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Correction: Delivering genomic medicine in the UK National Health Service: a systematic review and narrative synthesis.

Journal article

Pearce C. et al, (2019), Genetics in medicine : official journal of the American College of Medical Genetics, 21

Does the type of disease matter when receiving secondary findings? A qualitative vignette study on Finnish adults' views

Conference paper

Vornanen M. et al, (2019), EUROPEAN JOURNAL OF HUMAN GENETICS, 27, 716 - 716

Mainstreaming BRCA1 and BRCA2 testing: an interview study of healthcare professionals' views

Conference paper

Wright S. et al, (2019), EUROPEAN JOURNAL OF HUMAN GENETICS, 27, 664 - 665

Moving into the mainstream: Treatment focussed genetic testing a screening tool or diagnostic resource?

Conference paper

Hallowell N. et al, (2019), EUROPEAN JOURNAL OF HUMAN GENETICS, 27, 704 - 704

Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis.

Journal article

Pearce C. et al, (2019), Genetics in medicine : official journal of the American College of Medical Genetics

High-risk women's risk perception after receiving personalized polygenic breast cancer risk information.

Journal article

Forrest LE. et al, (2019), Journal of community genetics, 10, 197 - 206

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study.

Journal article

Vornanen M. et al, (2019), Journal of genetic counseling, 28, 343 - 354

Big data phenotyping in rare diseases: some ethical issues.

Journal article

Hallowell N. et al, (2019), Genetics in medicine : official journal of the American College of Medical Genetics, 21, 272 - 274

Enabling Global Clinical Collaborations on Identifiable Patient Data: The Minerva Initiative.

Journal article

Nellåker C. et al, (2019), Frontiers in genetics, 10

How should decision aids be used during counseling to help patients who are "genetically at risk"?

Journal article

Evans N. et al, (2019), AMA Journal of Ethics, 21, 865 - 872

'I would like to discuss it further with an expert': a focus group study of Finnish adults' perspectives on genetic incidental findings

Conference paper

Vornanen M. et al, (2018), EUROPEAN JOURNAL OF HUMAN GENETICS, 26, 816 - 816

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study.

Journal article

Vornanen M. et al, (2018), Journal of genetic counseling

Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.

Journal article

Young M-A. et al, (2018), Journal of genetic counseling, 27, 702 - 708

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