Detalhe da pesquisa
1.
Ethical preparedness in genomic medicine: how NHS clinical scientists navigate ethical issues.
J Med Ethics
; 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38320848
2.
Ethical preparedness and developments in genomic healthcare.
J Med Ethics
; 2023 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37268409
3.
Beyond regulatory approaches to ethics: making space for ethical preparedness in healthcare research.
J Med Ethics
; 49(5): 352-356, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35725300
4.
Discussion of off-target and tentative genomic findings may sometimes be necessary to allow evaluation of their clinical significance.
J Med Ethics
; 2023 Jun 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37339848
5.
Mitochondrial DNA variants in genomic data: diagnostic uplifts and predictive implications.
Nat Rev Genet
; 22(9): 547-548, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34050335
6.
Using a biomarker acutely to identify babies at risk of serious adverse effects from antibiotics: where is the 'Terrible Moral and Medical Dilemma'?
J Med Ethics
; 47(2): 117-118, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33335072
7.
Recent developments in genetic/genomic medicine.
Clin Sci (Lond)
; 133(5): 697-708, 2019 03 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30837331
8.
Expanded carrier screening for autosomal recessive conditions in health care: Arguments for a couple-based approach and examination of couples' views.
Prenat Diagn
; 39(5): 369-378, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30756401
9.
The moral argument for heritable genome editing requires an inappropriately deterministic view of genetics.
J Med Ethics
; 45(8): 526-527, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30862707
10.
Is it acceptable to contact an anonymous egg donor to facilitate diagnostic genetic testing for the donor-conceived child?
J Med Ethics
; 45(6): 357-360, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31189727
11.
Familial genetic risks: how can we better navigate patient confidentiality and appropriate risk disclosure to relatives?
J Med Ethics
; 45(8): 504-507, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31123189
12.
Focusing attention on physicians' climate-related duties may risk missing the bigger picture: towards a systems approach to health and climate.
J Med Ethics
; 2024 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-38589196
13.
Towards a national genomics medicine service: the challenges facing clinical-research hybrid practices and the case of the 100 000 genomes project.
J Med Ethics
; 44(6): 397-403, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29496751
14.
Rare variants in NR2F2 cause congenital heart defects in humans.
Am J Hum Genet
; 94(4): 574-85, 2014 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-24702954
15.
Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom.
Genet Med
; 18(9): 876-81, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26890453
16.
What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Prenat Diagn
; 36(3): 252-9, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26743561
17.
Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.
Genet Med
; 17(8): 668-78, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25503495
18.
Old consent and new developments: health professionals should ask and not presume.
J Med Ethics
; 46(6): 412-413, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31662484
19.
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Am J Hum Genet
; 98(3): 592, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28863274
20.
Systematic reanalysis of genomic data by diagnostic laboratories: a scoping review of ethical, economic, legal and (psycho)social implications.
Eur J Hum Genet
; 32(5): 489-497, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38480795