Research Flagships, Centres and Institutes
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Sub-communities within this community
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Australian Industrial Transformation Institute
AITI is a trans-disciplinary research venture, bringing social scientists, scientists and engineers together to work collaboratively with industry, government and communities. -
Flinders Centre for Innovation in Cancer
The Flinders Centre for Innovation in Cancer (FCIC) is a leading cancer centre in Australia, housing world-class care and survivorship services alongside innovative cancer prevention and early intervention research. -
Flinders Centre for Ophthalmology, Eye and Vision Research
The Flinders Centre for Ophthalmology, Eye and Vision Research aims to improve outcomes for patients with blinding eye conditions affecting our community.. -
Flinders Digital Health Research Centre
The Flinders Digital Health Research Centre is a multidisciplinary research entity, established as a cornerstone in Flinders University’s expansion in the health technology domain. -
Flinders Institute for Research in the Humanities
Flinders Institute for Research in the Humanities unites humanities-based researchers engaged in creative and reflective investigations of culture and thought. -
Southgate Institute for Health, Society and Equity
The Southgate Institute for Health, Society and Equity leads high quality scholarship on the social and economic determinants of health and health equity.
Recent Submissions
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The Australian Corneal Graft Registry 2018 Report
(South Australian Health and Medical Research Institute, 2018)The Australian Corneal Graft Registry 2018 Report is still being published and will be made available here shortly. The Australian Corneal Graft Registry (ACGR) opened in May 1985 and has now been operating for 33 ... -
Testosterone Pathway Genetic Polymorphisms in Relation to Primary Open-Angle Glaucoma: An Analysis in Two Large Datasets
(Investigative Ophthalmology and Visual Science, 2018-02)Purpose: Sex hormones may be associated with primary open-angle glaucoma (POAG), although the mechanisms are unclear. We previously observed that gene variants involved with estrogen metabolism were collectively associated ... -
PAX6 molecular analysis and genotype–phenotype correlations in families with aniridia from Australasia and Southeast Asia
(Molecular Vision, 2018-03-28)Purpose Aniridia is a congenital disorder caused by variants in the PAX6 gene. In this study, we assessed the involvement of PAX6 in patients with aniridia from Australasia and Southeast Asia. Methods Twenty-nine ... -
The effect of ice slurry ingestion on body temperature and cycling performance in competitive athletes
(Elsevier, 2018-02-02)The effects of pre cooling on endurance performance are widely known. In contrast, the approach of cooling during endurance exercise in combination with pre-exercise cooling has been poorly understood. The purpose of the ... -
Crowd-sourced Ontology for Photoleukocoria: Identifying Common Internet Search Terms for a Potentially Important Pediatric Ophthalmic Sign
(ARVO Journals, 2018-02-15)Purpose: Leukocoria is the most common presenting sign for pediatric eye disease including retinoblastoma and cataract, with worse outcomes if diagnosis is delayed. We investigated whether individuals could identify ... -
Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility
(Springer Nature, 2017-11-24)Glaucoma is a multi-factorial blinding disease in which genetic factors play an important role. Elevated intraocular pressure is a highly heritable risk factor for primary open angle glaucoma and currently the only target ... -
Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma
(Nature Publishing Group, 2018-02-18)Exfoliation syndrome (XFS) is the most common known risk factor for secondary glaucoma and a major cause of blindness worldwide. Variants in two genes, LOXL1 and CACNA1A, have previously been associated with XFS. To further ... -
DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma
(Taylor & Francis Group, 2017-12-21)Purpose: Recent genome-wide association studies reported strong association of genetic variation at the CDKN2B/CDKN2B-AS1 locus on 9p21 with normal-tension glaucoma (NTG) in multiple populations. The mechanism by which ... -
Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European Descent
(Investigative Ophthalmology and Visual Science, 2017-12)Purpose: The Zinc Finger Protein 469 (ZNF469) gene has been proposed as a candidate gene for keratoconus due to the association of an upstream polymorphism (rs9938149) with the disease in two independent studies, and the ... -
Angiopoietin-1 is required for Schlemm’s canal development in mice and humans
(American Society for Clinical Investigation, 2017-11)Primary congenital glaucoma (PCG) is a leading cause of blindness in children worldwide and is caused by developmental defects in 2 aqueous humor outflow structures, Schlemm’s canal (SC) and the trabecular meshwork. We ... -
Global causes of blindness and distance vision impairment 1990–2020: a systematic review and meta-analysis
(Elsevier, 2017-10-11)Background Contemporary data for causes of vision impairment and blindness form an important basis of recommendations in public health policies. Refreshment of the Global Vision Database with recently published data sources ... -
The Mobility Assessment Course for the Diagnosis of Spatial Neglect: Taking a Step Forward?
(Frontiers Media S.A., 2017-10-31)Spatial neglect after stroke can be a challenging syndrome to diagnose under standard neuropsychological assessment. There is now sufficient evidence that those affected might demonstrate neglect behavior in everyday ... -
Ideas, actors and institutions: lessons from South Australian Health in All Policies on what encourages other sectors’ involvement
(BioMed Central, 2017-10-16)Background This paper examines the extent to which actors from sectors other than health engaged with the South Australian Health in All Policies (HiAP) initiative, determines why they were prepared to do so and explains ... -
An integrative review of e-learning in the delivery of self-management support training for health professionals
(BioMed Central, 2017-10-10)Background E-learning involves delivery of education through Information and Communication Technology (ITC) using a wide variety of instructional designs, including synchronous and asynchronous formats. It can be as ... -
Teaching Communication Skills: An Australian Optometry Program’s New Course
(Association of Schools and Colleges of Optometry., 2014-09)After a review of the literature, the authors describe the experience of developing and teaching a new communication skills course at Flinders University in South Australia. A follow-up survey indicated that optometry ... -
The National Eye Survey of Trinidad and Tobago (NESTT): Rationale, Objectives and Methodology
(Taylor & Francis Group, 2017-01-20)Purpose: This paper describes the rationale, study design and procedures of the National Eye Survey of Trinidad and Tobago (NESTT). The main objective of this survey is to obtain prevalence estimates of vision impairment ... -
Number of People Blind or Visually Impaired by Cataract Worldwide and in World Regions, 1990 to 2010
(ARVO Journals, 2015-10)Purpose: To estimate prevalence and number of people visually impaired or blind due to cataract. Methods: Based on the Global Burden of Diseases Study 2010 and ongoing literature research, we examined how many people ... -
ACE 2016 Handbook : 45th Australian Conference of Economists
(Flinders University, 2016-07-11)Held at Flinders University 11-13 July 2016 -
Public Infrastructure and Private Sector Productivity, Tasmania 1990-2015
(Flinders University, 2016-07-11)The study utilises the recent advances in development of capital stock data at subnational level for Australian states and applies the series for analysis of the effect of the public infrastructure on the private sector ... -
TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases
(Public Library of Science, 2017-08-23)Fuchs’ endothelial corneal dystrophy (FECD) is a progressive, vision impairing disease. Common single nucleotide polymorphisms (SNPs) and a trinucleotide repeat polymorphism, thymine-guanine-cytosine (TGC), in the TCF4 ...
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