Skip to menu Skip to content Skip to footer

2013

Journal Article

Estimation and partition of heritability in human populations using whole-genome analysis methods

Vinkhuyzen, Anna A.E., Wray, Naomi R., Yang, Jiang, Goddard, Michael E. and Visscher, Peter M. (2013). Estimation and partition of heritability in human populations using whole-genome analysis methods. Annual Review of Genetics, Review in Advance: 47 (5), 93-113. doi: 10.1146/annurev-genet-111212-133258

Estimation and partition of heritability in human populations using whole-genome analysis methods

2013

Journal Article

Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression

Culverhouse, Robert C., Bowes, Lucy, Breslau, Naomi, Nurnberger, John I. Jr, Burmeister, Margit, Fergusson, David M., Munafo, Marcus, Saccone, Nancy L., Bierut, Laura J., 5-HTTLPR, Stress, and Depression Consortium, Wray, Naomi and Middeldorp, Christel (2013). Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression. BMC Psychiatry, 13 (1) 304, 1-12. doi: 10.1186/1471-244X-13-304

Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression

2013

Journal Article

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'

Robinson, E. B., Howrigan, D., Yang, J., Ripke, S., Anttila, V., Duncan, L. E., Jostins, L., Barrett, J. C., Medland, S. E., Macarthur, D. G., Breen, G., O'Donovan, M. C., Wray, N. R., Devlin, B., Daly, M. J., Visscher, P. M., Sullivan, P. F. and Neale, B. M. (2013). Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'. Molecular Psychiatry, 19 (8), 859-861. doi: 10.1038/mp.2013.125

Response to 'Predicting the diagnosis of autism spectrum disorder using gene pathway analysis'

2013

Journal Article

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Ripke, Stephan, O'Dushlaine, Colm, Chambert, Kimberly, Moran, Jennifer L., Kaehler, Anna K., Akterin, Susanne, Bergen, Sarah E., Collins, Ann L., Crowley, James J., Fromer, Menachem, Kim, Yunjung, Lee, Sang Hong, Magnusson, Patrik K. E., Sanchez, Nick, Stahl, Eli A., Williams, Stephanie, Wray, Naomi R., Xia, Kai, Bettella, Francesco, Borglum, Anders D., Bulik-Sullivan, Brendan K., Cormican, Paul, Craddock, Nick, de Leeuw, Christiaan, Durmishi, Naser, Gill, Michael, Golimbet, Vera, Hamshere, Marian L., Holmans, Peter ... Brown, Matthew A (2013). Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nature Genetics, 45 (10), 1150-U282. doi: 10.1038/ng.2742

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

2013

Journal Article

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, Bryan J., Goddard, Michael E., O'Donovan, Michael C., Purcell, Shaun M., Posthuma, Danielle, The International Schizophrenia Consortium, The Molecular Genetics of Schizophrenia Collaboration, Visscher, Peter M., Wray, Naomi R. and Keller, Matthew C. (2013). Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. American Journal of Human Genetics, 93 (3), 463-470. doi: 10.1016/j.ajhg.2013.07.007

Additive genetic variation in schizophrenia risk is shared by populations of African and European descent

2013

Journal Article

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

Lee, S. Hong, Ripke, Stephan, Neale, Benjamin M., Faraone, Stephen V., Purcell, Shaun M., Perlis, Roy H., Mowry, Bryan J., Thapar, Anita, Goddard, Michael E., Witte, John S., Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A., Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E., Asherson, Philip, Azevedo, Maria H., Backlund, Lena, Badner, Judith A., Bailey, Anthony J., Banaschewski, Tobias, Barchas, Jack D., Barnes, Michael R., Barrett, Thomas B., Bass, Nicholas ... Wray, Naomi R. (2013). Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics, 45 (9), 984-995. doi: 10.1038/ng.2711

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

2013

Journal Article

Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia

McGrath, John J., Mortensen, Preben Bo, Visscher, Peter M. and Wray, Naomi R. (2013). Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia. Schizophrenia Bulletin, 39 (5), 955-959. doi: 10.1093/schbul/sbt108

Where GWAS and epidemiology meet: opportunities for the simultaneous study of genetic and environmental risk factors in schizophrenia

2013

Journal Article

Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy

Lee, Sang Hong and Wray, Naomi R. (2013). Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy. PLoS One, 8 (8) e71494, e71494. doi: 10.1371/journal.pone.0071494

Novel genetic analysis for case-control genome-wide association studies: quantification of power and genomic prediction accuracy

2013

Journal Article

Research review: the role of cytokines in depression in adolescents: a systematic review

Mills, Natalie T., Scott, James G., Wray, Naomi R., Cohen-Woods, Sarah and Baune, Bernhard T. (2013). Research review: the role of cytokines in depression in adolescents: a systematic review. Journal of Child Psychology and Psychiatry, 54 (8), 816-835. doi: 10.1111/jcpp.12080

Research review: the role of cytokines in depression in adolescents: a systematic review

2013

Journal Article

Pitfalls of predicting complex traits from SNPs

Wray, Naomi R., Yang, Jian, Hayes, Ben J., Price, Alkes L., Goddard, Michael E. and Visscher, Peter M. (2013). Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics, 14 (7), 507-515. doi: 10.1038/nrg3457

Pitfalls of predicting complex traits from SNPs

2013

Journal Article

Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits

Stringer, Sven, Derks, Eske M., Kahn, Rene S., Hill, William G. and Wray, Naomi R. (2013). Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits. PLoS One, 8 (7) e68913, e68913.1-e68913.9. doi: 10.1371/journal.pone.0068913

Assumptions and properties of limiting pathway models for analysis of epistasis in complex traits

2013

Journal Article

Assessment of response to lithium maintenance treatment in bipolar disorder: a Consortium on Lithium Genetics (ConLiGen) report

Manchia, Mirko, Adli, Mazda, Akula, Nirmala, Ardau, Raffaella, Aubry, Jean-Michel, Backlund, Lena, Banzato, Claudio E. M., Baune, Bernhard T., Bellivier, Frank, Bengesser, Susanne, Biernacka, Joanna M., Brichant-Petitjean, Clara, Bui, Elise, Calkin, Cynthia V., Cheng, Andrew Tai Ann, Chillotti, Caterina, Cichon, Sven, Clark, Scott, Czerski, Piotr M., Dantas, Clarissa, Del Zompo, Maria, DePaulo, J. Raymond, Detera-Wadleigh, Sevilla D., Etain, Bruno, Falkai, Peter, Frisen, Louise, Frye, Mark A., Fullerton, Jan, Gard, Sebastien ... Alda, Martin (2013). Assessment of response to lithium maintenance treatment in bipolar disorder: a Consortium on Lithium Genetics (ConLiGen) report. PLoS One, 8 (6) e65636, e65636.1-e65636.9. doi: 10.1371/journal.pone.0065636

Assessment of response to lithium maintenance treatment in bipolar disorder: a Consortium on Lithium Genetics (ConLiGen) report

2013

Journal Article

Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

Byrne, E. M., Carrillo-Roa, T., Henders, A. K., Bowdler, L., McRae, A. F., Heath, A. C., Martin, N. G., Montgomery, G. W., Krause, L. and Wray, N. R. (2013). Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin. Translational Psychiatry, 3 (6) e269, e269.1-e269.6. doi: 10.1038/tp.2013.45

Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin

2013

Journal Article

A genome-wide association study of sleep habits and insomnia

Byrne, Enda M., Gehrman, Philip R., Medland, Sarah E., Nyholt, Dale R., Heath, Andrew C., Madden, Pamela A. F., Hickie, Ian B., Van Duijn, Cornelia M., Henders, Anjali K., Montgomery, Grant W., Martin, Nicholas G., Wray, Naomi R. and The Chronogen Consortium (2013). A genome-wide association study of sleep habits and insomnia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162 (5), 439-451. doi: 10.1002/ajmg.b.32168

A genome-wide association study of sleep habits and insomnia

2013

Journal Article

The neuroprogressive nature of major depressive disorder: Pathways to disease evolution and resistance, and therapeutic implications

Moylan, S., Maes, M., Wray, N. R. and Berk, M. (2013). The neuroprogressive nature of major depressive disorder: Pathways to disease evolution and resistance, and therapeutic implications. Molecular Psychiatry, 18 (5), 595-606. doi: 10.1038/mp.2012.33

The neuroprogressive nature of major depressive disorder: Pathways to disease evolution and resistance, and therapeutic implications

2013

Journal Article

A mega-analysis of genome-wide association studies for major depressive disorder

Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Wray, Naomi, Byrne, Enda M., Martin, Nicholas G., Gordon, Scott D., Henders, Anjali K., Montgomery, Grant M., Nyholt, Dale R. and Middeldorp, Christel M. (2013). A mega-analysis of genome-wide association studies for major depressive disorder. Molecular Psychiatry, 18 (4), 497-511. doi: 10.1038/mp.2012.21

A mega-analysis of genome-wide association studies for major depressive disorder

2013

Journal Article

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

Gratten, Jacob, Visscher, Peter M., Mowry, Bryan J. and Wray, Naomi R. (2013). Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics, 45 (3), 234-238. doi: 10.1038/ng.2555

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease

2013

Journal Article

ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

Nelson, Elliot C., Lynskey, Michael T., Heath, Andrew C., Wray, Naomi, Agrawal, Arpana, Shand, Fiona L., Henders, Anjali K., Wallace, Leanne, Todorov, Alexandre A., Schrage, Andrew J., Saccone, Nancy L., Madden, Pamela A. F., Degenhardt, Louisa, Martin, Nicholas G. and Montgomery, Grant W. (2013). ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. JAMA Psychiatry, 70 (3), 325-333. doi: 10.1001/jamapsychiatry.2013.282

ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure

2013

Journal Article

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Lee, S. Hong, Harold, Denise, Nyholt, Dale R., ANZGene Consortium, International Endogene Consortium, Genetic and Environmental Risk for Alzheimer’s disease (GERAD1) Consortium, Goddard, Michael E., Zondervan, Krina T., Williams, Julie, Montgomery, Grant W., Wray, Naomi R. and Visscher, Peter M. (2013). Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Human Molecular Genetics, 22 (4) dds491, 832-841. doi: 10.1093/hmg/dds491

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

2013

Journal Article

Estimation of SNP heritability from dense genotype data

Lee, S. Hong, Yang, Jian, Chen, Guo-Bo, Ripke, Stephan, Stahl, Eli A., Hultman, Christina M., Sklar, Pamela, Visscher, Peter M., Sullivan, Patrick F., Goddard, Michael E. and Wray, Naomi (2013). Estimation of SNP heritability from dense genotype data. American Journal Of Human Genetics, 93 (6), 1151-1155. doi: 10.1016/j.ajhg.2013.10.015

Estimation of SNP heritability from dense genotype data