Browsing publications by Dr Rebecca Darlay

Newcastle AuthorsTitleYearFull text
Dr Rebecca Darlay
Dr Kristin Ayers
Professor David Jones
Dr Peter Donaldson
Professor Heather Cordell
et al.
Immunochip analysis identifies amino acid residues in five separate HLA genes driving the association between the MHC and primary biliary cirrhosis2015
Dr Anna Mitchell
Katie MacArthur
Dr Jolanta Weaver
Dr Bijayeswar Vaidya
Dr Rebecca Darlay
et al.
Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus2015
Dr Michael Rushton
Dr Louise Reynard
Professor David Young
Dr Colin Shepherd
Dr Rebecca Darlay
et al.
Methylation of cartilage DNA is a mediator of genetic risk at several OA susceptibility loci2015
Dr Michael Rushton
Dr Louise Reynard
Professor David Young
Dr Colin Shepherd
Dr Fiona Gee
et al.
Methylation quantitative trait locus (meQTL) analysis of osteoarthritis links epigenetics with genetic risk2015
Dr Rebecca Darlay
The heritability of abortion in pedigree Charollais flocks2014
Dr Quentin Anstee
Dr Rebecca Darlay
Julian Leathart
Yilei Liu
Professor Alastair Burt
et al.
A candidate-gene approach to validation of genetic modifier associations using a large cohort with histologically characterised non-alcoholic fatty liver disease2013
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
Dr Valerie Wilson
Dr Rebecca Darlay
Dr Katrina Wood
Dr Eva-Maria Hunze
Dr Kevin Marchbank
et al.
Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy2013
Dr Quentin Anstee
Professor Heather Cordell
Dr Rebecca Darlay
Professor Chris Day
Professor Ann Daly
et al.
Mapping Expression Quantitative Traits Loci (EQTL) for PNPLA3 Gene Identifies Additional SNPs Associated with Non-Alcoholic Fatty Liver Disease (NAFLD) Independent of rs7384092013
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
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