Publications by Dr Rebecca Darlay - ePrints

Browsing publications by Dr Rebecca Darlay.

Newcastle Authors	Title	Year
Dr Rebecca Darlay Professor Heather Cordell	Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome	2024
Dr Rebecca Darlay Professor Bernard Keavney Professor Heather Cordell	Whole -genome survival analysis of 144 286 people from the UK Biobank identifies novel loci associated with blood pressure	2024
Professor Heather Cordell Dr Rebecca Darlay Professor David Jones	Corrigendum to: “An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs” [J Hepatol 75 (2021) 572-581, (S0168827821003342), (10.1016/j.jhep.2021.04.055)]	2023
Dr Rebecca Darlay Professor Heather Cordell Professor Quentin Anstee Professor Ann Daly	A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation	2022
Dr Wei-yu Lin Dr Sarah Fordham Dr Nicola Sunter Dr Claire Elstob Dr Yaobo Xu et al.	Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia (Nature Communications, (2021), 12, 1, (6233), 10.1038/s41467-021-26551-x)	2022
Professor Heather Cordell Dr Rebecca Darlay Professor David Jones	Corrigendum to ‘An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs’ [J Hepatol 2021;75(3):572–581]	2022
Dr Rebecca Darlay Professor Heather Cordell Professor Ann Daly Professor Chris Day Dr Steven Masson et al.	Corrigendum to: 'A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers' [J Hepatol 2022 (76) 275–282] (Journal of Hepatology (2022) 76(2) (275–282), (S0168827821021115), (10.1016/j.jhep.2021.10.005))	2022
Dr Olivier Govaere Dr Rebecca Darlay Dr Julien Peltier Dr Jeremy Palmer Dr Massimo Younes et al.	Macrophage Scavenger Receptor 1 mediates lipid-induced inflammation in non-alcoholic fatty liver disease	2022
David Langton Rohan Bhalekar Professor Tom Joyce Professor Stephen Rushton Dr Rebecca Darlay et al.	The influence of HLA genotype on the development of metal hypersensitivity following joint replacement	2022
Nardeen Eldafashi Dr Rebecca Darlay Dr Ruchi Shukla Misti McCain Robyn Watson et al.	A pdcd1 role in the genetic predisposition to nafld-hcc?	2021
Professor Heather Cordell James Fryett Dr Rebecca Darlay Professor David Jones	An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs	2021
Dr Rebecca Darlay Dr Steven Masson Professor Chris Day Professor Ann Daly Professor Heather Cordell et al.	Genome-wide association study and meta-analysis on alcohol-related liver cirrhosis identifies novel genetic risk factors	2021
Dr Wei-Yu Lin Dr Sarah Fordham Dr Nicola Sunter Dr Claire Elstob Dr Yaobo Xu et al.	Genome-wide association study identifies susceptibility loci for acute myeloid leukemia	2021
David Langton Professor Stephen Bourke Dr Rebecca Darlay Dr Carlos Echevarria	The influence of HLA genotype on the severity of COVID-19 infection	2021
Professor Quentin Anstee Dr Rebecca Darlay Dr Simon Cockell Dr Olivier Govaere Dr Dina Tiniakos et al.	Genome-Wide Association Study of Non-Alcoholic Fatty Liver and Steatohepatitis in a Histologically-Characterised Cohort	2020
Dr Olivier Govaere Dr Simon Cockell Dr Dina Tiniakos Dr Rachel Queen Dr Massimo Younes et al.	Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis	2020
Dr Rebecca Darlay Dr Kristin Ayers Dr Lynsey Hall Professor David Jones Professor Heather Cordell et al.	Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and Primary Biliary Cholangitis	2018
Dr Rebecca Darlay Aisling Stewart Dr Yaobo Xu Dr Heather Lambert Dr Mauro Santibanez Koref et al.	Erratum: Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux (Scientific reports (2017) 7 1 (14595))	2018
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 reflux	2017
Professor Quentin Anstee Dr Yang-Lin Liu Dr Rebecca Darlay Professor Heather Cordell Professor Ann Daly et al.	Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humans	2017
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 cirrhosis	2015
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 Locus	2015
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 loci	2015
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 risk	2015
Dr Richard Howey Dr Rebecca Darlay Professor Heather Cordell	Examination of previously identified associations within the Genetic Analysis Workshop 19 data	2014
Dr Rebecca Darlay	The heritability of abortion in pedigree Charollais flocks	2014
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 disease	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
Dr Valerie Wilson Dr Rebecca Darlay Dr Katrina Wood Professor Claire Harris Dr Eva-Maria Hunze et al.	Genotype/Phenotype Correlations in Complement Factor H Deficiency Arising From Uniparental Isodisomy	2013
Professor Quentin Anstee Dr Yang-Lin Liu Professor Heather Cordell Dr Rebecca Darlay Professor Chris Day et al.	Mapping Expression Quantitative Traits Loci (EQTL) for PNPLA3 Gene Identifies Additional SNPs Associated with Non-Alcoholic Fatty Liver Disease (NAFLD) Independent of rs738409	2013
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
Professor Quentin Anstee Dr Rebecca Darlay Julian Leathart Professor Helen Reeves Professor Alastair Burt et al.	Genome-Wide Association Analysis Confirms Importance of PNPLA3 and Identifies Novel Variants Associated With Histologically Progressive Steatohepatitis in NAFLD	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 Rebecca Darlay	Novel polymorphisms in ovine immune response genes and their association with abortion	2011
Professor Heather Cordell Dr Rebecca Darlay Dr Heather Lambert Professor Tim Goodship Dr Rajko Kenda et al.	Whole-Genome Linkage and Association Scan in Primary, Nonsyndromic Vesicoureteric Reflux	2010
Professor Judith Goodship Dr Rebecca Darlay Dr Rajko Kenda Professor Heather Cordell	Whole-genome linkage and association scan in primary, non-syndromic vesicoureteric reflux (VUR) and reflux nephropathy	2009