279 related articles for article (PubMed ID: 30629777)
1. Role and practice evolution for genetic counseling in the genomic era: The experience of Australian and UK genetics practitioners.
Dwarte T; Barlow-Stewart K; O'Shea R; Dinger ME; Terrill B
J Genet Couns; 2019 Apr; 28(2):378-387. PubMed ID: 30629777
[TBL] [Abstract][Full Text] [Related]
2. Informed Consent in the Genomics Era.
Rego S; Grove ME; Cho MK; Ormond KE
Cold Spring Harb Perspect Med; 2020 Aug; 10(8):. PubMed ID: 31570382
[TBL] [Abstract][Full Text] [Related]
3. Mainstreaming informed consent for genomic sequencing: A call for action.
Bunnik EM; Dondorp WJ; Bredenoord AL; de Wert G; Cornel MC
Eur J Cancer; 2021 May; 148():405-410. PubMed ID: 33784533
[TBL] [Abstract][Full Text] [Related]
4. Mainstreaming genomic testing: pre-test counselling and informed consent.
Cormack M; Irving KB; Cunningham F; Fennell AP
Med J Aust; 2024 May; 220(8):403-406. PubMed ID: 38479398
[No Abstract] [Full Text] [Related]
5. Personal genomic screening: How best to facilitate preparedness of future clients.
Fleming J; Terrill B; Dziadek M; Kirk EP; Roscioli T; Barlow-Stewart K
Eur J Med Genet; 2019 May; 62(5):397-404. PubMed ID: 31085343
[TBL] [Abstract][Full Text] [Related]
6. Genetic Counseling in the Era of Genomics: What's all the Fuss about?
Brett GR; Wilkins EJ; Creed ET; West K; Jarmolowicz A; Valente GM; Prawer Y; Lynch E; Macciocca I
J Genet Couns; 2018 Sep; 27(5):1010-1021. PubMed ID: 29368275
[TBL] [Abstract][Full Text] [Related]
7. "Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Tomlinson AN; Skinner D; Perry DL; Scollon SR; Roche MI; Bernhardt BA
J Genet Couns; 2016 Feb; 25(1):62-72. PubMed ID: 25911622
[TBL] [Abstract][Full Text] [Related]
8. The new genetics and informed consent: differentiating choice to preserve autonomy.
Bunnik EM; de Jong A; Nijsingh N; de Wert GM
Bioethics; 2013 Jul; 27(6):348-55. PubMed ID: 23718722
[TBL] [Abstract][Full Text] [Related]
9. Old Challenges or New Issues? Genetic Health Professionals' Experiences Obtaining Informed Consent in Diagnostic Genomic Sequencing.
Vears DF; Borry P; Savulescu J; Koplin JJ
AJOB Empir Bioeth; 2021; 12(1):12-23. PubMed ID: 33017265
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Clinical application of genomic high-throughput data: Infrastructural, ethical, legal and psychosocial aspects.
Umbach N; Beißbarth T; Bleckmann A; Duttge G; Flatau L; König A; Kuhn J; Perera-Bel J; Roschauer J; Schulze TG; Schweda M; Urban A; Zimmermann A; Sax U
Eur Neuropsychopharmacol; 2020 Feb; 31():1-15. PubMed ID: 31866110
[TBL] [Abstract][Full Text] [Related]
12. Attitudes toward offering genetic counseling for psychiatric conditions among genetics healthcare practitioners in the United Kingdom: A qualitative study.
Rowlatt AE; McAllister M; Cuthbert A
J Genet Couns; 2022 Feb; 31(1):279-290. PubMed ID: 34363721
[TBL] [Abstract][Full Text] [Related]
13. Genomic testing: a struggle for oncologists.
Hede K
J Natl Cancer Inst; 2014 Jun; 106(6):dju172. PubMed ID: 24907388
[No Abstract] [Full Text] [Related]
14. Models of consent to return of incidental findings in genomic research.
Appelbaum PS; Parens E; Waldman CR; Klitzman R; Fyer A; Martinez J; Price WN; Chung WK
Hastings Cent Rep; 2014; 44(4):22-32. PubMed ID: 24919982
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Managing the ethical challenges of next-generation sequencing in genomic medicine.
Clarke AJ
Br Med Bull; 2014 Sep; 111(1):17-30. PubMed ID: 25122627
[TBL] [Abstract][Full Text] [Related]
17. On the limits of genetic responsibility: communication and consent for tumour testing for Lynch syndrome.
Shipman HE; Arribas-Allyon M; Murray A; Gaff CL
Commun Med; 2013; 10(3):225-35. PubMed ID: 25233560
[TBL] [Abstract][Full Text] [Related]
18. Variation among Consent Forms for Clinical Whole Exome Sequencing.
Fowler SA; Saunders CJ; Hoffman MA
J Genet Couns; 2018 Feb; 27(1):104-114. PubMed ID: 28689263
[TBL] [Abstract][Full Text] [Related]
19. Responsibility, identity, and genomic sequencing: A comparison of published recommendations and patient perspectives on accepting or declining incidental findings.
Boardman F; Hale R
Mol Genet Genomic Med; 2018 Nov; 6(6):1079-1096. PubMed ID: 30370638
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]