Chen GB, Lee SH, Robinson MR, Trzaskowski M, Zhu ZX, Winkler TW, Day FR, Croteau-Chonka DC, Wood AR, Locke AE, Kutalik Z, Loos RJ, Frayling TM, Hirschhorn JN, Yang J, Wray NR; Genetic Investigation of Anthropometric Traits (GIANT) Consortium., Visscher PM. Across-cohort QC analyses of GWAS summary statistics from complex traits. Eur J Hum Genet. 2016 Jan;25(1):137-146. doi: 10.1038/ejhg.2016.106. PubMed PMID: 27552965; PubMed Central PMCID: PMC5159754.

Yang J, Lee SH, Wray NR, Goddard ME, Visscher PM. GCTA-GREML accounts for linkage disequilibrium when estimating genetic variance from genome-wide SNPs. Proc Natl Acad Sci U S A. 2016 Aug 9;113(32):E4579-80. doi: 10.1073/pnas.1602743113. PubMed PMID: 27457963; PubMed Central PMCID: PMC4987770.

van Rheenen W, Shatunov A, Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U, de Jong S, Robinson MR, Yang J, Fogh I, van Doormaal PT, Tazelaar GH, Koppers M, Blokhuis AM, Sproviero W, Jones AR, Kenna KP, van Eijk KR, Harschnitz O, Schellevis RD, Brands WJ, Medic J, Menelaou A, Vajda A, Ticozzi N, Lin K, Rogelj B, Vrabec K, Ravnik-Glavač M, Koritnik B, Zidar J, Leonardis L,  Grošelj LD, Millecamps S, Salachas F, Meininger V, de Carvalho M, Pinto S, Mora JS, Rojas-García R, Polak M, Chandran S, Colville S, Swingler R, Morrison KE, Shaw PJ, Hardy J, Orrell RW, Pittman A, Sidle K, Fratta P, Malaspina A, Topp S, Petri S, Abdulla S, Drepper C, Sendtner M, Meyer T, Ophoff RA, Staats KA, Wiedau-Pazos M, Lomen-Hoerth C, Van Deerlin VM, Trojanowski JQ, Elman L, McCluskey L, Basak AN, Tunca C, Hamzeiy H, Parman Y, Meitinger T, Lichtner P, Radivojkov-Blagojevic M, Andres CR, Maurel C, Bensimon G, Landwehrmeyer B, Brice  A, Payan CA, Saker-Delye S, Dürr A, Wood NW, Tittmann L, Lieb W, Franke A, Rietschel M, Cichon S, Nöthen MM, Amouyel P, Tzourio C, Dartigues JF, Uitterlinden AG, Rivadeneira F, Estrada K, Hofman A, Curtis C, Blauw HM, van der  Kooi AJ, de Visser M, Goris A, Weber M, Shaw CE, Smith BN, Pansarasa O, Cereda C, Del Bo R, Comi GP, D'Alfonso S, Bertolin C, Sorarù G, Mazzini L, Pensato V, Gellera C, Tiloca C, Ratti A, Calvo A, Moglia C, Brunetti M, Arcuti S, Capozzo R, Zecca C, Lunetta C, Penco S, Riva N, Padovani A, Filosto M, Muller B, Stuit RJ; PARALS Registry.; SLALOM Group.; SLAP Registry.; FALS Sequencing Consortium.; SLAGEN Consortium.; NNIPPS Study Group., Blair I, Zhang K, McCann EP, Fifita JA,  Nicholson GA, Rowe DB, Pamphlett R, Kiernan MC, Grosskreutz J, Witte OW, Ringer T, Prell T, Stubendorff B, Kurth I, Hübner CA, Leigh PN, Casale F, Chio A, Beghi  E, Pupillo E, Tortelli R, Logroscino G, Powell J, Ludolph AC, Weishaupt JH, Robberecht W, Van Damme P, Franke L, Pers TH, Brown RH, Glass JD, Landers JE, Hardiman O, Andersen PM, Corcia P, Vourc'h P, Silani V, Wray NR, Visscher PM, de  Bakker PI, van Es MA, Pasterkamp RJ, Lewis CM, Breen G, Al-Chalabi A, van den Berg LH, Veldink JH. Genome-wide association analyses identify new risk variants  and the genetic architecture of amyotrophic lateral sclerosis. Nat Genet. 2016 Sep;48(9):1043-8. doi: 10.1038/ng.3622. PubMed PMID: 27455348.

Zhu Z, Zhang F, Hu H, Bakshi A, Robinson MR, Powell JE, Montgomery GW, Goddard ME, Wray NR, Visscher PM, Yang J. Integration of summary data from GWAS and eQTL  studies predicts complex trait gene targets. Nat Genet. 2016 May;48(5):481-7. doi: 10.1038/ng.3538. PubMed PMID: 27019110.

Mehta D, Tropf FC, Gratten J, Bakshi A, Zhu Z, Bacanu SA, Hemani G, Magnusson  PK, Barban N, Esko T, Metspalu A, Snieder H, Mowry BJ, Kendler KS, Yang J, Visscher PM, McGrath JJ, Mills MC, Wray NR, Lee SH; Schizophrenia Working Group of the Psychiatric Genomics Consortium, LifeLines Cohort Study, and TwinsUK., Andreassen OA, Bramon E, Bruggeman R, Buxbaum JD, Cairns MJ, Cantor RM, Cloninger CR, Cohen D, Crespo-Facorro B, Darvasi A, DeLisi LE, Dinan T, Djurovic S, Donohoe G, Drapeau E, Escott-Price V, Freimer NB, Georgieva L, de Haan L, Henskens FA, Joa I, Julià A, Khrunin A, Lerer B, Limborska S, Loughland CM, Macek M Jr, Magnusson PK, Marsal S, McCarley RW, McIntosh AM, McQuillin A, Melegh B, Michie PT, Morris DW, Murphy KC, Myin-Germeys I, Olincy A, Van Os J, Pantelis C, Posthuma D, Quested D, Schall U, Scott RJ, Seidman LJ, Toncheva D, Tooney PA, Waddington J, Weinberger DR, Weiser M, Wu JQ. Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women. JAMA Psychiatry. 2016 May  1;73(5):497-505. doi: 10.1001/jamapsychiatry.2016.0129. PubMed PMID: 27007234.

Yang J, Bakshi A, Zhu Z, Hemani G, Vinkhuyzen AA, Lee SH, Robinson MR, Perry JR, Nolte IM, van Vliet-Ostaptchouk JV, Snieder H; LifeLines Cohort Study., Esko  T, Milani L, Mägi R, Metspalu A, Hamsten A, Magnusson PK, Pedersen NL, Ingelsson  E, Soranzo N, Keller MC, Wray NR, Goddard ME, Visscher PM. Genetic variance estimation with imputed variants finds negligible missing heritability for human  height and body mass index. Nat Genet. 2015 Oct;47(10):1114-20. doi: 10.1038/ng.3390. PubMed PMID: 26323059; PubMed Central PMCID: PMC4589513.

Shah S, Bonder MJ, Marioni RE, Zhu Z, McRae AF, Zhernakova A, Harris SE, Liewald D, Henders AK, Mendelson MM, Liu C, Joehanes R, Liang L; BIOS Consortium., Levy D, Martin NG, Starr JM, Wijmenga C, Wray NR, Yang J, Montgomery GW, Franke L, Deary IJ, Visscher PM. Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations. Am J Hum Genet. 2015 Jul 2;97(1):75-85. doi: 10.1016/j.ajhg.2015.05.014. PubMed PMID: 26119815; PubMed Central PMCID: PMC4572498.

Visscher PM, Hemani G, Vinkhuyzen AA, Chen GB, Lee SH, Wray NR, Goddard ME, Yang J. Statistical power to detect genetic (co)variance of complex traits using  SNP data in unrelated samples. PLoS Genet. 2014 Apr 10;10(4):e1004269. doi: 10.1371/journal.pgen.1004269. PubMed PMID: 24721987; PubMed Central PMCID: PMC3983037.

Lee SH, Yang J, Chen GB, Ripke S, Stahl EA, Hultman CM, Sklar P, Visscher PM,  Sullivan PF, Goddard ME, Wray NR. Estimation of SNP heritability from dense genotype data. Am J Hum Genet. 2013 Dec 5;93(6):1151-5. doi: 10.1016/j.ajhg.2013.10.015. PubMed PMID: 24314550; PubMed Central PMCID: PMC3852919.

Wray NR, Yang J, Hayes BJ, Price AL, Goddard ME, Visscher PM. Author reply to A commentary on Pitfalls of predicting complex traits from SNPs. Nat Rev Genet. 2013 Dec;14(12):894. doi: 10.1038/nrg3457-c2. PubMed PMID: 24240515; PubMed Central PMCID: PMC4266985.

Vinkhuyzen AA, Wray NR, Yang J, Goddard ME, Visscher PM. Estimation and partition of heritability in human populations using whole-genome analysis methods. Annu Rev Genet. 2013;47:75-95. doi: 10.1146/annurev-genet-111212-133258. Review. PubMed PMID: 23988118; PubMed Central PMCID: PMC4037293.

de Candia TR, Lee SH, Yang J, Browning BL, Gejman PV, Levinson DF, Mowry BJ,  Hewitt JK, Goddard ME, O'Donovan MC, Purcell SM, Posthuma D; International Schizophrenia Consortium.; Molecular Genetics of Schizophrenia Collaboration., Visscher PM, Wray NR, Keller MC. Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. Am J Hum Genet. 2013 Sep 5;93(3):463-70. doi: 10.1016/j.ajhg.2013.07.007. PubMed PMID: 23954163; PubMed Central PMCID: PMC3845872.

Wray NR, Yang J, Hayes BJ, Price AL, Goddard ME, Visscher PM. Pitfalls of predicting complex traits from SNPs. Nat Rev Genet. 2013 Jul;14(7):507-15. doi: 10.1038/nrg3457. Review. PubMed PMID: 23774735; PubMed Central PMCID: PMC4096801.

Lee SH, DeCandia TR, Ripke S, Yang J; Schizophrenia Psychiatric Genome-Wide Association Study Consortium (PGC-SCZ).; International Schizophrenia Consortium (ISC).; Molecular Genetics of Schizophrenia Collaboration (MGS)., Sullivan PF, Goddard ME, Keller MC, Visscher PM, Wray NR. Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nat Genet.  2012 Feb 19;44(3):247-50. doi: 10.1038/ng.1108. PubMed PMID: 22344220; PubMed Central PMCID: PMC3327879.

Wray NR, Yang J, Goddard ME, Visscher PM. The genetic interpretation of area  under the ROC curve in genomic profiling. PLoS Genet. 2010 Feb 26;6(2):e1000864.  doi: 10.1371/journal.pgen.1000864. PubMed PMID: 20195508; PubMed Central PMCID: PMC2829056.

Yang J, Wray NR, Visscher PM. Comparing apples and oranges: equating the power of case-control and quantitative trait association studies. Genet Epidemiol. 2010 Apr;34(3):254-7. doi: 10.1002/gepi.20456. PubMed PMID: 19918758.

Yang J, Visscher PM, Wray NR. Sporadic cases are the norm for complex disease. Eur J Hum Genet. 2010 Sep;18(9):1039-43. doi: 10.1038/ejhg.2009.177. Erratum in: Eur J Hum Genet. 2010 Sep;18(9):1044. PubMed PMID: 19826454; PubMed Central PMCID: PMC2987426.