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Matthew A. Brown
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Year
‘Sink or swim’: an evaluation of the clinical characteristics of individuals with high bone mass
CL Gregson, SA Steel, KP O’Rourke, K Allan, J Ayuk, A Bhalla, G Clunie, ...
Osteoporosis International 23, 643-654, 2012
642012
055 The impact of methotrexate and targeted immunosuppression on cellular and humoral immune responses to COVID-19 vaccine BNT162b2: a cohort study
SK Mahil, K Bechman, A Raharja, C Domingo-Vila, M Brown, A Cope, ...
The Journal of Investigative Dermatology 141 (10), S158, 2021
2021
1: CAS: 528: DC% 2BC3sXpt1Oms70% 3D: Efficacy and safety of adalimumab in patients with non-radiographic axial spondyloarthritis: results of a randomised placebo-controlled …
J Sieper, D van der Heijde, M Dougados, P Mease, W Maksymowych, ...
Ann Rheum Dis, 815-822, 2013
62013
10 years of GWAS discovery: biology, function, and translation
PM Visscher, NR Wray, Q Zhang, P Sklar, MI McCarthy, MA Brown, ...
The American Journal of Human Genetics 101 (1), 5-22, 2017
35012017
194
SY See, R Jhagroo, C Vigneault, M Brown, A Lally, D Hull, KV Ranga
American Journal of Kidney Diseases 4 (49), B73, 2007
2007
37 Schou M, Amdisen A, Thomsen K, et al Lithium 1229-1231.
MA Brown, AB Corrigan
The Medical Journal of Australia 155 (7-12), 493-494, 1991
1991
47XXY and 47XXX in Scleroderma and Myositis
RH Scofield, VM Lewis, J Cavitt, BT Kurien, S Assassi, J Martin, O Gorlova, ...
ACR Open Rheumatology 4 (6), 528-533, 2022
142022
757 Hypoxic tumour environment and its implication for cancer treatment
M Brown
EJC Supplements 5 (1), S227, 2003
2003
A “candidate-interactome” aggregate analysis of genome-wide association data in multiple sclerosis
R Mechelli, R Umeton, C Policano, V Annibali, G Coarelli, VAG Ricigliano, ...
PLoS One 8 (5), e63300, 2013
362013
A clinically challenging diagnosis in a returning traveller with pyrexia of unknown origin
P Khetarpal, S Jmor, G Wallis, N McCann, M Brown
A combined genome-wide association scan and proteomics aproach for the identification of genetic modifiers of pseudoexfoliation syndrome
K Burdon, S Sharma, P Danoy, P Leo, A Hewitt, M Brown, T Chataway, ...
41st Royal Australian and New Zealand College of Ophthalmologists Annual Meeting, 2009
2009
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome
T Aung, M Ozaki, T Mizoguchi, RR Allingham, Z Li, A Haripriya, S Nakano, ...
Nature genetics 47 (4), 387-392, 2015
1232015
A comparison of instructional data sources in computing: the case for more and better simulated data in the classroom
M Brown
Journal of Computing Sciences in Colleges 27 (5), 45-51, 2012
2012
A COMPARISON OF THE VARIATION OF BASIC LASER PARAMETERS FOR PHOTODYNAMIC THERAPY
BW STEWART, M LAPLANT, A TURNER, B LAMPKIN, M BROWN
LASERS IN SURGERY AND MEDICINE 7 (1), 75-75, 1987
1987
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
2016
A gene causing autosomal dominant kyphoscoliosis in an N-ethyl-N-nitrosourea (ENU) mutagenised mouse model is located on a 5 Mb interval on mouse chromosome 4 band A3
C Esapa, R Head, H Evans, G Thomas, M Brown, P Croucher, R Cox, ...
Endocrine Abstracts 25, 2011
2011
A gene pathogenicity tool 'GenePy' identifies missed biallelic diagnoses in the 100,000 Genomes Project
A gene pathogenicity tool “GenePy” identifies missed biallelic diagnoses in the 100,000 Genomes Project
EG Seaby, G Leggatt, G Cheng, NS Thomas, JJ Ashton, I Stafford, ...
Genetics in Medicine 26 (4), 101073, 2024
22024
A gene pathway analysis highlights the role of cellular adhesion molecules in multiple sclerosis susceptibility
V Damotte, L Guillot-Noel, NA Patsopoulos, L Madireddy, M El Behi, ...
Genes & Immunity 15 (2), 126-132, 2014
362014
A general framework for validation of variant detection approaches in clinical whole genome sequencing
J Ellingford, S Walker, E Serra, G Aldam, M Doherty, L Abrahams, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 289-289, 2024
2024
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