BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

246 related articles for article (PubMed ID: 23843345)

  • 1. Implications of genetic testing in noncompaction/hypertrabeculation.
    Shieh JT
    Am J Med Genet C Semin Med Genet; 2013 Aug; 163C(3):206-11. PubMed ID: 23843345
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Modern genomic techniques in the identification of genetic causes of cardiomyopathy.
    Spracklen TF; Keavney B; Laing N; Ntusi N; Shaboodien G
    Heart; 2022 Nov; 108(23):1843-1850. PubMed ID: 35140110
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The genetics of left ventricular noncompaction.
    Cannie D; Elliott P
    Curr Opin Cardiol; 2021 May; 36(3):301-308. PubMed ID: 33605617
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.
    Callis TE; Jensen BC; Weck KE; Willis MS
    Expert Rev Mol Diagn; 2010 Apr; 10(3):329-51. PubMed ID: 20370590
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children.
    Mehaney DA; Haghighi A; Embaby AK; Zeyada RA; Darwish RK; Elfeel NS; Abouelhoda M; El-Saiedi SA; Gohar NA; Seliem ZS
    Cardiol Young; 2022 Feb; 32(2):295-300. PubMed ID: 34036930
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genetic diagnostics for cardiomyopathies].
    Czepluch F; Wollnik B; Hasenfuß G
    Dtsch Med Wochenschr; 2017 May; 142(9):657-664. PubMed ID: 28454199
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.
    Teekakirikul P; Kelly MA; Rehm HL; Lakdawala NK; Funke BH
    J Mol Diagn; 2013 Mar; 15(2):158-70. PubMed ID: 23274168
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and Mechanistic Insights Into the Genetics of Cardiomyopathy.
    Burke MA; Cook SA; Seidman JG; Seidman CE
    J Am Coll Cardiol; 2016 Dec; 68(25):2871-2886. PubMed ID: 28007147
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical genetic testing in pediatric cardiomyopathy: Is bigger better?
    Ouellette AC; Mathew J; Manickaraj AK; Manase G; Zahavich L; Wilson J; George K; Benson L; Bowdin S; Mital S
    Clin Genet; 2018 Jan; 93(1):33-40. PubMed ID: 28369760
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications.
    Kalsner L; Twachtman-Bassett J; Tokarski K; Stanley C; Dumont-Mathieu T; Cotney J; Chamberlain S
    Mol Genet Genomic Med; 2018 Mar; 6(2):171-185. PubMed ID: 29271092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic cardiomyopathies.
    Wilcox JE; Hershberger RE
    Curr Opin Cardiol; 2018 May; 33(3):354-362. PubMed ID: 29561320
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype-phenotype correlations.
    Ader F; De Groote P; Réant P; Rooryck-Thambo C; Dupin-Deguine D; Rambaud C; Khraiche D; Perret C; Pruny JF; Mathieu-Dramard M; Gérard M; Troadec Y; Gouya L; Jeunemaitre X; Van Maldergem L; Hagège A; Villard E; Charron P; Richard P
    Clin Genet; 2019 Oct; 96(4):317-329. PubMed ID: 31245841
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy.
    Golbus JR; Puckelwartz MJ; Dellefave-Castillo L; Fahrenbach JP; Nelakuditi V; Pesce LL; Pytel P; McNally EM
    Circ Cardiovasc Genet; 2014 Dec; 7(6):751-759. PubMed ID: 25179549
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic advances in sarcomeric cardiomyopathies: state of the art.
    Ho CY; Charron P; Richard P; Girolami F; Van Spaendonck-Zwarts KY; Pinto Y
    Cardiovasc Res; 2015 Apr; 105(4):397-408. PubMed ID: 25634555
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Septal hypertrabeculation/noncompaction: cardiac and neurologic implications.
    Stöllberger C; Finsterer J
    Int J Cardiol; 2009 Feb; 132(2):173-5. PubMed ID: 19046611
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
    Wu W; Lu CX; Wang YN; Liu F; Chen W; Liu YT; Han YC; Cao J; Zhang SY; Zhang X
    J Am Heart Assoc; 2015 Jul; 4(7):. PubMed ID: 26163040
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics and Genomics of Single-Gene Cardiovascular Diseases: Common Hereditary Cardiomyopathies as Prototypes of Single-Gene Disorders.
    Marian AJ; van Rooij E; Roberts R
    J Am Coll Cardiol; 2016 Dec; 68(25):2831-2849. PubMed ID: 28007145
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnostic Considerations in the Epilepsies-Testing Strategies, Test Type Advantages, and Limitations.
    Chen WL; Mefford HC
    Neurotherapeutics; 2021 Jul; 18(3):1468-1477. PubMed ID: 34532824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy.
    Robyns T; Kuiperi C; Breckpot J; Devriendt K; Souche E; Van Cleemput J; Willems R; Nuyens D; Matthijs G; Corveleyn A
    Eur J Hum Genet; 2017 Dec; 25(12):1313-1323. PubMed ID: 29255176
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Establishment of Specialized Clinical Cardiovascular Genetics Programs: Recognizing the Need and Meeting Standards: A Scientific Statement From the American Heart Association.
    Ahmad F; McNally EM; Ackerman MJ; Baty LC; Day SM; Kullo IJ; Madueme PC; Maron MS; Martinez MW; Salberg L; Taylor MR; Wilcox JE
    Circ Genom Precis Med; 2019 Jun; 12(6):e000054. PubMed ID: 31117808
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.