Search results - ORA - Oxford University Research Archive

1

Journal article

Genomic sequencing in oncology: Considerations for integration in routine cancer care

Rahman, B, Lamb, A, Protheroe, A, et al.
2022-04-05

2

Journal article

Genomic health data generation in the UK: a 360 view

Ormondroyd, E, Border, P, Hayward, J, et al.
2021-10-19

3

Journal article

Incremental value of left atrial booster and reservoir strain in predicting atrial fibrillation in patients with hypertrophic cardiomyopathy: a cardiovascular magnetic resonance study

Raman, B, Smillie, RW, Mahmod, M, et al.
2021-10-11

4

Journal article

Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity

Harper, AR, Goel, A, Grace, C, et al.
2021-01-25

5

Journal article

Taking it to the bank: the ethical management of individual findings arising in secondary research

Graham, M, Hallowell, N, Solberg, B, et al.
2021-01-13

6

Journal article

Secondary findings in inherited heart conditions: a genotype-first feasibility study to assess phenotype, behavioural and psychosocial outcomes

Ormondroyd, E, Harper , AR, Thomson, KL, et al.
2020-07-20

7

Journal article

Whole-genome sequencing of patients with rare diseases in a national health system

Turro, E, Astle, WJ, Megy, K, et al.
2020-06-24

8

Journal article

A Re-evaluation of the South Asian MYBPC3Δ25 Intronic Deletion in Hypertrophic Cardiomyopathy

Harper, AR, Bowman, M, Hayesmoore, JBG, et al.
2020-03-12

9

Journal article

Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series

Taylor, J, Craft, J, Blair, E, et al.
2019-07-25

10

Journal article

Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease

Buchanan, J, Blair, E, Thomson, KL, et al.
2019-06-11

11

Journal article

Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield

Thomson, K, Ormondroyd, E, Harper, A, et al.
2018-12-11

12

Journal article

From genotype to phenotype: Clinical assessment and participant perspective of a secondary genomic finding associated with long QT syndrome

Mackley, M, McGuire, K, Taylor, J, et al.
2018-10-15

13

Journal article

Distinct ECG phenotypes identified in hypertrophic cardiomyopathy using machine learning associate with arrhythmic risk markers

Lyon, A, Ariga, R, Minchole, A, et al.
2018-03-13

14

Journal article

Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study

Mackley, M, Blair, E, Parker, M, et al.
2018-02-13

15

Thesis

A clinical and ethical evaluation of secondary findings in the era of clinical whole-genome sequencing

Mackley, M
2017

16

Journal article

“Not pathogenic until proven otherwise”: perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project

Ormondroyd, E, Mackley, M, Blair, E, et al.
2017-10-26

17

Journal article

Exploring the potential duty of care in clinical genomics under UK law.

Mitchell, C, Ploem, C, Chico, V, et al.
2017-08-01

18

Journal article

Insights from early experience of a Rare Disease Genomic Medicine Multidisciplinary Team: a qualitative study

Ormondroyd, E, Mackley, M, Blair, E, et al.
2017-03-22

19

Journal article

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies

Ormondroyd, E, Mackley, M, Fletcher, B, et al.
2016-09-01

20

Journal article

Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications.

Ormondroyd, E, Oates, S, Parker, M, et al.
2014-01-01

21

Journal article

Disclosure of genetics research results after the death of the patient participant: a qualitative study of the impact on relatives.

Ormondroyd, E, Moynihan, C, Watson, M, et al.
2007-08-01

22

Journal article

Communicating genetics research results to families: problems arising when the patient participant is deceased.

Ormondroyd, E, Moynihan, C, Ardern-Jones, A, et al.
2008-08-01

23

Journal article

Pre-symptomatic genetic testing for inherited cardiac conditions: A qualitative exploration of psychosocial and ethical implications

Ormondroyd, E, Oates, S, Parker, M, et al.
2014-01-01

24

Journal article

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.

Taylor, J, Martin, H, Lise, S, et al.
2015-05-18

25

Conference item

Evaluation of Clinical Diagnostic Potential of Next Generation Sequencing using Hypertrophic Cardiomyopathy as a Model

Taylor, J, Kaur, K, Broxholme, J, et al.
2010-09-01