Simon Williams

The University of Manchester

United Kingdom

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Articles (12)

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2022

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2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Collaborators (17)

Kathryn Hentges

Reader

The University of Manchester

UNITED KINGDOM

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Raymond T O'Keefe

The University of Manchester

UNITED KINGDOM

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Paul R. Kasher

The University of Manchester

UNITED KINGDOM

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Jørgen Vestbo

The University of Manchester

UNITED KINGDOM

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Walter Rossmanith

Medical University of Vienna

AUSTRIA

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Hugh J. McMillan

McGill University

CANADA

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Stephanie Baross

The University of Manchester

UNITED KINGDOM

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Yingjuan Liu

The University of Manchester

UNITED KINGDOM

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Richard Monaghan

The University of Manchester

UNITED KINGDOM

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James O'Sullivan

University of Manchester

UNITED KINGDOM

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Mun-Kit Choy

The University of Manchester

UNITED KINGDOM

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Alexandru Chelu

The University of Manchester

UNITED KINGDOM

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Hui Guo

Reader in Biostatistics

The University of Manchester

UNITED KINGDOM

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Simon Frain

The University of Manchester

UNITED KINGDOM

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Rachel Taylor

The University of Manchester

UNITED KINGDOM

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David Talavera

The University of Manchester

UNITED KINGDOM

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Wyatt Yue

UNITED KINGDOM

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Simon Williams

Research Interests

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Articles (12)

FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms

Clinical risk associated with COVID-19 among 86000 patients with congenital heart disease

Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease.

Joint analysis of functionally related genes yields further candidates associated with Tetralogy of Fallot

Bi-allelic mutation of CTNNB1 causes a severe form of syndromic microphthalmia, persistent foetal vasculature and vitreoretinal dysplasia

A novel RNA-mediated mechanism causing down-regulation of insulating promoter interactions in human embryonic stem cells

Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations

Rare GATA6 variants associated with risk of congenital heart disease phenotypes in 200,000 UK Biobank exomes.

Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot

Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot.

Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome

Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank.

Collaborators (17)

Kathryn Hentges

Raymond T O'Keefe

Paul R. Kasher

Jørgen Vestbo

Walter Rossmanith

Hugh J. McMillan

Stephanie Baross

Yingjuan Liu

Richard Monaghan

James O'Sullivan

Mun-Kit Choy

Alexandru Chelu

Hui Guo

Simon Frain

Rachel Taylor

David Talavera

Wyatt Yue

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