Publications by Dr Darroch Hall - ePrints

Browsing publications by Dr Darroch Hall.

Newcastle Authors	Title	Year
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 Size	2024
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 Angiogenesis	2017
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
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 Controls	2013
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
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 Zwolinski 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 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart 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
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 phenotypes	2009
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 study	2008
Dr Katrina Wood Dr Michael Jackson Dr Maria Lastowska Dr Darroch Hall Dr Helen Imrie et al.	Histological profile of tumours from MYCN transgenic mice	2008
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 hypertension	2007
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 families	2006