BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 33493017)

  • 1. Whole Sequencing of Most Prevalent Dilated Cardiomyopathy-Causing Genes as a Molecular Strategy to Improve Molecular Diagnosis Efficiency?
    Januel L; Chanavat V; Rollat-Farnier PA; Bardel C; Nony S; Millat G; Janin A
    DNA Cell Biol; 2021 Mar; 40(3):491-498. PubMed ID: 33493017
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy.
    Janin A; Chanavat V; Rollat-Farnier PA; Bardel C; Nguyen K; Chevalier P; Eicher JC; Faivre L; Piard J; Albert E; Nony S; Millat G
    Hum Mutat; 2020 Feb; 41(2):465-475. PubMed ID: 31730716
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing.
    Carnevale A; Rosas-Madrigal S; Rosendo-Gutiérrez R; López-Mora E; Romero-Hidalgo S; Avila-Vazzini N; Jacobo-Albavera L; Domínguez-Pérez M; Vargas-Alarcón G; Pérez-Villatoro F; Navarrete-Martínez JI; Villarreal-Molina MT
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1504. PubMed ID: 32969603
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genetic characterization of dilated cardiomyopathy patients undergoing heart transplantation in the Chinese population by whole-exome sequencing.
    Lian H; Song S; Chen W; Shi A; Jiang H; Hu S
    J Transl Med; 2023 Jul; 21(1):476. PubMed ID: 37461109
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy.
    Norton N; Li D; Rampersaud E; Morales A; Martin ER; Zuchner S; Guo S; Gonzalez M; Hedges DJ; Robertson PD; Krumm N; Nickerson DA; Hershberger RE;
    Circ Cardiovasc Genet; 2013 Apr; 6(2):144-53. PubMed ID: 23418287
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic analysis using targeted next-generation sequencing of sporadic Chinese patients with idiopathic dilated cardiomyopathy.
    Li M; Xia S; Xu L; Tan H; Yang J; Wu Z; He X; Li L
    J Transl Med; 2021 May; 19(1):189. PubMed ID: 33941202
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis.
    Seidel F; Holtgrewe M; Al-Wakeel-Marquard N; Opgen-Rhein B; Dartsch J; Herbst C; Beule D; Pickardt T; Klingel K; Messroghli D; Berger F; Schubert S; Kühnisch J; Klaassen S
    Circ Genom Precis Med; 2021 Aug; 14(4):e003250. PubMed ID: 34213952
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy.
    Horvat C; Johnson R; Lam L; Munro J; Mazzarotto F; Roberts AM; Herman DS; Parfenov M; Haghighi A; McDonough B; DePalma SR; Keogh AM; Macdonald PS; Hayward CS; Roberts A; Barton PJR; Felkin LE; Giannoulatou E; Cook SA; Seidman JG; Seidman CE; Fatkin D
    Genet Med; 2019 Jan; 21(1):133-143. PubMed ID: 29892087
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy - a pilot study.
    Zaklyazminskaya E; Mikhailov V; Bukaeva A; Kotlukova N; Povolotskaya I; Kaimonov V; Dombrovskaya A; Dzemeshkevich S
    Sci Rep; 2019 Nov; 9(1):16409. PubMed ID: 31712709
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
    Norton N; Li D; Rieder MJ; Siegfried JD; Rampersaud E; Züchner S; Mangos S; Gonzalez-Quintana J; Wang L; McGee S; Reiser J; Martin E; Nickerson DA; Hershberger RE
    Am J Hum Genet; 2011 Mar; 88(3):273-82. PubMed ID: 21353195
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.