Wray NR - Search Results

1

Conventional multipoint nonparametric linkage analysis is not necessarily inherently biased.

Visscher PM, Wray NR. Visscher PM, et al. Among authors: wray nr. Am J Hum Genet. 2004 Oct;75(4):718-20; author reply 723-7. doi: 10.1086/424755. Am J Hum Genet. 2004. PMID: 15338458 Free PMC article. No abstract available.

2

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

Wray NR, Goddard ME, Visscher PM. Wray NR, et al. Genome Res. 2007 Oct;17(10):1520-8. doi: 10.1101/gr.6665407. Epub 2007 Sep 4. Genome Res. 2007. PMID: 17785532 Free PMC article.

3

Genetic and phenotypic stability of measures of neuroticism over 22 years.

Wray NR, Birley AJ, Sullivan PF, Visscher PM, Martin NG. Wray NR, et al. Twin Res Hum Genet. 2007 Oct;10(5):695-702. doi: 10.1375/twin.10.5.695. Twin Res Hum Genet. 2007. PMID: 17903109

4

Heritability in the genomics era--concepts and misconceptions.

Visscher PM, Hill WG, Wray NR. Visscher PM, et al. Among authors: wray nr. Nat Rev Genet. 2008 Apr;9(4):255-66. doi: 10.1038/nrg2322. Epub 2008 Mar 4. Nat Rev Genet. 2008. PMID: 18319743 Review.

5

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

Wray NR, Middeldorp CM, Birley AJ, Gordon SD, Sullivan PF, Visscher PM, Nyholt DR, Willemsen G, de Geus EJ, Slagboom PE, Montgomery GW, Martin NG, Boomsma DI. Wray NR, et al. Arch Gen Psychiatry. 2008 Jun;65(6):649-58. doi: 10.1001/archpsyc.65.6.649. Arch Gen Psychiatry. 2008. PMID: 18519823 Free PMC article.

6

Prediction of individual genetic risk of complex disease.

Wray NR, Goddard ME, Visscher PM. Wray NR, et al. Curr Opin Genet Dev. 2008 Jun;18(3):257-63. doi: 10.1016/j.gde.2008.07.006. Epub 2008 Aug 28. Curr Opin Genet Dev. 2008. PMID: 18682292 Review.

7

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

Evans DM, Visscher PM, Wray NR. Evans DM, et al. Among authors: wray nr. Hum Mol Genet. 2009 Sep 15;18(18):3525-31. doi: 10.1093/hmg/ddp295. Epub 2009 Jun 24. Hum Mol Genet. 2009. PMID: 19553258

8

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.

International Schizophrenia Consortium; Purcell SM, Wray NR, Stone JL, Visscher PM, O'Donovan MC, Sullivan PF, Sklar P. International Schizophrenia Consortium, et al. Among authors: wray nr. Nature. 2009 Aug 6;460(7256):748-52. doi: 10.1038/nature08185. Epub 2009 Jul 1. Nature. 2009. PMID: 19571811 Free PMC article.

9

Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.

Raychaudhuri S, Korn JM, McCarroll SA; International Schizophrenia Consortium; Altshuler D, Sklar P, Purcell S, Daly MJ. Raychaudhuri S, et al. PLoS Genet. 2010 Sep 9;6(9):e1001097. doi: 10.1371/journal.pgen.1001097. PLoS Genet. 2010. PMID: 20838587 Free PMC article.

10

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

Gusev A, Lee SH, Trynka G, Finucane H, Vilhjálmsson BJ, Xu H, Zang C, Ripke S, Bulik-Sullivan B, Stahl E; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium; Kähler AK, Hultman CM, Purcell SM, McCarroll SA, Daly M, Pasaniuc B, Sullivan PF, Neale BM, Wray NR, Raychaudhuri S, Price AL; Schizophrenia Working Group of the Psychiatric Genomics Consortium; SWE-SCZ Consortium. Gusev A, et al. Among authors: wray nr. Am J Hum Genet. 2014 Nov 6;95(5):535-52. doi: 10.1016/j.ajhg.2014.10.004. Epub 2014 Nov 6. Am J Hum Genet. 2014. PMID: 25439723 Free PMC article.

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