Selected Publications

Nature reviews genetics

 
The contribution of genetic variants to disease depends on the ruler. John S Witte, Peter M Visscher, and Naomi R Wray. Nature Reviews Genetics, 15(11):765--776, 2014. [ DOI ]
 
Pitfalls of predicting complex traits from SNPs. Naomi R Wray, Jian Yang, Ben J Hayes, Alkes L Price, Michael E Goddard, and Peter M Visscher. Nature Reviews Genetics, 14(7):507--515, 2013. [ DOI ]
 
Reconciling the analysis of IBD and IBS in complex trait studies. Joseph E Powell, Peter M Visscher, and Michael E Goddard. Nature Reviews Genetics, 11(11):800--805, 2010. [ DOI ]
 
Heritability in the genomics era—concepts and misconceptions. Peter M Visscher, William G Hill, and Naomi R Wray. Nature Reviews Genetics, 9(4):255--266, 2008. [ DOI ]

Nature

 
New genetic loci link adipose and insulin biology to body fat distribution. Dmitry Shungin, Thomas W Winkler, Damien C Croteau-Chonka, Teresa Ferreira, Adam E Locke, Reedik Mägi, Rona J Strawbridge, Tune H Pers, Krista Fischer, Anne E Justice, et al. Nature, 518(7538):187--196, 2015. [ DOI ]
 
Genetic studies of body mass index yield new insights for obesity biology. Adam E Locke, Bratati Kahali, Sonja I Berndt, Anne E Justice, Tune H Pers, Felix R Day, Corey Powell, Sailaja Vedantam, Martin L Buchkovich, Jian Yang, et al. Nature, 518(7538):197--206, 2015. [ DOI ]
 
The UK10K project identifies rare variants in health and disease. UK10K Consortium et al. Nature, 526(7571):82--90, 2015. [ DOI ]
 
Detection and replication of epistasis influencing transcription in humans. Gibran Hemani, Konstantin Shakhbazov, Harm-Jan Westra, Tonu Esko, Anjali K Henders, Allan F McRae, Jian Yang, Greg Gibson, Nicholas G Martin, Andres Metspalu, et al. Nature, 2014. [ DOI ]
 
Life history trade-offs at a single locus maintain sexually selected genetic variation. Susan E Johnston, Jacob Gratten, Camillo Berenos, Jill G Pilkington, Tim H Clutton-Brock, Josephine M Pemberton, and Jon Slate. Nature, 2013. [ DOI ]
 
FTO genotype is associated with phenotypic variability of body mass index. Jian Yang, Ruth JF Loos, Joseph E Powell, Sarah E Medland, Elizabeth K Speliotes, Daniel I Chasman, Lynda M Rose, Gudmar Thorleifsson, Valgerdur Steinthorsdottir, Reedik Mägi, et al. Nature, 490(7419):267--272, 2012. [ DOI ]
 
Genetic contributions to stability and change in intelligence from childhood to old age. Ian J Deary, Jian Yang, Gail Davies, Sarah E Harris, Albert Tenesa, David Liewald, Michelle Luciano, Lorna M Lopez, Alan J Gow, Janie Corley, et al. Nature, 482(7384):212--215, 2012. [ DOI ]
 
Finding the missing heritability of complex diseases. Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti, et al. Nature, 461(7265):747--753, 2009. [ DOI ]
 
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Shaun M Purcell, Naomi R Wray, Jennifer L Stone, Peter M Visscher, Michael C O'Donovan, Patrick F Sullivan, Pamela Sklar, Shaun M Purcell, Jennifer L Stone, Patrick F Sullivan, et al. Nature, 460(7256):748--752, 2009. [ DOI ]
 
A viable herd of genetically uniform cattle. PM Visscher, D Smith, Stephen JG Hall, and JL Williams. Nature, 409(6818):303--303, 2001. [ DOI ]

Science

 
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Cornelius A Rietveld, Sarah E Medland, Jaime Derringer, Jian Yang, Tõnu Esko, Nicolas W Martin, Harm-Jan Westra, Konstantin Shakhbazov, Abdel Abdellaoui, Arpana Agrawal, et al. Science, 340(6139):1467--1471, 2013. [ DOI ]

Nature genetics

 
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets. Zhihong Zhu, Futao Zhang, Han Hu, Andrew Bakshi, Matthew R Robinson, Joseph E Powell, Grant W Montgomery, Michael E Goddard, Naomi R Wray, Peter M Visscher, et al. Nature Genetics, 2016. [ DOI ]
 
Population genetic differentiation of height and body mass index across Europe. Matthew R Robinson, Gibran Hemani, Carolina Medina-Gomez, Massimo Mezzavilla, Tonu Esko, Konstantin Shakhbazov, Joseph E Powell, Anna Vinkhuyzen, Sonja I Berndt, Stefan Gustafsson, et al. Nature Genetics, 2015. [ DOI ]
 
Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index. Jian Yang, Andrew Bakshi, Zhihong Zhu, Gibran Hemani, Anna AE Vinkhuyzen, Sang Hong Lee, Matthew R Robinson, John RB Perry, Ilja M Nolte, Jana V van Vliet-Ostaptchouk, et al. Nature genetics, 2015. [ DOI ]
 
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies. Brendan K Bulik-Sullivan, Po-Ru Loh, Hilary K Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark J Daly, Alkes L Price, Benjamin M Neale, Schizophrenia Working Group of the Psychiatric Genomics Consortium, et al. Nature genetics, 47(3):291--295, 2015. [ DOI ]
 
Advantages and pitfalls in the application of mixed-model association methods. Jian Yang, Noah A Zaitlen, Michael E Goddard, Peter M Visscher, and Alkes L Price. Nature genetics, 46(2):100--106, 2014. [ DOI ]
 
Defining the role of common variation in the genomic and biological architecture of adult human height. Andrew R Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H Pers, Stefan Gustafsson, Audrey Y Chu, Karol Estrada, Jian'an Luan, Zoltán Kutalik, et al. Nature genetics, 46(11):1173--1186, 2014. [ DOI ]
 
Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Jacob Gratten, Peter M Visscher, Bryan J Mowry, and Naomi R Wray. Nature genetics, 45(3):234--238, 2013. [ DOI ]
 
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Cross-Disorder Group of the Psychiatric Genomics Consortium et al. Nature genetics, 2013. [ DOI ]
 
Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. S Hong Lee, Teresa R DeCandia, Stephan Ripke, Jian Yang, Patrick F Sullivan, Michael E Goddard, Matthew C Keller, Peter M Visscher, Naomi R Wray, Schizophrenia Psychiatric Genome-Wide Association Study Consortium, et al. Nature genetics, 44(3):247--250, 2012. [ DOI ]
 
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Jian Yang, Teresa Ferreira, Andrew P Morris, Sarah E Medland, Pamela AF Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery, Michael N Weedon, Ruth J Loos, et al. Nature genetics, 44(4):369--375, 2012. [ DOI ]
 
Genome partitioning of genetic variation for complex traits using common SNPs. Jian Yang, Teri A Manolio, Louis R Pasquale, Eric Boerwinkle, Neil Caporaso, Julie M Cunningham, Mariza de Andrade, Bjarke Feenstra, Eleanor Feingold, M Geoffrey Hayes, et al. Nature genetics, 43(6):519--525, 2011. [ DOI ]
 
Common SNPs explain a large proportion of the heritability for human height. Jian Yang, Beben Benyamin, Brian P McEvoy, Scott Gordon, Anjali K Henders, Dale R Nyholt, Pamela A Madden, Andrew C Heath, Nicholas G Martin, Grant W Montgomery, et al. Nature genetics, 42(7):565--569, 2010. [ DOI ]

Annual Review of Genetics

 
Estimation and partitioning of heritability in human populations using whole genome analysis methods. Anna AE Vinkhuyzen, Naomi R Wray, Jian Yang, Michael E Goddard, and Peter M Visscher. Annual review of genetics, 47:75, 2013. [ DOI ]

Nature neurogenetics

 
Large-scale genomics unveils the genetic architecture of psychiatric disorders. Jacob Gratten, Naomi R Wray, Matthew C Keller, and Peter M Visscher. Nature neuroscience, 17(6):782--790, 2014. [ DOI ]

Molecular Psychiatry

 
Assessing the genetic overlap between BMI and cognitive function. RE Marioni, J Yang, D Dykiert, R Mõttus, A Campbell, Carla A Ibrahim-Verbaas, Jan Bressler, Stephanie Debette, Maaike Schuur, Albert V Smith, et al. Molecular psychiatry, 2016. [ DOI ]
 
The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Elise B Robinson, Andrew Kirby, Kosha Ruparel, Jian Yang, Lauren McGrath, Verneri Anttila, Benjamin M Neale, Kathleen Merikangas, Thomas Lehner, Patrick MA Sleiman, et al. Molecular psychiatry, 20(4):454--458, 2015. [ DOI ]
 
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. PA Thomson, JS Parla, AF McRae, M Kramer, K Ramakrishnan, J Yao, DC Soares, S McCarthy, SW Morris, L Cardone, et al. Molecular psychiatry, 19(6):668--675, 2014. [ DOI ]
 
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. NR Wray, ML Pergadia, DHR Blackwood, BWJH Penninx, SD Gordon, DR Nyholt, S Ripke, DJ MacIntyre, KA McGhee, AW Maclean, et al. Molecular psychiatry, 17(1):36--48, 2012. [ DOI ]
 
The emerging spectrum of allelic variation in schizophrenia: current evidence and strategies for the identification and functional characterization of common and rare variants. BJ Mowry and J Gratten. Molecular psychiatry, 18(1):38--52, 2012. [ DOI ]
 
A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. G Davies, SE Harris, CA Reynolds, A Payton, HM Knight, DC Liewald, LM Lopez, M Luciano, AJ Gow, J Corley, et al. Molecular psychiatry, 19(1):76--87, 2012. [ DOI ]
 
Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Gail Davies, Albert Tenesa, Antony Payton, Jian Yang, Sarah E Harris, David Liewald, Xiayi Ke, Stephanie Le Hellard, Andrea Christoforou, Michelle Luciano, et al. Molecular psychiatry, 16(10):996--1005, 2011. [ DOI ]
 
Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. PM Visscher, ME Goddard, EM Derks, and NR Wray. Molecular psychiatry, 17(5):474--485, 2011. [ DOI ]

Genome Research

 
Genetic and environmental exposures constrain epigenetic drift over the human life course. Sonia Shah, Allan F McRae, Riccardo E Marioni, Sarah E Harris, Jude Gibson, Anjali K Henders, Paul Redmond, Simon R Cox, Alison Pattie, Janie Corley, et al. Genome research, 24(11):1725--1733, 2014. [ DOI ]
 
Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence. Lavinia Gordon, Jihoon E Joo, Joseph E Powell, Miina Ollikainen, Boris Novakovic, Xin Li, Roberta Andronikos, Mark N Cruickshank, Karen N Conneely, Alicia K Smith, et al. Genome research, 22(8):1395--1406, 2012. [ DOI ]
 
Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Joseph E Powell, Anjali K Henders, Allan F McRae, Margaret J Wright, Nicholas G Martin, Emmanouil T Dermitzakis, Grant W Montgomery, and Peter M Visscher. Genome research, 22(3):456--466, 2012. [ DOI ]
 
Human population dispersal “Out of Africa” estimated from linkage disequilibrium and allele frequencies of SNPs. Brian P McEvoy, Joseph E Powell, Michael E Goddard, and Peter M Visscher. Genome research, 21(6):821--829, 2011. [ DOI ]
 
Prediction of individual genetic risk to disease from genome-wide association studies. Naomi R Wray, Michael E Goddard, and Peter M Visscher. Genome research, 17(10):1520--1528, 2007. [ DOI ]
 
Recent human effective population size estimated from linkage disequilibrium. Albert Tenesa, Pau Navarro, Ben J Hayes, David L Duffy, Geraldine M Clarke, Mike E Goddard, and Peter M Visscher. Genome research, 17(4):520--526, 2007. [ DOI ]

PLoS Biology

 
Synthetic associations created by rare variants do not explain most GWAS results. Naomi R Wray, Shaun M Purcell, and Peter M Visscher. PLoS biology, 9(1):e1000579, 2011. [ DOI ]

Trends in Genetics

 
Explaining additional genetic variation in complex traits. Matthew R Robinson, Naomi R Wray, and Peter M Visscher. Trends in Genetics, 30(4):124--132, 2014. [ DOI ]

American Journal of Human Genetics

 
Mixed model with correction for case-control ascertainment increases association power. Tristan J Hayeck, Noah A Zaitlen, Po-Ru Loh, Bjarni Vilhjalmsson, Samuela Pollack, Alexander Gusev, Jian Yang, Guo-Bo Chen, Michael E Goddard, Peter M Visscher, et al. The American Journal of Human Genetics, 96(5):720--730, 2015. [ DOI ]
 
Modeling linkage disequilibrium increases accuracy of polygenic risk scores. Bjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, Alexander Gusev, Sara Lindström, Stephan Ripke, Giulio Genovese, Po-Ru Loh, Gaurav Bhatia, Ron Do, et al. The American Journal of Human Genetics, 97(4):576--592, 2015. [ DOI ]
 
Dominance genetic variation contributes little to the missing heritability for human complex traits. Zhihong Zhu, Andrew Bakshi, Anna AE Vinkhuyzen, Gibran Hemani, Sang Hong Lee, Ilja M Nolte, Jana V van Vliet-Ostaptchouk, Harold Snieder, Tonu Esko, Lili Milani, et al. The American Journal of Human Genetics, 96(3):377--385, 2015. [ DOI ]
 
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations. Sonia Shah, Marc J Bonder, Riccardo E Marioni, Zhihong Zhu, Allan F McRae, Alexandra Zhernakova, Sarah E Harris, Dave Liewald, Anjali K Henders, Michael M Mendelson, et al. The American Journal of Human Genetics, 2015. [ DOI ]
 
Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder. Robert Maier, Gerhard Moser, Guo-Bo Chen, Stephan Ripke, William Coryell, James B Potash, William A Scheftner, Jianxin Shi, Myrna M Weissman, Christina M Hultman, et al. The American Journal of Human Genetics, 96(2):283--294, 2015. [ DOI ]
 
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. Teresa R de Candia, S Hong Lee, Jian Yang, Brian L Browning, Pablo V Gejman, Douglas F Levinson, Bryan J Mowry, John K Hewitt, Michael E Goddard, Michael C O’Donovan, et al. The American Journal of Human Genetics, 93(3):463--470, 2013. [ DOI ]
 
Inference of the genetic architecture underlying BMI and height with the use of 20,240 sibling pairs. Gibran Hemani, Jian Yang, Anna Vinkhuyzen, Joseph E Powell, Gonneke Willemsen, Jouke-Jan Hottenga, Abdel Abdellaoui, Massimo Mangino, Ana M Valdes, Sarah E Medland, et al. The American Journal of Human Genetics, 93(5):865--875, 2013. [ DOI ]
 
Five years of GWAS discovery. Peter M Visscher, Matthew A Brown, Mark I McCarthy, and Jian Yang. The American Journal of Human Genetics, 90(1):7--24, 2012. [ DOI ]
 
GCTA: a tool for genome-wide complex trait analysis. Jian Yang, S Hong Lee, Michael E Goddard, and Peter M Visscher. The American Journal of Human Genetics, 88(1):76--82, 2011. [ DOI ]
 
Estimating missing heritability for disease from genome-wide association studies. Sang Hong Lee, Naomi R Wray, Michael E Goddard, and Peter M Visscher. The American Journal of Human Genetics, 88(3):294--305, 2011. [ DOI ]
 
Genome partitioning of genetic variation for height from 11,214 sibling pairs. Peter M Visscher, Stuart Macgregor, Beben Benyamin, Gu Zhu, Scott Gordon, Sarah Medland, William G Hill, Jouke-Jan Hottenga, Gonneke Willemsen, Dorret I Boomsma, et al. The American Journal of Human Genetics, 81(5):1104--1110, 2007. [ DOI ]

Genome Biology

 
DNA methylation age of blood predicts all-cause mortality in later life. Riccardo E Marioni, Sonia Shah, Allan F McRae, Brian H Chen, Elena Colicino, Sarah E Harris, Jude Gibson, Anjali K Henders, Paul Redmond, Simon R Cox, et al. Genome biology, 16(1), 2015. [ DOI ]
 
Contribution of genetic variation to transgenerational inheritance of DNA methylation. Allan F McRae, Joseph E Powell, Anjali K Henders, Lisa Bowdler, Gibran Hemani, Sonia Shah, Jodie N Painter, Nicholas G Martin, Peter M Visscher, and Grant W Montgomery. Genome biology, 15(5), 2014. [ DOI ]

Proceedings of the National Academy of Sciences

 
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Cornelius A Rietveld, Tõnu Esko, Gail Davies, Tune H Pers, Patrick Turley, Beben Benyamin, Christopher F Chabris, Valur Emilsson, Andrew D Johnson, James J Lee, et al. Proceedings of the National Academy of Sciences, 111(38):13790--13794, 2014. [ DOI ]
 
The genetic architecture of economic and political preferences. Daniel J Benjamin, David Cesarini, Matthijs JHM van der Loos, Christopher T Dawes, Philipp D Koellinger, Patrik KE Magnusson, Christopher F Chabris, Dalton Conley, David Laibson, Magnus Johannesson, et al. Proceedings of the National Academy of Sciences, 109(21):8026--8031, 2012. [ DOI ]

International Journal of Epidemiology

 
Mendelian randomization study of height and risk of colorectal cancer. Aaron P Thrift, Jian Gong, Ulrike Peters, Jenny Chang-Claude, Anja Rudolph, Martha L Slattery, Andrew T Chan, Tonu Esko, Andrew R Wood, Jian Yang, et al. International journal of epidemiology, page dyv082, 2015. [ DOI ]
 
The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936. Riccardo E Marioni, Sonia Shah, Allan F McRae, Stuart J Ritchie, Graciela Muniz-Terrera, Sarah E Harris, Jude Gibson, Paul Redmond, Simon R Cox, Alison Pattie, et al. International journal of epidemiology, 2015. [ DOI ]

PLoS Genetics

 
The influence of age and sex on genetic associations with adult body size and shape: a large-scale genome-wide interaction study. Thomas W Winkler, Anne E Justice, Mariaelisa Graff, Llilda Barata, Mary F Feitosa, Su Chu, Jacek Czajkowski, Tõnu Esko, Tove Fall, Tuomas O Kilpeläinen, et al. PLoS Genet, 11(10):e1005378, 2015. [ DOI ]
 
Simultaneous Discovery, Estimation and Prediction Analysis of Complex Traits Using a Bayesian Mixture Model. Gerhard Moser, Sang Hong Lee, Ben J Hayes, Michael E Goddard, Naomi R Wray, and Peter M Visscher. PLoS genetics, 11(4), 2015. [ DOI ]
 
Statistical power to detect genetic (co) variance of complex traits using SNP data in unrelated samples. Peter M Visscher, Gibran Hemani, Anna AE Vinkhuyzen, Guo-Bo Chen, Sang Hong Lee, Naomi R Wray, Michael E Goddard, and Jian Yang. PLoS genetics, 10(4):e1004269, 2014. [ DOI ]
 
Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. Joseph E Powell, Anjali K Henders, Allan F McRae, Jinhee Kim, Gibran Hemani, Nicholas G Martin, Emmanouil T Dermitzakis, Greg Gibson, Grant W Montgomery, and Peter M Visscher. PLoS genetics, 9(5):e1003502, 2013. [ DOI ]
 
The genetic interpretation of area under the ROC curve in genomic profiling. Naomi R Wray, Jian Yang, Michael E Goddard, and Peter M Visscher. PLoS Genetics, 6(2):e1000864, 2010. [ DOI ]
 
The limits of individual identification from sample allele frequencies: theory and statistical analysis. Peter M Visscher and William G Hill. PLoS genetics, 5(10):e1000628, 2009. [ DOI ]
 
Data and theory point to mainly additive genetic variance for complex traits. William G Hill, Michael E Goddard, and Peter M Visscher. PLoS Genetics, 4(2):e1000008, 2008. [ DOI ]
 
Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Peter M Visscher, Sarah E Medland, Manuel AR Ferreira, Katherine I Morley, Gu Zhu, Belinda K Cornes, Grant W Montgomery, and Nicholas G Martin. PLoS genetics, 2(3):e41, 2006. [ DOI ]

Bioinformatics

 
Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Sang Hong Lee, Jian Yang, Michael E Goddard, Peter M Visscher, and Naomi R Wray. Bioinformatics, 28(19):2540--2542, 2012. [ DOI ]
 
Classification based upon gene expression data: bias and precision of error rates. Ian A Wood, Peter M Visscher, and Kerrie L Mengersen. Bioinformatics, 23(11):1363--1370, 2007. [ DOI ]

European Journal of Human Genetics

 
Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes. Naomi R Wray, Sang Hong Lee, and Kenneth S Kendler. European Journal of Human Genetics, 20(6):668--674, 2012. [ DOI ]
 
Genomic inflation factors under polygenic inheritance. Jian Yang, Michael N Weedon, Shaun Purcell, Guillaume Lettre, Karol Estrada, Cristen J Willer, Albert V Smith, Erik Ingelsson, Jeffrey R O'Connell, Massimo Mangino, et al. European Journal of Human Genetics, 19(7):807--812, 2011. [ DOI ]
 
On Jim Watson's APOE status: Genetic information is hard to hide. Dale R Nyholt, Chang-En Yu, and Peter M Visscher. European Journal of Human Genetics, 17(2):147, 2009. [ DOI ]
 
Sporadic cases are the norm for complex disease. Jian Yang, Peter M Visscher, and Naomi R Wray. European Journal of Human Genetics, 18(9):1039--1043, 2009. [ DOI ]

PLoS One

 
Human fertility, molecular genetics, and natural selection in modern societies. Felix C Tropf, Gert Stulp, Nicola Barban, Peter M Visscher, Jian Yang, Harold Snieder, and Melinda C Mills. PloS one, 10(6):e0126821, 2015. [ DOI ]
 
A comparative study of techniques for differential expression analysis on RNA-Seq data. Zong Hong Zhang, Dhanisha J Jhaveri, Vikki M Marshall, Denis C Bauer, Janette Edson, Ramesh K Narayanan, Gregory J Robinson, Andreas E Lundberg, Perry F Bartlett, Naomi R Wray, et al. PLoS one, 9(8), 2014. [ DOI ]
 
Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits. Sven Stringer, Eske M Derks, René S Kahn, William G Hill, and Naomi R Wray. PLoS one, 8(7), 2013. [ DOI ]
 
The Brisbane Systems Genetics Study: genetical genomics meets complex trait genetics. Joseph E Powell, Anjali K Henders, Allan F McRae, Anthony Caracella, Sara Smith, Margaret J Wright, John B Whitfield, Emmanouil T Dermitzakis, Nicholas G Martin, Peter M Visscher, et al. PLoS one, 7(4), 2012. [ DOI ]

Twin Research and Human Genetics

 
A commentary on ‘common SNPs explain a large proportion of the heritability for human height’by Yang et al.(2010). Peter M Visscher, Jian Yang, and Michael E Goddard. Twin Research and Human Genetics, 13(06):517--524, 2010. [ DOI ]
 
Power of the classical twin design revisited: II detection of common environmental variance. Peter M Visscher, Scott Gordon, and Michael C Neale. Twin Research and Human Genetics, 11(01):48--54, 2008. [ DOI ]
 
A note on the asymptotic distribution of likelihood ratio tests to test variance components. Peter M Visscher. Twin research and human genetics, 9(04):490--495, 2006. [ DOI ]

Epidemiology and Psychiatric Sciences

 
Novel directions for G × E analysis in psychiatry. AAE Vinkhuyzen and NR Wray. Epidemiology and Psychiatric Sciences, 24(01):12--19, 2015. [ DOI ]

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