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| Author | Identifier | Number of Items | Total Downloads |
|---|---|---|---|
| Brown, M |  https://orcid.org/0000-0003-0538-8211 |
38 | 2138 |
| Title | Author(s) | IrusType | Repository | Item URL | Total Downloads |
|---|---|---|---|---|---|
| A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk | Revez, J. A.; Bain, L.; Chapman, B.; Powell, J. E.; Jansen, R.; Duffy, D. L.; Tung, J. Y.; AAGC Collaborators; Penninx, B. W.; Visscher, P. M.; De Geus, E. J. C.; Boomsma, D. I.; Hinds, D. A.; Martin, N. G.; Montgomery, G. W.; Ferreira, M. A. R.; Danoy, P | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:314832 | 36 |
| Amyotrophic lateral sclerosis genetic studies: from genome-wide association mapping to genome sequencing | He, Ji; Mangelsdorf, Marie; Fan, Dongsheng; Bartlett, Perry; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:351652 | 149 |
| C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis | He, Ji; Tang, Lu; Benyamin, Beben; Shah, Sonia; Hemani, Gib; Liu, Rong; Ye, Shan; Liu, Xiaolu; Ma, Yan; Zhang, Huagang; Cremin, Katie; Leo, Paul; Wray, Naomi R.; Visscher, Peter M.; Xu, Huji; Brown, Matthew A.; Bartlett, Perry F.; Mangelsdorf, Marie; Fan, | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:365226 | 113 |
| Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family | Johnson, Stephanie R.; Leo, Paul; Conwell, Louise S.; Harris, Mark; Brown, Matthew A.; Duncan, Emma L. | Article | University of Queensland [UQ eSpace] | 12 | |
| Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips | Ritchie, Matthew E.; Liu, Ruijie; Carvalho, Benilton S.; The Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene); Irizarry, Rafael A.; Brown, Matthew A.; Csurhes, Peter A.; Danoy, Patrick; Greer, Judith M.; Hadler, Johanna; Pryce, K | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:244941 | 37 |
| Comparison of the performance of two commercial genome-wide association study genotyping platforms in Han Chinese samples | Jiang, Lei; Willner, Dana; Danoy, Patrick; Xu, Huji; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:291548 | 3 |
| Comprehensive genetic screening: the prevalence of MODY gene variants in a population-based childhood diabetes cohort | Johnson, Stephanie R.; Ellis, Jonathan J.; Leo, Paul; Anderson, Lisa K.; Ganti, Uma; Harris, Jessica E.; Curran, Jacqueline A.; McInerney-Leo, Aideen; Paramalingam, Nirubasini; Song, Xiaoxia; Conwell, Louise S.; Harris, Mark; Jones, Timothy W.; Brown, Mat | Article | University of Queensland [UQ eSpace] | 11 | |
| Discovery of candidate serum proteomic and metabolomic biomarkers in ankylosing spondylitis | Fischer, Roman; Trudgian, David C.; Wright, Cynthia; Thomas, Gethin; Bradbury, Linda A.; Brown, Matthew A.; Bowness, Paul; Kessler, Benedikt M. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:268955 | 9 |
| Ethics of genetic testing and research in sport: A position statement from the Australian Institute of Sport | Vlahovich, Nicole; Fricker, Peter A.; Brown, Matthew A.; Hughes, David | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:533330 | 2 |
| Genes determining nevus count and dermoscopic appearance in Australian melanoma cases and controls | Duffy, David L.; Jagirdar, Kasturee; Lee, Katie J.; McWhirter, Seamus R.; McMeniman, Erin K.; De’Ambrosis, Brian; Pflugfelder, Annette; Rayner, Jenna E.; Whiteman, David C.; Brown, Matthew A.; Martin, N.G.; Smithers, B.M.; Schaider, Helmut; Soyer, H | Article | University of Queensland [UQ eSpace] | 24 | |
| Genetic studies in osteoporosis - the end of the beginning | Duncan, Emma L.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:193904 | 24 |
| Genome-wide association study in Guillain-Barré syndrome | Blum, Stefan; Ji, Ying; Pennisi, David; Li, Zhixiu; Leo, Paul; McCombe, Pamela; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | 85 | |
| Genome-wide association study of extreme high bone mass: contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes | Gregson, Celia L.; Newell, Felicity; Leo, Paul J.; Clark, Graeme R.; Paternoster, Lavinia; Marshall, Mhairi; Forgetta, Vincenzo; Morris, John A.; Ge, Bing; Bao, Xiao; Duncan Bassett, J. H.; Williams, Graham R.; Youlten, Scott E.; Croucher, Peter I.; Davey | Article | University of Queensland [UQ eSpace] | 7 | |
| Immunopathogenesis of ankylosing spondylitis | Kenna, Tony J.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:325514 | 2 |
| Incidence and prevalence of NMOSD in Australia and New Zealand | Bukhari, Wajih; Prain, Kerri M.; Waters, Patrick; Woodhall, Mark; O'Gorman, Cullen M.; Clarke, Laura; Silvestrini, Roger A.; Bundell, Christine S.; Abernethy, David; Bhuta, Sandeep; Blum, Stefan; Boggild, Mike; Boundy, Karyn; Brew, Bruce J.; Brown, Matthe | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:676337 | 103 |
| Integrated genome-wide chromatin occupancy and expression analyses identify key myeloid pro-differentiation transcription factors repressed by Myb | Zhao, Liang; Glazov, Evgeny; Diwakar Ram Pattabiraman; Al-Owaidi, Faisal; Ping Zhang; Brown, Matthew A.; Paul Leo; Gonda, Thomas J. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:235055 | 38 |
| Interleukin-23 mediates the intestinal response to microbial beta-glucan and the development of spondyloarthritis pathology in SKG mice | Benham, Helen; Rehaume, Linda M.; Hasnain, Sumaira Z.; Velasco, Jared; Baillet, Athan C.; Ruutu, Merja; Kikly, Kristine; Wang, Ran; Tseng, Hsu-Wen; Thomas, Gethin P.; Brown, Matthew A.; Strutton, Geoffrey; McGuckin, Michael A.; Thomas, Ranjeny | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:327412 | 78 |
| Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm | Zheng, Hou-Feng; Duncan, Emma L.; Yerges-Armstrong, Laura M.; Eriksson, Joel; Bergström, Ulrica; Leo, Paul J.; Leslie, William D.; Goltzman, David; Blangero, John; Hanley, David A.; Carless, Melanie A.; Streeten, Elizabeth A.; Lorentzon, Mattias; Bro | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:305070 | 66 |
| Microbes, the gut and ankylosing spondylitis | Costello, Mary-Ellen; Elewaut, Dirk; Kenna, Tony J.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:326239 | 20 |
| Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFB | Andreas Zankl; Duncan, Emma L.; Leo, Paul J.; Clark, Graeme R.; Glazov, Evgeny A.; Addor, Marie-Claude; Herlin, Troels; Kim, Chong Ae; Leheup, Bruno P.; McGill, Jim; McTaggart, Steven; Mittas, Stephan; Mitche, Anna L.; Mortier, Geert R.; Robertson, Stephe | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:270109 | 3 |
| Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients | Jensen, Cathy J.; Stankovich, Jim; Van der Walt, Anneke; Bahlo, Melanie; Taylor, Bruce V.; van der Mei, Ingrid A. F.; Foote, Simon J.; Kilpatrick, Trevor J.; Johnson, Laura J.; Wilkins, Ella; Field, Judith; Danoy, Patrick; Brown, Matthew A.; Rubio, Justin | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:204271 | 34 |
| Mutation of perinatal myosin heavy chain | Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:117515 | 76 |
| NAD deficiency, congenital malformations, and niacin supplementation | Shi, Hongjun; Enriquez, Annabelle; Rapadas, Melissa; Martin, Ella M. M. A.; Wang, Roni; Moreau, Julie; Lim, Chai K.; Szot, Justin O.; Ip, Eddie; Hughes, James N.; Sugimoto, Kotaro; Humphreys, David T.; McInerney-Leo, Aideen M.; Leo, Paul J.; Maghzal, Ghas | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:682057 | 378 |
| Oncosis and apoptosis induction by activation of an overexpressed ion channel in breast cancer cells | Peters, A. A.; Jamaludin, S. Y. N.; Yapa, K. T. D. S.; Chalmers, S.; Wiegmans, A. P.; Lim, H. F.; Milevskiy, M. J. G.; Azimi, I.; Davis, F. M.; Northwood, K. S.; Pera, E.; Marcial, D. L.; Dray, E.; Waterhouse, N. J.; Cabot, P. J.; Gonda, T. J.; Kenny, P. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:690109 | 268 |
| Progress in spondylarthritis: progress in studies of the genetics of ankylosing spondylitis | Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:193754 | 28 |
| Promise and pitfalls of the Immunochip | Cortes, Adrian; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:250352 | 19 |
| Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia | Grozeva, Detelina; Kirov, George; Ivanov, Dobril; Jones, Ian R.; Jones, Lisa; Green, Elaine K.; St Clair, David M.; Young, Allan H.; Ferrier, Nicol; Farmer, Anne E.; McGuffin, Peter; Holmans, Peter A.; Owen, Michael J.; O'Donovan, Michael C.; Craddock, Ni | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:239017 | 69 |
| Rare, potentially pathogenic variants in ZNF469 are not enriched in keratoconus in a large Australian cohort of European descent | Lucas, Sionne E. M.; Zhou, Tiger; Blackburn, Nicholas B.; Mills, Richard A.; Ellis, Jonathan; Leo, Paul; Souzeau, Emmanuelle; Ridge, Bronwyn; Charlesworth, Jac C.; Brown, Matthew A.; Lindsay, Richard; Craig, Jamie E.; Burdon, Kathryn P. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:709472 | 32 |
| Schizophrenia genetic variants are not associated with intelligence | Terwisscha van Scheltinga, A. F.; Bakker, S. C.; Van Haren, N. E. M.; Derks, E. M.; Buizer-Voskamp, J. E.; Cahn, W.; Ripke, S.; Ophoff, R. A.; Kahn, R. S.; Psychiatric Genomic-Wide Association Study (GWAS) Consortium; Visscher, P. M.; Mowry, B. J.; Brown, | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:323725 | 1 |
| Seven newly identified loci for autoimmune thyroid disease | Cooper, Jason D.; Simmonds, Matthew J.; Walker, Neil M.; Burren, Oliver; Brand, Oliver J.; Guo, Hui; Wallace, Chris; Stevens, Helen; Coleman, Gillian; Wellcome Trust Case Control Consortium; Brown, Matthew A.; Franklyn, Jayne A.; Gough, Stephen C. L.; Tod | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:297645 | 1 |
| Successful approaches in genetics of musculoskeletal diseases | Brown, MA | Conference Papers/Posters | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:119235 | 134 |
| T‐cell receptor immunosequencing reveals altered repertoire diversity and disease‐associated clonal expansions in ankylosing spondylitis patients | Hanson, Aimee L.; Nel, Hendrik J.; Bradbury, Linda; Phipps, Julie; Thomas, Ranjeny; Lê Cao, Kim‐Anh; Kenna, Tony J.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | 98 | |
| The role of IL-17-secreting mast cells in inflammatory joint disease | Kenna, Tony J.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:305076 | 1 |
| Using the maternal-fetal genotype incompatibility test to assess non-inherited maternal DRB1 coding alleles as rheumatoid arthritis risk factors | Hseih, Hsin-Ju; Palmer, Christina G. S.; Harney, Sinead; Chen, Hsiu-Wen; Bauman, Lara; Brown, Matthew A.; Sinsheimer, Janet S. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:138369 | 5 |
| Utility of temporal artery biopsy samples for genome-wide analysis of giant cell arteritis | Cremin, K.; Leo, P.; Harris, J. E.; De Smit, E.; Bradbury, L.; McKelvie, P.; Hill, C. L.; Brown, M. A.; Hewitt, A. W. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:336914 | 40 |
| Variability inworking memory performance explained by epistasis vs polygenic scores in the ZNF804A pathway | Nicodemus, Kristin K.; Hargreaves, April; Morris, Derek; Anney, Richard; Gill, Michael; Corvin, Aiden; Donohoe, Gary; for the Schizophrenia Psychiatric Genome-wide Association Study (GWAS) Consortium and The Wellcome Trust Case Control Consortium 2; Brown | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:356736 | 61 |
| Whole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia | Glazov, Evgeny A.; Zankl, Andreas; Donskoi, Marina; Kenna,Tony J.; Thomas, Gethin P.; Clark, Graeme R.; Duncan, E. L.; Brown, Matthew A. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:241466 | 33 |
| Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism | Johnson, S. R.; Leo, P. J.; McInerney-Leo, A. M.; Anderson, L. K.; Marshall, M.; McGown, I.; Newell, F.; Brown, M. A.; Conwell, L. S.; Harris, M.; Duncan, E. L. | Article | University of Queensland [UQ eSpace] | https://espace.library.uq.edu.au/view/UQ:720407 | 38 |
