Dr Ana Topf Dr Helen Griffin Dr Elise Glen Rachel Soemedi Dr Danielle Brown et al. | Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot | 2014 |
|
Dr Elise Glen Dr Ana Topf Professor Judith Goodship
| A Nonsense Mutation in the IKBKG Gene in Mares with Incontinentia Pigmenti | 2013 |
|
Professor Judith Goodship Dr Darroch Hall Dr Ana Topf Valentina Mamasoula Dr Helen Griffin et al. | A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot | 2012 |
|
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 |
|
Rachel Soemedi Dr Ana Topf Dr Ian Wilson Dr Rebecca Darlay Dr Thahira Rahman et al. | Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls | 2012 |
|
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 |
|
Dr Helen Griffin Dr Ana Topf Dr Elise Glen Dr John O'Sullivan Professor Sir John Burn et al. | Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants | 2010 |
|