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 *

171 related articles for article (PubMed ID: 27550507)

  • 1. Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
    Quinlan-Jones E; Kilby MD; Greenfield S; Parker M; McMullan D; Hurles ME; Hillman SC
    Prenat Diagn; 2016 Oct; 36(10):935-941. PubMed ID: 27550507
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Understanding variations in secondary findings reporting practices across U.S. genome sequencing laboratories.
    Ackerman SL; Koenig BA
    AJOB Empir Bioeth; 2018; 9(1):48-57. PubMed ID: 29131714
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Medical genetics and the genome].
    Gerdes AM; Vogel I
    Ugeskr Laeger; 2014 Nov; 176(46):. PubMed ID: 25394930
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Committee Opinion No.682: Microarrays and Next-Generation Sequencing Technology: The Use of Advanced Genetic Diagnostic Tools in Obstetrics and Gynecology.
    Committee on Genetics and the Society for Maternal-Fetal Medicine
    Obstet Gynecol; 2016 Dec; 128(6):e262-e268. PubMed ID: 27875474
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.
    Joseph G; Chen F; Harris-Wai J; Puck JM; Young C; Koenig BA
    Pediatrics; 2016 Jan; 137 Suppl 1(Suppl 1):S36-46. PubMed ID: 26729702
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and Outcomes.
    Lindor NM; Schahl KA; Johnson KJ; Hunt KS; Mensink KA; Wieben ED; Klee E; Black JL; Highsmith WE; Thibodeau SN; Ferber MJ; Aypar U; Ji Y; Graham RP; Fiksdal AS; Sarangi V; Ormond KE; Riegert-Johnson DL; McAllister TM; Farrugia G; McCormick JB
    Mayo Clin Proc; 2015 Oct; 90(10):1327-37. PubMed ID: 26434960
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
    Westerfield LE; Stover SR; Mathur VS; Nassef SA; Carter TG; Yang Y; Eng CM; Van den Veyver IB
    Prenat Diagn; 2015 Oct; 35(10):1022-9. PubMed ID: 26275793
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.
    Bayefsky MJ; White A; Wakim P; Hull SC; Wasserman D; Chen S; Berkman BE
    Prenat Diagn; 2016 Dec; 36(13):1250-1256. PubMed ID: 27862072
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Points to consider for informed consent for genome/exome sequencing.
    ACMG Board of Directors
    Genet Med; 2013 Sep; 15(9):748-9. PubMed ID: 23970068
    [No Abstract]   [Full Text] [Related]  

  • 10. "I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
    Townsend A; Adam S; Birch PH; Lohn Z; Rousseau F; Friedman JM
    Am J Med Genet A; 2012 Oct; 158A(10):2519-25. PubMed ID: 22903777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
    Levenseller BL; Soucier DJ; Miller VA; Harris D; Conway L; Bernhardt BA
    J Genet Couns; 2014 Aug; 23(4):552-65. PubMed ID: 23846343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Views of genetics health professionals on the return of genomic results.
    Grove ME; Wolpert MN; Cho MK; Lee SS; Ormond KE
    J Genet Couns; 2014 Aug; 23(4):531-8. PubMed ID: 23728783
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ethical and counseling challenges in prenatal exome sequencing.
    Harris S; Gilmore K; Hardisty E; Lyerly AD; Vora NL
    Prenat Diagn; 2018 Nov; 38(12):897-903. PubMed ID: 30171820
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Criteria for reporting incidental findings in clinical exome sequencing - a focus group study on professional practices and perspectives in Belgian genetic centres.
    Saelaert M; Mertes H; Moerenhout T; De Baere E; Devisch I
    BMC Med Genomics; 2019 Aug; 12(1):123. PubMed ID: 31429751
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Reporting Incidental Findings in Clinical Whole Exome Sequencing: Incorporation of the 2013 ACMG Recommendations into Current Practices of Genetic Counseling.
    Smith LA; Douglas J; Braxton AA; Kramer K
    J Genet Couns; 2015 Aug; 24(4):654-62. PubMed ID: 25403901
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal whole-exome sequencing: parental attitudes.
    Kalynchuk EJ; Althouse A; Parker LS; Saller DN; Rajkovic A
    Prenat Diagn; 2015 Oct; 35(10):1030-6. PubMed ID: 26151551
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Informed consent for exome sequencing in diagnostics: exploring first experiences and views of professionals and patients.
    Rigter T; van Aart CJ; Elting MW; Waisfisz Q; Cornel MC; Henneman L
    Clin Genet; 2014 May; 85(5):417-22. PubMed ID: 24117109
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
    Mackley MP; Fletcher B; Parker M; Watkins H; Ormondroyd E
    Genet Med; 2017 Mar; 19(3):283-293. PubMed ID: 27584911
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Informed consent for exome sequencing research in families with genetic disease: the emerging issue of incidental findings.
    Bergner AL; Bollinger J; Raraigh KS; Tichnell C; Murray B; Blout CL; Telegrafi AB; James CA
    Am J Med Genet A; 2014 Nov; 164A(11):2745-52. PubMed ID: 25251809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues.
    Minear MA; Alessi S; Allyse M; Michie M; Chandrasekharan S
    Annu Rev Genomics Hum Genet; 2015; 16():369-98. PubMed ID: 26322648
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.