BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

694 related articles for article (PubMed ID: 31983221)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 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. The genetics of dilated cardiomyopathy: a prioritized candidate gene study of LMNA, TNNT2, TCAP, and PLN.
    Hirtle-Lewis M; Desbiens K; Ruel I; Rudzicz N; Genest J; Engert JC; Giannetti N
    Clin Cardiol; 2013 Oct; 36(10):628-33. PubMed ID: 24037902
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Determining the Likelihood of Disease Pathogenicity Among Incidentally Identified Genetic Variants in Rare Dilated Cardiomyopathy-Associated Genes.
    Yang Q; Berkman AM; Ezekian JE; Rosamilia M; Rosenfeld JA; Liu P; Landstrom AP
    J Am Heart Assoc; 2022 Oct; 11(19):e025257. PubMed ID: 36129056
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy.
    Ramchand J; Wallis M; Macciocca I; Lynch E; Farouque O; Martyn M; Phelan D; Chong B; Lockwood S; Weintraub R; Thompson T; Trainer A; Zentner D; Vohra J; Chetrit M; Hare DL; James P
    J Am Heart Assoc; 2020 Jan; 9(2):e013346. PubMed ID: 31931689
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers.
    Verdonschot JAJ; Robinson EL; James KN; Mohamed MW; Claes GRF; Casas K; Vanhoutte EK; Hazebroek MR; Kringlen G; Pasierb MM; van den Wijngaard A; Glatz JFC; Heymans SRB; Krapels IPC; Nahas S; Brunner HG; Szklarczyk R
    Mol Genet Genomic Med; 2020 Feb; 8(2):e1049. PubMed ID: 31880413
    [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. Massive parallel sequencing questions the pathogenic role of missense variants in dilated cardiomyopathy.
    Dalin MG; Engström PG; Ivarsson EG; Unneberg P; Light S; Schaufelberger M; Gilljam T; Andersson B; Bergo MO
    Int J Cardiol; 2017 Feb; 228():742-748. PubMed ID: 27886618
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
    Villard E; Perret C; Gary F; Proust C; Dilanian G; Hengstenberg C; Ruppert V; Arbustini E; Wichter T; Germain M; Dubourg O; Tavazzi L; Aumont MC; DeGroote P; Fauchier L; Trochu JN; Gibelin P; Aupetit JF; Stark K; Erdmann J; Hetzer R; Roberts AM; Barton PJ; Regitz-Zagrosek V; ; Aslam U; Duboscq-Bidot L; Meyborg M; Maisch B; Madeira H; Waldenström A; Galve E; Cleland JG; Dorent R; Roizes G; Zeller T; Blankenberg S; Goodall AH; Cook S; Tregouet DA; Tiret L; Isnard R; Komajda M; Charron P; Cambien F
    Eur Heart J; 2011 May; 32(9):1065-76. PubMed ID: 21459883
    [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. 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]  

  • 20. Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
    Domínguez F; Cuenca S; Bilińska Z; Toro R; Villard E; Barriales-Villa R; Ochoa JP; Asselbergs F; Sammani A; Franaszczyk M; Akhtar M; Coronado-Albi MJ; Rangel-Sousa D; Rodriguez-Palomares JF; Jiménez-Jáimez J; Garcia-Pinilla JM; Ripoll-Vera T; Mogollón-Jiménez MV; Fontalba-Romero A; Garcia-Medina D; Palomino-Doza J; de Gonzalo-Calvo D; Cicerchia M; Salazar-Mendiguchia J; Salas C; Pankuweit S; Hey TM; Mogensen J; Barton PJ; Charron P; Elliott P; Garcia-Pavia P;
    J Am Coll Cardiol; 2018 Nov; 72(20):2471-2481. PubMed ID: 30442290
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 35.