Articles with public access mandates - Matthew A. Brown - National Institute for Health Research, UKLearn more
NoteFor this mandate, articles should be available from specific locations.
OverallNHMRCNIHMRCNIHRVersus Arthritis, UKWellcomeARCBHFNSFCCIHREuropean CommissionCancer Research UKSwedish Research CouncilGovernment of SpainDFGFWOUK Research & InnovationFRQSGenome CanadaINSERMSNSFHHMISFINWOBBSRCCSOESRCZonMwRCNBMBFHealth Data Research, UKVAEPSRCParkinson's UKANRJDRFMedical Research Future Fund, AustraliaNSFDoDNSERCFraunhofer-GesellschaftDSFMotor Neurone Disease Association, UKDoris Duke Charitable FoundationGovernment of ItalyIFOPADOEGatesNASAFWFDNRFAcademy of FinlandTelethonFORTEKnut and Alice Wallenberg FoundationA*StarBlood Cancer UKDiabetes UKMultiple Sclerosis Society, UKSTFCWorldwide Cancer Research, UKARRSResearch Grants Council, Hong KongMichael J Fox FoundationJST
Available based on mandate: 69
Estimates of the rate of infection and asymptomatic COVID-19 disease in a population sample from SE England
PM Wells, KJ Doores, S Couvreur, RM Nunez, J Seow, C Graham, ...
Journal of Infection 81 (6), 931-936, 2020
Polygenic risk scores have high diagnostic capacity in ankylosing spondylitis
Z Li, X Wu, PJ Leo, E De Guzman, N Akkoc, M Breban, GJ Macfarlane, ...
Annals of the rheumatic diseases 80 (9), 1168-1174, 2021
Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy
PS Graham, G Kaidonis, S Abhary, MC Gillies, M Daniell, RW Essex, ...
BMC Medical Genetics 19, 1-8, 2018
Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes
CL Gregson, F Newell, PJ Leo, GR Clark, L Paternoster, M Marshall, ...
Bone 114, 62-71, 2018
Genomewide association study of acute anterior uveitis identifies new susceptibility loci
XF Huang, Z Li, E De Guzman, P Robinson, L Gensler, MM Ward, ...
Investigative Ophthalmology & Visual Science 61 (6), 3-3, 2020
Mutations in known monogenic high bone mass loci only explain a small proportion of high bone mass cases
CL Gregson, L Wheeler, SA Hardcastle, LH Appleton, KA Addison, ...
Journal of Bone and Mineral Research 31 (3), 640-649, 2016
A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD‐Dependent BMP Signaling Pathway as a Potential Anabolic Target for …
CL Gregson, DJM Bergen, P Leo, RB Sessions, L Wheeler, A Hartley, ...
Journal of Bone and Mineral Research 35 (1), 92-105, 2020
ERAP1 association with ankylosing spondylitis is attributable to common genotypes rather than rare haplotype combinations
AR Roberts, LH Appleton, A Cortes, M Vecellio, J Lau, L Watts, MA Brown, ...
Proceedings of the National Academy of Sciences 114 (3), 558-561, 2017
Comprehensive analysis of the major histocompatibility complex in systemic sclerosis identifies differential HLA associations by clinical and serological subtypes
M Acosta-Herrera, M Kerick, E Lopéz-Isac, S Assassi, L Beretta, ...
Annals of the rheumatic diseases 80 (8), 1040-1047, 2021
Polymorphism in a lincRNA associates with a doubled risk of pneumococcal bacteremia in Kenyan children
A Rautanen, M Pirinen, TC Mills, KA Rockett, A Strange, AW Ndungu, ...
The American Journal of Human Genetics 98 (6), 1092-1100, 2016
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease
PC Robinson, PJ Leo, JJ Pointon, J Harris, K Cremin, LA Bradbury, ...
NPJ genomic medicine 1 (1), 1-6, 2016
Risk‐mitigating behaviours in people with inflammatory skin and joint disease during the COVID‐19 pandemic differ by treatment type: a cross‐sectional patient survey
SK Mahil, M Yates, SM Langan, ZZN Yiu, T Tsakok, N Dand, KJ Mason, ...
British Journal of Dermatology 185 (1), 80-90, 2021
Genetics and the axial spondyloarthritis spectrum
MA Brown, H Xu, Z Li
Rheumatology 59 (Supplement_4), iv58-iv66, 2020
Biallelic mutation of ARHGEF18, involved in the determination of epithelial apicobasal polarity, causes adult-onset retinal degeneration
G Arno, KJ Carss, S Hull, C Zihni, AG Robson, A Fiorentino, G Black, ...
The American Journal of Human Genetics 100 (2), 334-342, 2017
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
A Goris, J van Setten, F Diekstra, S Ripke, NA Patsopoulos, SJ Sawcer, ...
Human molecular genetics 23 (7), 1916-1922, 2014
Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2)
T Karaderi, SM Keidel, JJ Pointon, LH Appleton, MA Brown, DM Evans, ...
Annals of the rheumatic diseases 73 (11), 2054-2058, 2014
Describing the burden of the COVID‐19 pandemic in people with psoriasis: findings from a global cross‐sectional study
SK Mahil, M Yates, ZZN Yiu, SM Langan, T Tsakok, N Dand, KJ Mason, ...
Journal of the European Academy of Dermatology and Venereology 35 (10), e636 …, 2021
A method to exploit the structure of genetic ancestry space to enhance case-control studies
CA Bodea, BM Neale, S Ripke, M Barclay, L Peyrin-Biroulet, ...
The American Journal of Human Genetics 98 (5), 857-868, 2016
Heterogeneity of axial spondyloarthritis: genetics, sex and structural damage matter
Z Li, SM Van Der Linden, MA Khan, H Baumberger, H van Zandwijk, ...
RMD open 8 (1), e002302, 2022
MHC associations of ankylosing spondylitis in East Asians are complex and involve non-HLA-B27 HLA contributions
G Wang, TH Kim, Z Li, A Cortes, K Kim, SY Bang, P Leo, MA Brown, H Xu
Arthritis research & therapy 22, 1-8, 2020
Publication and funding information is determined automatically by a computer program