS; Kearns SD; Karthik F; Etheridge SP; Monroe TO; Pottinger TD; Kannankeril PJ; Shoemaker MB; Fountain D; Roden DM; Faulkner M; MacLeod HM; Burns KM; Yandell M; Tristani-Firouzi M; George AL; McNally EM
Genome Med; 2024 Jan; 16(1):13. PubMed ID: 38229148
[TBL] [Abstract][Full Text] [Related]
10. 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; 137(25):2705-2715. PubMed ID: 29915097
[TBL] [Abstract][Full Text] [Related]
11. 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; 36(4):768-78. PubMed ID: 25500949
[TBL] [Abstract][Full Text] [Related]
12. Applying High-Resolution Variant Classification to Cardiac Arrhythmogenic Gene Testing in a Demographically Diverse Cohort of Sudden Unexplained Deaths.
Lin Y; Williams N; Wang D; Coetzee W; Zhou B; Eng LS; Um SY; Bao R; Devinsky O; McDonald TV; Sampson BA; Tang Y
Circ Cardiovasc Genet; 2017 Dec; 10(6):. PubMed ID: 29247119
[TBL] [Abstract][Full Text] [Related]
13. Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program.
Siskind T; Williams N; Sebastin M; Marion R; McDonald TV; Walsh C; Sampson B; Tang Y; Clark BC
J Community Genet; 2022 Dec; 13(6):629-639. PubMed ID: 36203036
[TBL] [Abstract][Full Text] [Related]
14. Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation.
Papadakis M; Raju H; Behr ER; De Noronha SV; Spath N; Kouloubinis A; Sheppard MN; Sharma S
Circ Arrhythm Electrophysiol; 2013 Jun; 6(3):588-96. PubMed ID: 23671135
[TBL] [Abstract][Full Text] [Related]
15. Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases.
Salfati EL; Spencer EG; Topol SE; Muse ED; Rueda M; Lucas JR; Wagner GN; Campman S; Topol EJ; Torkamani A
Genome Med; 2019 Dec; 11(1):83. PubMed ID: 31847883
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Confirmation of Cause of Death Via Comprehensive Autopsy and Whole Exome Molecular Sequencing in People With Epilepsy and Sudden Unexpected Death.
Chahal CAA; Tester DJ; Fayyaz AU; Jaliparthy K; Khan NA; Lu D; Khan M; Sahoo A; Rajendran A; Knight JA; Simpson MA; Behr ER; So EL; St Louis EK; Reichard RR; Edwards WD; Ackerman MJ; Somers VK
J Am Heart Assoc; 2021 Dec; 10(23):e021170. PubMed ID: 34816733
[TBL] [Abstract][Full Text] [Related]
18. Phenotype-driven molecular autopsy for sudden cardiac death.
Cann F; Corbett M; O'Sullivan D; Tennant S; Hailey H; Grieve JH; Broadhurst P; Rankin R; Dean JC
Clin Genet; 2017 Jan; 91(1):22-29. PubMed ID: 27000522
[TBL] [Abstract][Full Text] [Related]
19. 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; 40(10):831-838. PubMed ID: 30380018
[TBL] [Abstract][Full Text] [Related]
20. Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders.
Junttila MJ; Holmström L; Pylkäs K; Mantere T; Kaikkonen K; Porvari K; Kortelainen ML; Pakanen L; Kerkelä R; Myerburg RJ; Huikuri HV
Circulation; 2018 Jun; 137(25):2716-2726. PubMed ID: 29915098
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
