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 *

96 related articles for article (PubMed ID: 29704685)

  • 1. Is it research or is it clinical? Revisiting an old frontier through the lens of next-generation sequencing technologies.
    Bertier G; Cambon-Thomsen A; Joly Y
    Eur J Med Genet; 2018 Oct; 61(10):634-641. PubMed ID: 29704685
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical exome sequencing in France and Quebec: what are the challenges? What does the future hold?
    Bertier G; Joly Y
    Life Sci Soc Policy; 2018 Aug; 14(1):17. PubMed ID: 30066179
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Guidelines for NGS procedures applied to prenatal diagnosis by the Spanish Society of Gynecology and Obstetrics and the Spanish Association of Prenatal Diagnosis.
    Abulí A; Antolín E; Borrell A; Garcia-Hoyos M; García Santiago F; Gómez Manjón I; Maíz N; González González C; Rodríguez-Revenga L; Valenzuena Palafoll I; Suela J
    J Med Genet; 2024 Jul; 61(8):727-733. PubMed ID: 38834294
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recommendations for Next-Generation Sequencing Germline Variant Confirmation: A Joint Report of the Association for Molecular Pathology and National Society of Genetic Counselors.
    Crooks KR; Farwell Hagman KD; Mandelker D; Santani A; Schmidt RJ; Temple-Smolkin RL; Lincoln SE
    J Mol Diagn; 2023 Jul; 25(7):411-427. PubMed ID: 37207865
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases.
    Schuler BA; Nelson ET; Koziura M; Cogan JD; Hamid R; Phillips JA
    J Clin Invest; 2022 Apr; 132(7):. PubMed ID: 35362483
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Towards a European consensus for reporting incidental findings during clinical NGS testing.
    Hehir-Kwa JY; Claustres M; Hastings RJ; van Ravenswaaij-Arts C; Christenhusz G; Genuardi M; Melegh B; Cambon-Thomsen A; Patsalis P; Vermeesch J; Cornel MC; Searle B; Palotie A; Capoluongo E; Peterlin B; Estivill X; Robinson PN
    Eur J Hum Genet; 2015 Dec; 23(12):1601-6. PubMed ID: 26036857
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Normative Issues in Next Generation Sequencing Gene Testing.
    Kim NK
    Dev Reprod; 2023 Apr; 27(1):47-56. PubMed ID: 38075441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next-generation sequencing strategies in venous thromboembolism: in whom and for what purpose?
    Trégouët DA; Morange PE
    J Thromb Haemost; 2024 Jul; 22(7):1826-1834. PubMed ID: 38641321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Systematic Review of Value Criteria for Next-Generation Sequencing/Comprehensive Genomic Profiling to Inform Value Framework Development.
    Augustovski F; Colaci C; Mills M; Chavez D; Argento F; Alfie V; Pichon Riviere A; Kanavos P; Alcaraz A
    Value Health; 2024 May; 27(5):670-685. PubMed ID: 38403113
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cost of cancer diagnosis using next-generation sequencing targeted gene panels in routine practice: a nationwide French study.
    Marino P; Touzani R; Perrier L; Rouleau E; Kossi DS; Zhaomin Z; Charrier N; Goardon N; Preudhomme C; Durand-Zaleski I; Borget I; Baffert S;
    Eur J Hum Genet; 2018 Mar; 26(3):314-323. PubMed ID: 29367707
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Is it the time to integrate novel sequencing technologies into clinical practice?
    VanOudenhove J; Halene S; Mendez L
    Curr Opin Hematol; 2023 Mar; 30(2):70-77. PubMed ID: 36602939
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Next-Generation Sequencing and the Return of Results.
    Knoppers BM; Nguyen MT; Sénécal K; Tassé AM; Zawati MH
    Cold Spring Harb Perspect Med; 2016 Oct; 6(10):. PubMed ID: 27599532
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Privacy and ethical challenges in next-generation sequencing.
    Martinez-Martin N; Magnus D
    Expert Rev Precis Med Drug Dev; 2019; 4(2):95-104. PubMed ID: 32775691
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications.
    van der Geest MA; Maeckelberghe ELM; van Gijn ME; Lucassen AM; Swertz MA; van Langen IM; Plantinga M
    Eur J Hum Genet; 2024 May; 32(5):489-497. PubMed ID: 38480795
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next-Generation Sequencing-Based Cancer Panel Data Conversion Using International Standards to Implement a Clinical Next-Generation Sequencing Research System: Single-Institution Study.
    Park P; Shin SY; Park SY; Yun J; Shin C; Jung J; Choi KS; Cha HS
    JMIR Med Inform; 2020 Apr; 8(4):e14710. PubMed ID: 32329738
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical implementation of germ line cancer pharmacogenetic variants during the next-generation sequencing era.
    Gillis NK; Patel JN; Innocenti F
    Clin Pharmacol Ther; 2014 Mar; 95(3):269-80. PubMed ID: 24136381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dealing with ambivalence in the practice of advanced genetic healthcare: towards an ethical choreography.
    Kuiper JML; Borry P; Vears DF; Van Esch H; Cornel MC; Van Hoyweghen I
    Eur J Hum Genet; 2023 Dec; 31(12):1387-1392. PubMed ID: 37592172
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic testing in healthcare: a hybrid space where clinical practice and research need to co-exist.
    Horton R; Lucassen A
    Expert Rev Mol Diagn; 2019 Nov; 19(11):963-967. PubMed ID: 31603004
    [No Abstract]   [Full Text] [Related]  

  • 19. Management of Incidental Findings in the Era of Next-generation Sequencing.
    Blackburn HL; Schroeder B; Turner C; Shriver CD; Ellsworth DL; Ellsworth RE
    Curr Genomics; 2015 Jun; 16(3):159-74. PubMed ID: 26069456
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel.
    Messner DA; Al Naber J; Koay P; Cook-Deegan R; Majumder M; Javitt G; Deverka P; Dvoskin R; Bollinger J; Curnutte M; Chandrasekharan S; McGuire A
    Appl Transl Genom; 2016 Sep; 10():19-24. PubMed ID: 27668172
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.