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For: Brion M, Blanco-Verea A, Sobrino B, Santori M, Gil R, Ramos-Luis E, Martinez M, Amigo J, Carracedo A. Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders. Electrophoresis 2014;35:3111-6. [PMID: 24981977 DOI: 10.1002/elps.201400148] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Blanco-verea A, Ramos-luis E, García-seara J, Carracedo Á, González-juanatey JR, Brion M. Una nueva delección de calsequestrina 2 que causa taquicardia ventricular polimórfica catecolaminérgica y muerte súbita cardiaca. Revista Española de Cardiología 2019;72:681-3. [DOI: 10.1016/j.recesp.2018.07.013] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 Hertz CL, Christiansen SL, Ottesen GL, Frank-hansen R, Bundgaard H, Morling N. Post-mortem investigation of young deceased individuals with ischemic heart disease—outcome of supplementary genetic testing for dyslipidemia. Int J Legal Med 2016;130:947-8. [DOI: 10.1007/s00414-015-1282-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
3 Hellenthal N, Gaertner-rommel A, Klauke B, Paluszkiewicz L, Stuhr M, Kerner T, Farr M, Püschel K, Milting H. Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases. Europace. [DOI: 10.1093/europace/euw247] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.0] [Reference Citation Analysis]
4 Wei J, Ni X, Dai Y, Chen X, Ding S, Bao J, Xing L. Identification of genes associated with sudden cardiac death: a network- and pathway-based approach. J Thorac Dis 2021;13:3610-27. [PMID: 34277054 DOI: 10.21037/jtd-21-361] [Reference Citation Analysis]
5 Jaouadi H, Bouyacoub Y, Chabrak S, Kraoua L, Zaroui A, Elouej S, Nagara M, Dallali H, Delague V, Levy N, Benkhalifa R, Mechmeche R, Zaffran S, Abdelhak S. Multiallelic rare variants support an oligogenic origin of sudden cardiac death in the young. Herz 2021;46:94-102. [PMID: 31970460 DOI: 10.1007/s00059-019-04883-1] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
6 Poloni G, De Bortoli M, Calore M, Rampazzo A, Lorenzon A. Arrhythmogenic right-ventricular cardiomyopathy: molecular genetics into clinical practice in the era of next generation sequencing. J Cardiovasc Med (Hagerstown) 2016;17:399-407. [PMID: 26990921 DOI: 10.2459/JCM.0000000000000385] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
7 Martinez-Matilla M, Blanco-Verea A, Santori M, Ansede-Bermejo J, Ramos-Luis E, Gil R, Bermejo AM, Lotufo-Neto F, Hirata MH, Brisighelli F, Paramo M, Carracedo A, Brion M. Genetic susceptibility in pharmacodynamic and pharmacokinetic pathways underlying drug-induced arrhythmia and sudden unexplained deaths. Forensic Sci Int Genet 2019;42:203-12. [PMID: 31376648 DOI: 10.1016/j.fsigen.2019.07.010] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Wang C, Duan S, Lv G, Lai X, Chen R, Lin H, Qiu S, Tang J, Kuang W, Xu C. Using whole exome sequencing and bioformatics in the molecular autopsy of a sudden unexplained death syndrome (SUDS) case. Forensic Sci Int 2015;257:e20-5. [PMID: 26385840 DOI: 10.1016/j.forsciint.2015.08.022] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
9 Morini E, Sangiuolo F, Caporossi D, Novelli G, Amati F. Application of Next Generation Sequencing for personalized medicine for sudden cardiac death. Front Genet 2015;6:55. [PMID: 25784923 DOI: 10.3389/fgene.2015.00055] [Cited by in Crossref: 14] [Cited by in F6Publishing: 10] [Article Influence: 2.0] [Reference Citation Analysis]
10 Suárez-Rama JJ, Arrojo M, Sobrino B, Amigo J, Brenlla J, Agra S, Paz E, Brión M, Carracedo Á, Páramo M, Costas J. Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility. J Psychiatr Res 2015;66-67:38-44. [PMID: 25943950 DOI: 10.1016/j.jpsychires.2015.04.013] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 1.9] [Reference Citation Analysis]
11 Castiglione V, Modena M, Aimo A, Chiti E, Botto N, Vittorini S, Guidi B, Vergaro G, Barison A, Rossi A, Passino C, Giannoni A, Di Paolo M, Emdin M. Molecular Autopsy of Sudden Cardiac Death in the Genomics Era. Diagnostics (Basel) 2021;11:1378. [PMID: 34441312 DOI: 10.3390/diagnostics11081378] [Reference Citation Analysis]
12 Blanco-Verea A, Ramos-Luis E, García-Seara J, Carracedo Á, González-Juanatey JR, Brion M. A Novel Calsequestrin 2 Deletion Causing Catecholaminergic Polymorphic Ventricular Tachycardia and Sudden Cardiac Death. Rev Esp Cardiol (Engl Ed) 2019;72:681-3. [PMID: 30139651 DOI: 10.1016/j.rec.2018.07.005] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Farrugia A, Keyser C, Hollard C, Raul J, Muller J, Ludes B. Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths. Forensic Science International 2015;254:5-11. [DOI: 10.1016/j.forsciint.2015.06.023] [Cited by in Crossref: 26] [Cited by in F6Publishing: 19] [Article Influence: 3.7] [Reference Citation Analysis]
14 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. Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young. Genome Res 2016;26:1170-7. [PMID: 27435932 DOI: 10.1101/gr.195800.115] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 2.7] [Reference Citation Analysis]
15 Brion M, Sobrino B, Martinez M, Blanco-Verea A, Carracedo A. Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young. Forensic Sci Int Genet 2015;18:160-70. [PMID: 26243589 DOI: 10.1016/j.fsigen.2015.07.010] [Cited by in Crossref: 24] [Cited by in F6Publishing: 17] [Article Influence: 3.4] [Reference Citation Analysis]
16 Scheiper S, Ramos-Luis E, Blanco-Verea A, Niess C, Beckmann BM, Schmidt U, Kettner M, Geisen C, Verhoff MA, Brion M, Kauferstein S. Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses. Forensic Sci Int 2018;293:70-6. [PMID: 30415094 DOI: 10.1016/j.forsciint.2018.09.034] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
17 Santori M, Blanco-verea A, Gil R, Cortis J, Becker K, Schneider PM, Carracedo A, Brion M. Broad-based molecular autopsy: a potential tool to investigate the involvement of subtle cardiac conditions in sudden unexpected death in infancy and early childhood. Arch Dis Child 2015;100:952-6. [DOI: 10.1136/archdischild-2015-308200] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 2.6] [Reference Citation Analysis]