Detalhe da pesquisa
1.
Towards implementation of comprehensive breast cancer risk prediction tools in health care for personalised prevention.
Prev Med
; 159: 107075, 2022 06.
Artigo
Inglês
| MEDLINE | ID: mdl-35526672
2.
Implications of using whole genome sequencing to test unselected populations for high risk breast cancer genes: a modelling study.
Hered Cancer Clin Pract
; 14: 12, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27252788
3.
Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases.
J Inherit Metab Dis
; 37(6): 889-98, 2014 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-25022222
4.
What ethical and legal principles should guide the genotyping of children as part of a personalised screening programme for common cancer?
J Med Ethics
; 40(3): 163-7, 2014 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-23454719
5.
Incorporating genomics into breast and prostate cancer screening: assessing the implications.
Genet Med
; 15(6): 423-32, 2013 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-23412607
6.
Systematic review of birth prevalence of neural tube defects in India.
Birth Defects Res A Clin Mol Teratol
; 97(7): 437-43, 2013 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-23873811
7.
Preparing clinicians for genomic medicine.
Postgrad Med J
; 92(1089): 369-71, 2016 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-27001864
8.
Extending the reach of public health genomics: what should be the agenda for public health in an era of genome-based and "personalized" medicine?
Genet Med
; 12(12): 785-91, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21189494
9.
Legal and ethical implications of inherited cardiac disease in clinical practice within the UK.
J Med Ethics
; 36(12): 762-6, 2010 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-21112937
10.
Genetics in ophthalmology: equity in service provision?
J Public Health (Oxf)
; 32(2): 259-66, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-19951987
11.
A toolkit for incorporating genetics into mainstream medical services: Learning from service development pilots in England.
BMC Health Serv Res
; 10: 125, 2010 May 14.
Artigo
Inglês
| MEDLINE | ID: mdl-20470377
12.
Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Genet Med
; 11(3): 139-46, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19367186
13.
Beyond public health genomics: proposals from an international working group.
Eur J Public Health
; 24(6): 877-9, 2014 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-25168910
14.
Mainstreaming of genomic medicine in gastroenterology, present and future: a nationwide survey of UK gastroenterology trainees.
BMJ Open
; 9(10): e030505, 2019 10 22.
Artigo
Inglês
| MEDLINE | ID: mdl-31640999
15.
Risk stratification, genomic data and the law.
J Community Genet
; 9(3): 195-199, 2018 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-29470710
16.
Competences, education and support for new roles in cancer genetics services: outcomes from the cancer genetics pilot projects.
Fam Cancer
; 6(2): 171-80, 2007.
Artigo
Inglês
| MEDLINE | ID: mdl-17520353
17.
Realising the benefits of genetics for health.
Lancet
; 376(9750): 1370-1, 2010 Oct 23.
Artigo
Inglês
| MEDLINE | ID: mdl-20971348
18.
Genomics education for medical professionals - the current UK landscape.
Clin Med (Lond)
; 16(4): 347-52, 2016 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-27481379
19.
Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?
J Pers Med
; 5(2): 191-212, 2015 Jun 09.
Artigo
Inglês
| MEDLINE | ID: mdl-26068647
20.
From Mendel to the Human Genome Project: the implications for nurse education.
Nurse Educ Today
; 23(5): 380-5; discussion 386-7, 2003 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-12831804