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 *

110 related articles for article (PubMed ID: 27848942)

  • 21. Lynch Syndrome Limbo: Patient Understanding of Variants of Uncertain Significance.
    Solomon I; Harrington E; Hooker G; Erby L; Axilbund J; Hampel H; Semotiuk K; Blanco A; Klein WMP; Giardiello F; Leonard L
    J Genet Couns; 2017 Aug; 26(4):866-877. PubMed ID: 28127677
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
    McGillivray G; Rosenfeld JA; McKinlay Gardner RJ; Gillam LH
    Prenat Diagn; 2012 Apr; 32(4):389-95. PubMed ID: 22467169
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Disclosure of cardiac variants of uncertain significance results in an exome cohort.
    Lawal TA; Lewis KL; Johnston JJ; Heidlebaugh AR; Ng D; Gaston-Johansson FG; Klein WMP; Biesecker BB; Biesecker LG
    Clin Genet; 2018 May; 93(5):1022-1029. PubMed ID: 29383714
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
    Rosell AM; Pena LD; Schoch K; Spillmann R; Sullivan J; Hooper SR; Jiang YH; Mathey-Andrews N; Goldstein DB; Shashi V
    J Genet Couns; 2016 Oct; 25(5):1019-31. PubMed ID: 26868367
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cancer patients' understandings of genetic variants of uncertain significance in clinical care.
    Amano Y; Raz A; Timmermans S; Shkedi-Rafid S
    J Community Genet; 2022 Aug; 13(4):381-388. PubMed ID: 35616809
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Patient hopes for diagnostic genomic sequencing: roles of uncertainty and social status.
    Khan CM; Moore EG; Leos C; Rini C
    Eur J Hum Genet; 2016 Jun; 24(6):803-8. PubMed ID: 26395557
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Variants of uncertain significance in BRCA1 and BRCA2 assessment of in silico analysis and a proposal for communication in genetic counselling.
    Moghadasi S; Hofland N; Wouts JN; Hogervorst FB; Wijnen JT; Vreeswijk MP; van Asperen CJ
    J Med Genet; 2013 Feb; 50(2):74-9. PubMed ID: 23231788
    [TBL] [Abstract][Full Text] [Related]  

  • 28. From the laboratory to the clinic: sharing BRCA VUS reclassification tools with practicing genetics professionals.
    Augusto BM; Lake P; Scherr CL; Couch FJ; Lindor NM; Vadaparampil ST
    J Community Genet; 2018 Jul; 9(3):209-215. PubMed ID: 29124491
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Approach to the patient with a variant of uncertain significance on genetic testing.
    Newey PJ
    Clin Endocrinol (Oxf); 2022 Oct; 97(4):400-408. PubMed ID: 35996232
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.
    Lynch JA; Sharp RR; Aufox SA; Bland ST; Blout C; Bowen DJ; Buchanan AH; Halverson C; Harr M; Hebbring SJ; Henrikson N; Hoell C; Holm IA; Jarvik G; Kullo IJ; Kochan DC; Larson EB; Lazzeri A; Leppig KA; Madden J; Marasa M; Myers MF; Peterson J; Prows CA; Kulchak Rahm A; Ralston J; Milo Rasouly H; Scrol A; Smith ME; Sturm A; Stuttgen K; Wiesner G; Williams MS; Wynn J; Williams JL
    J Pers Med; 2020 May; 10(2):. PubMed ID: 32413979
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Perceptions of provider's epistemic authority in response to variant of uncertain significance-related recommendations.
    Makhnoon S; Mork M; Arun B; Volk RJ; Peterson SK
    J Genet Couns; 2020 Oct; ():. PubMed ID: 33090616
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Impact of presymptomatic genetic testing on young adults: a systematic review.
    Godino L; Turchetti D; Jackson L; Hennessy C; Skirton H
    Eur J Hum Genet; 2016 Apr; 24(4):496-503. PubMed ID: 26173961
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Quality assessment of genetic counseling process in the context of presymptomatic testing for late-onset disorders: a thematic analysis of three review articles.
    Paneque M; Sequeiros J; Skirton H
    Genet Test Mol Biomarkers; 2012 Jan; 16(1):36-45. PubMed ID: 21819246
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Experiences of patients seeking to participate in variant of uncertain significance reclassification research.
    Makhnoon S; Garrett LT; Burke W; Bowen DJ; Shirts BH
    J Community Genet; 2019 Apr; 10(2):189-196. PubMed ID: 30027524
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Understanding variants of uncertain significance in the era of multigene panels: Through the eyes of the patient.
    Reuter C; Chun N; Pariani M; Hanson-Kahn A
    J Genet Couns; 2019 Aug; 28(4):878-886. PubMed ID: 31050105
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Toward the diagnosis of rare childhood genetic diseases: what do parents value most?
    Pollard S; Weymann D; Dunne J; Mayanloo F; Buckell J; Buchanan J; Wordsworth S; Friedman JM; Stockler-Ipsiroglu S; Dragojlovic N; Elliott AM; Harrison M; Lynd LD; Regier DA
    Eur J Hum Genet; 2021 Oct; 29(10):1491-1501. PubMed ID: 33903739
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Predictive Genetic Testing of Children for Adult-Onset Conditions: Negotiating Requests with Parents.
    Fenwick A; Plantinga M; Dheensa S; Lucassen A
    J Genet Couns; 2017 Apr; 26(2):244-250. PubMed ID: 27680566
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Views of Israeli healthcare professionals regarding communication of genetic variants of uncertain significance to patients.
    Levin Fridman A; Raz A; Timmermans S; Shkedi-Rafid S
    J Genet Couns; 2022 Aug; 31(4):912-921. PubMed ID: 35122362
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
    Nisselle A; Macciocca I; McKenzie F; Vuong H; Dunlop K; McClaren B; Metcalfe S; Gaff C;
    J Genet Couns; 2019 Apr; 28(2):367-377. PubMed ID: 30779404
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic counselling in the era of genomic medicine.
    Patch C; Middleton A
    Br Med Bull; 2018 Jun; 126(1):27-36. PubMed ID: 29617718
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.