191 related articles for article (PubMed ID: 23852418)
21. 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]
22. Titin mutations and muscle disease.
Kellermayer D; Smith JE; Granzier H
Pflugers Arch; 2019 May; 471(5):673-682. PubMed ID: 30919088
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.
Andreasen C; Nielsen JB; Refsgaard L; Holst AG; Christensen AH; Andreasen L; Sajadieh A; Haunsø S; Svendsen JH; Olesen MS
Eur J Hum Genet; 2013 Sep; 21(9):918-28. PubMed ID: 23299917
[TBL] [Abstract][Full Text] [Related]
25. Second Hits in Dilated Cardiomyopathy.
Marstrand P; Picard K; Lakdawala NK
Curr Cardiol Rep; 2020 Jan; 22(2):8. PubMed ID: 31980956
[TBL] [Abstract][Full Text] [Related]
26. Identification by next-generation sequencing of 2 novel cases of noncompaction cardiomyopathy associated with 1p36 deletions.
Peña-Peña ML; Trujillo-Quintero JP; García-Medina D; Cantero-Pérez EM; De Uña-Iglesias D; Monserrat L
Rev Esp Cardiol (Engl Ed); 2020 Sep; 73(9):780-782. PubMed ID: 32192878
[No Abstract] [Full Text] [Related]
27. FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
Ader F; De Groote P; Réant P; Rooryck-Thambo C; Dupin-Deguine D; Rambaud C; Khraiche D; Perret C; Pruny JF; Mathieu-Dramard M; Gérard M; Troadec Y; Gouya L; Jeunemaitre X; Van Maldergem L; Hagège A; Villard E; Charron P; Richard P
Clin Genet; 2019 Oct; 96(4):317-329. PubMed ID: 31245841
[TBL] [Abstract][Full Text] [Related]
28. A Reliable Targeted Next-Generation Sequencing Strategy for Diagnosis of Myopathies and Muscular Dystrophies, Especially for the Giant Titin and Nebulin Genes.
Zenagui R; Lacourt D; Pegeot H; Yauy K; Juntas Morales R; Theze C; Rivier F; Cances C; Sole G; Renard D; Walther-Louvier U; Ferrer-Monasterio X; Espil C; Arné-Bes MC; Cintas P; Uro-Coste E; Martin Negrier ML; Rigau V; Bieth E; Goizet C; Claustres M; Koenig M; Cossée M
J Mol Diagn; 2018 Jul; 20(4):533-549. PubMed ID: 29792937
[TBL] [Abstract][Full Text] [Related]
29. Use of high-throughput targeted exome-sequencing to screen for copy number variation in hypertrophic cardiomyopathy.
Lopes LR; Murphy C; Syrris P; Dalageorgou C; McKenna WJ; Elliott PM; Plagnol V
Eur J Med Genet; 2015 Nov; 58(11):611-6. PubMed ID: 26455666
[TBL] [Abstract][Full Text] [Related]
30. Dystrophin: from non-ischemic cardiomyopathy to ischemic cardiomyopathy.
Zheng QS; Guo WG; Lu ZF; Shi XQ; Su FF; Li H
Med Hypotheses; 2008 Sep; 71(3):434-8. PubMed ID: 18562127
[TBL] [Abstract][Full Text] [Related]
31. A 'second truncation' in TTN causes early onset recessive muscular dystrophy.
Harris E; Töpf A; Vihola A; Evilä A; Barresi R; Hudson J; Hackman P; Herron B; MacArthur D; Lochmüller H; Bushby K; Udd B; Straub V
Neuromuscul Disord; 2017 Nov; 27(11):1009-1017. PubMed ID: 28716623
[TBL] [Abstract][Full Text] [Related]
32. The next step toward personalized recommendations for genetic cardiomyopathies.
Stroeks SLVM; Verdonschot JAJ
Eur J Hum Genet; 2023 Nov; 31(11):1201-1203. PubMed ID: 37280362
[No Abstract] [Full Text] [Related]
33. Molecular genetics and pathogenesis of cardiomyopathy.
Kimura A
J Hum Genet; 2016 Jan; 61(1):41-50. PubMed ID: 26178429
[TBL] [Abstract][Full Text] [Related]
34. Interpreting secondary cardiac disease variants in an exome cohort.
Ng D; Johnston JJ; Teer JK; Singh LN; Peller LC; Wynter JS; Lewis KL; Cooper DN; Stenson PD; Mullikin JC; Biesecker LG;
Circ Cardiovasc Genet; 2013 Aug; 6(4):337-46. PubMed ID: 23861362
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Genetic cardiomyopathies.
Wilcox JE; Hershberger RE
Curr Opin Cardiol; 2018 May; 33(3):354-362. PubMed ID: 29561320
[TBL] [Abstract][Full Text] [Related]
37. Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity.
Richard P; Ader F; Roux M; Donal E; Eicher JC; Aoutil N; Huttin O; Selton-Suty C; Coisne D; Jondeau G; Damy T; Mansencal N; Casalta AC; Michel N; Haentjens J; Faivre L; Lavoute C; Nguyen K; Tregouët DA; Habib G; Charron P
Clin Genet; 2019 Mar; 95(3):356-367. PubMed ID: 30471092
[TBL] [Abstract][Full Text] [Related]
38. Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death.
Lahrouchi N; Lodder EM; Mansouri M; Tadros R; Zniber L; Adadi N; Clur SB; van Spaendonck-Zwarts KY; Postma AV; Sefiani A; Ratbi I; Bezzina CR
Eur J Hum Genet; 2017 Jun; 25(6):783-787. PubMed ID: 28295041
[TBL] [Abstract][Full Text] [Related]
39. A PLN nonsense variant causes severe dilated cardiomyopathy in a novel autosomal recessive inheritance mode.
Li Z; Chen P; Xu J; Yu B; Li X; Wang DW; Wang DW
Int J Cardiol; 2019 Mar; 279():122-125. PubMed ID: 30638982
[TBL] [Abstract][Full Text] [Related]
40. Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy.
Roncarati R; Viviani Anselmi C; Krawitz P; Lattanzi G; von Kodolitsch Y; Perrot A; di Pasquale E; Papa L; Portararo P; Columbaro M; Forni A; Faggian G; Condorelli G; Robinson PN
Eur J Hum Genet; 2013 Oct; 21(10):1105-11. PubMed ID: 23463027
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]