191 related articles for article (PubMed ID: 23852418)
1. Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.
Punetha J; Hoffman EP
Circ Cardiovasc Genet; 2013 Aug; 6(4):427-34. PubMed ID: 23852418
[No Abstract] [Full Text] [Related]
2. Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies.
Lu C; Wu W; Liu F; Yang K; Li J; Liu Y; Wang R; Si N; Gao P; Liu Y; Zhang S; Zhang X
J Transl Med; 2018 Aug; 16(1):241. PubMed ID: 30165862
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Identification of a Novel Titin Variant Underlying Myocardial Involvement in Neurofibromatosis Type 1.
Kizawa M; Nakagama Y; Shindo T; Ogawa S; Inuzuka R
Can J Cardiol; 2018 Oct; 34(10):1369.e5-1369.e7. PubMed ID: 30269836
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation of dystrophin in a Becker muscular dystrophy family with severe cardiac involvement: from genetics to clinicopathology.
Chen L; Ren J; Chen X; Chen K; Rao M; Zhang N; Yu W; Song J
Cardiovasc Pathol; 2018; 36():64-70. PubMed ID: 30103083
[TBL] [Abstract][Full Text] [Related]
6. Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.
Vrijenhoek T; Kraaijeveld K; Elferink M; de Ligt J; Kranendonk E; Santen G; Nijman IJ; Butler D; Claes G; Costessi A; Dorlijn W; van Eyndhoven W; Halley DJ; van den Hout MC; van Hove S; Johansson LF; Jongbloed JD; Kamps R; Kockx CE; de Koning B; Kriek M; Lekanne Dit Deprez R; Lunstroo H; Mannens M; Mook OR; Nelen M; Ploem C; Rijnen M; Saris JJ; Sinke R; Sistermans E; van Slegtenhorst M; Sleutels F; van der Stoep N; van Tienhoven M; Vermaat M; Vogel M; Waisfisz Q; Marjan Weiss J; van den Wijngaard A; van Workum W; Ijntema H; van der Zwaag B; van IJcken WF; den Dunnen J; Veltman JA; Hennekam R; Cuppen E
Eur J Hum Genet; 2015 Sep; 23(9):1142-50. PubMed ID: 25626705
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Cardiomyopathies: Genetic overlap between peripartum and dilated cardiomyopathies.
Lim GB
Nat Rev Cardiol; 2016 Mar; 13(3):121. PubMed ID: 26794013
[No Abstract] [Full Text] [Related]
9. Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patients.
Alimohamed MZ; Johansson LF; Posafalvi A; Boven LG; van Dijk KK; Walters L; Vos YJ; Westers H; Hoedemaekers YM; Sinke RJ; Sijmons RH; Sikkema-Raddatz B; Jongbloed JDH; van der Zwaag PA
Int J Cardiol; 2021 Jun; 332():99-104. PubMed ID: 33662488
[TBL] [Abstract][Full Text] [Related]
10. Titin in muscular dystrophy and cardiomyopathy: Urinary titin as a novel marker.
Misaka T; Yoshihisa A; Takeishi Y
Clin Chim Acta; 2019 Aug; 495():123-128. PubMed ID: 30959043
[TBL] [Abstract][Full Text] [Related]
11. Truncating mutations on myofibrillar myopathies causing genes as prevalent molecular explanations on patients with dilated cardiomyopathy.
Janin A; N'Guyen K; Habib G; Dauphin C; Chanavat V; Bouvagnet P; Eschalier R; Streichenberger N; Chevalier P; Millat G
Clin Genet; 2017 Dec; 92(6):616-623. PubMed ID: 28436997
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Stergiopoulos K; Lima FV; Yang J
N Engl J Med; 2016 Jun; 374(26):2601. PubMed ID: 27355548
[No Abstract] [Full Text] [Related]
14. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Biteker M
N Engl J Med; 2016 Jun; 374(26):2601. PubMed ID: 27355547
[No Abstract] [Full Text] [Related]
15. Shared Genetic Predisposition in Peripartum and Dilated Cardiomyopathies.
Ware JS; Seidman JG; Arany Z
N Engl J Med; 2016 Jun; 374(26):2601-2. PubMed ID: 27355546
[No Abstract] [Full Text] [Related]
16. Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy.
van Spaendonck-Zwarts KY; Posafalvi A; van den Berg MP; Hilfiker-Kleiner D; Bollen IA; Sliwa K; Alders M; Almomani R; van Langen IM; van der Meer P; Sinke RJ; van der Velden J; Van Veldhuisen DJ; van Tintelen JP; Jongbloed JD
Eur Heart J; 2014 Aug; 35(32):2165-73. PubMed ID: 24558114
[TBL] [Abstract][Full Text] [Related]
17. Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy.
Mazzarotto F; Olivotto I; Walsh R
Cardiovasc Drugs Ther; 2020 Apr; 34(2):241-253. PubMed ID: 32080787
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. 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]
20. Genetic Variation in Cardiomyopathy and Cardiovascular Disorders.
McNally EM; Puckelwartz MJ
Circ J; 2015; 79(7):1409-15. PubMed ID: 26040335
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]