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Tropf FC, Stulp G, Barban N, Visscher PM, Yang J, Snieder H, Mills MC (2015), Human Fertility, Molecular Genetics, and Natural Selection in Modern Societies. Plos One 10.

Hayeck TJ, Zaitlen NA, Loh PR, Vilhjalmsson B, Pollack S, Gusev A, Yang J, Chen GB, et al. (2015), Mixed Model with Correction for Case-Control Ascertainment Increases Association Power. American Journal of Human Genetics 96:720-730.

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Robinson EB, Kirby A, Ruparel K, Yang J, McGrath L, Anttila V, Neale BM, Merikangas K, et al. (2015), The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Molecular Psychiatry 20:454-458.


Wood AR, Esko T, Yang J, Vedantam S, Pers TH, Gustafsson S, Chun AY, Estrada K, et al. (2014), Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics 46:1173-1186.

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Tada H, Won HH, Melander O, Yang J, Peloso GM, Kathiresan S (2014), Multiple Associated Variants Increase the Heritability Explained for Plasma Lipids and Coronary Artery Disease. Circulation-Cardiovascular Genetics 7:583-587.

Robinson EB, Howrigan D, Yang J, Ripke S, Anttila V, Duncan LE, Jostins L, Barrett JC, et al. (2014), Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. Molecular Psychiatry 19:859-861.

Jiang L, Yin J, Ye LY, Yang J, Hemani G, Liu AJ, Zou HJ, He DY, et al. (2014), Novel Risk Loci for Rheumatoid Arthritis in Han Chinese and Congruence With Risk Variants in Europeans. Arthritis & Rheumatology 66:1121-1132.

Visscher PM, Hemani G, Vinkhuyzen AAE, Chen GB, Lee SH, Wray NR, Goddard ME, Yang J (2014), Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples. Plos Genetics 10.

Trzaskowski M, Yang J, Visscher PM, Plomin R (2014), DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12. Molecular Psychiatry 19:380-384.

Okada Y, Wu D, Trynka G, Raj T, Terao C, Ikari K, Kochi Y, Ohmura K, et al. (2014), Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature 506:376-381.

Benyamin B, St Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJA, Kirkpatrick RM, Cents RAM, et al. (2014), Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry 19:253-258.

Yang J, Zaitlen NA, Goddard ME, Visscher PM, Price AL (2014), Advantages and pitfalls in the application of mixed-model association methods. Nature Genetics 46:100-106.

Zhou KX, Donnelly L, Yang J, Li MX, Deshmukh H, Van Zuydam N, Ahlqvist E, Spencer CC, et al. (2014), Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis. Lancet Diabetes & Endocrinology 2:481-487.


Wray NR, Yang J, Hayes BJ, Price AL, Goddard ME, Visscher PM (2013), Author reply to A commentary on Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics 14:894.

Vinkhuyzen AAE, Wray NR, Yang J, Goddard ME, Visscher PM (2013), Estimation and Partition of Heritability in Human Populations Using Whole-Genome Analysis Methods. Annual Review of Genetics 47:75-95.

Hemani G, Yang J, Vinkhuyzen A, Powell JE, Willemsen G, Hottenga JJ, Abdellaoui A, Mangino M, et al. (2013), Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics 93:865-875.

Davis LK, Yu DM, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, et al. (2013), Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture. Plos Genetics 9.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ, Hewitt JK, et al. (2013), Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent. American Journal of Human Genetics 93:463-470.

Wray NR, Yang J, Hayes BJ, Price AL, Goddard ME, Visscher PM (2013), Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics 14:507-515.

Trzaskowski M, Davis OSP, DeFries JC, Yang J, Visscher PM, Plomin R (2013), DNA Evidence for Strong Genome-Wide Pleiotropy of Cognitive and Learning Abilities. Behavior Genetics 43:267-273.

Cortes A, Hadler J, Pointon JP, Robinson PC, Karaderi T, Leo P, Cremin K, Pryce K, et al. (2013), Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nature Genetics 45:730-738.

Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, et al. (2013), GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment. Science 340:1467-1471.

Randall JC, Winkler TW, Kutalik Z, Berndt SI, Jackson AU, Monda KL, Kilpelainen TO, Esko T, et al. (2013), Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits. Plos Genetics 9.

den Hoed M, Eijgelsheim M, Esko T, Brundel B, Peal DS, Evans DM, Nolte IM, Segre AV, et al. (2013), Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics 45:621-631.

Murad NAA, Cullen JK, McKenzie M, Ryan MT, Thorburn D, Gueven N, Kobayashi J, Birrell G, et al. (2013), Mitochondrial dysfunction in a novel form of autosomal recessive ataxia. Mitochondrion 13:235-245.

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Lu Y, Vitart V, Burdon KP, Khor CC, Bykhovskaya Y, Mirshahi A, Hewitt AW, Koehn D, et al. (2013), Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Nature Genetics 45:155-163.


van der Harst P, Zhang WH, Leach IM, Rendon A, Verweij N, Sehmi J, Paul DS, Elling U, et al. (2012), Seventy-five genetic loci influencing the human red blood cell. Nature 492:369-375.

Yang J, Loos RJF, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, et al. (2012), FTO genotype is associated with phenotypic variability of body mass index. Nature 490:267-272.

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 28:2540-2542.


McQuillan R, Eklund N, Pirastu N, Kuningas M, McEvoy BP, Esko T, Corre T, Davies G, et al. (2012), Evidence of Inbreeding Depression on Human Height. Plos Genetics 8.

Vinkhuyzen AAE, Pedersen NL, Yang J, Lee SH, Magnusson PKE, Iacono WG, McGue M, Madden PAF, et al. (2012), Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry 2:e102.

Yang J, Ferreira T, Morris AP, Medland SE, Madden PAF, Heath AC, Martin NG, Montgomery GW, et al. (2012), Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics 44:369-375.

Lee SH, DeCandia TR, Ripke S, Yang J, Sullivan PF, Goddard ME, Keller MC, Visscher PM, et al. (2012), Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics 44:247-250.

Deary IJ, Yang J, Davies G, Harris SE, Tenesa A, Liewald D, Luciano M, Lopez LM, et al. (2012), Genetic contributions to stability and change in intelligence from childhood to old age. Nature 482:212-215.

Visscher PM, Brown MA, McCarthy MI, Yang J (2012), Five Years of GWAS Discovery. American Journal of Human Genetics 90:7-24.


Davies G, Tenesa A, Payton A, Yang J, Harris SE, Liewald D, Ke X, Le Hellard S, et al. (2011), Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Molecular Psychiatry 16:996-1005.

Goddard ME, Lee H, Yang J, Wray NR, Visscher PM (2011), Population Structure Can Inflate SNP-Based Heritability Estimates Response. American Journal of Human Genetics 89:193-195.

Yang J, Weedon MN, Purcell S, Lettre G, Estrada K, Willer CJ, Smith AV, Ingelsson E, et al. (2011), Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics 19:807-812.

Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, et al. (2011), Genome partitioning of genetic variation for complex traits using common SNPs. Nature Genetics 43:519-525.

Yang J, Lee SH, Goddard ME, Visscher PM (2011), GCTA: A Tool for Genome-wide Complex Trait Analysis. American Journal of Human Genetics 88:76-82.


Visscher PM, McEvoy B, Yang J (2010), From Galton to GWAS: quantitative genetics of human height. Genetics Research 92:371-379.

Visscher PM, Yang J, Goddard ME (2010), A Commentary on 'Common SNPs Explain a Large Proportion of the Heritability for Human Height' by Yang et al. (2010). Twin Research and Human Genetics 13:517-524.

Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, et al. (2010), Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics 42:949-960.

Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Allen HL, Lindgren CM, et al. (2010), Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics 42:937-948.

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Yang J, Visscher PM, Wray NR (2010), Sporadic cases are the norm for complex disease. European Journal of Human Genetics 18:1039-1043.

Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, Madden PA, Heath AC, et al. (2010), Common SNPs explain a large proportion of the heritability for human height. Nature Genetics 42:565-569.

Zheng WJ, Yang J, Zhu J (2010), QTLNetworkR: an interactive R package for QTL visualization. Journal of Zhejiang University-Science B 11:512-515.

Yang J, Wray NR, Visscher PM (2010), Comparing Apples and Oranges: Equating the Power of Case-Control and Quantitative Trait Association Studies. Genetic Epidemiology 34:254-257.

Wray NR, Yang J, Goddard ME, Visscher PM (2010), The Genetic Interpretation of Area under the ROC Curve in Genomic Profiling. Plos Genetics 6.

Before 2010

Yang J, Zou YY, Zhu J (2009), Identifying differentially expressed genes in human acute leukemia and mouse brain microarray datasets utilizing QTModel. Functional & Integrative Genomics 9:59-66.

Zou YY, Su ZX, Yang J, Zeng YW, Gu X (2009), Uncovering Genetic Regulatory Network Divergence Between Duplicate Genes Using Yeast eQTL Landscape. Journal of Experimental Zoology Part B-Molecular and Developmental Evolution 312B:722-733.

Yang J, Wu W, Zhu J (2008), Mapping interspecific genetic architecture in a host-parasite interaction system. Genetics 178:1737-1743.

Yang J, Hu CC, Hu H, Yu RD, Xia Z, Ye XZ, Zhu J (2008), QTLNetwork: mapping and visualizing genetic architecture of complex traits in experimental populations. Bioinformatics 24:721-723.

Liu GF, Yang J, Xu HM, Hayat Y, Zhu J (2008), Genetic analysis of grain yield conditioned on its component traits in rice (Oryza sativa L.). Australian Journal of Agricultural Research 59:189-195.

Hayat Y, Yang J, Xu HM, Zhu J (2008), Influence of outliers on QTL mapping for complex traits. Journal of Zhejiang University-Science B 9:931-937.

Yang J, Zhu J, Williams RW (2007), Mapping the genetic architecture of complex traits in experimental populations. Bioinformatics 23:1527-1536.

Hu CC, Ye XZ, Zhang Y, Yu RD, Yang J, Zhu J (2007), 3D graphical visualization of the genetic architectures underlying complex traits in multiple environments. Journal of Zhejiang University-Science A 8:563-567.

Yang J, Zhu J (2005), Methods for predicting superior genotypes under multiple environments based on QTL effects. Theoretical and Applied Genetics 110:1268-1274.