Detalhe da pesquisa
1.
Providing recurrence risk counselling for parents after diagnosis of a serious genetic condition caused by an apparently de novo mutation in their child: a qualitative investigation of the PREGCARE strategy with UK clinical genetics practitioners.
J Med Genet
; 60(9): 925-931, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36931705
2.
Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory records.
J Med Genet
; 60(7): 669-678, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36572524
3.
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
4.
Artificial intelligence and medical research databases: ethical review by data access committees.
BMC Med Ethics
; 24(1): 49, 2023 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37422629
5.
The impact of artificial intelligence on the person-centred, doctor-patient relationship: some problems and solutions.
BMC Med Inform Decis Mak
; 23(1): 73, 2023 04 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37081503
6.
"I don't think people are ready to trust these algorithms at face value": trust and the use of machine learning algorithms in the diagnosis of rare disease.
BMC Med Ethics
; 23(1): 112, 2022 11 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36384545
7.
Taking it to the bank: the ethical management of individual findings arising in secondary research.
J Med Ethics
; 47(10): 689-696, 2021 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-33441306
8.
Nitroglycerin for treatment of retained placenta: A randomised, placebo-controlled, multicentre, double-blind trial in the UK.
PLoS Med
; 16(12): e1003001, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31887169
9.
Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis.
Genet Med
; 21(12): 2846, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31235794
10.
Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis.
Genet Med
; 21(12): 2667-2675, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31186523
11.
Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure.
Hum Genomics
; 12(1): 24, 2018 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29695297
12.
Patients' Views of Treatment-Focused Genetic Testing (TFGT): Some Lessons for the Mainstreaming of BRCA1 and BRCA2 Testing.
J Genet Couns
; 2018 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29752676
13.
Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.
J Genet Couns
; 27(3): 702-708, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29168041
14.
AIgorithmic Ethics: A Technically Sweet Solution to a Non-Problem.
Am J Bioeth
; 22(7): 28-30, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35737495
15.
The Psychosocial Impact of Undergoing Prophylactic Total Gastrectomy (PTG) to Manage the Risk of Hereditary Diffuse Gastric Cancer (HDGC).
J Genet Couns
; 26(4): 752-762, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27837291
16.
Therapeutic appropriation: a new concept in the ethics of clinical research.
J Med Ethics
; 42(12): 805-808, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27733438
17.
If you build it, they will come: unintended future uses of organised health data collections.
BMC Med Ethics
; 17(1): 54, 2016 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27600117
18.
Revealing the results of whole-genome sequencing and whole-exome sequencing in research and clinical investigations: some ethical issues.
J Med Ethics
; 41(4): 317-21, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25038088
19.
Treating childhood intermittent distance exotropia: a qualitative study of decision making.
BMC Ophthalmol
; 15: 112, 2015 Aug 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26296859
20.
Big data phenotyping in rare diseases: some ethical issues.
Genet Med
; 21(2): 272-274, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29907800