200 related articles for article (PubMed ID: 26516846)
1. Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death.
Campuzano O; Sanchez-Molero O; Mademont-Soler I; Riuró H; Allegue C; Coll M; Pérez-Serra A; Mates J; Picó F; Iglesias A; Brugada R
Int J Mol Sci; 2015 Oct; 16(10):25773-87. PubMed ID: 26516846
[TBL] [Abstract][Full Text] [Related]
2. Post-mortem genetic analysis in juvenile cases of sudden cardiac death.
Campuzano O; Sanchez-Molero O; Allegue C; Coll M; Mademont-Soler I; Selga E; Ferrer-Costa C; Mates J; Iglesias A; Sarquella-Brugada G; Cesar S; Brugada J; Castellà J; Medallo J; Brugada R
Forensic Sci Int; 2014 Dec; 245():30-7. PubMed ID: 25447171
[TBL] [Abstract][Full Text] [Related]
3. Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis.
Campuzano O; Sanchez-Molero O; Fernandez A; Mademont-Soler I; Coll M; Perez-Serra A; Mates J; Del Olmo B; Pico F; Nogue-Navarro L; Sarquella-Brugada G; Iglesias A; Cesar S; Carro E; Borondo JC; Brugada J; Castellà J; Medallo J; Brugada R
Sports Med; 2017 Oct; 47(10):2101-2115. PubMed ID: 28255936
[TBL] [Abstract][Full Text] [Related]
4. Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood.
Santori M; Blanco-Verea A; Gil R; Cortis J; Becker K; Schneider PM; Carracedo A; Brion M
Arch Dis Child; 2015 Oct; 100(10):952-6. PubMed ID: 26272908
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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. PubMed ID: 29350269
[TBL] [Abstract][Full Text] [Related]
8. The role of clinical, genetic and segregation evaluation in sudden infant death.
Campuzano O; Allegue C; Sarquella-Brugada G; Coll M; Mates J; Alcalde M; Ferrer-Costa C; Iglesias A; Brugada J; Brugada R
Forensic Sci Int; 2014 Sep; 242():9-15. PubMed ID: 25016126
[TBL] [Abstract][Full Text] [Related]
9. Genetic analysis in post-mortem samples with micro-ischemic alterations.
Campuzano O; Sanchez-Molero O; Mademont-Soler I; Coll M; Allegue C; Ferrer-Costa C; Mates J; Perez-Serra A; Del Olmo B; Iglesias A; Sarquella-Brugada G; Brugada J; Borondo JC; Castella J; Medallo J; Brugada R
Forensic Sci Int; 2017 Feb; 271():120-125. PubMed ID: 28086167
[TBL] [Abstract][Full Text] [Related]
10. Interpreting Genetic Variants in Titin in Patients With Muscle Disorders.
Savarese M; Maggi L; Vihola A; Jonson PH; Tasca G; Ruggiero L; Bello L; Magri F; Giugliano T; Torella A; Evilä A; Di Fruscio G; Vanakker O; Gibertini S; Vercelli L; Ruggieri A; Antozzi C; Luque H; Janssens S; Pasanisi MB; Fiorillo C; Raimondi M; Ergoli M; Politano L; Bruno C; Rubegni A; Pane M; Santorelli FM; Minetti C; Angelini C; De Bleecker J; Moggio M; Mongini T; Comi GP; Santoro L; Mercuri E; Pegoraro E; Mora M; Hackman P; Udd B; Nigro V
JAMA Neurol; 2018 May; 75(5):557-565. PubMed ID: 29435569
[TBL] [Abstract][Full Text] [Related]
11. Next-generation sequencing of 34 genes in sudden unexplained death victims in forensics and in patients with channelopathic cardiac diseases.
Hertz CL; Christiansen SL; Ferrero-Miliani L; Fordyce SL; Dahl M; Holst AG; Ottesen GL; Frank-Hansen R; Bundgaard H; Morling N
Int J Legal Med; 2015 Jul; 129(4):793-800. PubMed ID: 25467552
[TBL] [Abstract][Full Text] [Related]
12. Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy.
Akinrinade O; Heliö T; Lekanne Deprez RH; Jongbloed JDH; Boven LG; van den Berg MP; Pinto YM; Alastalo TP; Myllykangas S; Spaendonck-Zwarts KV; van Tintelen JP; van der Zwaag PA; Koskenvuo J
Sci Rep; 2019 Mar; 9(1):4093. PubMed ID: 30858397
[TBL] [Abstract][Full Text] [Related]
13. A missense variant in the titin gene in Doberman pinscher dogs with familial dilated cardiomyopathy and sudden cardiac death.
Meurs KM; Friedenberg SG; Kolb J; Saripalli C; Tonino P; Woodruff K; Olby NJ; Keene BW; Adin DB; Yost OL; DeFrancesco TC; Lahmers S; Tou S; Shelton GD; Granzier H
Hum Genet; 2019 May; 138(5):515-524. PubMed ID: 30715562
[TBL] [Abstract][Full Text] [Related]
14. Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations.
Alcalde M; Nogué-Navarro L; Tiron C; Fernandez-Falgueras A; Iglesias A; Simon A; Buxó M; Pérez-Serra A; Puigmulé M; López L; Picó F; Del Olmo B; Corona M; Campuzano O; Moral S; Castella J; Coll M; Brugada R
Forensic Sci Int Genet; 2022 May; 58():102688. PubMed ID: 35316720
[TBL] [Abstract][Full Text] [Related]
15. Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology.
Campuzano O; Sarquella-Brugada G; Mademont-Soler I; Allegue C; Cesar S; Ferrer-Costa C; Coll M; Mates J; Iglesias A; Brugada J; Brugada R
PLoS One; 2014; 9(12):e114894. PubMed ID: 25494010
[TBL] [Abstract][Full Text] [Related]
16. Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations.
Zhu YB; Luo JW; Jiang F; Liu G
Mol Med Rep; 2018 May; 17(5):7073-7080. PubMed ID: 29568937
[TBL] [Abstract][Full Text] [Related]
17. 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; 12(7):e0180056. PubMed ID: 28704380
[TBL] [Abstract][Full Text] [Related]
18. Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases.
Hertz CL; Christiansen SL; Larsen MK; Dahl M; Ferrero-Miliani L; Weeke PE; Pedersen O; Hansen T; Grarup N; Ottesen GL; Frank-Hansen R; Banner J; Morling N
Eur J Hum Genet; 2016 Jun; 24(6):817-22. PubMed ID: 26350513
[TBL] [Abstract][Full Text] [Related]
19. Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses.
Scheiper S; Ramos-Luis E; Blanco-Verea A; Niess C; Beckmann BM; Schmidt U; Kettner M; Geisen C; Verhoff MA; Brion M; Kauferstein S
Forensic Sci Int; 2018 Dec; 293():70-76. PubMed ID: 30415094
[TBL] [Abstract][Full Text] [Related]
20. Unveiling a sudden unexplained death case by whole exome sequencing and bioinformatic analysis.
Modena M; Castiglione V; Aretini P; Mazzanti CM; Chiti E; Giannoni A; Emdin M; Di Paolo M
Mol Genet Genomic Med; 2020 Apr; 8(4):e1182. PubMed ID: 32101375
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
