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 *

256 related articles for article (PubMed ID: 23643378)

  • 1. Incidental variants are critical for genomics.
    Biesecker LG
    Am J Hum Genet; 2013 May; 92(5):648-51. PubMed ID: 23643378
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genomic test validation for incidental findings.
    Park JY; Fortina P; Kricka LJ
    Clin Chem; 2014 Feb; 60(2):292-3. PubMed ID: 23818443
    [No Abstract]   [Full Text] [Related]  

  • 3. Management of Incidental Findings in Clinical Genomic Sequencing.
    Krier JB; Green RC
    Curr Protoc Hum Genet; 2015 Oct; 87():9.23.1-9.23.16. PubMed ID: 26439717
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium.
    Berg JS; Amendola LM; Eng C; Van Allen E; Gray SW; Wagle N; Rehm HL; DeChene ET; Dulik MC; Hisama FM; Burke W; Spinner NB; Garraway L; Green RC; Plon S; Evans JP; Jarvik GP;
    Genet Med; 2013 Nov; 15(11):860-7. PubMed ID: 24195999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
    Shickh S; Clausen M; Mighton C; Gutierrez Salazar M; Zakoor KR; Kodida R; Reble E; Elser C; Eisen A; Panchal S; Aronson M; Graham T; Armel SR; Morel CF; Fattouh R; Glogowski E; Schrader KA; Hamilton JG; Offit K; Robson M; Carroll JC; Isaranuwatchai W; Kim RH; Lerner-Ellis J; Thorpe KE; Laupacis A; Bombard Y;
    BMJ Open; 2019 Oct; 9(10):e031092. PubMed ID: 31594892
    [TBL] [Abstract][Full Text] [Related]  

  • 6. American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
    Rehder CW; David KL; Hirsch B; Toriello HV; Wilson CM; Kearney HM
    Genet Med; 2013 Feb; 15(2):150-2. PubMed ID: 23328890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review.
    Elfatih A; Mohammed I; Abdelrahman D; Mifsud B
    Physiol Genomics; 2021 Sep; 53(9):373-384. PubMed ID: 34250816
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Choices of incidental findings of individuals undergoing genome wide sequencing, a single center's experience.
    Bishop CL; Strong KA; Dimmock DP
    Clin Genet; 2017 Jan; 91(1):137-140. PubMed ID: 27392285
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.
    Anderson JA; Hayeems RZ; Shuman C; Szego MJ; Monfared N; Bowdin S; Zlotnik Shaul R; Meyn MS
    Clin Genet; 2015 Apr; 87(4):301-10. PubMed ID: 25046648
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recommendations for returning genomic incidental findings? We need to talk!
    Burke W; Antommaria AH; Bennett R; Botkin J; Clayton EW; Henderson GE; Holm IA; Jarvik GP; Khoury MJ; Knoppers BM; Press NA; Ross LF; Rothstein MA; Saal H; Uhlmann WR; Wilfond B; Wolf SM; Zimmern R
    Genet Med; 2013 Nov; 15(11):854-9. PubMed ID: 23907645
    [TBL] [Abstract][Full Text] [Related]  

  • 11. To disclose, or not to disclose? Perspectives of clinical genomics professionals toward returning incidental findings from genomic research.
    AlFayyad I; Al-Tannir M; Abu-Shaheen A; AlGhamdi S
    BMC Med Ethics; 2021 Jul; 22(1):101. PubMed ID: 34315465
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The DNA of a nation.
    Marx V
    Nature; 2015 Aug; 524(7566):503-5. PubMed ID: 26310768
    [No Abstract]   [Full Text] [Related]  

  • 13. Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
    Abdul-Karim R; Berkman BE; Wendler D; Rid A; Khan J; Badgett T; Hull SC
    Pediatrics; 2013 Mar; 131(3):564-71. PubMed ID: 23400601
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study.
    Saelaert M; Mertes H; Moerenhout T; De Baere E; Devisch I
    BMC Med Ethics; 2020 Jan; 21(1):9. PubMed ID: 32000764
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Incidental findings of uncertain significance: To know or not to know--that is not the question.
    Hofmann B
    BMC Med Ethics; 2016 Feb; 17():13. PubMed ID: 26873084
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.
    Thauvin-Robinet C; Thevenon J; Nambot S; Delanne J; Kuentz P; Bruel AL; Chassagne A; Cretin E; Pelissier A; Peyron C; Gautier E; Lehalle D; Jean-Marçais N; Callier P; Mosca-Boidron AL; Vitobello A; Sorlin A; Tran Mau-Them F; Philippe C; Vabres P; Demougeot L; Poé C; Jouan T; Chevarin M; Lefebvre M; Bardou M; Tisserant E; Luu M; Binquet C; Deleuze JF; Verstuyft C; Duffourd Y; Faivre L
    Eur J Hum Genet; 2019 Aug; 27(8):1197-1214. PubMed ID: 31019283
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.
    Daack-Hirsch S; Driessnack M; Hanish A; Johnson VA; Shah LL; Simon CM; Williams JK
    Clin Genet; 2013 Jul; 84(1):11-8. PubMed ID: 23590238
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach.
    Feng YA; Stanaway IB; Connolly JJ; Denny JC; Luo Y; Weng C; Wei WQ; Weiss ST; Karlson EW; Smoller JW
    BMC Genomics; 2022 May; 23(1):385. PubMed ID: 35590255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Searching for secondary findings: considering actionability and preserving the right not to know.
    Isidor B; Julia S; Saugier-Veber P; Weil-Dubuc PL; Bézieau S; Bieth E; Bonnefont JP; Munnich A; Bourdeaut F; Bourgain C; Chassaing N; Corradini N; Haye D; Plaisancie J; Dupin-Deguine D; Calvas P; Mignot C; Cogné B; Manouvrier S; Pasquier L; Héron D; Boycott KM; Turrini M; Vears DF; Nizon M; Vincent M
    Eur J Hum Genet; 2019 Oct; 27(10):1481-1484. PubMed ID: 31186543
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
    Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
    Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.