Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 217

1.

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;130(4):1011-1021. doi: 10.1007/s00414-016-1317-4. Epub 2016 Feb 4. Erratum in: Int J Legal Med. 2016 Jul;130(4):1023.

PMID:
26846766
2.

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. doi: 10.1016/j.forsciint.2015.06.023. Epub 2015 Jul 3.

PMID:
26164358
3.

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;132(4):1057-1065. doi: 10.1007/s00414-018-1775-y. Epub 2018 Jan 19.

PMID:
29350269
4.

Mutations in the SCN5A gene: evidence for a link between long QT syndrome and sudden death?

Kiehne N, Kauferstein S.

Forensic Sci Int Genet. 2007 Jun;1(2):170-4. doi: 10.1016/j.fsigen.2007.01.009. Epub 2007 Feb 26.

PMID:
19083750
5.

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. doi: 10.1161/CIRCGENETICS.115.001370. Epub 2016 Apr 25.

PMID:
27114410
6.

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. doi: 10.1016/j.forsciint.2014.01.014. Epub 2014 Feb 15.

PMID:
24631775
7.

Postmortem Analysis of 4 Mutation Hotspots of KCNQ1, KCNH2, and SCN5A Genes in Sudden Unexplained Death in Southwest of China.

Jia PL, Wang YB, Fu H, Huang WL, Zhong SR, Ma L, Li YH, Dong Y, Sun ZC, Yang L, Qu PF, Zhao S, Qu YQ, Xi YM, Wang SW, Tang X, Lei PP.

Am J Forensic Med Pathol. 2018 Sep;39(3):218-222. doi: 10.1097/PAF.0000000000000411.

PMID:
29851656
8.

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. doi: 10.1007/s00246-014-1082-4. Epub 2014 Dec 13.

9.

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. doi: 10.1111/j.1540-8167.2012.02371.x. Epub 2012 Aug 6.

PMID:
22882672
10.

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. doi: 10.1016/j.mayocp.2012.02.017.

11.

Influence of genetic modifiers on sudden cardiac death cases.

Jenewein T, Neumann T, Erkapic D, Kuniss M, Verhoff MA, Thiel G, Kauferstein S.

Int J Legal Med. 2018 Mar;132(2):379-385. doi: 10.1007/s00414-017-1739-7. Epub 2017 Dec 6.

PMID:
29214556
12.

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. doi: 10.1016/j.hrthm.2014.01.017. Epub 2014 Jan 17.

PMID:
24440382
13.

Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.

Suktitipat B, Sathirareuangchai S, Roothumnong E, Thongnoppakhun W, Wangkiratikant P, Vorasan N, Krittayaphong R, Pithukpakorn M, Boonyapisit W.

PLoS One. 2017 Jul 13;12(7):e0180056. doi: 10.1371/journal.pone.0180056. eCollection 2017.

14.

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. doi: 10.1007/s00414-015-1237-8. Epub 2015 Jul 31.

15.

Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.

Tester DJ, Ackerman MJ.

J Am Coll Cardiol. 2007 Jan 16;49(2):240-6. Epub 2006 Dec 29.

16.

Genetic analysis of sudden unexplained death: a multidisciplinary approach.

Kauferstein S, Kiehne N, Jenewein T, Biel S, Kopp M, König R, Erkapic D, Rothschild M, Neumann T.

Forensic Sci Int. 2013 Jun 10;229(1-3):122-7. doi: 10.1016/j.forsciint.2013.03.050. Epub 2013 Apr 30.

PMID:
23683917
17.

Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?

Liu C, Tester DJ, Hou Y, Wang W, Lv G, Ackerman MJ, Makielski JC, Cheng J.

Forensic Sci Int. 2014 Mar;236:38-45. doi: 10.1016/j.forsciint.2013.12.033. Epub 2014 Jan 7.

PMID:
24529773
18.

Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.

J E, T D, M S, M KN, J D, M NW.

Int J Legal Med. 2017 Mar;131(2):333-338. doi: 10.1007/s00414-016-1446-9. Epub 2016 Sep 9.

PMID:
27613431
19.

The role of known variants of KCNQ1, KCNH2, KCNE1, SCN5A, and NOS1AP in water-related deaths.

Tzimas I, Zingraf JC, Bajanowski T, Poetsch M.

Int J Legal Med. 2016 Nov;130(6):1575-1579. Epub 2016 Jul 26.

PMID:
27460199
20.

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. doi: 10.1093/europace/euv285. Epub 2015 Oct 25.

Supplemental Content

Support Center