Browsing publications by Dr Rebecca Darlay

Newcastle AuthorsTitleYearFull text
Dr Rebecca Darlay
Aisling Stewart
Dr Yaobo Xu
Dr Mauro Santibanez Koref
Professor John Sayer
et al.
Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux2017
Professor Quentin Anstee
Dr Rebecca Darlay
Professor Heather Cordell
Professor Ann Daly
Professor Chris Day
et al.
Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans2017
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 Richard Howey
Dr Rebecca Darlay
Professor Heather Cordell
Examination of previously identified associations within the Genetic Analysis Workshop 19 data2014
Dr Rebecca Darlay
The heritability of abortion in pedigree Charollais flocks2014
Professor 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
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