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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

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

Research or clinical care: what's the difference?

Journal article

Hallowell N., (2018), Journal of medical ethics, 44, 359 - 360

High-risk individuals' perceptions of reproductive genetic testing for CDH1 mutations.

Journal article

Hallowell N. et al, (2017), Familial cancer, 16, 531 - 535

Primary care physicians' views about gatekeeping in clinical research recruitment: A qualitative study.

Journal article

Guillemin M. et al, (2017), AJOB empirical bioethics, 8, 99 - 105

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