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 |
|
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Dr Rebecca Darlay
Rachel Soemedi
et al. | Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot | 2013 |
|
Professor Heather Cordell
Dr Ana Topf
Valentina Mamasoula
Rachel Soemedi
Dr Ruairidh Martin
et al. | Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 | 2013 |
|
Rachel Soemedi
Dr Ian Wilson
Dr Rebecca Darlay
Dr Ana Topf
Dr Simon Zwolinski
et al. | Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease | 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 Anna Mitchell
Professor Heather Cordell
Rachel Soemedi
Professor Simon Pearce
| Programmed Death Ligand 1 (PD-L1) Gene Variants Contribute to Autoimmune Addison's Disease and Graves' Disease Susceptibility | 2009 |
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