196 related articles for article (PubMed ID: 26351163)
1. [Application of next-generation semiconductor sequencing technologies in genetic diagnosis of inherited cardiomyopathies].
Zhao Y; Zhang H; Xia XS
Yi Chuan; 2015 Jul; 37(7):635-44. PubMed ID: 26351163
[TBL] [Abstract][Full Text] [Related]
2. [Genetic diagnostics for cardiomyopathies].
Czepluch F; Wollnik B; Hasenfuß G
Dtsch Med Wochenschr; 2017 May; 142(9):657-664. PubMed ID: 28454199
[TBL] [Abstract][Full Text] [Related]
3. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
Teekakirikul P; Kelly MA; Rehm HL; Lakdawala NK; Funke BH
J Mol Diagn; 2013 Mar; 15(2):158-70. PubMed ID: 23274168
[TBL] [Abstract][Full Text] [Related]
4. Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
Wu W; Lu CX; Wang YN; Liu F; Chen W; Liu YT; Han YC; Cao J; Zhang SY; Zhang X
J Am Heart Assoc; 2015 Jul; 4(7):. PubMed ID: 26163040
[TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing entering the clinical arena.
Haas J; Katus HA; Meder B
Mol Cell Probes; 2011; 25(5-6):206-11. PubMed ID: 21914469
[TBL] [Abstract][Full Text] [Related]
6. A Variant Detection Pipeline for Inherited Cardiomyopathy-Associated Genes Using Next-Generation Sequencing.
Oliveira TG; Mitne-Neto M; Cerdeira LT; Marsiglia JD; Arteaga-Fernandez E; Krieger JE; Pereira AC
J Mol Diagn; 2015 Jul; 17(4):420-30. PubMed ID: 25937619
[TBL] [Abstract][Full Text] [Related]
7. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
Waldmüller S; Schroeder C; Sturm M; Scheffold T; Imbrich K; Junker S; Frische C; Hofbeck M; Bauer P; Bonin M; Gawaz M; Gramlich M
Mol Cell Probes; 2015 Oct; 29(5):308-14. PubMed ID: 25979592
[TBL] [Abstract][Full Text] [Related]
8. Targeted next-generation sequencing can replace Sanger sequencing in clinical diagnostics.
Sikkema-Raddatz B; Johansson LF; de Boer EN; Almomani R; Boven LG; van den Berg MP; van Spaendonck-Zwarts KY; van Tintelen JP; Sijmons RH; Jongbloed JD; Sinke RJ
Hum Mutat; 2013 Jul; 34(7):1035-42. PubMed ID: 23568810
[TBL] [Abstract][Full Text] [Related]
9. Genetics of inherited cardiomyopathies.
Bowles KR; Bowles NE
Expert Rev Cardiovasc Ther; 2004 Sep; 2(5):683-97. PubMed ID: 15350170
[TBL] [Abstract][Full Text] [Related]
10. Genetic cardiomyopathies.
Wilcox JE; Hershberger RE
Curr Opin Cardiol; 2018 May; 33(3):354-362. PubMed ID: 29561320
[TBL] [Abstract][Full Text] [Related]
11. Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.
Robyns T; Kuiperi C; Breckpot J; Devriendt K; Souche E; Van Cleemput J; Willems R; Nuyens D; Matthijs G; Corveleyn A
Eur J Hum Genet; 2017 Dec; 25(12):1313-1323. PubMed ID: 29255176
[TBL] [Abstract][Full Text] [Related]
12. Targeted next-generation sequencing detects novel gene-phenotype associations and expands the mutational spectrum in cardiomyopathies.
Forleo C; D'Erchia AM; Sorrentino S; Manzari C; Chiara M; Iacoviello M; Guaricci AI; De Santis D; Musci RL; La Spada A; Marangelli V; Pesole G; Favale S
PLoS One; 2017; 12(7):e0181842. PubMed ID: 28750076
[TBL] [Abstract][Full Text] [Related]
13. Molecular Diagnosis of Inherited Cardiac Diseases in the Era of Next-Generation Sequencing: A Single Center's Experience Over 5 Years.
Janin A; Januel L; Cazeneuve C; Delinière A; Chevalier P; Millat G
Mol Diagn Ther; 2021 May; 25(3):373-385. PubMed ID: 33954932
[TBL] [Abstract][Full Text] [Related]
14. Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies.
Millat G; Chanavat V; Rousson R
Clin Chim Acta; 2014 Jun; 433():266-71. PubMed ID: 24721642
[TBL] [Abstract][Full Text] [Related]
15. Evolving Approaches to Genetic Evaluation of Specific Cardiomyopathies.
Teo LY; Moran RT; Tang WH
Curr Heart Fail Rep; 2015 Dec; 12(6):339-49. PubMed ID: 26472190
[TBL] [Abstract][Full Text] [Related]
16. Massive parallel sequencing applied to the molecular autopsy in sudden cardiac death in the young.
Brion M; Sobrino B; Martinez M; Blanco-Verea A; Carracedo A
Forensic Sci Int Genet; 2015 Sep; 18():160-70. PubMed ID: 26243589
[TBL] [Abstract][Full Text] [Related]
17. Targeted next-generation sequencing in Slovak cardiomyopathy patients.
Nagyova E; Radvanszky J; Hyblova M; Simovicova V; Goncalvesova E; Asselbergs FW; Kadasi L; Szemes T; Minarik G
Bratisl Lek Listy; 2019; 120(1):46-51. PubMed ID: 30685992
[TBL] [Abstract][Full Text] [Related]
18. Arrhythmogenic right-ventricular cardiomyopathy: molecular genetics into clinical practice in the era of next generation sequencing.
Poloni G; De Bortoli M; Calore M; Rampazzo A; Lorenzon A
J Cardiovasc Med (Hagerstown); 2016 Jun; 17(6):399-407. PubMed ID: 26990921
[TBL] [Abstract][Full Text] [Related]
19. Genetic advances in sarcomeric cardiomyopathies: state of the art.
Ho CY; Charron P; Richard P; Girolami F; Van Spaendonck-Zwarts KY; Pinto Y
Cardiovasc Res; 2015 Apr; 105(4):397-408. PubMed ID: 25634555
[TBL] [Abstract][Full Text] [Related]
20. Modern genomic techniques in the identification of genetic causes of cardiomyopathy.
Spracklen TF; Keavney B; Laing N; Ntusi N; Shaboodien G
Heart; 2022 Nov; 108(23):1843-1850. PubMed ID: 35140110
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
