BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 22468808)

  • 21. Expanding DNA diagnostic panel testing: is more better?
    Klee EW; Hoppman-Chaney NL; Ferber MJ
    Expert Rev Mol Diagn; 2011 Sep; 11(7):703-9. PubMed ID: 21902532
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Concepts for the return of secondary genetic findings in medical diagnostics and research].
    Fisher E; Achilles S; Tönnies H; Schmidtke J
    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz; 2015 Feb; 58(2):166-73. PubMed ID: 25487853
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Special report: exome sequencing for clinical diagnosis of patients with suspected genetic disorders.
    Blue Cross and Blue Shield Association
    Technol Eval Cent Assess Program Exec Summ; 2013 Aug; 28(3):1-4. PubMed ID: 24066368
    [No Abstract]   [Full Text] [Related]  

  • 24. Dual testing strategy in autism increases diagnostic yield: Chromosomal microarray and whole-exome sequencing combination may be best for children with multiple physical anomalies, study suggests.
    Levenson D
    Am J Med Genet A; 2016 Jan; 170A(1):7-8. PubMed ID: 26768328
    [No Abstract]   [Full Text] [Related]  

  • 25. Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2012 Mar; 33(3):586-90. PubMed ID: 22213110
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exome sequencing deciphers rare diseases.
    Maxmen A
    Cell; 2011 Mar; 144(5):635-7. PubMed ID: 21376225
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Diagnostic clinical genome and exome sequencing.
    Biesecker LG; Green RC
    N Engl J Med; 2014 Jun; 370(25):2418-25. PubMed ID: 24941179
    [No Abstract]   [Full Text] [Related]  

  • 28. Dysmorphology in the era of whole exome sequencing.
    Robin NH
    Curr Opin Pediatr; 2011 Dec; 23(6):579-80. PubMed ID: 21946345
    [No Abstract]   [Full Text] [Related]  

  • 29. Next-generation sequencing and its applications in molecular diagnostics.
    Su Z; Ning B; Fang H; Hong H; Perkins R; Tong W; Shi L
    Expert Rev Mol Diagn; 2011 Apr; 11(3):333-43. PubMed ID: 21463242
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Revealing the human mutome.
    Chen JM; Férec C; Cooper DN
    Clin Genet; 2010 Oct; 78(4):310-20. PubMed ID: 20569258
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome diagnostics: next-generation sequencing, new genome-wide association studies and clinical challenges.
    Ziogas DE; Roukos DH
    Expert Rev Mol Diagn; 2011 Sep; 11(7):663-6. PubMed ID: 21902524
    [No Abstract]   [Full Text] [Related]  

  • 32. [Introduction to human genome sequencing in diagnostics].
    Piatkowski J; Skalniak A; Bodzioch M; Pach D; Hubalewska-Dydejczyk A
    Przegl Lek; 2013; 70(7):458-62. PubMed ID: 24167948
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratory.
    Strom SP; Lee H; Das K; Vilain E; Nelson SF; Grody WW; Deignan JL
    Genet Med; 2014 Jul; 16(7):510-5. PubMed ID: 24406459
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sequencing set to alter clinical landscape.
    Hayden EC
    Nature; 2012 Feb; 482(7385):288. PubMed ID: 22337027
    [No Abstract]   [Full Text] [Related]  

  • 35. [Application of DNA microarray-based high throughput gene analysis system for molecular diagnosis].
    Takahashi Y; Goto J; Tsuji S
    Tanpakushitsu Kakusan Koso; 2005 Dec; 50(16 Suppl):2115-21. PubMed ID: 16411439
    [No Abstract]   [Full Text] [Related]  

  • 36. [Cancer genome analysis through next-generation sequencing].
    Aburatani H
    Gan To Kagaku Ryoho; 2011 Jan; 38(1):1-6. PubMed ID: 21368453
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Next-generation sequencing entering the clinical arena.
    Haas J; Katus HA; Meder B
    Mol Cell Probes; 2011; 25(5-6):206-11. PubMed ID: 21914469
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Next-generation DNA sequencing in clinical diagnostics].
    Lacoste C; Fabre A; Pécheux C; Lévy N; Krahn M; Malzac P; Bonello-Palot N; Badens C; Bourgeois P
    Arch Pediatr; 2017 Apr; 24(4):373-383. PubMed ID: 28242148
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing.
    Walker RH; Schulz VP; Tikhonova IR; Mahajan MC; Mane S; Arroyo Muniz M; Gallagher PG
    Mov Disord; 2012 Apr; 27(4):539-43. PubMed ID: 22038564
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new ocular phenotype associated with an unexpected but known systemic disorder and mutation: novel use of genomic diagnostics and exome sequencing.
    Majewski J; Wang Z; Lopez I; Al Humaid S; Ren H; Racine J; Bazinet A; Mitchel G; Braverman N; Koenekoop RK
    J Med Genet; 2011 Sep; 48(9):593-6. PubMed ID: 21862673
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.