171 related articles for article (PubMed ID: 27855642)
1. Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families.
Hanley A; Walsh KA; Joyce C; McLellan MA; Clauss S; Hagen A; Shea MA; Tucker NR; Lin H; Fahy GJ; Ellinor PT
BMC Med Genet; 2016 Nov; 17(1):83. PubMed ID: 27855642
[TBL] [Abstract][Full Text] [Related]
2. Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death.
Sveinbjornsson G; Olafsdottir EF; Thorolfsdottir RB; Davidsson OB; Helgadottir A; Jonasdottir A; Jonasdottir A; Bjornsson E; Jensson BO; Arnadottir GA; Kristinsdottir H; Stephensen SS; Oskarsson G; Gudbjartsson T; Sigurdsson EL; Andersen K; Danielsen R; Arnar DO; Jonsdottir I; Thorsteinsdottir U; Sulem P; Thorgeirsson G; Gudbjartsson DF; Holm H; Stefansson K
Circ Genom Precis Med; 2018 Aug; 11(8):e002151. PubMed ID: 30354339
[TBL] [Abstract][Full Text] [Related]
3. Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.
Xu JH; Gu JY; Guo YH; Zhang H; Qiu XB; Li RG; Shi HY; Liu H; Yang XX; Xu YJ; Qu XK; Yang YQ
Int Heart J; 2017 Aug; 58(4):521-529. PubMed ID: 28690296
[TBL] [Abstract][Full Text] [Related]
4. Whole exome sequencing identifies a KCNJ12 mutation as a cause of familial dilated cardiomyopathy.
Yuan HX; Yan K; Hou DY; Zhang ZY; Wang H; Wang X; Zhang J; Xu XR; Liang YH; Zhao WS; Xu L; Zhang L
Medicine (Baltimore); 2017 Aug; 96(33):e7727. PubMed ID: 28816949
[TBL] [Abstract][Full Text] [Related]
5. Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.
Zaragoza MV; Fung L; Jensen E; Oh F; Cung K; McCarthy LA; Tran CK; Hoang V; Hakim SA; Grosberg A
PLoS One; 2016; 11(5):e0155421. PubMed ID: 27182706
[TBL] [Abstract][Full Text] [Related]
6. Whole exome sequencing identified 1 base pair novel deletion in BCL2-associated athanogene 3 (BAG3) gene associated with severe dilated cardiomyopathy (DCM) requiring heart transplant in multiple family members.
Rafiq MA; Chaudhry A; Care M; Spears DA; Morel CF; Hamilton RM
Am J Med Genet A; 2017 Mar; 173(3):699-705. PubMed ID: 28211974
[TBL] [Abstract][Full Text] [Related]
7. Exome Sequencing Identifies a Novel DES Mutation (R227C) in a Chinese Dilated Cardiomyopathy Family.
Yu R; Liu L; Chen C; Shen JM
Cardiology; 2017; 137(2):78-82. PubMed ID: 28171858
[TBL] [Abstract][Full Text] [Related]
8. Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
Ellesøe SG; Johansen MM; Bjerre JV; Hjortdal VE; Brunak S; Larsen LA
Congenit Heart Dis; 2016 May; 11(3):283-90. PubMed ID: 26679770
[TBL] [Abstract][Full Text] [Related]
9. Association Between Mutations in the NKX2.5 Homeobox, Atrial Septal Defects, Ventricular Noncompaction and Sudden Cardiac Death.
Palomino Doza J; Salguero-Bodes R; de la Parte M; Arribas-Ynsaurriaga F
Rev Esp Cardiol (Engl Ed); 2018 Jan; 71(1):53-55. PubMed ID: 28330612
[No Abstract] [Full Text] [Related]
10. A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.
Yuan F; Qiu XB; Li RG; Qu XK; Wang J; Xu YJ; Liu X; Fang WY; Yang YQ; Liao DN
Int J Mol Med; 2015 Feb; 35(2):478-86. PubMed ID: 25503402
[TBL] [Abstract][Full Text] [Related]
11. Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy.
Zhao Y; Feng Y; Zhang YM; Ding XX; Song YZ; Zhang AM; Liu L; Zhang H; Ding JH; Xia XS
Int J Mol Med; 2015 Dec; 36(6):1479-86. PubMed ID: 26458567
[TBL] [Abstract][Full Text] [Related]
12. Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians.
Chami N; Tadros R; Lemarbre F; Lo KS; Beaudoin M; Robb L; Labuda D; Tardif JC; Racine N; Talajic M; Lettre G
Can J Cardiol; 2014 Dec; 30(12):1655-61. PubMed ID: 25448463
[TBL] [Abstract][Full Text] [Related]
13. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy.
Al-Hassnan ZN; Shinwari ZM; Wakil SM; Tulbah S; Mohammed S; Rahbeeni Z; Alghamdi M; Rababh M; Colak D; Kaya N; Al-Fayyadh M; Alburaiki J
BMC Med Genet; 2016 Jan; 17():3. PubMed ID: 26768247
[TBL] [Abstract][Full Text] [Related]
14. Novel Genetic Variants in BAG3 and TNNT2 in a Swedish Family with a History of Dilated Cardiomyopathy and Sudden Cardiac Death.
Fernlund E; Österberg AW; Kuchinskaya E; Gustafsson M; Jansson K; Gunnarsson C
Pediatr Cardiol; 2017 Aug; 38(6):1262-1268. PubMed ID: 28669108
[TBL] [Abstract][Full Text] [Related]
15. Genotype-phenotype associations in dilated cardiomyopathy: meta-analysis on more than 8000 individuals.
Kayvanpour E; Sedaghat-Hamedani F; Amr A; Lai A; Haas J; Holzer DB; Frese KS; Keller A; Jensen K; Katus HA; Meder B
Clin Res Cardiol; 2017 Feb; 106(2):127-139. PubMed ID: 27576561
[TBL] [Abstract][Full Text] [Related]
16. TBX20 loss-of-function mutation associated with familial dilated cardiomyopathy.
Zhao CM; Bing-Sun ; Song HM; Wang J; Xu WJ; Jiang JF; Qiu XB; Yuan F; Xu JH; Yang YQ
Clin Chem Lab Med; 2016 Feb; 54(2):325-32. PubMed ID: 26118961
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system.
Zhao Y; Cao H; Song Y; Feng Y; Ding X; Pang M; Zhang Y; Zhang H; Ding J; Xia X
Int J Mol Med; 2016 Jun; 37(6):1511-20. PubMed ID: 27082122
[TBL] [Abstract][Full Text] [Related]
19. Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.
Millat G; Bouvagnet P; Chevalier P; Sebbag L; Dulac A; Dauphin C; Jouk PS; Delrue MA; Thambo JB; Le Metayer P; Seronde MF; Faivre L; Eicher JC; Rousson R
Eur J Med Genet; 2011; 54(6):e570-5. PubMed ID: 21846512
[TBL] [Abstract][Full Text] [Related]
20. Patient-specific induced-pluripotent stem cells-derived cardiomyocytes recapitulate the pathogenic phenotypes of dilated cardiomyopathy due to a novel DES mutation identified by whole exome sequencing.
Tse HF; Ho JC; Choi SW; Lee YK; Butler AW; Ng KM; Siu CW; Simpson MA; Lai WH; Chan YC; Au KW; Zhang J; Lay KW; Esteban MA; Nicholls JM; Colman A; Sham PC
Hum Mol Genet; 2013 Apr; 22(7):1395-403. PubMed ID: 23300193
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
