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Browsing publications by
Dr Darroch Hall
Newcastle Authors
Title
Year
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 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
Rachel Soemedi
Dr Ian Wilson
Dr Rebecca Darlay
Dr Ana Topf
Dr Simon Zwolinksi
et al.
Contribution of Global Rare Copy-Number Variants to the Risk of Sporadic Congenital Heart Disease
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 1q21.1Rearrangements and GJA5 Duplications in 2437 CongenitalHeart Disease Patients and 6760 Controls
2012
Dr Darroch Hall
Dr Thahira Rahman
Dr Peter Avery
Professor Bernard Keavney
Common variation in the CD36 (fatty acid translocase) gene is associated with left-ventricular mass
2011
Dr Thahira Rahman
Dr Darroch Hall
Dr Peter Avery
Professor Bernard Keavney
Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness
2011
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 Michael Cunnington
Dr Darroch Hall
Dr Peter Avery
Professor Bernard Keavney
Genetic Polymorphisms Linked to Coronary Artery Disease Are Not Associated With Carotid Artery Intima-Media Thickness, Less Ventricular Size or Intermediate Risk Phenotypes
2009
Dr Helen Griffin
Dr Darroch Hall
Dr Ana Topf
James Eden
Professor Sir John Burn
et al.
Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation
2009
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