Genomic health data generation in the UK: a 360 view by Ormondroyd, E, Border, P, Hayward, J, Papanikitas, A

Pre-symptomatic genetic testing for inherited cardiac conditions: A qualitative exploration of psychosocial and ethical implications by Ormondroyd, E, Oates, S, Parker, M, Blair, E, Watkins, H

Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications. by Ormondroyd, E, Oates, S, Parker, M, Blair, E, Watkins, H

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies by Ormondroyd, E, Mackley, M, Fletcher, B, Parker, M, Watkins, H

From genotype to phenotype: Clinical assessment and participant perspective of a secondary genomic finding associated with long QT syndrome by Mackley, M, McGuire, K, Taylor, J, Watkins, H, Ormondroyd, E

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study by Mackley, M, Blair, E, Parker, M, Taylor, J, Watkins, H, Ormondroyd, E

Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease by Buchanan, J, Blair, E, Thomson, KL, Ormondroyd, E, Watkins, H, Taylor, JC, Wordsworth, S

Communicating genetics research results to families: problems arising when the patient participant is deceased. by Ormondroyd, E, Moynihan, C, Ardern-Jones, A, Eeles, R, Foster, C, Davolls, S, Watson, M

Disclosure of genetics research results after the death of the patient participant: a qualitative study of the impact on relatives. by Ormondroyd, E, Moynihan, C, Watson, M, Foster, C, Davolls, S, Ardern-Jones, A, Eeles, R

Genomic sequencing in oncology: Considerations for integration in routine cancer care by Rahman, B, Lamb, A, Protheroe, A, Shah, K, Solomons, J, Williams, J, Ormondroyd, E

“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and th... by Ormondroyd, E, Mackley, M, Blair, E, Craft, J, Knight, J, Taylor, J, Taylor, J, Watkins, H

Genetic therapies for cardiomyopathy: survey of attitudes of the patient community for the CureHeart project by Ormondroyd, E, Grace, C, Borsari, W, Goel, A, McDonough, B, Rose, J, Seidman, C, Watkins, H

Whole-genome sequencing of patients with rare diseases in a national health system by Turro, E, Astle, WJ, Megy, K, Bennett, DL, Ormondroyd, E, Roberts, I, Roy, NBA, Themistocleous, A, Watkins, H

Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study by Ormondroyd, E, Mackley, M, Blair, E, Craft, J, Knight, J, Taylor, J, Taylor, J, Wilkie, A, Watkins, H

Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes by Ormondroyd, E, Harper , AR, Thomson, KL, Mackley, MP, Martin, J, Penkett, CJ, Salatino, S, Stark, H, Stephens, J, Watkins, H

Distinct ECG phenotypes identified in hypertrophic cardiomyopathy using machine learning associate with arrhythmic risk markers by Lyon, A, Ariga, R, Minchole, A, Mahmod, M, Ormondroyd, E, Laguna, P, de Freitas, N, Neubauer, S, Watkins, H, Rodriguez, B

Taking it to the bank: the ethical management of individual findings arising in secondary research by Graham, M, Hallowell, N, Solberg, B, Haukkala, A, Holliday, J, Kerasidou, A, Littlejohns, T, Ormondroyd, E, Skolbekken, J-A, Vornanen, M

Evaluation of Clinical Diagnostic Potential of Next Generation Sequencing using Hypertrophic Cardiomyopathy as a Model by Taylor, J, Kaur, K, Broxholme, J, Copley, R, Thistleton, J, Reid, S, Ormondroyd, E, Seller, A, Blair, E, Ragoussis, I, Watkins, H

Public and patient involvement in research to support genome services development in the UK by Hunter, A, Lewis, C, Hill, M, Chitty, LS, Leeson-Beevers, K, McInnes-Dean, H, Harvey, K, Pichini, A, Ormondroyd, E, Thomson, K

Exploring the potential duty of care in clinical genomics under UK law. by Mitchell, C, Ploem, C, Chico, V, Ormondroyd, E, Hall, A, Wallace, S, Fay, M, Goodwin, D, Bell, J, Phillips, S, Taylor, J, Hennekam, R, Kaye, J