BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 21483645)

  • 1. Rare variant mutations identified in pediatric patients with dilated cardiomyopathy.
    Rampersaud E; Siegfried JD; Norton N; Li D; Martin E; Hershberger RE
    Prog Pediatr Cardiol; 2011 Jan; 31(1):39-47. PubMed ID: 21483645
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study.
    Shen C; Xu L; Sun X; Sun A; Ge J
    Ann Transl Med; 2022 Feb; 10(3):129. PubMed ID: 35284542
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genetic analysis in 418 index patients with idiopathic dilated cardiomyopathy: overview of 10 years' experience.
    van Spaendonck-Zwarts KY; van Rijsingen IA; van den Berg MP; Lekanne Deprez RH; Post JG; van Mil AM; Asselbergs FW; Christiaans I; van Langen IM; Wilde AA; de Boer RA; Jongbloed JD; Pinto YM; van Tintelen JP
    Eur J Heart Fail; 2013 Jun; 15(6):628-36. PubMed ID: 23349452
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Genetic testing for dilated cardiomyopathy in clinical practice.
    Lakdawala NK; Funke BH; Baxter S; Cirino AL; Roberts AE; Judge DP; Johnson N; Mendelsohn NJ; Morel C; Care M; Chung WK; Jones C; Psychogios A; Duffy E; Rehm HL; White E; Seidman JG; Seidman CE; Ho CY
    J Card Fail; 2012 Apr; 18(4):296-303. PubMed ID: 22464770
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.
    Ehlermann P; Weichenhan D; Zehelein J; Steen H; Pribe R; Zeller R; Lehrke S; Zugck C; Ivandic BT; Katus HA
    BMC Med Genet; 2008 Oct; 9():95. PubMed ID: 18957093
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Reevaluating the Genetic Contribution of Monogenic Dilated Cardiomyopathy.
    Mazzarotto F; Tayal U; Buchan RJ; Midwinter W; Wilk A; Whiffin N; Govind R; Mazaika E; de Marvao A; Dawes TJW; Felkin LE; Ahmad M; Theotokis PI; Edwards E; Ing AY; Thomson KL; Chan LLH; Sim D; Baksi AJ; Pantazis A; Roberts AM; Watkins H; Funke B; O'Regan DP; Olivotto I; Barton PJR; Prasad SK; Cook SA; Ware JS; Walsh R
    Circulation; 2020 Feb; 141(5):387-398. PubMed ID: 31983221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.
    Morales A; Painter T; Li R; Siegfried JD; Li D; Norton N; Hershberger RE
    Circulation; 2010 May; 121(20):2176-82. PubMed ID: 20458009
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic Variants Are Not Rare in ICD Candidates with Dilated Cardiomyopathy: Time for Next-Generation Sequencing?
    Sousa A; Canedo P; Campelo M; Moura B; Leite S; Baixia M; Belo A; Rocha-Gonçalves F; Machado JC; Silva-Cardoso J; Martins E; Fatima Investigators
    Cardiol Res Pract; 2019; 2019():2743650. PubMed ID: 31179125
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evidence-Based Assessment of Genes in Dilated Cardiomyopathy.
    Jordan E; Peterson L; Ai T; Asatryan B; Bronicki L; Brown E; Celeghin R; Edwards M; Fan J; Ingles J; James CA; Jarinova O; Johnson R; Judge DP; Lahrouchi N; Lekanne Deprez RH; Lumbers RT; Mazzarotto F; Medeiros Domingo A; Miller RL; Morales A; Murray B; Peters S; Pilichou K; Protonotarios A; Semsarian C; Shah P; Syrris P; Thaxton C; van Tintelen JP; Walsh R; Wang J; Ware J; Hershberger RE
    Circulation; 2021 Jul; 144(1):7-19. PubMed ID: 33947203
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy.
    Long PA; Evans JM; Olson TM
    J Cardiovasc Dev Dis; 2017 Aug; 4(3):. PubMed ID: 29367541
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.
    Hershberger RE; Norton N; Morales A; Li D; Siegfried JD; Gonzalez-Quintana J
    Circ Cardiovasc Genet; 2010 Apr; 3(2):155-61. PubMed ID: 20215591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Common susceptibility variants examined for association with dilated cardiomyopathy.
    Rampersaud E; Kinnamon DD; Hamilton K; Khuri S; Hershberger RE; Martin ER
    Ann Hum Genet; 2010 Mar; 74(2):110-6. PubMed ID: 20201937
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic Determinants and Genotype-Phenotype Correlations in Vietnamese Patients With Dilated Cardiomyopathy.
    Nguyen TV; Tran Vu MT; Do TNP; Tran THN; Do TH; Nguyen TMH; Tran Huynh BN; Le LA; Nguyen Pham NT; Nguyen TDA; Nguyen TMN; Le NHP; Pham Nguyen V; Ho Huynh TD
    Circ J; 2021 Aug; 85(9):1469-1478. PubMed ID: 34011823
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
    Núñez L; Gimeno-Blanes JR; Rodríguez-García MI; Monserrat L; Zorio E; Coats C; McGregor CG; Hernandez del Rincón JP; Castro-Beiras A; Hermida-Prieto M
    Circ J; 2013; 77(9):2358-65. PubMed ID: 23782526
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.