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All papers authored by Naomi R. Wray

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2021 Guiyan Ni, J. van Os, S. van der Auwera, Jian Zeng

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, Joana A. Revez

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, Ying Wang, Zhili Zheng, Tian Ge, Restuadi Restuadi, Jacqueline Kiewa, Dale R. Nyholt

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, Jonathan R. I. Coleman

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, Jordan W. Smoller

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, Peter M. Visscher and 464 other authors

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

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2020 F. C. Garton

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, B. B. Trabjerg

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, N. R. Wray

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Cardiovascular disease, psychiatric diagnosis and sex differences in the multistep hypothesis of amyotrophic lateral sclerosis

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Peter A. C. ‘t Hoen, Maarten van Iterson, Joyce van Meurs, Peter A. C. ’t Hoen, Marleen M.-J. van Greevenbroek, Carla J. H. van der Kallen, Diana van Heemst, Leonard H. van den Berg, Jeroen van Rooij, Ruud van der Breggen, Michiel van Galen, Erik W. van Zwet, Mawussé Agbessi, Anke R. Hammerschlag

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, Habibul Ahsan and 112 other authors

Refining attention-deficit/hyperactivity disorder and autism spectrum disorder genetic loci by integrating summary data from genome-wide association, gene expression and DNA methylation studies

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Costanza L. Vallerga, Futao Zhang, Javed Fowdar

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, Allan F. McRae

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, Ting Qi, Marta F. Nabais, Qian Zhang, Irfahan Kassam, Anjali K. Henders, Leanne Wallace, Grant Montgomery

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, Yu-Hsuan Chuang, Steve Horvath

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, Beate Ritz, Glenda Halliday

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and 15 other authors

Analysis of DNA methylation associates the cystine–glutamate antiporter SLC7A11 with risk of Parkinson’s disease

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Betina B. Trabjerg

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, Fleur C. Garton

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, Wouter van Rheenen

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, Robert D. Henderson, Preben Bo Mortensen

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, Naomi R. Wray

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ALS in Danish Registries

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2019 Anna E. Bauer

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, Xiaoqin Liu, Enda M. Byrne, Patrick F. Sullivan, Naomi R. Wray

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, Mette Nyegaard

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, Katherine L. Musliner

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, Katja G. Ingstrup, Benedicte M. W. Johannsen, Merete L. Mægbæk, Yunpeng Wang, Merete Nordentoft

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, Ole Mors and 6 other authors

Genetic risk scores for major psychiatric disorders and the risk of postpartum psychiatric disorders

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2018 Jerry Guintivano, Holly Krohn, Carol Lewis, Enda M. Byrne, Anjali K. Henders, Alexander Ploner

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, Katherine Kirk

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, Nicholas G. Martin

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, Jeannette Milgrom, Naomi R. Wray

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, Patrick F. Sullivan, Samantha Meltzer-Brody

PPD ACT: an app-based genetic study of postpartum depression

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Robert M. Maier

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, Zhihong Zhu, Sang Hong Lee, Maciej Trzaskowski, Douglas M. Ruderfer, Eli A. Stahl, Stephan Ripke, Naomi R. Wray

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, Peter M. Visscher

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, Matthew R. Robinson

Improving genetic prediction by leveraging genetic correlations among human diseases and traits

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This paper is made freely available by the publisher.

2017 Aurélien Macé, Marcus A. Tuke, Patrick Deelen

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, Kati Kristiansson

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, Hannele Mattsson, Margit Nõukas, Yadav Sapkota, Ursula Schick, Eleonora Porcu, Sina Rüeger, Aaron F. McDaid

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, David Porteous, Thomas W. Winkler

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and 91 other authors

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits

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Beben Benyamin, Ji He, Qiongyi Zhao

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, Jacob Gratten, Fleur Garton, Paul J. Leo, Zhijun Liu, Marie Mangelsdorf, Ammar Al-Chalabi

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, Lisa Anderson, Timothy J. Butler, Lu Chen, Xiang-Ding Chen, Katie Cremin, Hong-Weng Deng and 49 other authors

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

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2016 Z. Hawi, T. D. R. Cummins, J. Tong

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, M. Arcos-Burgos, Q. Zhao

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, N. Matthews, D. P. Newman, B. Johnson, A. Vance, H. S. Heussler, F. Levy, S. Easteal, N. R. Wray

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, E. Kenny, D. Morris

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and 3 other authors

Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study

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Rick A. A. van der Spek, Anneke J. van der Kooi, Leonard H. van den Berg, Perry Tc C. van Doormaal, Kristel R. van Eijk, Mamede de Carvalho, Marianne de Visser, Paul I. W. de Bakker, Michael A. van Es, W. van Rheenen, Simone de Jong, Wouter Van Rheenen, Annelot M. Dekker, Russell L. Mclaughlin

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, R. A. A. Van Der Spek and 190 other authors

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

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Guo-Bo Chen

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, Matthew R. Robinson, Maciej Trzaskowski, Zhi-Xiang Zhu, Thomas W. Winkler, Andrew R. Wood, Ruth J. F. Loos, Jian Yang

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, Naomi R. Wray

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, Sang Hong Lee, Peter M. Visscher

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, Damien C. Croteau-Chonka, Zoltán Kutalik, Timothy M. Frayling and 2 other authors

Across-cohort QC analyses of GWAS summary statistics from complex traits.

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2015 S. Schizophrenia Working Group of Psychiatric Genomics Consortium (Ripke, Bm Neale, A. Corvin, Jt Walters, Kh Farh, Pa Holmans, P. Lee, Da Collier, H. Huang, Th Pers, I. Agartz, E. Agerbo, M. Albus, M. Alexander, F. Amin and 304 other authors

Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis

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Jian Yang

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, Andrew Bakshi, Zhihong Zhu, R. Magi, Gibran Hemani, LifeLines Cohort Study, Anna A. E. Vinkhuyzen, Sang Hong Lee, Magnusson Pke, Matthew R. Robinson, John R. B. Perry, Pedersen Nl, Ilja M. Nolte, Keller Mc, Jana V. van Vliet-Ostaptchouk and 24 other authors

Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index

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Jake M. Najman, Rosa Alati, William Bor, Alexandra Clavarino, Abdullah Mamun, John J. McGrath, David McIntyre, Michael O'Callaghan, James Scott, Greg Shuttlewood, Gail M. Williams, Naomi R. Wray

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Cohort profile update: the Mater-University of Queensland Study of Pregnancy (MUSP)

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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, Janie Corley, Adele Taylor, Lee Murphy

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, John M. Starr, Steve Horvath and 3 other authors

The epigenetic clock is correlated with physical and cognitive fitness in the Lothian Birth Cohort 1936

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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, Alison Pattie, Janie Corley, Lee Murphy

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, Nicholas G. Martin, Grant W. Montgomery and 17 other authors

DNA methylation age of blood predicts all-cause mortality in later life

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2014 Natalie T. Mills, Margaret J. Wright, Anjali K. Henders, Darryl W. Eyles, Bernhard T. Baune, John J. McGrath, Edna M. Byrne, Narelle K. Hansell

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, Eva Birosova, James G. Scott, Nicholas G. Martin

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, Grant W. Montgomery, Naomi R. Wray

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, Anna A. E. Vinkhuyzen

Heritability of Transforming Growth Factor-β1 and Tumor Necrosis Factor-Receptor Type 1 Expression and Vitamin D Levels in Healthy Adolescent Twins

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