Naomi Wray is an ARC Future Fellow and an NHMRC Honorary Senior Research Fellow. Her early training was in quantitative genetics with application in livestock, which provides a strong theoretical foundation for her research today. She holds a BSc in Animal Science from the University of Edinburgh (1984), an MS in Animal Breeding and Statistics from Cornell (1986) and a PhD in Quantitative Genetics from the University of Edinburgh (1989). Her career path from livestock genetics through epidemiology of childhood leukaemia to psychiatric genetics has been underpinned at each stage by a strong interest in underlying theory and practical applications. She moved to Australia in 2005 to join the Queensland Institute of Medical Research where she established and led the Psychiatric Genetics Laboratory. She joined QBI in 2011 to establish the Statistical and Psychiatric Genetics Laboratory.
My broad interest is to understand the genetic contribution to individual differences between people. My research programme focuses on methodology in statistical and quantitative genetics (particularly associated with prediction of genetic risk) and application of new methods to genetically informative data sets of psychiatric disorders. My portfolio of current and recent grants reflects this mix of theory and application in psychiatric genetics.
Join our new study on the genetics of major depression
Recent genetic studies have made important progress in our understanding of the genetic factors underlying schizophrenia. Our analyses of genome-wide genotypes currently available for major depressive disorder (MDD) suggest that similar inroads could be made, but that much larger samples are needed. The international community is gearing up to collect 100,000 cases with MDD and DNA for genome-wide genotyping. Together with Professor Nick Martin from the Queensland Institute for Medical Research, Professor Ian Hickie of the Brain and Mind Research Institute, University of Sydney and Professor Julio Licinio of the South Australia Health and Medical Research Institute we are establishing a collection of MDD cases in Australia. The online questionnaire takes about 45 minutes to complete and asks if you are willing to provide a sample of saliva. The questions relate to all aspects of depression like sleep/wake patterns and seasonality of mood. And for those who have taken anti-depressants we ask about efficacy of specific drugs and their side-effects. Evidence from other diseases clearly shows that genetic factors underpin differences between individuals in their response to drug treatment. Understanding these differences may contribute to personalizing treatment options in the long term. To join the online recruitment click here, we need as participants both those affected and those unaffected by depression.
- Psychiatric GWAS Consortium for Major Depressive Disorder
- Psychiatric GWAS Consortium for Schizophrenia
- Psychiatric GWAS Consortium Cross Disorder Group
- Western Australian Family Study of Schizophrenia
- Genetics of Anxiety (Jack Hettema, Virginia Commonwealth University)
- Consortium of Lithium Genetics
- Mater University Study of Pregnancy (MUSP)
- Queensland Institute of Medical Research
Wray NR, Goddard ME, Visscher PM (2007) Prediction of individual genetic risk to disease from genome-wide association studies. Genome Research 17: 1520-8
Purcell SM, Wray NR, Stone JL, Visscher PM, O’Donovan MC, Sullivan PF, Sklar P. International Schizophrenia Consortium (2009) Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460: 748-752
Wray NR, Visscher PM (2010) Narrowing the boundaries of the genetic architecture of schizophrenia. Schizophrenia Bulletin 36: 14-23.
Wray NR, Yang J, Goddard ME, Visscher PM (2010) The genetic interpretation of area under the ROC curve in genomic profiling. PLoS Genetics e1000864
Wray NR, Purcell SM, Visscher PM (2011): Synthetic associations created by rare variants do not explain most GWAS results. PLoS biology 9(1):e1000579
Wray NR, Pergadia ML, .., Sullivan PF (2012): Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Molecular Psychiatry 17: 36-48
Lee S.H ,DeCandia T.R, Ripke S, … Wray NR (2012) Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics 44: 247-50.
Lee SH, Yang J, Goddard ME, Visscher PM, Wray NR (2012) Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics. 28:2540-2
Gratten J, Visscher PM, Mowry BJ, Wray NR (2013) Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics 45:234-8
Wray NR, Yang J, Hayes BJ, Price AL, Goddard ME, Visscher PM (2013) Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics 14 507-15
Lee SH, Ripke S, Neale B,.> 300 authors…, Sullivan PF, Smoller JW, Kendler KS, Wray NR (2013) Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. In press.
Group Members Based at Queensland Institute of Medical Research
Child and Adolescent Psychiatrist, PhD student