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Browsing publications by Dr Darroch Hall.

Newcastle AuthorsTitleYearFull text
Dr Rachael Redgrave
Dr Esha Singh
Dr Simon Tual-Chalot
Dr Catherine Park
Dr Darroch Hall
et al.
Exogenous Transforming Growth Factor-β1 and Its Helminth-Derived Mimic Attenuate the Heart's Inflammatory Response to Ischemic Injury and Reduce Mature Scar Size2023
Dr Rachael Redgrave
Dr Simon Tual-Chalot
Dr Benjamin Davison
Dr Esha Singh
Dr Darroch Hall
et al.
Cardiosphere-Derived Cells Require Endoglin for Paracrine-Mediated Angiogenesis2017
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 Fallot2014
Valentina Mamasoula
Dr Tomasz Pierscionek
Dr Darroch Hall
Dr Ana Topf
Dr Danielle Brown
et al.
Association between C677T Polymorphism of Methylene Tetrahydrofolate Reductase and Congenital Heart Disease: Meta-Analysis of 7,697 Cases and 13,125 Controls2013
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 Fallot2013
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 4p162013
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 Fallot2012
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 Disease2012
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 malformation2012
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 controls2012
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 mass2011
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 Thickness2011
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 malformation2011
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 Phenotypes2009
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 malformation2009
Dr Michael Cunnington
Dr Darroch Hall
Dr Peter Avery
Hannah Watkins
Professor Bernard Keavney
et al.
Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes2009
Dr Thahira Rahman
Michelle Baker
Dr Darroch Hall
Dr Peter Avery
Professor Bernard Keavney
et al.
Common genetic variation in the type A endothelin-1 receptor is associated with ambulatory blood pressure: A family study2008
Dr Katrina Wood
Dr Michael Jackson
Dr Maria Lastowska
Dr Darroch Hall
Dr Helen Imrie
et al.
Histological profile of tumours from MYCN transgenic mice2008
Michelle Baker
Dr Thahira Rahman
Dr Darroch Hall
Dr Peter Avery
Hannah Watkins
et al.
The C-532T polymorphism of the angiotensinogen gene is associated with pulse pressure: A possible explanation for heterogeneity in genetic association studies of AGT and hypertension2007
Dr Darroch Hall
Dr Thahira Rahman
Dr Peter Avery
Professor Bernard Keavney
INSIG-2 promoter polymorphism and obesity related phenotypes: Association study in 1428 members of 248 families2006