Research output per year
Research output per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
Master of Science, Genomics, The University of Manchester
Award Date: 2 Oct 2017
Bachelor of Medicine and Bachelor of Surgery, MB ChB
Award Date: 6 Jul 1982
Areas of expertise
- R Medicine (General)
- QH426 Genetics
Fingerprint
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Research output
- 5 Article
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The impact of COVID-19 vaccination on patients with congenital heart disease in England: a case-control study
CVD-COVID-UK/COVID-IMPACT consortium , 11 Oct 2024, In: Heart. 9 p.Research output: Contribution to journal › Article › peer-review
Open Access -
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease
Williams, S. G., Frain, S., Guo, H., Carr, M. J., Ashcroft, D. M. & Keavney, B. D., 14 Dec 2023, In: Open Heart. 10, 2, e002415.Research output: Contribution to journal › Article › peer-review
Open Access -
Data-independent acquisition mass spectrometry in severe rheumatic heart disease (RHD) identifies a proteomic signature showing ongoing inflammation and effectively classifying RHD cases
RHDGen Network Consortium, 22 Mar 2022, In: Clinical Proteomics. 19, 1, p. 7Research output: Contribution to journal › Article › peer-review
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Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease
Byrne, D., Williams, S. G., Nakev, A., Frain, S., Baross, S., Vestbo, J., Keavney, B. & Talavera, D., 4 Nov 2022, In: Scientific Reports. 12, 1, 18703.Research output: Contribution to journal › Article › peer-review
Open Access -
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank
Williams, S., Nakev, A., Guo, H., Frain, S., Tenin, G., Liakhovitskaia, A., Priest, J., Hentges, K. & Keavney, B., 1 Sept 2020, In: European Journal of Human Genetics. 28, p. 1265–1273Research output: Contribution to journal › Article › peer-review
Open Access