Research Topics
Genomes and Genes
| Naomi R WraySummaryAffiliation: Queensland Institute of Medical Research Country: Australia Publications
| Collaborators
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Detail Information
Publications
Narrowing the boundaries of the genetic architecture of schizophreniaNaomi R Wray
Genetic Epidemiology and Queensland Statistical Genetics, Queensland Institute of Medical Research, 330 Herston Road, Brisbane 4029, Australia
Schizophr Bull 36:14-23. 2010..The first generation of studies have generated hypotheses that should be testable in the near future and will further narrow the boundaries on genetic architectures that are consistent with empirical data...
Prediction of individual genetic risk of complex diseaseNaomi R Wray
Genetic Epidemiology and Queensland Statistical Genetics, Queensland Institute of Medical Research, Brisbane, Australia
Curr Opin Genet Dev 18:257-63. 2008..We conclude that with larger GWAS sample sizes or by combining studies, accurate prediction of genetic risk will be possible, even if the causal mutations or the mechanisms by which they affect susceptibility are unknown...
Multi-locus models of genetic risk of diseaseNaomi R Wray
Genetic Epidemiology and, Queensland Institute of Medical Research, Herston Road, Brisbane, Queensland 4006, Australia
Genome Med 2:10. 2010..To reconcile the two descriptions requires a model of how risks from individual loci combine to determine an individual's overall risk...
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learnedN R Wray
Genetic Epidemiology, Molecular Epidemiology, Psychiatric Genetics and Queensland Statistical Genetics Laboratories, Queensland Institute of Medical Research, Brisbane, QLD, Australia
Mol Psychiatry 17:36-48. 2012..Larger study cohorts characterized for genetic and environmental risk factors accumulated prospectively are likely to be needed to dissect more fully the etiology of MDD...
The genetic interpretation of area under the ROC curve in genomic profilingNaomi R Wray
Genetic Epidemiology and Queensland Statistical Genetics, Queensland Institute of Medical Research, Brisbane, Australia
PLoS Genet 6:e1000864. 2010..We provide a strategy to estimate proportion of genetic variance explained on the liability scale from estimates of AUC, disease prevalence, and heritability (or sibling recurrence risk) available as an online calculator...
Accurate, Large-Scale Genotyping of 5HTTLPR and Flanking Single Nucleotide Polymorphisms in an Association Study of Depression, Anxiety, and Personality MeasuresNaomi R Wray
Genetic and Molecular Epidemiology Laboratories, Queensland Institute of Medical Research, 300 Herston Road, Brisbane 4006, Australia
Biol Psychiatry 66:468-76. 2009..However, the original 5HTTLPR assay is prone to bias toward short allele calling...
Association study of candidate variants from brain-derived neurotrophic factor and dystrobrevin-binding protein 1 with neuroticism, anxiety, and depressionNaomi R Wray
Queensland Institute of Medical Research, Brisbane, Australia
Psychiatr Genet 18:219-25. 2008..Here, association between variants of BDNF and DTNBP1, and multiple anxiety and depression phenotypes is explored...
Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the NetherlandsNaomi R Wray
Department of Genetic Epidemiology, Queensland Institute of Medical Research, 300 Herston Rd, Brisbane, Australia 4029
Arch Gen Psychiatry 65:649-58. 2008..Studying this personality dimension can give insights into the etiology of these important psychiatric disorders...
Association study of candidate variants of COMT with neuroticism, anxiety and depressionNaomi R Wray
Queensland Institute of Medical Research, Brisbane, Australia
Am J Med Genet B Neuropsychiatr Genet 147:1314-8. 2008..Haplotype T-G-G showed weak association (P = 0.042) with PDAG before correction for multiple testing; association between this haplotype and schizophrenia has been previously reported in an Australian sample...
Genetic and phenotypic stability of measures of neuroticism over 22 yearsNaomi R Wray
Genetic Epidermology, Queensland Institute of Medical Research, Brisbane, Australia
Twin Res Hum Genet 10:695-702. 2007..33 for a single measure to .43 for mean score because of the reduction in the estimate of the environmental variance, and this will increase power in genetic linkage or association studies of neuroticism...
Prediction of individual genetic risk to disease from genome-wide association studiesNaomi R Wray
Genetic Epidemiology, Queensland Institute of Medical Research, Queensland 4029, Brisbane, Australia
Genome Res 17:1520-8. 2007..Whether an individual with known genetic risk develops the disease depends on known and unknown environmental factors...
Anxiety and comorbid measures associated with PLXNA2Naomi R Wray
Queensland Institute of Medical Research, Royal Brisbane Hospital, Brisbane, QLD 4029, Australia
Arch Gen Psychiatry 64:318-26. 2007..Common genetic liabilities have been reported between psychiatric and psychological measures, but few examples exist of common genetic variants...
Do 5HTTLPR and stress interact in risk for depression and suicidality? Item response analyses of a large sampleWilliam L Coventry
Genetic Epidemiology Unit, Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Am J Med Genet B Neuropsychiatr Genet 153:757-65. 2010..01) and are not significantly associated with any of the genotype main effects (5HTTLPR, 5HTTLPR + rs25531) or interactions (stress x genotype). We find no evidence to support the hypothesis of any 5HTTLPR genotype by stress interaction...
Genetic and environmental influences on the co-morbidity between depression, panic disorder, agoraphobia, and social phobia: a twin studyMiriam A Mosing
Queensland Institute of Medical Research, Brisbane, QLD 4029, Australia
Depress Anxiety 26:1004-11. 2009..However, the relative importance of genetic and environmental etiology of the covariation between these disorders, particularly the relationship between PD and AG, is less clear...
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPsS Hong Lee
Queensland Brain Institute, University of Queensland, Brisbane, Australia
Nat Genet 44:247-50. 2012..6 × 10(-8)). These results are consistent with a polygenic genetic architecture and imply more individual SNP associations will be detected for this disease as sample size increases...
Use of monozygotic twins to investigate the relationship between 5HTTLPR genotype, depression and stressful life events: an application of Item Response TheoryNaomi R Wray
Genetic and Molecular Epidemiology Laboratories, Queensland Institute of Medical Research, Brisbane, 4006, Australia
Novartis Found Symp 293:48-59; discussion 59-70. 2008..The use of MZT provides a novel framework for examining genotype x environment interaction in the absence of measures on SLE...
A versatile gene-based test for genome-wide association studiesJimmy Z Liu
Genetics and Population Health Division, Queensland Institute of Medical Research, Brisbane, Queensland 4006, Australia
Am J Hum Genet 87:139-45. 2010..We have implemented the approach in both an easy-to-use web interface, which only requires the uploading of markers with their association p-values, and a separate downloadable application...
A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personalityKarin J H Verweij
Genetic Epidemiology, Molecular Epidemiology, and Queensland Statistical Genetics Laboratories, Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Biol Psychol 85:306-17. 2010....
Comparing apples and oranges: equating the power of case-control and quantitative trait association studiesJian Yang
Queensland Institute of Medical Research, Brisbane, Australia
Genet Epidemiol 34:254-7. 2010..With equal sample size, when v=K, the power of CC association study is much less than that of QT association study because of the information lost by transforming a quantitative continuous trait to a binary trait...
Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association studyJorim J Tielbeek
Genetic Epidemiology, Molecular Epidemiology, and Queensland Statistical Genetics Laboratories, Queensland Institute of Medical Research, Brisbane, Queensland, Australia
PLoS ONE 7:e45086. 2012..Biosocial criminological research allows a more empirically grounded understanding of criminal behavior, which could ultimately inform and improve current treatment strategies...
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in AustraliaManuel A R Ferreira
Queensland Institute of Medical Research, Brisbane, QLD, Australia
Eur J Hum Genet 19:458-64. 2011..In conclusion, we confirm the association between asthma risk and variants in ORMDL3 and identify a novel risk variant in IL1RL1. Follow-up of the 17q21 deletion in larger cohorts is warranted...
Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosisS Hong Lee
Consortium membership lists are provided in the Supplementary Information
Hum Mol Genet 22:832-41. 2013..We provide strong evidence that a substantial proportion of variation in liability is explained by common SNPs, and thereby give insights into the genetic architecture of the diseases...
Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypesNaomi R Wray
Queensland Institute of Medical Research, Brisbane, Australia
Eur J Hum Genet 20:668-74. 2012..2 in the presence of 10% reciprocal misdiagnosis. Strategies for minimizing the effects of misdiagnosis in cross-disorder genetic studies are discussed...
A better coefficient of determination for genetic profile analysisSang Hong Lee
Queensland Institute of Medical Research, Brisbane, QLD 4072, Australia
Genet Epidemiol 36:214-24. 2012..Furthermore, even when using ascertained case-control studies that are typical in human disease studies, we can obtain an R(2) measure on the liability scale that can be compared directly to heritability...
Sporadic cases are the norm for complex diseaseJian Yang
Queensland Institute of Medical Research, Brisbane, Queensland, Australia
Eur J Hum Genet 18:1039-43. 2010....
Estimating missing heritability for disease from genome-wide association studiesSang Hong Lee
Queensland Institute of Medical Research, 300 Herston Road, Herston, Queensland 4006, Australia
Am J Hum Genet 88:294-305. 2011..We apply the method to data from the Wellcome Trust Case Control Consortium and show that a substantial proportion of variation in liability for Crohn disease, bipolar disorder, and type I diabetes is tagged by common SNPs...
Heritability in the genomics era--concepts and misconceptionsPeter M Visscher
Queensland Institute of Medical Research, Royal Brisbane Hospital Post Office, Brisbane 4029, Queensland, Australia
Nat Rev Genet 9:255-66. 2008..Recent reports of substantial heritability for gene expression and new estimation methods using marker data highlight the relevance of heritability in the genomics era...
Interpreting the role of de novo protein-coding mutations in neuropsychiatric diseaseJacob Gratten
The University of Queensland, Queensland Brain Institute, Brisbane, Queensland, Australia
Nat Genet 45:234-8. 2013..Here, we consider several challenges for the interpretation of such mutations in the context of their role in neuropsychiatric disease...
Shared temperament risk factors for anorexia nervosa: a twin studyTracey D Wade
School of Psychology, Flinders University, P O Box 2100, Adelaide, SA 5001, Australia
Psychosom Med 70:239-44. 2008..To answer two questions about the nature of the relationship between anorexia nervosa (AN) and dimensional temperament traits: Which traits are comorbid with AN? Which traits share transmitted liabilities with AN?..
Haplotype analysis and a novel allele-sharing method refines a chromosome 4p locus linked to bipolar affective disorderStephanie Le Hellard
Medical Genetics Section, School of Clinical and Molecular Medicine, Molecular Medicine Centre, University of Edinburgh, Scotland, United Kingdom
Biol Psychiatry 61:797-805. 2007..Previously, we described significant linkage of BPAD to a chromosome 4p locus within a large pedigree (F22). Others subsequently have found evidence for linkage of BPAD and SCZ to this region...
Empirical evaluation of the genetic similarity of samples from twin registries in Australia and the Netherlands using 359 STRP markersPatrick F Sullivan
Department of Genetics, University of North Carolina, Chapel Hill, North Carolina 27599 7264, United States of America
Twin Res Hum Genet 9:600-2. 2006..30% between the Australian and the Netherlands cohorts, a smaller value than between many European groups. We conclude that it is reasonable to combine the Australian and the Netherlands samples for joint genetic analyses...
Allele frequencies and the r2 measure of linkage disequilibrium: impact on design and interpretation of association studiesNaomi R Wray
Department of Medical Sciences, University of Edinburgh, United Kingdom
Twin Res Hum Genet 8:87-94. 2005..5. For r(2) >/= .8 and allele frequency at one locus of .1, the maximum difference in allele frequency at the second locus is only +/- .02. The impact on the design and interpretation of association studies is discussed...
Conventional multipoint nonparametric linkage analysis is not necessarily inherently biasedPeter M Visscher
Am J Hum Genet 75:718-20; author reply 723-7. 2004
Sex differences in symptoms of depression in unrelated individuals and opposite-sex twin and sibling pairsChristel M Middeldorp
Department of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands
Twin Res Hum Genet 9:632-6. 2006..This signifies that men and women are alike in their symptom profiles for major depression and genes for depression are probably expressed in the same way in the two sexes...
Response to Amar J. Klar: The chromosome 1;11 translocation provides the best evidence supporting genetic etiology for schizophrenia and bipolar affective disordersJ Kirsty Millar
Genetics 163:833-5; author reply 837-8. 2003
