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 *

295 related articles for article (PubMed ID: 29892087)

  • 1. 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]  

  • 2. Digenic Inheritance of LAMA4 and MYH7 Mutations in Patient with Infantile Dilated Cardiomyopathy.
    Abdallah AM; Carlus SJ; Al-Mazroea AH; Alluqmani M; Almohammadi Y; Bhuiyan ZA; Al-Harbi KM
    Medicina (Kaunas); 2019 Jan; 55(1):. PubMed ID: 30650640
    [No Abstract]   [Full Text] [Related]  

  • 3. Role of Titin Missense Variants in Dilated Cardiomyopathy.
    Begay RL; Graw S; Sinagra G; Merlo M; Slavov D; Gowan K; Jones KL; Barbati G; Spezzacatene A; Brun F; Di Lenarda A; Smith JE; Granzier HL; Mestroni L; Taylor M;
    J Am Heart Assoc; 2015 Nov; 4(11):. PubMed ID: 26567375
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy.
    Minoche AE; Horvat C; Johnson R; Gayevskiy V; Morton SU; Drew AP; Woo K; Statham AL; Lundie B; Bagnall RD; Ingles J; Semsarian C; Seidman JG; Seidman CE; Dinger ME; Cowley MJ; Fatkin D
    Genet Med; 2019 Mar; 21(3):650-662. PubMed ID: 29961767
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Retrospective Analysis of Clinical Genetic Testing in Pediatric Primary Dilated Cardiomyopathy: Testing Outcomes and the Effects of Variant Reclassification.
    Quiat D; Witkowski L; Zouk H; Daly KP; Roberts AE
    J Am Heart Assoc; 2020 Jun; 9(11):e016195. PubMed ID: 32458740
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Clinical and Genetic Investigations of 109 Index Patients With Dilated Cardiomyopathy and 445 of Their Relatives.
    Hey TM; Rasmussen TB; Madsen T; Aagaard MM; Harbo M; Mølgaard H; Nielsen SK; Haas J; Meder B; Møller JE; Eiskjær H; Mogensen J
    Circ Heart Fail; 2020 Oct; 13(10):e006701. PubMed ID: 33019804
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.
    Koskenvuo JW; Saarinen I; Ahonen S; Tommiska J; Weckström S; Seppälä EH; Tuupanen S; Kangas-Kontio T; Schleit J; Heliö K; Hathaway J; Gummesson A; Dahlberg P; Ojala TH; Vepsäläinen V; Kytölä V; Muona M; Sistonen J; Salmenperä P; Gentile M; Paananen J; Myllykangas S; Alastalo TP; Heliö T
    PLoS One; 2021; 16(2):e0245681. PubMed ID: 33534821
    [TBL] [Abstract][Full Text] [Related]  

  • 14.
    Cowan JR; Salyer L; Wright NT; Kinnamon DD; Amaya P; Jordan E; Bamshad MJ; Nickerson DA; Hershberger RE
    Circ Genom Precis Med; 2020 Aug; 13(4):e002892. PubMed ID: 32603605
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of
    Sedaghat-Hamedani F; Rebs S; El-Battrawy I; Chasan S; Krause T; Haas J; Zhong R; Liao Z; Xu Q; Zhou X; Akin I; Zitron E; Frey N; Streckfuss-Bömeke K; Kayvanpour E
    Int J Mol Sci; 2021 Nov; 22(23):. PubMed ID: 34884792
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Considering complexity in the genetic evaluation of dilated cardiomyopathy.
    Jordan E; Hershberger RE
    Heart; 2021 Jan; 107(2):106-112. PubMed ID: 33109712
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy.
    Hershberger RE; Pinto JR; Parks SB; Kushner JD; Li D; Ludwigsen S; Cowan J; Morales A; Parvatiyar MS; Potter JD
    Circ Cardiovasc Genet; 2009 Aug; 2(4):306-13. PubMed ID: 20031601
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.