Articles with public access mandates - Matthew A. BrownLearn more
Available somewhere: 291
Review
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
Mandates: British Heart Foundation, UK Medical Research Council, National Institute …
Review
Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
NA Patsopoulos, ...
Annals of neurology 70 (6), 897-912, 2011
Mandates: US National Institutes of Health
Review
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
Mandates: British Heart Foundation, Blood Cancer UK, UK Medical Research Council …
Review
WNT16 Influences Bone Mineral Density, Cortical Bone Thickness, Bone Strength, and Osteoporotic Fracture Risk
HF Zheng, JH Tobias, E Duncan, DM Evans, J Eriksson, L Paternoster, ...
PLoS genetics 8 (7), e1002745, 2012
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk
EL Duncan, P Danoy, JP Kemp, PJ Leo, E McCloskey, GC Nicholson, ...
PLoS genetics 7 (4), e1001372, 2011
Mandates: Canadian Institutes of Health Research, Fonds de recherche du Québec - Santé …
Review
Crystal structures of the endoplasmic reticulum aminopeptidase-1 (ERAP1) reveal the molecular basis for N-terminal peptide trimming
G Kochan, T Krojer, D Harvey, R Fischer, L Chen, M Vollmar, F von Delft, ...
Proceedings of the National Academy of Sciences 108 (19), 7745-7750, 2011
Mandates: Canadian Institutes of Health Research, Genome Canada, Versus Arthritis, UK
Review
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer
E Ruark, K Snape, P Humburg, C Loveday, I Bajrami, R Brough, ...
Nature 493 (7432), 406-410, 2013
Mandates: Cancer Research UK
Review
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
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
β‐glucan triggers spondylarthritis and Crohn's disease–like ileitis in SKG mice
M Ruutu, G Thomas, R Steck, MA Degli‐Esposti, MS Zinkernagel, ...
Arthritis & rheumatism 64 (7), 2211-2222, 2012
Mandates: National Health and Medical Research Council, Australia
Review
Common variants at 12q14 and 12q24 are associated with hippocampal volume
Nature genetics 44 (5), 545-551, 2012
Mandates: US National Institutes of Health, Austrian Science Fund, National Institute …
Review
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype
MAR Ferreira, MC Matheson, CS Tang, R Granell, W Ang, J Hui, AK Kiefer, ...
Journal of allergy and clinical immunology 133 (6), 1564-1571, 2014
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis
MD Mayes, L Bossini-Castillo, O Gorlova, JE Martin, X Zhou, WV Chen, ...
The American Journal of Human Genetics 94 (1), 47-61, 2014
Mandates: US National Institutes of Health, Versus Arthritis, UK, Government of Spain
Review
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
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans
J Halbritter, AA Bizet, M Schmidts, JD Porath, DA Braun, HY Gee, ...
The American Journal of Human Genetics 93 (5), 915-925, 2013
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Review
Genome-wide association study to identify genetic determinants of severe asthma
YI Wan, NRG Shrine, MS Artigas, LV Wain, JD Blakey, MF Moffatt, A Bush, ...
Thorax 67 (9), 762-768, 2012
Mandates: US National Institutes of Health, National Health and Medical Research …
Review
NAD deficiency, congenital malformations, and niacin supplementation
H Shi, A Enriquez, M Rapadas, EMMA Martin, R Wang, J Moreau, CK Lim, ...
New England Journal of Medicine 377 (6), 544-552, 2017
Mandates: Australian Research Council, National Health and Medical Research Council …
Review
Association of Variants at 1q32 and STAT3 with Ankylosing Spondylitis Suggests Genetic Overlap with Crohn's Disease
P Danoy, K Pryce, J Hadler, LA Bradbury, C Farrar, J Pointon, ...
PLoS genetics 6 (12), e1001195, 2010
Mandates: US National Institutes of Health, Versus Arthritis, UK
Review
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma
P Gharahkhani, KP Burdon, R Fogarty, S Sharma, AW Hewitt, S Martin, ...
Nature genetics 46 (10), 1120-1125, 2014
Mandates: US National Institutes of Health, Australian Research Council, National …
Review
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Human molecular genetics 20 (2), 345-353, 2011
Mandates: Parkinson's UK
Review
Common variants at the MHC locus and at chromosome 16q24. 1 predispose to Barrett's esophagus
Esophageal Adenocarcinoma Genetics Consortium, ...
Nature genetics 44 (10), 1131-1136, 2012
Mandates: US National Institutes of Health, National Health and Medical Research …
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