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.
Not available based on mandate: 12
HLA alleles associated with risk of ankylosing spondylitis and rheumatoid arthritis influence the gut microbiome
M Asquith, PR Sternes, ME Costello, L Karstens, S Diamond, TM Martin, ...
Arthritis & rheumatology 71 (10), 1642-1650, 2019
Incidence and prevalence of NMOSD in Australia and New Zealand
W Bukhari, KM Prain, P Waters, M Woodhall, MOG Cullen, L Clarke, ...
Journal of Neurology, Neurosurgery & Psychiatry 88 (8), 632-638, 2017
Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene
KP Burdon, RD Fogarty, W Shen, S Abhary, G Kaidonis, B Appukuttan, ...
Diabetologia 58, 2288-2297, 2015
Biomarker development for axial spondyloarthritis
MA Brown, Z Li, KAL Cao
Nature Reviews Rheumatology 16 (8), 448-463, 2020
The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis
PC Robinson, PJ Leo, JJ Pointon, J Harris, K Cremin, LA Bradbury, ...
Genes & Immunity 17 (1), 46-51, 2016
Factors predicting axial spondyloarthritis among first-degree relatives of probands with ankylosing spondylitis: a family study spanning 35 years
SM Van Der Linden, MA Khan, Z Li, H Baumberger, H Van Zandwijk, ...
Annals of the rheumatic diseases 81 (6), 831-837, 2022
HLA-B27, axial spondyloarthritis and survival
Z Li, MK Khan, SM van der Linden, B Winkens, PM Villiger, H Baumberger, ...
Annals of the rheumatic diseases 82 (12), 1558-1567, 2023
round table unites to tackle culture change in an effort to improve animal research reporting
NJ Osborne, M Ritskes-Hoitinga, A Ahluwahlia, S Alam, M Brown, ...
BMC veterinary research 13, 1-2, 2017
A RUNX3 enhancer polymorphism associated with ankylosing spondylitis influences recruitment of Interferon Regulatory Factor 5 and factors of the Nucleosome …
M Vecellio, A Cortes, S Bonham, C Selmi, JC Knight, R Fischer, ...
bioRxiv, 832840, 2019
A rare SMAD9 mutation identifies the BMP signalling pathway as a potential osteoanabolic target
CL Gregson, D Bergen, P Leo, RB Sessions, L Wheeler, A Hartley, ...
bioRxiv, 560565, 2019
Loss-of-function nuclear factor kB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans
MH Jansen, E Staples, J Stephens, KJ Carss, D Biasci, H Baxendale, ...
Allergy 91, 6749, 2018
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics …
CR Marshall, DP Howrigan, D Merico, B Thiruvahindrapuram, W Wu, ...
bioRxiv, 040493, 2016
Available based on mandate: 69
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility
International Multiple Sclerosis Genetics Consortium*†, ANZgene, ...
Science 365 (6460), eaav7188, 2019
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci
D Ellinghaus, L Jostins, SL Spain, A Cortes, J Bethune, B Han, YR Park, ...
Nature genetics 48 (5), 510-518, 2016
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
HF Zheng, V Forgetta, YH Hsu, K Estrada, A Rosello‐Diez, PJ Leo, ...
Nature 526 (7571), 112-117, 2015
Physical, cognitive, and mental health impacts of COVID-19 after hospitalisation (PHOSP-COVID): a UK multicentre, prospective cohort study
RA Evans, H McAuley, EM Harrison, A Shikotra, A Singapuri, M Sereno, ...
The Lancet Respiratory Medicine 9 (11), 1275-1287, 2021
Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
Clinical characteristics with inflammation profiling of long COVID and association with 1-year recovery following hospitalisation in the UK: a prospective observational study
RA Evans, OC Leavy, M Richardson, O Elneima, HJC McAuley, ...
The Lancet Respiratory Medicine 10 (8), 761-775, 2022
Major histocompatibility complex associations of ankylosing spondylitis are complex and involve further epistasis with ERAP1
A Cortes, SL Pulit, PJ Leo, JJ Pointon, PC Robinson, MH Weisman, ...
Nature communications 6 (1), 7146, 2015
Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study
K Trajanoska, JA Morris, L Oei, HF Zheng, DM Evans, DP Kiel, C Ohlsson, ...
bmj 362, 2018
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