Naomi R Wray

发表

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Han Xu, Stephan Ripke, Chongzhi Zang, 2014, American journal of human genetics.

Author Correction: Bayesian reassessment of the epigenetic architecture of complex traits

Archie Campbell, Peter M Visscher, Gibran Hemani, 2020, Nature Communications.

Improved polygenic prediction by Bayesian multiple regression on summary statistics

Andres Metspalu, Gerhard Moser, Loïc Yengo, 2019, Nature Communications.

Across-cohort QC analyses of GWAS summary statistics from complex traits

Zoltán Kutalik, Sang Hong Lee, Jian Yang, 2016, European Journal of Human Genetics.

Performance of risk prediction for inflammatory bowel disease based on genotyping platform and genomic risk score method

Sang Hong Lee, Peter M Visscher, Naomi R Wray, 2017, BMC Medical Genetics.

Concepts, estimation and interpretation of SNP-based heritability

Jian Yang, Peter M Visscher, Michael E Goddard, 2017, Nature Genetics.

Integrative analysis of omics summary data reveals putative mechanisms underlying complex traits

Ting Qi, Nicholas G Martin, Jian Yang, 2018, Nature Communications.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Jakob Grove, Esben Agerbo, Robert Plomin, 2018, Nature Genetics.

Translation elongation factor eEF1A2 is a potential oncoprotein that is overexpressed in two-thirds of breast tumours

Naomi R Wray, N. Wray, H. Newbery, 2005, BMC Cancer.

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk.

Peter M Visscher, Naomi R Wray, David M. Evans, 2009, Human molecular genetics.

Contrasting regional architectures of schizophrenia and other complex diseases using fast variance components analysis

Alexander Gusev, Sang Hong Lee, Gaurav Bhatia, 2015 .

A resource-efficient tool for mixed model association analysis of large-scale data

Ting Qi, Jian Yang, Peter M Visscher, 2019, Nature Genetics.

Large-scale genomics unveils the genetic architecture of psychiatric disorders

Peter M Visscher, Matthew C Keller, Naomi R Wray, 2014, Nature Neuroscience.

Prediction of individual genetic risk to disease from genome-wide association studies.

Peter M Visscher, Michael E Goddard, Naomi R Wray, 2007, Genome research.

Overlap of expression Quantitative Trait Loci (eQTL) in human brain and blood

Joseph E Powell, Naomi R Wray, N. Wray, 2014, BMC Medical Genomics.

Explaining additional genetic variation in complex traits.

Peter M Visscher, Naomi R Wray, P. Visscher, 2014, Trends in genetics : TIG.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936

Steve Horvath, Paul Redmond, Peter M Visscher, 2015, International journal of epidemiology.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

Yadav Sapkota, Thomas Meitinger, Andres Metspalu, 2017, Nature Communications.

Comparison of Genotypic and Phenotypic Correlations: Cheverud’s Conjecture in Humans

Kathryn E Kemper, Naomi R Wray, Maciej Trzaskowski, 2018, Genetics.

Genome‐wide gene‐environment interaction in depression: A systematic evaluation of candidate genes

Alexander Teumer, Niamh Mullins, Stephan Ripke, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Prediction of individual genetic risk of complex disease.

Peter M Visscher, Michael E Goddard, Naomi R Wray, 2008, Current opinion in genetics & development.

Genetic and Phenotypic Stability of Measures of Neuroticism Over 22 Years

Nicholas G Martin, Peter M Visscher, Patrick F Sullivan, 2007, Twin Research and Human Genetics.

Estimation of SNP heritability from dense genotype data.

Stephan Ripke, Jian Yang, Peter M Visscher, 2013, American journal of human genetics.

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs

Stephan Ripke, Jian Yang, Peter M Visscher, 2012, Nature Genetics.

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands.

Nicholas G Martin, Peter M Visscher, Patrick F Sullivan, 2008, Archives of general psychiatry.

which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Multi-locus models of genetic risk of disease

Michael E Goddard, Naomi R Wray, N. Wray, 2009 .

Improving genetic prediction by leveraging genetic correlations among human diseases and traits

Stephan Ripke, Sang Hong Lee, Jian Yang, 2018, Nature Communications.

Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits

Jian Yang, Naomi R Wray, Allan F McRae, 2016, Genome Medicine.

Hypermethylation in the ZBTB20 gene is associated with major depressive disorder

Fei Gao, Alexis Battle, Jun Wang, 2014, Genome Biology.

Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.

Esben Agerbo, Manuel Mattheisen, Stephan Ripke, 2015, JAMA psychiatry.

Epigenetic Signatures of Cigarette Smoking

Paolo Vineis, Allan C Just, Luigi Ferrucci, 2016, Circulation. Cardiovascular genetics.

Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: Genome‐wide association study of both common and rare variants

Jun Li, Ning Ji, Li Yang, 2013, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.