Dr Paul Brennan Professor Judith Goodship Alexander Henderson Linda Sneddon
| Analysis of 51 proposed hypertrophic cardiomyopathy genes from genome sequencing data in sarcomere negative cases has negligible diagnostic yield | 2019 |
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Dr David Bourn Dr Richard Fisher Professor Judith Goodship Dr Tara Montgomery Linda Sneddon et al. | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language (Nature Communications, (2018), 9, 1, (4619), 10.1038/s41467-018-06014-6) | 2019 |
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Dr David Bourn Professor Sir John Burn Dr Richard Fisher Professor Judith Goodship Alexander Henderson et al. | Prevalence and architecture of de novo mutations in developmental disorders | 2017 |
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Dr David Bourn Professor Sir John Burn Dr Richard Fisher Professor Judith Goodship Dr Alistair Henderson et al. | Large-scale discovery of novel genetic causes of developmental disorders | 2015 |
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Dr Elise Glen Dr Ana Topf Dr Darroch Hall Dr John O'Sullivan Linda Sneddon et al. | Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation | 2012 |
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Linda Sneddon Professor Peter Thomson
| Occupation and risk of upper aerodigestive tract cancer: The ARCAGE study | 2012 |
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Dr Elise Glen Dr Ana Topf Dr Darroch Hall Dr John O'Sullivan Linda Sneddon et al. | Non-synonymous SMAD6 mutations impaired inhibition of BMP signalling in patients with congenital cardiovascular malformation | 2011 |
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Linda Sneddon
| The association between change in body mass index and upper aerodigestive tract cancers in the ARCAGE project: multicenter case-control study | 2011 |
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