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7 research outputs found

Ethics, Policy, and Educational Issues in Genetic Testing

Author: American College of Medical Genetics Board of Directors
ASHG/ACMG Report
Association of Women's Health Obstetric, and Neonatal Nursing
Clayton E.W.
Feetham S.L.
Feetham S.L.
French M.E.
Goldberg I.V.
Guttmacher A.
Health Resources and Services Administration and the National Institutes of Health
Human Genetics Commission
International Society of Nurses in Genetics
Kirk M.
Lea D.H.
Masny A.
Masny A.
National Center for Human Genome Research
National Coalition for Health Professional Education in Genetics
National Health Service Department of Health
Oncology Nursing Society
Public Health Genetics Unit
Reede J.Y.
Report of a Working Party of the Clinical Genetics Society (UK)
Skirton H.
U.S. Department of Health and Human Services Office for Civil Rights
Willard H.F.
Wolf L.E.
World Health Organisation
Publication venue: 'Wiley'
Publication date
Field of study

Crossref

Bioconstitutional Imaginaries and the Comparative Politics of Genetic Self-knowledge

Crossref

A framework for genetic service provision for haemophilia and other inherited bleeding disorders

Author: British Medical Association
Department of Health
European Society of Human Genetics Public ad Professional Policy Committee
Genetic Interest Group
Genetic Interest Group
Human Genetics Commission
Miller R.
NHS Executive
Nuffield Council on Bioethics
RCN Haemophilia Nurses Association
Report of Working Party of the Clinical Genetics Society (UK)
Robertson J.
Royal College of Obstetrics and Gynaecology
The Haemophilia Alliance
UKHCDO Genetics Working Party
Publication venue: 'Wiley'
Publication date
Field of study

Crossref

Redefining a technology: public and private genetic testing in Aotearoa New Zealand

Author: Akrich
Cartwright
Cockburn
Department of Health UK
Dew
Everts
Foucault
Gauld
Genetic Technologies Ltd
Healy
Hughes
Human Genetics Commission
Kelsey
Kerr
Law
Lippman
MacKenzie
Melucci
Nelkin
Nettleton
NHC
NHC
Oudshoorn
Petersen
Polzer
Rose
Scott
Taussig
White
Williams-Jones
Winner
Publication venue: 'Wiley'
Publication date
Field of study

Crossref

Informed choice and public health screening for children: the case of blood spot screening

Author: Broclain D
Department of Health
Dodge J
Faden RR
Grant DB
Green J
Hargreaves K
Human Genetics Commission
Jones S
National Screening Committee
National Screening Committee
Newson A
Oliver S
Petticrew MP
Pollitt RJ
Smith I
Stewart R
UK Newborn Screening Programme Centre
Zenner D
Publication venue: 'Wiley'
Publication date
Field of study

Crossref

Securing our genetic health: engendering trust in UK Biobank

Author: Austin
Bailey
Barbour
Barnett
Boyes
Bud
Callan
Chadwick
Condit
Condit
Conrad
Conrad
Coote
Department of Health
Evans
Everett
Frow
GeneWatch UK
Gibson
Giddens
Hansen
Holtzman
House of Commons Select Committee on Science and Technology
House of Lords Select Committee on Science and Technology
House of Lords Select Committee on Science and Technology
Human Genetics Commission
Human Genetics Commission
Institute of Ideas
Interim Advisory Group
Joss
Kaye
Kaye
Keller
Marshall
Martin
Martin
Miller
Miringoff
MRC
MRC The Wellcome Trust and Department of Health
Nelkin
Nelkin
Nisbet
Office of Science and Technology and The Wellcome Trust
Parliamentary Office of Science and Technology
People Science and Policy Ltd
Petersen
Petersen
Petersen
Petersen
Petryna
Pálsson
Radford
Rose
Rose
Taylor-Gooby
The Wellcome Trust and MRC
The Wellcome Trust and MRC
Titmus
Turney
Van Dijck
Weldon
Whitt
World Health Organization
Publication venue: 'Wiley'
Publication date
Field of study

Crossref

Patients' understanding of genetic susceptibility testing in mainstream medicine: qualitative study on thrombophilia.

Author: A Bharadwaj
A Clarke
A Petersen
B Glaser
B Meiser
B Meiser
C Novas
C Shaw
CM McBride
D Kevles
Department of Health
Department of Health
Department of Health
E Vidler
E Watson
EA Hellmann
F Henwood
F Walter
G Elwyn
G Hollman
HC Gooding
Human Genetics Commission
I Shaw
I Walker
J Clarke
J Emery
J Smith
John L Campbell
Joint Committee on Medical Genetics
K Armstrong
L Rutten
L Wilkins-Haug
LF Ross
M Baars
M Broadstock
Maggie H Shepherd
National Statistics
NHS Modernization Agency
P Yoon
Paula M Saukko
PM Saukko
R Robins
S Middeldorp
S Middeldorp
S Ramanadhan
S Shepperd
SE Humphries
Sian Ellard
Suzanne H Richards
T Marteau
T Marteau
UK Genetic Testing Network
W Grody
Publication venue: 'Springer Science and Business Media LLC'
Publication date: 01/01/2007
Field of study

UK and US policy initiatives have suggested that, in the future, patients and clinicians in mainstream medicine could use genetic information to prevent common illnesses. There are no studies on patients' experience and understanding of the process of testing for common genetic susceptibilities in mainstream medicine.This article is freely available via Open Access. Click on the ‘Additional Link’ above to access the full-text from the publisher’s site.PDA/02/06/098/Department of Health/United Kingdo

RD&E Research Repository

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