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Plos One|June 21, 2018
Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 26, 2017
Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosisYuan Zhou, Jennifer S Graves, Steve Simpson, et al.
Investigative Ophthalmology & Visual Science|December 12, 2017
Rare, Potentially Pathogenic Variants in ZNF469 Are Not Enriched in Keratoconus in a Large Australian Cohort of European DescentSionne E M Lucas, Tiger Zhou, Nicholas B Blackburn, et al.
BMC Medical Genomics|July 17, 2010
Transcriptomic epidemiology of smoking: the effect of smoking on gene expression in lymphocytesJac C Charlesworth, Joanne E Curran, Matthew P Johnson, et al.
Arthritis Research & Therapy|October 22, 2014
An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3Jane Zochling, Felicity Newell, Jac C Charlesworth, et al.
Scientific Reports|November 12, 2022
Ensemble machine learning identifies genetic loci associated with future worsening of disability in people with multiple sclerosisValery Fuh-Ngwa, Yuan Zhou, Phillip E Melton, et al.
BMJ Open Ophthalmology|September 26, 2022
Pathogenic genetic variants identified in Australian families with paediatric cataractJohanna L Jones, Bennet J McComish, Sandra E Staffieri, et al.
Plos One|June 6, 2012
An X chromosome association scan of the Norfolk Island genetic isolate provides evidence for a novel migraine susceptibility locus at Xq12Bridget H Maher, Rod A Lea, Miles Benton, et al.
Human Molecular Genetics|May 1, 2007
Genetic determinants of mitochondrial contentJoanne E Curran, Matthew P Johnson, Thomas D Dyer, et al.
Genetic Epidemiology|November 30, 2007
Model selection and Bayesian methods in statistical genetics: summary of group 11 contributions to Genetic Analysis Workshop 15Michael D Swartz, Duncan C Thomas, E Warwick Daw, et al.
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