These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 35284542)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
    Norton N; Robertson PD; Rieder MJ; Züchner S; Rampersaud E; Martin E; Li D; Nickerson DA; Hershberger RE;
    Circ Cardiovasc Genet; 2012 Apr; 5(2):167-74. PubMed ID: 22337857
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 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. 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]  

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

    [Next]    [New Search]
    of 8.