Simon Frain

ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 8

Top Venues

Open heart

European journal of human genetics : EJHG

University of Manchester

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Manchester Oct 18 2017

United Kingdom

Honorary Research Associate :: Division of Cardiovascular Sciences

Publications

Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Simon Frain, Hui Guo, Matthew J Carr, Darren M Ashcroft, Bernard D Keavney
Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease. Open heart 10 (2) (2023)
Simon G Williams, Apostol Nakev, Hui Guo, Simon Frain, Gennadiy Tenin, Anna Liakhovitskaia, Priyanka Saha, James R Priest, Kathryn E Hentges, Bernard D Keavney
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank. European journal of human genetics : EJHG 28 (9) (2020)

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Publication Activity (10 Years)

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Simon Frain