BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

385 related articles for article (PubMed ID: 24671342)

  • 1. Genetic counselors' views and experiences with the clinical integration of genome sequencing.
    Machini K; Douglas J; Braxton A; Tsipis J; Kramer K
    J Genet Couns; 2014 Aug; 23(4):496-505. PubMed ID: 24671342
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomic counseling in the newborn period: experiences and views of genetic counselors.
    Nardini MD; Matthews AL; McCandless SE; Baumanis L; Goldenberg AJ
    J Genet Couns; 2014 Aug; 23(4):506-15. PubMed ID: 24659383
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Dynamic software design for clinical exome and genome analyses: insights from bioinformaticians, clinical geneticists, and genetic counselors.
    Shyr C; Kushniruk A; van Karnebeek CD; Wasserman WW
    J Am Med Inform Assoc; 2016 Mar; 23(2):257-68. PubMed ID: 26117142
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
    Arora S; Haverfield E; Richard G; Haga SB; Mills R
    J Genet Couns; 2016 Apr; 25(2):337-43. PubMed ID: 26283062
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Impacts of genesurance considerations on genetic counselors' practice and attitudes.
    Thoreson E; Murphy L; Lemons J; Farach L; Wilson K; Woodson A; Wagner C
    J Genet Couns; 2020 Dec; 29(6):1210-1220. PubMed ID: 32432815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Reporting results from whole-genome and whole-exome sequencing in clinical practice: a proposal for Canada?
    Zawati MH; Parry D; Thorogood A; Nguyen MT; Boycott KM; Rosenblatt D; Knoppers BM
    J Med Genet; 2014 Jan; 51(1):68-70. PubMed ID: 24078715
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Content Analysis of Informed Consent for Whole Genome Sequencing Offered by Direct-to-Consumer Genetic Testing Companies.
    Niemiec E; Borry P; Pinxten W; Howard HC
    Hum Mutat; 2016 Dec; 37(12):1248-1256. PubMed ID: 27647801
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
    Vassy JL; Lautenbach DM; McLaughlin HM; Kong SW; Christensen KD; Krier J; Kohane IS; Feuerman LZ; Blumenthal-Barby J; Roberts JS; Lehmann LS; Ho CY; Ubel PA; MacRae CA; Seidman CE; Murray MF; McGuire AL; Rehm HL; Green RC;
    Trials; 2014 Mar; 15():85. PubMed ID: 24645908
    [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. 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]  

  • 13. Cost-Effectiveness of Whole-Genome vs Whole-Exome Sequencing Among Children With Suspected Genetic Disorders.
    Nurchis MC; Radio FC; Salmasi L; Heidar Alizadeh A; Raspolini GM; Altamura G; Tartaglia M; Dallapiccola B; Pizzo E; Gianino MM; Damiani G
    JAMA Netw Open; 2024 Jan; 7(1):e2353514. PubMed ID: 38277144
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-Genome and Whole-Exome Sequencing in Pediatric Oncology: An Assessment of Parent and Young Adult Patient Knowledge, Attitudes, and Expectations.
    Oberg JA; Ruiz J; Ali-Shaw T; Schlechtweg KA; Ricci A; Kung AL; Chung WK; Appelbaum PS; Glade Bender JL; Levine JM
    JCO Precis Oncol; 2018; 2():. PubMed ID: 32913997
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of Exome and Genome Sequencing Technologies for the Complete Capture of Protein-Coding Regions.
    Lelieveld SH; Spielmann M; Mundlos S; Veltman JA; Gilissen C
    Hum Mutat; 2015 Aug; 36(8):815-22. PubMed ID: 25973577
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Defining critical educational components of informed consent for genetic testing: views of US-based genetic counselors and medical geneticists.
    Hallquist MLG; Borensztein MJ; Coughlin CR; Buchanan AH; Andrew Faucett W; Peay HL; Smith ME; Tricou EP; Uhlmann WR; Wain KE; Ormond KE
    Eur J Hum Genet; 2023 Oct; 31(10):1165-1174. PubMed ID: 37308598
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic counseling for consumer-driven whole exome and whole genome sequencing: A commentary on early experiences.
    Schmidt JL; Maas R; Altmeyer SR
    J Genet Couns; 2019 Apr; 28(2):449-455. PubMed ID: 30861266
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study.
    Park J; Zayhowski K; Newson AJ; Ormond KE
    J Genet Couns; 2019 Apr; 28(2):292-303. PubMed ID: 30741463
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
    Bernhardt BA; Kellom K; Barbarese A; Faucett WA; Wapner RJ
    J Genet Couns; 2014 Dec; 23(6):938-47. PubMed ID: 24569858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A scoping study to explore the cost-effectiveness of next-generation sequencing compared with traditional genetic testing for the diagnosis of learning disabilities in children.
    Beale S; Sanderson D; Sanniti A; Dundar Y; Boland A
    Health Technol Assess; 2015 Jun; 19(46):1-90. PubMed ID: 26132578
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.