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Are neurobehavioural and neuromotor impairments associated with FMR1 gene expansion? The gene that causes Fragile X syndrome is found at the end of the X chromosome and is present in all humans. In many cases there is a small to medium change in this gene that may cause psychological and motor difficulties in later adulthood. The core aim of this project is to identify early age-related changes that would indicate later neurological decline.
Identification of genetic polymorphisms of synaptically expressed genes that contribute to variation in normal brain function. This project focuses on understanding brain functions. Brain and mind disorders are by far the largest contributors to the burden of disability, far exceeding any other disorder. This research will contribute to knowledge through addressing the national research priority promoting and maintaining good health. The research outcomes will form the scientific knowledge base ....Identification of genetic polymorphisms of synaptically expressed genes that contribute to variation in normal brain function. This project focuses on understanding brain functions. Brain and mind disorders are by far the largest contributors to the burden of disability, far exceeding any other disorder. This research will contribute to knowledge through addressing the national research priority promoting and maintaining good health. The research outcomes will form the scientific knowledge base essential for the translation of the project into public benefit through their application in development of new testing paradigms for a range of brain and mind disorders. Read moreRead less
Searching for genes influencing reading ability using multivariate genomic linkage analysis and allelic association analysis. Following from the replicated linkages of reading disability to loci on chromosomes 6 & 18, this study examines linkage of these same regions to a range of reading measures in an unselected sample of twins and siblings. Preliminary univariate linkage scans of two neuropsychological reading indices suggest linkage to loci on two chromosomes. Our next step is to include rea ....Searching for genes influencing reading ability using multivariate genomic linkage analysis and allelic association analysis. Following from the replicated linkages of reading disability to loci on chromosomes 6 & 18, this study examines linkage of these same regions to a range of reading measures in an unselected sample of twins and siblings. Preliminary univariate linkage scans of two neuropsychological reading indices suggest linkage to loci on two chromosomes. Our next step is to include reading measures of orthographic skill and phonological decoding in a multivariate linkage analysis with the other reading indices and with measures of IQ and academic achievement. Multivariate linkage increases the power of detecting quantitative traits and assists in defining the phenotype related to the locus. We then aim to identify the functional gene through allelic association analysis. Identification of QTLs for reading ability may lead to practical outcomes such as the behavioural and biomedical management of reading deficits, which may then benefit areas such as scholastic achievement.Read moreRead less
Locating genes for elementary and complex cognitive abilities using genetic linkage and association analysis. This study aims to identify genes influencing cognitive ability by using multiple measures of cognition in combination with genetic linkage and association analyses. Multiple measures can increase the statistical power of finding a gene and provide a more comprehensive framework for charting the functional role of genes. The outcome of locating genes for cognition will provide insight i ....Locating genes for elementary and complex cognitive abilities using genetic linkage and association analysis. This study aims to identify genes influencing cognitive ability by using multiple measures of cognition in combination with genetic linkage and association analyses. Multiple measures can increase the statistical power of finding a gene and provide a more comprehensive framework for charting the functional role of genes. The outcome of locating genes for cognition will provide insight into biological functions of the brain which affect human intellect, and will have downstream practical applications which could include better educational, behavioural and biomedical management of learning and memory disorders, and of other intellectual disabilities.Read moreRead less
Quantitative and Molecular Genetic Analysis of Cognition. This study attempts to unravel the pathways through which genes may exert their influence on cognitive processes by identifying some of the genes associated with normal variation in cognitive ability. Using the cognitive phenotypes we have collected, both linkage and association analysis will be used to find QTLs (locations on the chromosomes at which specific genes contribute to a quantitative trait) associated with processing speed and ....Quantitative and Molecular Genetic Analysis of Cognition. This study attempts to unravel the pathways through which genes may exert their influence on cognitive processes by identifying some of the genes associated with normal variation in cognitive ability. Using the cognitive phenotypes we have collected, both linkage and association analysis will be used to find QTLs (locations on the chromosomes at which specific genes contribute to a quantitative trait) associated with processing speed and other specific abilities. The research will enhance our understanding of the biological mechanisms influencing brain function and paves the way for the genetic dissection of the brain.Read moreRead less
Variation in the arginine vasopressin 1a receptor (AVPR1a) gene, the social environment, general health and wellbeing. The project aims to investigate how the arginine vasopressin 1a gene affects gene expression and influences social behaviour and ultimately health and wellbeing. This research will contribute to understanding the importance of individual differences in social policy and interventions aimed at improving health and wellbeing.