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Ethical Considerations in Research with Genomic Data.

Journal article

Horton R. and Lucassen A., (2022), The New bioethics : a multidisciplinary journal of biotechnology and the body, 1 - 15

Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants.

Journal article

Loong L. et al, (2022), Genetics in medicine : official journal of the American College of Medical Genetics, 24, 552 - 563

Re-imagining ‘the patient’: Linked lives and lessons from genomic medicine

Journal article

Weller S. et al, (2022), Social Science & Medicine, 297, 114806 - 114806

Public Trust and Trustworthiness in Biobanking: The Need for More Reflexivity.

Journal article

Samuel G. et al, (2022), Biopreservation and biobanking

Sustainable biobanks: a case study for a green global bioethics.

Journal article

Samuel G. et al, (2022), Global bioethics = Problemi di bioetica, 33, 50 - 64

In the family: access to, and communication of, familial information in clinical practice.

Journal article

Lucassen A. and Clarke A., (2021), Human genetics

Care of men with cancer-predisposing BRCA variants.

Journal article

Horton R. et al, (2021), BMJ (Clinical research ed.), 375

Couple-based expanded carrier screening provided by general practitioners to couples in the Dutch general population: psychological outcomes and reproductive intentions.

Journal article

Birnie E. et al, (2021), Genetics in medicine : official journal of the American College of Medical Genetics, 23, 1761 - 1768

Mitochondrial DNA variants in genomic data: diagnostic uplifts and predictive implications.

Journal article

Macken WL. et al, (2021), Nature reviews. Genetics, 22, 547 - 548

Patient data ownership: who owns your health?

Journal article

Liddell K. et al, (2021), Journal of law and the biosciences, 8

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study.

Journal article

International Mismatch Repair Consortium None., (2021), The Lancet. Oncology, 22, 1014 - 1022

Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations.

Journal article

Garrett A. et al, (2021), Journal of medical genetics, 58, 297 - 304

The ethics of genomic medicine: redefining values and norms in the UK and France

Journal article

Gaille M. and Horn R., (2021), European Journal of Human Genetics, 29, 780 - 788

What is the meaning of a 'genomic result' in the context of pregnancy?

Journal article

Shkedi-Rafid S. et al, (2021), European journal of human genetics : EJHG, 29, 225 - 230

Cancer Variant Interpretation Group UK (CanVIG-UK): an exemplar national subspecialty multidisciplinary network.

Journal article

Garrett A. et al, (2020), Journal of medical genetics, 57, 829 - 834

Exploring patient deliberation prior to predictive genetic testing in the absence of immediate clinical utility

Conference paper

Ballard LM. et al, (2020), EUROPEAN JOURNAL OF HUMAN GENETICS, 28, 110 - 110

Towards personalized genetic counselling: exploring subgroups among counselees based on different facets of empowerment before the first visit

Conference paper

Voorwinden J. et al, (2020), EUROPEAN JOURNAL OF HUMAN GENETICS, 28, 109 - 110

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