Professor Peter Visscher

Visscher, P. M., van der Beek, S. and Haley, C. S. (2021). Marker assisted selection. Animal Breeding. (pp. 119-136) edited by A.E. Clark. Boca Raton, FL, United States: CRC Press. doi: 10.1201/9781315137483-9

Yang, J., Lee, (Sang) Hong, Goddard, M. E. and Visscher, Peter (2013). Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations. Genome-Wide Association Studies and Genomic Prediction. (pp. 215-236) edited by Cedric Gondro, Julius van der Werf and Ben Hayes. New York, NY U.S.A.: Humana Press. doi: 10.1007/978-1-62703-447-0_9

Wray, Naomi R. and Visscher, Peter M. (2007). Mapping common disease genes. Mapping common disease genes. (pp. 59-79) CAMBRIDGE: CAMBRIDGE UNIV PRESS. doi: 10.1017/CBO9780511543555.005

Hatton, Alesha A., Cheng, Fei-Fei, Lin, Tian, Shen, Ren-Juan, Chen, Jie, Zheng, Zhili, Qu, Jia, Lyu, Fan, Harris, Sarah E., Cox, Simon R., Jin, Zi-Bing, Martin, Nicholas G., Fan, Dongsheng, Montgomery, Grant W., Yang, Jian, Wray, Naomi R., Marioni, Riccardo E., Visscher, Peter M. and McRae, Allan F. (2024). Genetic control of DNA methylation is largely shared across European and East Asian populations. Nature Communications, 15 (1) 2713, 1-12. doi: 10.1038/s41467-024-47005-0

Dai, Qile, Zhou, Geyu, Zhao, Hongyu, Võsa, Urmo, Franke, Lude, Battle, Alexis, Teumer, Alexander, Lehtimäki, Terho, Raitakari, Olli T., Esko, Tõnu, Agbessi, Mawussé, Ahsan, Habibul, Alves, Isabel, Andiappan, Anand Kumar, Arindrarto, Wibowo, Awadalla, Philip, Battle, Alexis, Beutner, Frank, Jan Bonder, Marc, Boomsma, Dorret I., Christiansen, Mark W., Claringbould, Annique, Deelen, Patrick, Favé, Marie-Julie, Frayling, Timothy, Gharib, Sina A., Gibson, Greg, Heijmans, Bastiaan T., Hemani, Gibran ... Yang, Jingjing (2023). OTTERS: a powerful TWAS framework leveraging summary-level reference data. Nature Communications, 14 (1) 1271, 1-13. doi: 10.1038/s41467-023-36862-w

Wang, Xiaotong, Hivert, Valentin, Groot, Shiane, Wang, Ying, Yengo, Loic, McGrath, John J., Kemper, Kathryn E., Visscher, Peter M., Wray, Naomi R. and Revez, Joana A. (2023). Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D. PLoS Genetics, 19 (11) e1011033, e1011033. doi: 10.1371/journal.pgen.1011033

Enbody, Erik D., Sendell-Price, Ashley T., Sprehn, C. Grace, Rubin, Carl-Johan, Visscher, Peter M., Grant, B. Rosemary, Grant, Peter R. and Andersson, Leif (2023). Community-wide genome sequencing reveals 30 years of Darwin’s finch evolution. Science, 381 (6665) eadf6218, 1-10. doi: 10.1126/science.adf6218

Campos, Adrian I., Namba, Shinichi, Lin, Shu-Chin, Nam, Kisung, Sidorenko, Julia, Wang, Huanwei, Kamatani, Yoichiro, The Biobank Japan Project, Wang, Ling-Hua, Lee, Seunggeun, Lin, Yen-Feng, Feng, Yen-Chen Anne, Okada, Yukinori, Visscher, Peter M. and Yengo, Loic (2023). Boosting the power of genome-wide association studies within and across ancestries by using polygenic scores. Nature Genetics, 55 (10), 1769-1776. doi: 10.1038/s41588-023-01500-0

Wang, Hao, Makowski, Carolina, Zhang, Yanxiao, Qi, Anna, Kaufmann, Tobias, Smeland, Olav B., Fiecas, Mark, Yang, Jian, Visscher, Peter M. and Chen, Chi-Hua (2023). Chromosomal inversion polymorphisms shape human brain morphology. Cell Reports, 42 (8) 112896, 112896. doi: 10.1016/j.celrep.2023.112896

Wu, Yang, Qi, Ting, Wray, Naomi R., Visscher, Peter M., Zeng, Jian and Yang, Jian (2023). Joint analysis of GWAS and multi-omics QTL summary statistics reveals a large fraction of GWAS signals shared with molecular phenotypes. Cell Genomics, 3 (8) 100344, 100344. doi: 10.1016/j.xgen.2023.100344

Wang, Xiaotong, Walker, Alicia, Revez, Joana A., Ni, Guiyan, Visscher, Peter M., Wray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till F.M., Bacanu, Silviu-Alin, Bækvad-Hansen, Marie, Beekman, Aartjan T.F., Bigdeli, Tim B., Binder, Elisabeth B., Bryois, Julien, Buttenschøn, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan R.I., Colodro-Conde, Lucía ... Sullivan, Patrick F. (2023). Polygenic risk prediction: why and when out-of-sample prediction R2 can exceed SNP-based heritability. The American Journal of Human Genetics, 110 (7), 1207-1215. doi: 10.1016/j.ajhg.2023.06.006

Chundru, V. Kartik, Marioni, Riccardo E., Pendergast, James G. D., Lin, Tian, Beveridge, Allan J., Martin, Nicholas G, Montgomery, Grant W., Hume, David A., Deary, Ian J., Visscher, Peter M., Wray, Naomi R. and McRae, Allan F. (2023). Rare genetic variants underlie outlying levels of DNA methylation and gene-expression. Human Molecular Genetics, 32 (11), 1912-1921. doi: 10.1093/hmg/ddad028

Makowski, Carolina, Wang, Hao, Srinivasan, Anjali, Qi, Anna, Qiu, Yuqi, van der Meer, Dennis, Frei, Oleksandr, Zou, Jingjing, Visscher, Peter M., Yang, Jian and Chen, Chi-Hua (2023). Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Proceedings of the National Academy of Sciences, 120 (11) e2214834120, e2214834120. doi: 10.1073/pnas.2214834120

Abdellaoui, Abdel, Yengo, Loic, Verweij, Karin J. H. and Visscher, Peter M. (2023). 15 years of GWAS discovery: realizing the promise. The American Journal of Human Genetics, 110 (2), 179-194. doi: 10.1016/j.ajhg.2022.12.011

Qiao, Zhen, Sidorenko, Julia, Revez, Joana A., Xue, Angli, Lu, Xueling, Pärna, Katri, Snieder, Harold, Visscher, Peter M., Wray, Naomi R., Yengo, Loic and Lifelines Cohort Study (2023). Estimation and implications of the genetic architecture of fasting and non-fasting blood glucose. Nature Communications, 14 (1) 451, 1-11. doi: 10.1038/s41467-023-36013-1

Li, Ang, Liu, Shouye, Bakshi, Andrew, Jiang, Longda, Chen, Wenhan, Zheng, Zhili, Sullivan, Patrick F., Visscher, Peter M., Wray, Naomi R., Yang, Jian and Zeng, Jian (2023). mBAT-combo: a more powerful test to detect gene-trait associations from GWAS data. American Journal of Human Genetics, 110 (1), 30-43. doi: 10.1016/j.ajhg.2022.12.006

Lopera-Maya, Esteban A., Li, Shuang, de Brouwer, Remco, Nolte, Ilja M., van Breen, Justin, Bosman, Laurens P., Verstraelen, Tom E., van Lint, Freya H. M., Cox, Moniek G. P. J., Groeneweg, Judith A., Mast, Thomas P., van der Zwaag, Paul A., Volders, Paul G. A., Evertz, Reinder, Wong, Lisa, de Groot, Natasja M. S., Zeppenfeld, Katja, van der Heijden, Jeroen F., van den Berg, Maarten P., Wilde, Arthur A. M., Asselbergs, Folkert W., Hauer, Richard N. W., te Riele, Anneline S. J. M., van Tintelen, J. Peter, Aguirre-Gamboa, Raul, Kuivenhoven, Jan A., Maya, Esteban A. Lopera, Visscher, Peter M., Vonk, Judith M. ... Sanna, Serena (2023). Phenotypic and Genetic Factors Associated with Absence of Cardiomyopathy Symptoms in PLN:c.40_42delAGA Carriers. Journal of Cardiovascular Translational Research, 16 (6), 1251-1266. doi: 10.1007/s12265-022-10347-5

Pang, Shichao, Yengo, Loic, Nelson, Christopher P., Bourier, Felix, Zeng, Lingyao, Li, Ling, Kessler, Thorsten, Erdmann, Jeanette, Mägi, Reedik, Läll, Kristi, Metspalu, Andres, Mueller-Myhsok, Bertram, Samani, Nilesh J., Visscher, Peter M. and Schunkert, Heribert (2023). Genetic and modifiable risk factors combine multiplicatively in common disease. Clinical Research in Cardiology, 112 (2), 247-257. doi: 10.1007/s00392-022-02081-4

Border, Richard, O’Rourke, Sean, de Candia, Teresa, Goddard, Michael E., Visscher, Peter M., Yengo, Loic, Jones, Matt and Keller, Matthew C. (2022). Author Correction: Assortative mating biases marker-based heritability estimators (Nature Communications, (2022), 13, 1, (660), 10.1038/s41467-022-28294-9). Nature Communications, 13 (1) 1903, 1903. doi: 10.1038/s41467-022-29652-3

Higham, Jonathan, Kerr, Lyndsay, Zhang, Qian, Walker, Rosie M., Harris, Sarah E., Howard, David M., Hawkins, Emma L., Sandu, Anca-Larisa, Steele, J. Douglas, Waiter, Gordon D., Murray, Alison D., Evans, Kathryn L., McIntosh, Andrew M., Visscher, Peter M., Deary, Ian J., Cox, Simon R. and Sproul, Duncan (2022). Local CpG density affects the trajectory and variance of age-associated DNA methylation changes. Genome Biology, 23 (1) 216, 1-28. doi: 10.1186/s13059-022-02787-8

Visscher, Peter M. and Yengo, Loic (2022). The effect of the scale of grant scoring on ranking accuracy. F1000Research, 11 1197, 1-18. doi: 10.12688/f1000research.125400.1

Couvy-Duchesne, Baptiste, Zhang, Futao, Kemper, Kathryn E., Sidorenko, Julia, Wray, Naomi R., Visscher, Peter M., Colliot, Olivier and Yang, Jian (2022). Parsimonious model for mass-univariate vertexwise analysis. Journal of Medical Imaging, 9 (5) ARTN 052404, 1-19. doi: 10.1117/1.JMI.9.5.052404

Orliac, Etienne J., Banos, Daniel Trejo, Ojavee, Sven E., Läll, Kristi, Mägi, Reedik, Visscher, Peter M. and Robinson, Matthew R. (2022). Improving GWAS discovery and genomic prediction accuracy in biobank data. Proceedings of the National Academy of Sciences of the United States of America, 119 (31) e2121279119, 1-8. doi: 10.1073/pnas.2121279119

Charlesworth, Brian, Goddard, Michael E., Meyer, Karin, Visscher, Peter M., Weir, Bruce S. and Wray, Naomi R. (2022). Author Correction: From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill. Nature Genetics, 54 (9), 1448-1448. doi: 10.1038/s41588-022-01160-6

Charlesworth, Brian, Goddard, Michael E., Meyer, Karin, Visscher, Peter M., Weir, Bruce S. and Wray, Naomi R. (2022). From Mendel to quantitative genetics in the genome era: the scientific legacy of W. G. Hill. Nature Genetics, 54 (7), 934-939. doi: 10.1038/s41588-022-01103-1

Visscher, Peter M. (2022). Genetics of cognitive performance, education and learning: from research to policy?. npj Science of Learning, 7 (1) 8, 8. doi: 10.1038/s41539-022-00124-z

Makowski, Carolina, van der Meer, Dennis, Dong, Weixiu, Wang, Hao, Wu, Yan, Zou, Jingjing, Liu, Cin, Rosenthal, Sara B., Hagler, Donald J., Fan, Chun Chieh, Kremen, William S., Andreassen, Ole A., Jernigan, Terry L., Dale, Anders M., Zhang, Kun, Visscher, Peter M., Yang, Jian and Chen, Chi-Hua (2022). Discovery of genomic loci of the human cerebral cortex using genetically informed brain atlases. Science, 375 (6580) A27, 522-528. doi: 10.1126/science.abe8457

Border, Richard, O’Rourke, Sean, de Candia, Teresa, Goddard, Michael E., Visscher, Peter M., Yengo, Loic, Jones, Matt and Keller, Matthew C. (2022). Assortative mating biases marker-based heritability estimators. Nature Communications, 13 (1) 660. doi: 10.1038/s41467-022-28294-9

Bivol, Svetlana, Mellick, George D., Gratten, Jacob, Parker, Richard, Mulcahy, Aoibhe, Mosley, Philip E., Poortvliet, Peter C., Campos, Adrian I., Mitchell, Brittany L., Garcia-Marin, Luis M., Cross, Simone, Ferguson, Mary, Lind, Penelope A., Loesch, Danuta Z., Visscher, Peter M., Medland, Sarah E., Scherzer, Clemens R., Martin, Nicholas G. and Rentería, Miguel E. (2022). Australian Parkinson’s Genetics Study (APGS): pilot (n=1532). BMJ Open, 12 (2) e052032, e052032. doi: 10.1136/bmjopen-2021-052032

Chen, Wenhan, Wu, Yang, Zheng, Zhili, Qi, Ting, Visscher, Peter M., Zhu, Zhihong and Yang, Jian (2021). Improved analyses of GWAS summary statistics by reducing data heterogeneity and errors. Nature Communications, 12 (1) 7117, 7117. doi: 10.1038/s41467-021-27438-7

Stevenson, Anna J, Gadd, Danni A, Hillary, Robert F, McCartney, Daniel L, Campbell, Archie, Walker, Rosie M, Evans, Kathryn L, Harris, Sarah E, Spires-Jones, Tara L, McRae, Allan F, Visscher, Peter M, McIntosh, Andrew M, Deary, Ian J and Marioni, Riccardo E (2021). Creating and validating a DNA methylation-based proxy for interleukin-6. Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 76 (12), 2284-2292. doi: 10.1093/gerona/glab046

Patxot, Marion, Banos, Daniel Trejo, Kousathanas, Athanasios, Orliac, Etienne J., Ojavee, Sven E., Moser, Gerhard, Holloway, Alexander, Sidorenko, Julia, Kutalik, Zoltan, Mägi, Reedik, Visscher, Peter M., Rönnegård, Lars and Robinson, Matthew R. (2021). Probabilistic inference of the genetic architecture underlying functional enrichment of complex traits. Nature Communications, 12 (1) 6972, 6972. doi: 10.1038/s41467-021-27258-9

Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Wood, David L.A., Krause, Lutz, Tyson, Gene W., Restuadi, Restuadi, Wallace, Leanne, McLaren, Tiana, Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Frenk, Mira Levis, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Holtmann, Gerald, Strike, Lachlan T., de Zubicaray, Greig I. ... Gratten, Jacob (2021). Autism-related dietary preferences mediate autism-gut microbiome associations. Cell, 184 (24), 5916-5931.e17. doi: 10.1016/j.cell.2021.10.015

Ni, Guiyan, Zeng, Jian, Revez, Joana A., Wang, Ying, Zheng, Zhili, Ge, Tian, Restuadi, Restuadi, Kiewa, Jacqueline, Nyholt, Dale R., Coleman, Jonathan R.I., Smoller, Jordan W., Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2021). A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts. Biological Psychiatry, 90 (9), 611-620. doi: 10.1016/j.biopsych.2021.04.018

Turley, Patrick, Meyer, Michelle N., Wang, Nancy, Cesarini, David, Hammonds, Evelynn, Martin, Alicia R., Neale, Benjamin M., Rehm, Heidi L., Wilkins-Haug, Louise, Benjamin, Daniel J., Hyman, Steven, Laibson, David and Visscher, Peter M. (2021). Problems with using polygenic scores to select embryos. Obstetrical and Gynecological Survey, 76 (10), 609-610. doi: 10.1097/OGX.0000000000000972

Visscher, Peter M., Yengo, Loic, Cox, Nancy J. and Wray, Naomi R. (2021). Discovery and implications of polygenicity of common diseases. Science, 373 (6562), 1468-1473. doi: 10.1126/science.abi8206

Lumbers, R. Thomas, Shah, Sonia, Lin, Honghuang, Czuba, Tomasz, Henry, Albert, Swerdlow, Daniel I., Mälarstig, Anders, Andersson, Charlotte, Verweij, Niek, Holmes, Michael V., Ärnlöv, Johan, Svensson, Per, Hemingway, Harry, Sallah, Neneh, Almgren, Peter, Aragam, Krishna G., Asselin, Geraldine, Backman, Joshua D., Biggs, Mary L., Bloom, Heather L., Boersma, Eric, Brandimarto, Jeffrey, Brown, Michael R., Brunner‐La Rocca, Hans‐Peter, Carey, David J., Chaffin, Mark D., Chasman, Daniel I., Chazara, Olympe, Chen, Xing ... Regeneron Genetics Center (2021). The genomics of heart failure: design and rationale of the HERMES consortium. ESC Heart Failure, 8 (6) ehf2.13517, 5531-5541. doi: 10.1002/ehf2.13517

Hemani, Gibran, Powell, Joseph E., Wang, Huanwei, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Goddard, Michael E., Gibson, Greg, Yang, Jian and Visscher, Peter M. (2021). Phantom epistasis between unlinked loci. Nature, 596 (7871), E1-E3. doi: 10.1038/s41586-021-03765-z

Yengo, Loic, Yang, Jian, Keller, Matthew C., Goddard, Michael E., Wray, Naomi R. and Visscher, Peter M. (2021). Genomic partitioning of inbreeding depression in humans. American Journal of Human Genetics, 108 (8), 1488-1501. doi: 10.1016/j.ajhg.2021.06.005

Turley, Patrick, Meyer, Michelle N., Wang, Nancy, Cesarini, David, Hammonds, Evelynn, Martin, Alicia R., Neale, Benjamin M., Rehm, Heidi L., Wilkins-Haug, Louise, Benjamin, Daniel J., Hyman, Steven, Laibson, David and Visscher, Peter M. (2021). Problems with using polygenic scores to select embryos. New England Journal of Medicine, 385 (1), 78-86. doi: 10.1056/NEJMsr2105065

Palmer, Rohan H. C., Benca-Bachman, Chelsie E., Huggett, Spencer B., Bubier, Jason A., McGeary, John E., Ramgiri, Nikhil, Srijeyanthan, Jenani, Yang, Jingjing, Visscher, Peter M., Yang, Jian, Knopik, Valerie S. and Chesler, Elissa J. (2021). Multi-omic and multi-species meta-analyses of nicotine consumption. Translational Psychiatry, 11 (1) 98, 98. doi: 10.1038/s41398-021-01231-y

Hivert, Valentin, Wray, Naomi R. and Visscher, Peter M. (2021). Gene action, genetic variation, and GWAS: A user-friendly web tool. PLoS Genetics, 17 (5) e1009548, 1-9. doi: 10.1371/journal.pgen.1009548

Restuadi, Restuadi, Garton, Fleur C., Benyamin, Beben, Lin, Tian, Williams, Kelly L., Vinkhuyzen, Anna, van Rheenen, Wouter, Zhu, Zhihong, Laing, Nigel G., Mather, Karen A., Sachdev, Perminder S., Ngo, Shyuan T., Steyn, Frederik J., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Needham, Merrilee, Mathers, Susan, Nicholson, Garth, Rowe, Dominic B., Henderson, Robert D., McCombe, Pamela A., Pamphlett, Roger, Blair, Ian P., Wray, Naomi R. and McRae, Allan F. (2021). Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia. European Journal of Human Genetics, 30 (5), 1-8. doi: 10.1038/s41431-021-00885-y

Mur, Jure, McCartney, Daniel L., Chasman, Daniel I., Visscher, Peter M., Muniz-Terrera, Graciela, Cox, Simon R., Russ, Tom C. and Marioni, Riccardo E. (2021). Variation in VKORC1 is associated with vascular dementia. Journal of Alzheimer's Disease, 80 (3), 1329-1337. doi: 10.3233/JAD-201256

Hivert, Valentin, Sidorenko, Julia, Rohart, Florian, Goddard, Michael E., Yang, Jian, Wray, Naomi R., Yengo, Loic and Visscher, Peter M. (2021). Estimation of non-additive genetic variance in human complex traits from a large sample of unrelated individuals. The American Journal of Human Genetics, 108 (5), 786-798. doi: 10.1016/j.ajhg.2021.02.014

Guo, Jing, Bakshi, Andrew, Wang, Ying, Jiang, Longda, Yengo, Loic, Goddard, Michael E., Visscher, Peter M. and Yang, Jian (2021). Quantifying genetic heterogeneity between continental populations for human height and body mass index. Scientific Reports, 11 (1) 5240, 1-9. doi: 10.1038/s41598-021-84739-z

Wu, Yeda, Murray, Graham K., Byrne, Enda M., Sidorenko, Julia, Visscher, Peter M. and Wray, Naomi R. (2021). GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Nature Communications, 12 (1) 1146, 1-17. doi: 10.1038/s41467-021-21280-7

Zeng, Jian, Xue, Angli, Jiang, Longda, Lloyd-Jones, Luke R., Wu, Yang, Wang, Huanwei, Zheng, Zhili, Yengo, Loic, Kemper, Kathryn E., Goddard, Michael E., Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2021). Widespread signatures of natural selection across human complex traits and functional genomic categories. Nature Communications, 12 (1) 1164, 1-12. doi: 10.1038/s41467-021-21446-3

Kemper, Kathryn E., Yengo, Loic, Zheng, Zhili, Abdellaoui, Abdel, Keller, Matthew C., Goddard, Michael E., Wray, Naomi R., Yang, Jian and Visscher, Peter M. (2021). Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals. Nature Communications, 12 (1) 1050, 1050. doi: 10.1038/s41467-021-21283-4

Yap, Chloe X., Alvares, Gail A., Henders, Anjali K., Lin, Tian, Wallace, Leanne, Farrelly, Alaina, McLaren, Tiana, Berry, Jolene, Vinkhuyzen, Anna A. E., Trzaskowski, Maciej, Zeng, Jian, Yang, Yuanhao, Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren, Leslie, Jodie, Levis Frenk, Mira, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Visscher, Peter M., Dawson, Paul A., Dissanayake, Cheryl ... Gratten, Jacob (2021). Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank. Molecular Autism, 12 (1) 12, 12. doi: 10.1186/s13229-020-00407-5

Xue, Angli, Jiang, Longda, Zhu, Zhihong, Wray, Naomi R., Visscher, Peter M., Zeng, Jian and Yang, Jian (2021). Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes. Nature Communications, 12 (1) 6450, 6450. doi: 10.1038/s41467-020-20237-6

Xue, Angli, Jiang, Longda, Zhu, Zhihong, Wray, Naomi R., Visscher, Peter M., Zeng, Jian and Yang, Jian (2021). Correction: Genome-wide analyses of behavioural traits are subject to bias by misreports and longitudinal changes. Nature Communications, 12 (1) 988, 988. doi: 10.1038/s41467-021-21294-1

Blokland, Gabriëlla A.M., Grove, Jakob, Chen, Chia-Yen, Cotsapas, Chris, Tobet, Stuart, Handa, Robert, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T.R., Farh, Kai-How, Holmans, Peter A., Lee, Phil, Bulik-Sullivan, Brendan, Collier, David A., Huang, Hailiang, Pers, Tune H., Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bergen, Sarah E., Bevilacqua, Elizabeth, Bigdeli, Tim B. ... iPSYCH (2021). Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Biological Psychiatry, 91 (1), 102-117. doi: 10.1016/j.biopsych.2021.02.972

Becker, Joel, Burik, Casper A. P., Goldman, Grant, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Belsky, Daniel W., Karlsson Linnér, Richard, Ahlskog, Rafael, Kleinman, Aaron, Hinds, David A., Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Huber, Karen E., Litterman, Nadia K., McCreight, Jennifer C., McIntyre, Matthew H., Mountain, Joanna L., Northover, Carrie A. M., Pitts, Steven J., Sathirapongsasuti, J. Fah, Sazonova, Olga V., Shelton, Janie F. ... Okbay, Aysu (2021). Resource profile and user guide of the Polygenic Index Repository. Nature Human Behaviour, 5 (12), 1744-1758. doi: 10.1038/s41562-021-01119-3

Wray, Naomi R., Lin, Tian, Austin, Jehannine, McGrath, John J., Hickie, Ian B., Murray, Graham K. and Visscher, Peter M. (2021). From basic science to clinical application of polygenic risk scores : a primer. JAMA Psychiatry, 78 (1), 101-109. doi: 10.1001/jamapsychiatry.2020.3049

Croese, John, Miller, Gregory C., Marquart, Louise, Llewellyn, Stacey, Gupta, Rohit, Becker, Luke, Clouston, Andrew D., Welch, Christine, Sidorenko, Julia, Wallace, Leanne, Visscher, Peter M., Remedios, Matthew L., McCarthy, James S., OʼRourke, Peter, Radford-Smith, Graham, Loukas, Alex, Norrie, Mark, Masson, John W., Gearry, Richard B., Rahman, Tony and Giacomin, Paul R. (2020). Randomized, placebo controlled trial of experimental hookworm infection for improving gluten tolerance in celiac disease. Clinical and Translational Gastroenterology, 11 (12) e00274, 1-11. doi: 10.14309/ctg.0000000000000274

Trejo Banos, Daniel, McCartney, Daniel L., Patxot, Marion, Anchieri, Lucas, Battram, Thomas, Christiansen, Colette, Costeira, Ricardo, Walker, Rosie M., Morris, Stewart W., Campbell, Archie, Zhang, Qian, Porteous, David J., McRae, Allan F., Wray, Naomi R., Visscher, Peter M., Haley, Chris S., Evans, Kathryn L., Deary, Ian J., McIntosh, Andrew M., Hemani, Gibran, Bell, Jordana T., Marioni, Riccardo E. and Robinson, Matthew R. (2020). Bayesian reassessment of the epigenetic architecture of complex traits. Nature Communications, 11 (1) 2865, 2865. doi: 10.1038/s41467-020-16520-1

Svardal, Hannes, Rusuwa, Bosco, Linderoth, Tyler, Kiran, Anmol, Charmantier, Anne, Lattorff, H. Michael G., Cagan, Alex, Ommeh, Sheila C., Kamng'ona, Arox, Katongo, Cyprian, Santos, M. Emília, Durbin, Richard, Kumwenda, Benjamin, Visscher, Peter M. and Von Der Heyden, Sophie (2020). Evolutionary genomics at the human-environment interface in Africa. Molecular Biology and Evolution, 37 (10), 3076-3080. doi: 10.1093/molbev/msaa132

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Witte, John S., Visscher, Peter M. and Wray, Naomi R. (2014). The contribution of genetic variants to disease depends on the ruler. Nature Reviews Genetics, 15 (11), 765-776. doi: 10.1038/nrg3786

Rietveld, Cornelius A., Conley, Dalton, Eriksson, Nicholas, Esko, Tonu, Medland, Sarah E., Vinkhuyzen, Anna A. E., Yang, Jian, Boardman, Jason D., Chabris, Christopher F., Dawes, Christopher T., Domingue, Benjamin W., Hinds, David A., Johannesson, Magnus, Kiefer, Amy K., Laibson, David, Magnusson, Patrik K. E., Mountain, Joanna L., Oskarsson, Sven, Rostapshova, Olga, Teumer, Alexander, Tung, Joyce Y., Visscher, Peter M., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014). Replicability and robustness of genome-wide-association studies for behavioral traits. Psychological Science, 25 (11), 1975-1986. doi: 10.1177/0956797614545132

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Benyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 (1) 5926, 4926.1-4926.10. doi: 10.1038/ncomms5926

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Brion, Marie-Jo A., Benyamin, Beben, Visscher, Peter M. and Smith, George Davey (2014). Beyond the Single SNP: Emerging Developments in Mendelian Randomization in the “Omics” Era. Current Epidemiology Reports, 1 (4), 228-236. doi: 10.1007/s40471-014-0024-2

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Al-Chalabi, Ammar and Visscher, Peter M. (2014). Motor neuron disease: common genetic variants and the heritability of ALS. Nature Reviews Neurology, 10 (10), 549-550. doi: 10.1038/nrneurol.2014.166

Chen, Guo-Bo, Lee, Sang Hong, Brion, Marie-Jo A., Montgomery, Grant W., Wray, Naomi R., Radford-Smith, Graham L., Visscher, Peter M., The International IBD Genetics Consortium, Australia and New Zealand IBDGC, Belgium Genetic Consortium, Initiative on Crohn and Colitis, NIDDK IBDGC, United Kingdom IBDGC and Wellcome Trust Case Control Consortium (2014). Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data. Human Molecular Genetics, 23 (17) ddu174, 4710-4720. doi: 10.1093/hmg/ddu174

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McRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5) ARTN R73, 1-10. doi: 10.1186/gb-2014-15-5-r73

Robinson, Matthew R., Wray, Naomi R. and Visscher, Peter M. (2014). Explaining additional genetic variation in complex traits. Trends in Genetics, 30 (4), 124-132. doi: 10.1016/j.tig.2014.02.003

Trzaskowski, M., Yang, J., Visscher, P. M. and Plomin, R. (2014). DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12. Molecular Psychiatry, 19 (3), 380-384. doi: 10.1038/mp.2012.191

Yang, Jian, Zaitlen, Noah A., Goddard, Michael E., Visscher, Peter M. and Price, Alkes L. (2014). Advantages and pitfalls in the application of mixed-model association methods. Nature Genetics, 46 (2), 100-106. doi: 10.1038/ng.2876

Benyamin, B., St Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franic, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J., Harris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., de Geus, E. J. C., Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe, V. W. V., Starr, J. M. ... Visscher, P. M. (2014). Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19 (2), 253-258. doi: 10.1038/mp.2012.184

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Catts, Stanley V., Gratten, Jacob, Lee, S. Hong, Wray, Naomi R., Visscher, Peter M., Mowry, Bryan J., Nertney, Deborah A., Psychosis Endophenotypes International Consortium and Wellcome Trust Case-Control Consortium 2 (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature, 511 (7510), 421-427. doi: 10.1038/nature13595

Marioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014). Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study. Behavior Genetics, 44 (2), 91-96. doi: 10.1007/s10519-014-9644-z

Jiang, Lei, Yin, Jian, Ye, Lingying, Yang, Jian, Hemani, Gibran, Liu, Ai-Jun, Zou, Hejian, He, Dongyi, Sun, Lingyun, Zeng, Xiaofeng, Li, Zhanguo, Zheng Yi, Lin, Yiping, Liu, Yi, Fang, Yongfei, Xu, Jianhua, Li, Yinong, Dai, Shengming, Guan, Jianlong, Jiang, Lindi, Wei, Qianghua, Wang, Yi, Li, Yang, Huang, Cibo, Zuo, Xiaoxia, Liu, Yu, Wu, Xin, Zhang, Libin, Zhou, Ling ... Xu, Huji (2014). Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeans. Arthritis and Rheumatology, 66 (5), 1121-1132. doi: 10.1002/art.38353

Visscher, Peter M., Hemani, Gibran, Vinkhuyzen, Anna A. E., Chen, Guo-Bo, Lee, Sang Hong, Wray, Naomi R., Goddard, Michael E. and Yang, Jian (2014). Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples. PLoS Genetics, 10 (4) e1004269, e1004269.1-e1004269.10. doi: 10.1371/journal.pgen.1004269

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Okada, Yukinori, Wu, Di, Trynka, Gosia, Raj, Towfique, Terao, Chikashi, Ikari, Katsunori, Kochi, Yuta, Ohmura, Koichiro, Suzuki, Akari, Yoshida, Shinji, Graham, Robert R., Manoharan, Arun, Ortmann, Ward, Bhangale, Tushar, Denny, Joshua C., Carroll, Robert J., Eyler, Anne E., Greenberg, Jeffrey D., Kremer, Joel M., Pappas, Dimitrios A., Jiang, Lei, Yin, Jian, Ye, Lingying, Su, Ding-Feng, Yang, Jian, Xie, Gang, Keystone, Ed, Westra, Harm-Jan, Esko, Tonu ... Brown, Matthew A. (2014). Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature, 506 (7488), 376-381. doi: 10.1038/nature12873

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Gratten, Jacob, Wray, Naomi R., Keller, Matthew C. and Visscher, Peter M. (2014). Large-scale genomics unveils the genetic architecture of psychiatric disorders. Nature Neuroscience, 17 (6), 782-790. doi: 10.1038/nn.3708

Derks, Eske M., Ayub, Muhammad, Chambert, Kimberly, Del Favero, Jurgen, Johnstone, Mandy, Macgregor, Stuart, Maclean, Alan, McKechanie, Andrew G., McRae, Allan F., Moran, Jennifer L., Pickard, Benjamin S., Purcell, Shaun, Sklar, Pamela, St Clair, David M., Wray, Naomi R., Visscher, Peter M. and Blackwood, Douglas H. R. (2013). A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability. American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 162 (8), 847-854. doi: 10.1002/ajmg.b.32189

Wray, Naomi R., Yang, Jian, Hayes, Ben J., Price, Alkes L., Goddard, Michael E. and Visscher, Peter M. (2013). Author reply to A commentary on Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics, 14 (12), 894-894. doi: 10.1038/nrg3457-c2

Terwisscha van Scheltinga, A. F., Bakker, S. C., Van Haren, N. E. M., Derks, E. M., Buizer-Voskamp, J. E., Cahn, W., Ripke, S., Ophoff, R. A., Kahn, R. S., Psychiatric Genomic-Wide Association Study (GWAS) Consortium, Visscher, P. M., Mowry, B. J., Brown, M. A. and McGrath, J. J. (2013). Schizophrenia genetic variants are not associated with intelligence. Psychological Medicine, 43 (12), 2563-2570. doi: 10.1017/S0033291713000196

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

Hemani, Gibran, Yang, Jian, Vinkhuyzen, Anna, Powell, Joseph E., Willemsen, Gonneke, Hottenga, Jouke-Jan, Abdellaoui, Abdel, Mangino, Massimo, Valdes, Ana M., Medland, Sarah E., Madden, Pamela A., Heath, Andrew C., Henders, Anjali K., Nyholt, Dale R., de Geus, Eco J. C., Magnusson, Patrik K. E., Ingelsson, Erik, Montgomery, Grant W., Spector, Timothy D., Boomsma, Dorret I., Pedersen, Nancy L., Martin, Nicholas G. and Visscher, Peter M. (2013). Inference of the Genetic Architecture Underlying BMI and Height with the Use of 20,240 Sibling Pairs. American Journal of Human Genetics, 93 (5), 865-875. doi: 10.1016/j.ajhg.2013.10.005

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

Revez, J. A., Bain, L., Chapman, B., Powell, J. E., Jansen, R., Duffy, D. L., Tung, J. Y., AAGC Collaborators, Penninx, B. W., Visscher, P. M., De Geus, E. J. C., Boomsma, D. I., Hinds, D. A., Martin, N. G., Montgomery, G. W., Ferreira, M. A. R., Danoy, Patrick and Brown, Matthew A. (2013). A new regulatory variant in the interleukin-6 receptor gene associates with asthma risk. Genes and Immunity, 14 (7), 441-446. doi: 10.1038/gene.2013.38

Visscher, Peter and Gibson, Greg (2013). What if we had whole-genome sequence data for millions of individuals?. Genome Medicine, 5 (80) 80, 80.1-80.3. doi: 10.1186/gm484

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

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

Hu, Yi-Juan, Berndt, Sonja I., Gustafsson, Stefan, Ganna, Andrea, Hirschhorn, Joel, North, Kari E., Ingelsson, Erik, Lin, Dan-Yu, Collins, Francis S., Berndt, Sonja I., Gustafsson, Stefan, Ma¨gi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, To˜nu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian’an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W. ... Ingelsson, Erik (2013). Meta-analysis of gene-level associations for rare variants based on single-variant statistics. American Journal of Human Genetics, 93 (2), 236-248. doi: 10.1016/j.ajhg.2013.06.011

Feulner, Philine G. D., Gratten, Jacob, Kijas, James W., Visscher, Peter M., Pemberton, Josephine M. and Slate, Jon (2013). Introgression and the fate of domesticated genes in a wild mammal population. Molecular Ecology, 22 (16), 4210-4221. doi: 10.1111/mec.12378

Visscher, Peter M. (2013). Commentary: height and Mendel's theory: the long and the short of it. International Journal of Epidemiology, 42 (4) dyt069, 944-945. doi: 10.1093/ije/dyt069

Gibson, Greg and Visscher, Peter M. (2013). From personalized to public health genomics. Genome Medicine, 5 (60) 60, 1-2. doi: 10.1186/gm464

Trzaskowski, Maciej, Davis, Oliver S. P., DeFries, John C., Yang, Jian, Visscher, Peter M. and Plomin, Robert (2013). DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities. Behavior Genetics, 43 (4), 267-273. doi: 10.1007/s10519-013-9594-x

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

Thomson, P. A., Parla, J. S., McRae, A. F., Kramer, M., Ramakrushnan, K., Yao, J., Soares, D. C., McCarthy, S., Morris, S. W., Cardone, L., Cass, S., Ghiban, E., Hennah, W., Evans, K. L., Rebolini, D., Millar, J. K., Harris, S. E., Starr, J. M., MacIntyre, J., Generation Scotland, McIntosh, A. M., Watson, J. D., Deary, I. J., Visscher, P. M., Blackwood, D. H., McCombie, W. R. and Porteous, D. J. (2013). 708 common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. Molecular Psychiatry, Advance online publication (6), 1-8. doi: 10.1038/mp.2013.68

Wei, Zhi, Wang, Wei, Bradfield, Jonathan, Li, Jin, Cardinale, Christopher, Frackelton, Edward, Kim, Cecilia, Mentch, Frank, Van Steen, Kristel, Visscher, Peter M., Baldassano, Robert N., Hakonarson, Hakon and International IBD Genetics Consortium (2013). Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease. American Journal of Human Genetics, 92 (6), 1008-1012. doi: 10.1016/j.ajhg.2013.05.002

McIntosh, Andrew M., Gow, Alan, Luciano, Michelle, Davies, Gail, Liewald, David C., Harris, Sarah E., Corley, Janie, Hall, Jeremy, Starr, John M., Porteous, David J., Tenesa, Albert, Visscher, Peter M. and Deary, Ian J. (2013). Polygenic risk for schizophrenia is associated with cognitive change between childhood and old age. Biological Psychiatry, 73 (10), 938-943. doi: 10.1016/j.biopsych.2013.01.011

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013). Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 (5) e1003502, e1003502.1-e1003502.10. doi: 10.1371/journal.pgen.1003502

Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helena, The Tobacco and Genetics Consortium, The Bipolar Disorder Psychiatric Genomics Consortium, The Schizophrenia Psychiatric Genomics Consortium, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M., McGrath, John J., Mowry, Bryan and Visscher, Peter (2013). All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PloS Genetics, 9 (4), e1003449. doi: 10.1371/journal.pgen.1003449

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

Vimaleswaran, Karani S., Berry, Diane J., Lu, Chen, Tikkanen, Emmi, Pilz, Stefan, Hiraki, Linda T., Cooper, Jason D., Dastani, Zari, Li, Rui, Houston, Denise K., Wood, Andrew R., Michaëlsson, Karl, Vandenput, Liesbeth, Zgaga, Lina, Yerges-Armstrong, Laura M., McCarthy, Mark I., Dupuis, Josée, Kaakinen, Marika, Kleber, Marcus E., Jameson, Karen, Arden, Nigel, Raitakari, Olli, Viikari, Jorma, Lohman, Kurt K., Ferrucci, Luigi, Melhus, Håkan, Ingelsson, Erik, Byberg, Liisa, Lind, Lars ... Hirschhorn, J. N. (2013). Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Medicine, 10 (2) e1001383, e1001383. doi: 10.1371/journal.pmed.1001383

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

Goldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221

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

Brion, Marie-Jo A., Shakhbazov, Konstantin and Visscher, Peter M. (2013). Calculating statistical power in Mendelian randomization studies. International Journal of Epidemiology, 42 (5) dyt179, 1497-1501. doi: 10.1093/ije/dyt179

Parnell, Grant P., Gatt, Prudence N., McKay, Fiona C., Schibeci, Stephen, Krupa, Malgorzata, Powell, Joseph E., Visscher, Peter M., Montgomery, Grant W., Lechner-Scott, Jeannette, Broadley, Simon, Liddle, Christopher, Slee, Mark, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2013). Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season. Multiple Sclerosis, 20 (6), 675-685. doi: 10.1177/1352458513507819

Davies, G., Harris, S. E., Reynolds, C. A., Payton, A., Knight, H. M., Liewald, D. C., Lopez, L. M., Luciano, M., Gow, A. J., Corley, J., Henderson, R., Murray, C., Pattie, A., Fox, H. C., Redmond, P., Lutz, M. W., Chiba-Falek, O., Linnertz, C., Saith, S., Haggarty, P., McNeill, G., Ke, X., Ollier, W., Horan, M., Roses, A. D., Ponting, C. P., Porteous, D. J., Tenesa, A., Pickles, A. ... Deary, I. J. (2012). A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. Molecular Psychiatry, 19 (1), 76-87. doi: 10.1038/mp.2012.159

Witte, John S. and Visscher, Peter M. (2012). Reclassify controls at your own risk. Epidemiology, 23 (6), 910-911. doi: 10.1097/EDE.0b013e31826cc118

Lee, S. H., Yang, J., Goddard, M. E., Visscher, P. M. and Wray, N. R. (2012). Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics, 28 (19) bts474, 2540-2542. doi: 10.1093/bioinformatics/bts474

Lips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., International Schizophrenia Consortium, Holmans, P. A., O'Donovan, M. C., Purcell, S. M., Smit, A. B., Verhage, M., Sullivan, P. F., Visscher, P. M. and Posthuma, D. (2012). Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry, 17 (10), 996-1006. doi: 10.1038/mp.2011.117

Verweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x

Calvin, Catherine M., Deary, Ian J., Webbink, Dinand, Smith, Pauline, Fernandes, Cres, Lee, Sang Hong, Luciano, Michelle and Visscher, Peter M. (2012). Multivariate genetic analyses of cognition and academic achievement from two population samples of 174,000 and 166,000 school children. Behavior Genetics, 42 (5), 699-710. doi: 10.1007/s10519-012-9549-7

Kemper, Kathryn E., Daetwyler, Hans D., Visscher, Peter M. and Goddard, Michael E. (2012). Comparing linkage and association analyses in sheep points to a better way of doing GWAS. Genetics Research, 94 (4), 191-203. doi: 10.1017/S0016672312000365

Gordon, Lavinia, Joo, Jihoon E., Powell, Joseph E., Ollikainen, Miina, Novakovic, Boris, Li, Xin, Andronikos, Roberta, Cruickshank, Mark N., Conneely, Karen N., Smith, Alicia K., Alisch, Reid S., Morley, Ruth, Visscher, Peter M., Craig, Jeffrey M. and Saffery, Richard (2012). Neonatal DNA methylation profile in human twins is specified by a complex interplay between intrauterine environmental and genetic factors, subject to tissue-specific influence. Genome Research, 22 (8), 1395-1406. doi: 10.1101/gr.136598.111

McQuillan, Ruth, Eklund, Niina, Pirastu, Nicola, Kuningas, Maris, McEvoy, Brian P., Esko, Tonu, Corre, Tanguy, Davies, Gail, Kaakinen, Marika, Lyytikainen, Leo-Pekka, Kristiansson, Kati, Havulinna, Aki S., Gogele, Martin, Vitart, Veronique, Tenesa, Albert, Aulchenko, Yurii, Hayward, Caroline, Johansson, Asa, Boban, Mladen, Ulivi, Sheila, Robino, Antonietta, Boraska, Vesna, Igl, Wilmar, Wild, Sarah H., Zgaga, Lina, Amin, Najaf, Theodoratou, Evropi, Polasek, Ozren, Girotto, Giorgia ... Wilson, James F. (2012). Evidence of inbreeding depression on human height. Plos Genetics, 8 (7) e1002655, e1002655. doi: 10.1371/journal.pgen.1002655

Lee, S. Hong, DeCandia, Teresa R., Ripke, Stephan, Yang, Jian, Sullivan, Patrick F., Goddard, Michael E., Keller, Matthew C., Visscher, Peter M. and Wray, Naomi R. (2012). Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs (vol 44, pg 247, 2012). Nature Genetics, 44 (7), 831-831. doi: 10.1038/ng0712-831a

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion (vol 2, e125, 2012). Translational Psychiatry, 2 (5) e125, e125-e125. doi: 10.1038/tp.2012.49

Benjamin, Daniel J., Cesarini, David, van der Loos, Matthijs, Dawes, Christopher T., Koellinger, Philipp d., Magnusson, Patrik K. E., Chabris, Christopher F., Conley, Dalton, Laibson, David, Johannesson, Magnus and Visscher, Peter M. (2012). The genetic architecture of economic and political preferences. Proceedings of the National Academy of Sciences of the United States of America, 109 (21), 8026-8031. doi: 10.1073/pnas.1120666109

Kemper, Kathryn E., Visscher, Peter M. and Goddard, Michael E. (2012). Genetic architecture of body size in mammals. Genome Biology, 13 (4) 244, 1-13. doi: 10.1186/gb-2012-13-4-244

Lee, Sang Hong, Goddard, Michael E., Wray, Naomi R. and Visscher, Peter M. (2012). A better coefficient of determination for genetic profile analysis. Genetic Epidemiology, 36 (3), 214-224. doi: 10.1002/gepi.21614

Yang, Jian, Ferreira, Teresa, Morris, Andrew P., Medland, Sarah E., Madden, Pamela A. F., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Weedon, Michael N., Loos, Ruth J., Frayling, Timothy M., McCarthy, Mark I., Hirschhorn, Joel N., Goddard, Michael E., Visscher, Peter M., Genetic Invest ANthropometric Trai and DIAbet Genetics Replication Meta-A (2012). Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. Nature Genetics, 44 (4), 369-375. doi: 10.1038/ng.2213

Vinkhuyzen, A. A. E., Pedersen, N. L., Yang, J., Lee, S. H., Magnusson, P. K. E., Iacono, W. G., McGue, M., Madden, P. A. F., Heath, A. C., Luciano, M., Payton, A., Horan, M., Ollier, W., Pendleton, N., Deary, I. J., Montgomery, G. W., Martin, N. G., Visscher, P. M. and Wray, N. R. (2012). Common SNPs explain some of the variation in the personality dimensions of neuroticism and extraversion. Translational Psychiatry, 2 (e102) 201227, e102-e102. doi: 10.1038/tp.2012.27

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Caracella, Anthony, Smith, Sara, Wright, Margaret J., Whitfield, John B., Dermitzakis, Emmanouil T., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2012). The Brisbane systems genetics study: genetical genomics meets complex trait genetics. PLoS One, 7 (4) e35430, e35430.1-e35430.9. doi: 10.1371/journal.pone.0035430

Ayoub, Mohammed Akli, Angelicheva, Dora, Vile, David, Chandler, David, Morar, Bharti, Cavanaugh, Juleen A., Visscher, Peter M., Jablensky, Assen, Pfleger, Kevin D. G. and Kalaydjieva, Luba (2012). Deleterious GRM1 mutations in schizophrenia. PLoS One, 7 (3) e32849, e32849. doi: 10.1371/journal.pone.0032849

Lee, S. Hong, DeCandia, Teresa R., Ripke, Stephan, Yang, Jian, Sullivan, Patrick F ., Goddard, Michael E ., Keller, Matthew C ., Visscher, Peter M ., Wray, Naomi R., Schizophrenia Psychiat Genome-Wide, Int Schizophrenia Consortium ISC, Mol Genetics Schizophrenia and Mowry, Bryan (2012). Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs. Nature Genetics, 44 (3), 247-250. doi: 10.1038/ng.1108

Powell, Joseph E., Henders, Anjali K., McRae, Allan F., Wright, Margaret J., Martin, Nicholas G., Dermitzakis, Emmanouil T., Montgomery, Grant W. and Visscher, Peter M. (2012). Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. Genome Research, 22 (3), 456-466. doi: 10.1101/gr.126540.111

Deary, Ian J., Yang, Jian, Davies, Gail, Harris, Sarah E., Tenesa, Albert, Liewald, David, Luciano, Michelle, Lopez, Lorna M., Gow, Alan J., Corley, Janie, Redmond, Paul, Fox, Helen C., Rowe, Suzanne J., Haggarty, Paul, McNeill, Gerald, Goddard, Michael E., Porteous, David J., Whalley, Lawrence J., Starr, John M. and Visscher, Peter M. (2012). Genetic contributions to stability and change in intelligence from childhood to old age. Nature, 482 (7384), 212-215. doi: 10.1038/nature10781

Richards, A. L., Jones, L., Moskvina, V., Kirov, G., Gejman, P. V., Levinson, D. F., Sanders, A. R., Molecular Genetics of Schizophrenia Collaboration, International Schizophrenia Consortium (ISC), Purcell, S., Visscher, P. M., Craddock, N., Owen, M. J., O'Donovan, M. C., Holmans, P. and Mowry, B.J. (2012). Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Molecular Psychiatry, 17 (2), 193-201. doi: 10.1038/mp.2011.11

Jia, Peilin, Wang, Lily, Fanous, Ayman H., Chen, Xiangning, Kendler, Kenneth S., Zhao, Zhongming, Morris, Derek W., O'Dushlaine, Colm T., Kenny, Elaine, Quinn, Emma M., Gill, Michael, Corvin, Aiden, O'Donovan, Michael C., Kirov, George K., Craddock, Nick J., Holmans, Peter A., Williams, Nigel M., Georgieva, Lucy, Nikolov, Ivan, Norton, N., Williams, H., Toncheva, Draga, Milanova, Vihra, Owen, Michael J., Hultman, Christina M., Lichtenstein, Paul, Thelander, Emma F., Sullivan, Patrick, McQuillin, Andrew ... Sklar, Pamela (2012). A bias-reducing pathway enrichment analysis of genome-wide association data confirmed association of the MHC region with schizophrenia. Journal of Medical Genetics, 49 (2), 96-103. doi: 10.1136/jmedgenet-2011-100397

Stolk L., Perry J.R.B., Chasman D.I., He C., Mangino M., Sulem P., Barbalic M., Broer L., Byrne E.M., Ernst F., Esko T., Franceschini N., Gudbjartsson D.F., Hottenga J.-J., Kraft P., McArdle P.F., Porcu E., Shin S.-Y., Smith A.V., Van Wingerden S., Zhai G., Zhuang W.V., Albrecht E., Alizadeh B.Z., Aspelund T., Bandinelli S., Lauc L.B., Beckmann J.S., Boban M. ... Lunetta K.L. (2012). Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Nature Genetics, 44 (3), 260-268. doi: 10.1038/ng.1051

Visscher, Peter, Goddard, M. E., Derks, E. M. and Wray, Naomi (2012). Evidence-based psychiatric genetics, AKA the false dichotomy between common and rare variant hypotheses. Molecular Psychiatry, 17 (5), 474-485. doi: 10.1038/mp.2011.65

Visscher, Peter M., Brown, Matthew .A, McCarthy, Mark I. and Yang, Jian (2012). Five years of GWAS discovery. American Journal of Human Genetics, 90 (1), 7-24. doi: 10.1016/j.ajhg.2011.11.029

Chen, X., Lee, G., Maher, B. S., Fanous, A. H., Chen, J., Zhao, Z., Guo, A., van den Oord, E., Sullivan, P. F., Shi, J., Levinson, D. F., Gejman, P. V., Sanders, A., Duan, J., Owen, M. J., Craddock, N. J., O'Donovan, M. C., Blackman, J., Lewis, D., Kirov, G. K., Qin, W., Schwab, S., Wildenauer, D., Chowdari, K., Nimgaonkar, V., Straub, R. E., Weinberger, D. R., O'Neill, F. A., Walsh, D. ... Visscher, Peter M. (2011). GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia. Molecular Psychiatry, 16 (11), 1117-1129. doi: 10.1038/mp.2010.96

Benyamin, Beben, Middelberg, Rita P., Lind, Penelope A., Valle, Anne M., Gordon, Scott, Nyholt, Dale R., Medland, Sarah E., Henders, Anjali K., Heath, Andrew C., Madden, Pamela A. F., Visscher, Peter M., O'Connor, Daniel T., Montgomery, Grant W., Martin, Nicholas G. and Whitfield, John B. (2011). GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Human Molecular Genetics, 20 (22) ddr375, 4504-4514. doi: 10.1093/hmg/ddr375

Davies, G., Tenesa, A., Payton, A., Yang, J., Harris, S. E., Liewald, D., Ke, X., Le Hellard, S., Christoforou, A., Luciano, M., McGhee, K., Lopez, L., Gow, A. J., Corley, J., Redmond, P., Fox, H. C., Haggarty, P., Whalley, L. J., McNeill, G., Goddard, M. E., Espeseth, T., Lundervold, A. J., Reinvang, I., Pickles, A., Steen, V. M., Ollier, W., Porteous, D. J., Horan, M., Starr, J. M. ... Deary, I. J. (2011). Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Molecular Psychiatry, 16 (10), 996-1005. doi: 10.1038/mp.2011.85

Danoy, Patrick, Wei, Meng, Hadler, Johanna, Jiang, Lei, He, Dongyi, Sun, Linyun, Zeng, Xiaofeng, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011). Association of variants in MMEL1 and CTLA4 with rheumatoid arthritis in the Han Chinese population. Annals of the Rheumatic Diseases, 70 (10), 1793-1797. doi: 10.1136/ard.2010.144576

Keller, Matthew C., Visscher, Peter M. and Goddard, Michael E. (2011). Quantification of inbreeding due to distant ancestors and its detection using dense single nucleotide polymorphism data. Genetics, 189 (1), 237-249. doi: 10.1534/genetics.111.130922

Ferreira, Manuel A. R., Matheson, Melanie C., Duffy, David L., Marks, Guy B., Hui, Jennie, Le Souef, Peter, Danoy, Patrick, Baltic, Svetlana, Nyholt, Dale R., Jenkins, Mark, Hayden, Catherine, Willemsen, Gonneke, Ang, Wei, Kuokkanen, Mikko, Beilby, John, Cheah, Faang, de Geus, Eco J.C., Ramasamy, Adaikalavan, Vedantam, Sailaka, Salomaa, Veikko, Madden, Pamela A., Heath, Andrew C., Hopper, John L., Visscher, Peter M., Musk, Bill, Leeder, Stephen R., Jarvelin, Marjo-Riitta, Pennell, Craig, Boomsma, Dorret I. ... Wright, Margaret J. (2011). Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Lancet, 378 (9795), 1006-1014. doi: 10.1016/S0140-6736(11)60874-X

Maugeri, Narelle, Powell, Joseph E., 't Hoen, Peter A. C., de Geus, Eco J. C., Willemsen, Gonneke, Kattenberg, Mathijs, Henders, Anjali K., Wallace, Leanne, Penninx, Brenda, Hottenga, Jouke-Jan, Medland, Sarah E., Saviouk, Viatcheslav, Martin, Nicholas G., Visscher, Peter M., van Ommen, Gert-Jan B., Frazer, Ian H., Boomsma, Dorret I., Montgomery, Grant W. and Ferreira, Manuel A. R (2011). LPAR1 and ITGA4 Regulate Peripheral Blood Monocyte Counts. Human Mutation, 32 (8), 873-876. doi: 10.1002/humu.21536

Goddard, Michael E., Lee, Hong, Yang, Jian, Wray, Naomi R. and Visscher, Peter M. (2011). Response to Browning and Browning. American Journal of Human Genetics, 89 (1), 193-195. doi: 10.1016/j.ajhg.2011.05.022

Demirkan, Ayse, Amin, Najaf, Isaacs, Aaron, Jarvelin, Marjo-Riitta, Whitfield, John B., Wichmann, Heinz-Erich, Kyvik, Kirsten Ohm, Rudan, Igor, Gieger, Christian, Hicks, Andrew A., Johansson, Asa, Hottenga, Jouke-Jan, Smith, Johannes J., Wild, Sarah H., Pedersen, Nancy L., Willemsen, Gonneke, Mangino, Massimo, Hayward, Caroline, Uitterlinden, Andre G., Hofman, Albert, Witteman, Jacqueline, Montgomery, Grant W., Pietilainen, Kirsi H., Rantanen, Taina, Kaprio, Jaakko, Doering, Angela, Pramstaller, Peter P., Gyllensten, Ulf, de Geus, Eco J. C. ... van Duijn, Cornelia M. (2011). Genetic architecture of circulating lipid levels. European Journal of Human Genetics, 19 (7), 813-819. doi: 10.1038/ejhg.2011.21

Yang, Jian, Weedon, Michael N., Purcell, Shaun, Lettre, Guillaume, Estrada, Karol, Willer, Cristen J., Smith, Albert V., Ingelsson, Erik, O'Connell, Jeffrey R., Mangino, Massimo, Maegi, Reedik, Madden, Pamela A., Heath, Andrew C., Nyholt, Dale R., Martin, Nicholas G., Montgomery, Grant W., Frayling, Timothy M., Hirschhorn, Joel N., McCarthy, Mark I., Goddard, Michael E. and Visscher, Peter M. (2011). Genomic inflation factors under polygenic inheritance. European Journal of Human Genetics, 19 (7), 807-812. doi: 10.1038/ejhg.2011.39

Yang, Jian, Manolio, Teri A., Pasquale, Louis R., Boerwinkle, Eric, Caporaso, Neil, Cunningham, Julie M., de Andrade, Mariza, Feenstra, Bjarke, Feingold, Eleanor, Hayes, M. Geoffrey, Hill, William G., Landi, Maria Teresa, Alonso, Alvaro, Lettre, Guillaume, Lin, Peng, Ling, Hua, Lowe, William, Mathias, Rasika A., Melbye, Mads, Pugh, Elizabeth, Cornelis, Marilyn C., Weir, Bruce S., Goddard, Michael E. and Visscher, Peter M. (2011). Genome partitioning of genetic variation for complex traits using common SNPs. Nature Genetics, 43 (6), 519-U44. doi: 10.1038/ng.823

McEvoy, Brian P., Powell, Joseph E., Goddard, Michael E. and Visscher, Peter M. (2011). Human population dispersal "Out of Africa" estimated from linkage disequilibrium and allele frequencies of SNPs. Genome Research, 21 (6), 821-829. doi: 10.1101/gr.119636.110

Smith, Nicholas L., Huffman, Jennifer E., Strachan, David P., Huang, Jie, Dehghan, Abbas, Trompet, Stella, Lopez, Lorna M., Shin, So-Youn, Baumert, Jens, Vitart, Veronique, Bis, Joshua C., Wild, Sarah H., Rumley, Ann, Yang, Qiong, Uitterlinden, Andre G., Stott, David. J., Davies, Gail, Carter, Angela M., Thorand, Barbara, Polasek, Ozren, McKnight, Barbara, Campbell, Harry, Rudnicka, Alicja R., Chen, Ming-Huei, Buckley, Brendan M., Harris, Sarah E., Peters, Annette, Pulanic, Drazen, Lumley, Thomas ... Hayward, Caroline (2011). Genetic Predictors of Fibrin D-Dimer Levels in Healthy Adults. Circulation, 123 (17), 1864-+. doi: 10.1161/CIRCULATIONAHA.110.009480

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2011). Does teenage childbearing reduce investment in human capital?. Journal of Population Economics, 24 (2), 701-730. doi: 10.1007/s00148-009-0270-7

Painter, Jodie N., Anderson, Carl A., Nyholt, Dale R., Macgregor, Stuart, Lin, Jianghai, Lee, Sang Hong, Lambert, Ann, Zhao, Zhen Z., Roseman, Fenella, Guo, Qun, Gordon, Scott D., Wallace, Leanne, Henders, Anjali K., Visscher, Peter M., Kraft, Peter, Martin, Nicholas G., Morris, Andrew P., Treloar, Susan A., Kennedy, Stephen H., Missmer, Stacey A., Montgomery, Grant W. and Zondervan, Krina T. (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Obstetrical and Gynecological Survey, 66 (4), 214-216. doi: 10.1097/OGX.0b013e318210cea1

Ferreira, Manuel A. R., McRae, Allan F., Medland, Sarah E., Nyholt, Dale R., Gordon, Scott D., Wright, Margaret J., Henders, Anjali K., Madden, Pamela A., Visscher, Peter M., Wray, Naomi R., Heath, Andrew C., Montgomery, Grant W., Duffy, David L. and Martin, Nicholas G. (2011). Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. European Journal of Human Genetics, 19 (4), 458-464. doi: 10.1038/ejhg.2010.191

Lee, Sang Hong, Wray, Naomi R., Goddard, Michael E. and Visscher, Peter M. (2011). Estimating missing heritability for disease from genome-wide association studies. American Journal of Human Genetics, 88 (3), 294-305. doi: 10.1016/j.ajhg.2011.02.002

Davidson, Stuart I., Liu, Yu, Danoy, Patrick A., Wu, Xin, Thomas, Gethin P., Jiang, Lei, Sun, Linyun, Wang, Niansong, Han, Jun, Han, Huanxing, Visscher, Peter M., Brown, Matthew A. and Xu, Huji (2011). Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese. Annals of the Rheumatic Diseases, 70 (2), 289-292. doi: 10.1136/ard.2010.133322

Wray, Naomi, Purcell, Shaun M. and Visscher, Peter (2011). Synthetic Associations Created by Rare Variants Do Not Explain Most GWAS Results. PLoS Biology, 9 (1) e1000579, e1000579.1-e1000579.11. doi: 10.1371/journal.pbio.1000579

Yang, Jian, Lee, S. Hong, Goddard, Michael E. and Visscher, Peter M. (2011). GCTA: a tool for genome-wide complex trait analysis. American Journal of Human Genetics, 88 (1), 76-82. doi: 10.1016/j.ajhg.2010.11.011

Painter, JN, Anderson, CA, Nyholt, DR, Macgregor, S, Lin, JH, Lee, SH, Lambert, A, Zhao, ZZ, Roseman, F, Guo, Q, Gordon, SD, Wallace, L, Henders, AK, Visscher, PM, Kraft, P, Martin, NG, Morris, AP, Treloar, SA, Kennedy, SH, Missmer, SA, Montgomery, GW and Zondervan, KT (2011). Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Nature Genetics, 43 (1), 51-54. doi: 10.1038/ng.731

Lee, Sang Hong, Nyholt, Dale R., Macgregor, Stuart, Henders, Anjali K., Zondervan, Krina T., Montgomery, Grant W. and Visscher, Peter M. (2010). A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies. Genetic Epidemiology, 34 (8), 854-862. doi: 10.1002/gepi.20541

Visscher, Peter M., Yang, Jian and Goddard, Michael E. (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 (6), 517-524. doi: 10.1375/twin.13.6.517

Powell, Joseph E., Visscher, Peter M. and Goddard, Michael E. (2010). Reconciling the analysis of IBD and IBS in complex trait studies. Nature Reviews Genetics, 11 (11), 800-805. doi: 10.1038/nrg2865

Gratten, J., Wilson, A. J., McRae, A. F., Beraldi, D., Visscher, P. M., Pemberton, J. M. and Slate, J. (2010). No evidence for warming climate theory of coat colour change in Soay sheep: A comment on Maloney et al.. Biology Letters, 6 (5), 678-679. doi: 10.1098/rsbl.2010.0160

Allen, Hana Lango, Estrada, Karol, Lettre, Guillaume, Berndt, Sonja I., Weedon, Michael N., Rivadeneira, Fernando, Willer, Cristen J., Jackson, Anne U., Vedantam, Sailaja, Raychaudhuri, Soumya, Nyholt, Dale, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2010). Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature, 467 (7317), 832-838. doi: 10.1038/nature09410

Visscher, Peter M., McEvoy, Brian and Yang, Jian (2010). From Galton to GWAS: Quantitative genetics of human height. Genetics Research, 92 (5-6), 371-379. doi: 10.1017/S0016672310000571

Raychaudhuri, Soumya, Korn, Joshua M., McCarroll, Steven A., Altshuler, David, Sklar, Pamela, Purcell, Shaun, Purcell, Shaun, Purcell, Shaun, Stone, Jennifer, Bergen, Sarah, O'Dushlaine, Colm, Ruderfer, Douglas, Sklar, Pamela, Scolnick, Edward, Chambert, Kimberly, O'Donovan, Michael, Kirov, George, Craddock, Nick, Holmans, Peter, Williams, Nigel, Georgieva, Lucy, Nikolov, Ivan, Norton, Nadine, Williams, H., Toncheva, Draga, Milanova, Vihra, Owen, Michael, Hultman, Christina, Lichtenstein, Paul ... Pato, Carlos N. (2010). Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function. PLoS Genetics, 6 (9) e1001097, e1001097. doi: 10.1371/journal.pgen.1001097

Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2010). Corrigendum to: Sporadic cases are the norm for complex disease (European Journal of Human Genetics (2010) 18 (1039-1043) DOI: 10.1038/ejhg.2009.177). European Journal of Human Genetics, 18 (9), 1044-1044. doi: 10.1038/ejhg.2009.233

Visscher, Peter M. and Posthuma, Danielle (2010). Statistical Power to Detect Genetic Loci Affecting Environmental Sensitivity. Behavior Genetics, 40 (5), 728-733. doi: 10.1007/s10519-010-9362-0

Yang, Jian, Visscher, Peter M. and Wray, Naomi R. (2010). Sporadic cases are the norm for complex disease. European Journal of Human Genetics, 18 (9), 1039-1043. doi: 10.1038/ejhg.2009.177

McEvoy, Brian P., Lind, Joanne M., Wang, Eric T., Moyzis, Robert K., Visscher, Peter M., Pellekaan, Sheila M. van Holst and Wilton, Alan N. (2010). Whole-Genome Genetic Diversity in a Sample of Australians with Deep Aboriginal Ancestry. American Journal of Human Genetics, 87 (2), 297-305. doi: 10.1016/j.ajhg.2010.07.008

McEvoy, B. P., Zhao, Z. Z., Macgregor, S., Bellis, C., Lea, R. A., Cox, H., Montgomery, G. W., Griffiths, L. R. and Visscher, P. M. (2010). European and Polynesian admixture in the Norfolk Island population. Heredity, 105 (2), 229-234. doi: 10.1038/hdy.2009.175

Liu, Jimmy Z., McRae, Allan F., Nyholt, Dale R., Medland, Sarah E., Wray, Naomi R., Brown, Kevin M., AMFS Investigators, Hayward, Nicholas K., Montgomery, Grant W., Visscher, Peter M., Martin, Nicholas G. and Macgregor, Stuart (2010). A versatile gene-based test for genome-wide association studies. American Journal of Human Genetics, 87 (1), 139-145. doi: 10.1016/j.ajhg.2010.06.009

Yang, Jian, Benyamin, Beben, McEvoy, Brian P., Gordon, Scott, Henders, Anjali K., Nyholt, Dale R., Madden, Pamela A., Heath, Andrew C., Martin, Nicholas G., Montgomery, Grant W., Goddard, Michael E. and Visscher, Peter M. (2010). Common SNPs explain a large proportion of the heritability for human height. Nature Genetics, 42 (7), 565-569. doi: 10.1038/ng.608

Calvin, Catherine M., Fernandes, Cres, Smith, Pauline, Visscher, Peter M. and Deary, Ian J. (2010). Sex, intelligence and educational achievement in a national cohort of over 175,000 11-year-old schoolchildren in England. Intelligence, 38 (4), 424-432. doi: 10.1016/j.intell.2010.04.005

Lee, Sang Hong, Goddard, Michael E., Visscher, Peter M. and van der Werf, Julius H. J. (2010). Using the realized relationship matrix to disentangle confounding factors for the estimation of genetic variance components of complex traits. Genetics Selection Evolution, 42 (1) 22, 22.1-22.14. doi: 10.1186/1297-9686-42-22

Houlihan, Lorna M., Davies, Gail, Tenesa, Albert, Harris, Sarah E., Luciano, Michelle, Gow, Alan J., McGhee, Kevin A., Liewald, David C., Porteous, David J., Starr, John M., Lowe, Gordon D., Visscher, Peter M. and Deary, Ian J. (2010). Common variants of large effect in F12, KNG1, and HRG are associated with ctivated partial thromboplastin time. American Journal of Human Genetics, 86 (4), 626-631. doi: 10.1016/j.ajhg.2010.02.016

Yang, Jian, Wray, Naomi R. and Visscher, Peter M. (2010). Comparing apples and oranges: Equating the power of case-control and quantitative trait association studies. Genetic Epidemiology, 34 (3), 254-257. doi: 10.1002/gepi.20456

Wray, Naomi R., Yang, Jian, Goddard, Michael E. and Visscher, Peter M. (2010). The Genetic Interpretation of Area under the ROC Curve in Genomic Profiling. PLoS Genetics, 6 (2) e1000864, e1000864.1-e1000864.9. doi: 10.1371/journal.pgen.1000864

Wray, Naomi R. and Visscher, Peter M. (2010). Narrowing the Boundaries of the Genetic Architecture of Schizophrenia. Schizophrenia Bulletin, 36 (1), 14-23. doi: 10.1093/schbul/sbp137

Macgregor, Stuart, Bellis, Claire, Lea, Rod A., Cox, Hannah, Dyer, Tom, Blangero, John, Visscher, Peter M. and Griffiths, Lyn R. (2010). Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island. European Journal of Human Genetics, 18 (1), 67-72. doi: 10.1038/ejhg.2009.111

Idaghdour, Youssef, Czika, Wendy, Shianna, Kevin V., Lee, Sang H., Visscher, Peter M., Martin, Hilary C., Miclaus, K, Jadallah, Sami J., Goldstein, David B., Wolfinger, Russell D. and Gibson, Greg (2010). Geographical genomics of human leukocyte gene expression variation in southern Morocco. Nature Genetics, 42 (1), 62-67. doi: 10.1038/ng.495

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2010). Does education reduce the probability of being overweight?. Journal of Health Economics, 29 (1), 29-38. doi: 10.1016/j.jhealeco.2009.11.013

Posthuma, Danielle, de Koning, Dirk-Jan, Dolan, Conor, Goddard, Michael E. and Visscher, Peter M. (2009). A Note on Permutation Tests for Genetic Association Analysis of Quantitative Traits When Variances Are Heterogeneous. Genetic Epidemiology, 33 (8), 710-716. doi: 10.1002/gepi.20423

McEvoy, Brian P. and Visscher, Peter M. (2009). Genetics of human height. Economics and Human Biology, 7 (3), 294-306. doi: 10.1016/j.ehb.2009.09.005

Goddard, Michael E., Wray, Naomi R., Verbyla, Klara and Visscher, Peter M. (2009). Estimating Effects and Making Predictions from Genome-Wide Marker Data. Statistical Science, 24 (4), 517-529. doi: 10.1214/09-STS306

Visscher, Peter M. and Montgomery, Grant W. (2009). Genome-wide Association Studies and Human Disease From Trickle to Flood. Jama-Journal of the American Medical Association, 302 (18), 2028-2029. doi: 10.1001/jama.2009.1643

Benyamin, B, Ferreira, MAR, Willemsen, G, Gordon, S, Middelberg, RPS, McEvoy, BP, Hottenga, JJ, Henders, AK, Campbell, MJ, Wallace, L, Frazer, IH, Heath, AC, de Geus, EJC, Nyholt, DR, Visscher, PM, Penninx, BW, Boomsma, DI, Martin, NG, Montgomery, GW and Whitfield, JB (2009). Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Nature Genetics, 41 (11), 1173-1175. doi: 10.1038/ng.456

Nagamine, Yoshitaka, Pong-Wong, Ricardo, Visscher, Peter M. and Haley, Chris S. (2009). Detection of multiple quantitative trait loci and their pleiotropic effects in outbred pig populations. Genetics Selection Evolution, 41 (1) 44. doi: 10.1186/1297-9686-41-44

Manolio, T.A., Collins, F.S., Cox, N.J., Goldstein, D.B., Hindorff, L.A., Hunter, D.J., McCarthy, M.I., Ramos, E.M., Cardon, L.R., Chakravarti, A., Cho, J.H., Guttmacher, A.E., Kong, A., Kruglyak, L., Mardis, E., Rotimi,C.N., Slatkin, M., Valle, D., Whittemore, A.S., Boehnke, M., Clarke, A.G., Eichler, E.E., Gibson, G.C., Haines, J.L., Mackay, T.F.C., McCarroll, S.A. and Visscher, P.M. (2009). Finding the missing heritability of complex diseases. Nature, 461 (7265), 747-753. doi: 10.1038/nature08494

Visscher, Peter M. and Hill, William G. (2009). The Limits of Individual Identification from Sample Allele Frequencies: Theory and Statistical Analysis. Plos Genetics, 5 (10) e1000628, e1000628. doi: 10.1371/journal.pgen.1000628

Jamie E. Craig, Alex W. Hewitt, Amy E. McMellon, Anjali K. Henders, Lingjun Ma, Leanne Wallace, Shiwani Sharma, Kathryn P. Burdon, Peter M. Visscher, Grant W. Montgomery and Stuart MacGregor (2009). Rapid inexpensive genome-wide association using pooled whole blood. Genome Research, 19 (11), 2075-2080. doi: 10.1101/gr.094680.109

E. M. Byrne, A. F. McRae, D. L. Duffy, Z. Z. Zhao, N. G. Martin, J. B. Whitfield, P. M. Visscher and G. W. Montgomery (2009). Family-based mitochondrial association study of traits related to type 2 diabetes and the metabolic syndrome in adolescents. Diabetologia, 52 (11), 2359-2368. doi: 10.1007/s00125-009-1510-9

Byrne, EM, McRae, AF, Duffy, DL, Zhao, ZZ, Martin, NG, Wright, MJ, Montgomery, GW and Visscher, PM (2009). Association Study of Common Mitochondrial Variants and Cognitive Ability. BEHAVIOR GENETICS, 39 (5), 504-512. doi: 10.1007/s10519-009-9276-x

Matthew C. Keller, Allan F. McRae, Julie M. McGaughran, Peter M. Visscher, Nicholas G. Martin and Grant W. Montgomery (2009). Non-pathological paternal isodisomy of chromosome 2 detected from a genome-wide SNP scan.. American Journal of Medical Genetics. Part A, 149A (8), 1823-1826. doi: 10.1002/ajmg.a.32973

Visscher, Peter M. (2009). Whole genome approaches to quantitative genetics. Genetica, 136 (2), 351-358. doi: 10.1007/s10709-008-9301-7

Calvin, Catherine, Fernandes, Cres, Smith, Pauline, Visscher, Peter M. and Deary, Ian J. (2009). Is there still a cognitive cost of being a twin in the UK?. Intelligence, 37 (3), 243-248. doi: 10.1016/j.intell.2008.12.005

Brian P. McEvoy, Grant W. Montgomery, Allan F. McRae, Samuli Ripatti, Markus Perola, Tim D. Spector, Lynn Cherkas, Kourosh R. Ahmadi, Dorret Boomsma, Gonneke Willemsen, Jouke J. Hottenga, Nancy L. Pedersen, Patrik K.E. Magnusson, Kirsten Ohm Kyvik, Kaare Christensen, Jaakko Kaprio, Kauko Heikkilä, Aarno Palotie, Elisabeth Widen, Juha Muilu, Ann-Christine Syvänen, Ulrika Liljedahl, Orla Hardiman, Simon Cronin, Leena Peltonen, Nicholas G. Martin and Peter M. Visscher (2009). Geographical structure and differential natural selection among North European populations. Genome Research, 19 (5), 804-814. doi: 10.1101/gr.083394.108

Hayes, B. J., Visscher, P. M. and Goddard, M. E. (2009). Increased accuracy of artificial selection by using the realized relationship matrix. (vol 91, pg 47, 2009). Genetics Research, 91 (2), 143-143. doi: 10.1017/S0016672309000111

Allison, David B., Visscher, Peter M., Rosa, Guilherme J. M. and Amos, Christopher I. (2009). Statistical genetics & statistical genomics: Where biology, epistemology, statistics, and computation collide. Computational Statistics & Data Analysis, 53 (5), 1531-1534. doi: 10.1016/j.csda.2009.01.005

Houlihan, L. M., Harris, S. E., Luciano, M., Gow, A. J., Starr, J. M., Visscher, P. M. and Deary, I. J. (2009). Replication study of candidate genes for cognitive abilities: the Lothian Birth Cohort 1936. Genes Brain and Behavior, 8 (2), 238-247. doi: 10.1111/j.1601-183X.2008.00470.x

Luciano, Michelle, Gow, Alan J., Harris, Sarah E., Hayward, Caroline, Allerhand, Mike, Starr, John M., Visscher, Peter M. and Deary, Ian J. (2009). Cognitive Ability at Age 11 and 70 Years, Information Processing Speed, and APOE Variation: The Lothian Birth Cohort 1936 Study. Psychology and Aging, 24 (1), 129-138. doi: 10.1037/a0014780

M. Luciano, F. Miyajima, P. A. Lind, T. C. Bates, M. Horan, S. E. Harris, M. J. Wright, W. E. Ollier, C. Hayward, N. Pendleton, A. J. Gow, P. M. Visscher, J. M. Starr, I. J. Deary, N. G. Martin and A. Payton (2009). Variation in the dysbindin gene and normal cognitive function in three independent population samples. Genes, Brain and Behavior, 8 (2), 218-227. doi: 10.1111/j.1601-183X.2008.00462.x

Benyamin, Beben, Visscher, Peter M. and McRae, Allan F. (2009). Family-based genome-wide association studies. Pharmacogenomics, 10 (2), 181-190. doi: 10.2217/14622416.10.2.181

Hayes, B. J., Visscher, P. M. and Goddard, M. E. (2009). Increased accuracy of artificial selection by using the realized relationship matrix. Genetics Research, 91 (1), 47-60. doi: 10.1017/S0016672308009981

Chenoweth, SF and Visscher, PM (2009). Association Mapping in Outbred Populations: Power and Efficiency When Genotyping Parents and Phenotyping Progeny. Genetics, 181 (2), 755-765. doi: 10.1534/genetics.108.099218

Zachary A Kaminsky, Thomas Tang, Sun-Chong Wang, Carolyn Ptak, Gabriel H T Oh, Albert H C Wong, Laura A Feldcamp, Carl Virtanen, Jonas Halfvarson, Curt Tysk, Allan F McRae, Peter M Visscher, Grant W Montgomery, Irving I Gottesman, Nicholas G Martin and Art Petronis (2009). DNA methylation profiles in monozygotic and dizygotic twins. Nature Genetics, 41 (2), 240-245. doi: 10.1038/ng.286

Beben Benyamin, Allan F. McRae, Gu Zhu, Scott Gordon, Anjali K. Henders, Aarno Palotie, Leena Peltonen, Nicholas G. Martin, Grant W. Montgomery, John B. Whitfield and Peter M. Visscher (2009). Variants in TF and HFE Explain 40% of Genetic Variation in Serum-Transferrin Levels. American Journal of Human Genetics, 84 (1), 60-65. doi: 10.1016/j.ajhg.2008.11.011

Evans, David M., Visscher, Peter M. and Wray, Naomi R. (2009). Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. Human Molecular Genetics, 18 (18), 3525-3531. doi: 10.1093/hmg/ddp295

Luciano, Michelle, Gow, Alan J., Taylor, Michelle D., Hayward, Caroline, Harris, Sarah E., Campbell, Harry, Porteous, David J., Starr, John M., Visscher, Peter M. and Deary, Ian J. (2009). Apolipoprotein E is not Related to Memory Abilities at 70 Years of Age. Behavior Genetics, 39 (1), 6-14. doi: 10.1007/s10519-008-9236-x

Knight, Helen M., Pickard, Benjamin S., Maclean, Alan, Malloy, Mary P., Soares, Dinesh C., McRae, Allan F., Condie, Alison, White, Angela, Hawkins, William, McGhee, Kevin, van Beck, Margaret, MacIntyre, Donald J., Starr, John M., Deary, Ian J., Visscher, Peter M., Porteous, David J., Cannon, Ronald E., St Clair, David, Muir, Walter J. and Blackwood, Douglas H. R. (2009). A cytogenetic abnormality and rare coding variants identify ABCA13 as a candidate gene in schizophrenia, bipolar disorder, and depression. American Journal of Human Genetics, 85 (6), 833-846. doi: 10.1016/j.ajhg.2009.11.003

Sved, John A., McRae, Allan F. and Visscher, Peter M. (2008). Divergence between human populations estimated from linkage disequilibrium. American Journal of Human Genetics, 83 (6), 737-743. doi: 10.1016/j.ajhg.2008.10.019

Hasselbalch, Ann L., Benyamin, Beben, Visscher, Peter M., Heitmann, Berit L., Kyvik, Kirsten O. and Sorensen, Thorkild I. A. (2008). Common genetic components of obesity traits and serum leptin. Obesity, 16 (12), 2723-2729. doi: 10.1038/oby.2008.440

Byrne, Enda M., Mcrae, Allan F., Zhao, Zhen-Zhen, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). The use of common mitochondrial variants to detect and characterise population structure in the Australian population: Implications for genome-wide association studies. European Journal of Human Genetics, 16 (11), 1396-1403. doi: 10.1038/ejhg.2008.117

Webbink, Dinand, Posthuma, Danielle, Boomsma, Dorret I., de Geus, Eco J. C. and Visscher, Peter M. (2008). Do twins have lower cognitive ability than singletons?. Intelligence, 36 (6), 539-547. doi: 10.1016/j.intell.2007.12.002

Hur, Y-M, Kaprio, J., Iacono, W. G., Boomsma, D. I., McGgue, M., Silventoinen, K., Martin, N. G., Luciano, M., Visscher, P. M., Rose, R. J., He, M., Ando, J., Ooki, S., Nonaka, K., Lin, C. C. H., Lajunen, H. R., Cornes, B. K., Bartels, M., van Beijsterveldt, C. E. M., Cherny, S. S. and Mitchell, K. (2008). Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins. International Journal of Obesity, 32 (10), 1455-1467. doi: 10.1038/ijo.2008.144

Lee, Sang Hong, van der Werf, Julius H. J., Hayes, Ben J., Goddard, Michael E. and Visscher, Peter M. (2008). Predicting unobserved phenotypes for complex traits from whole-genome SNP data. PLoS Genetics, 4 (10) e1000231, e1000231. doi: 10.1371/journal.pgen.1000231

Macgregor, Stuart, Hottenga, Jouke-Jan, Lind, Penelope A., Suchiman, H. Eka D., Willemsen, Gonneke, Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G., Visscher, Peter M. and Boomsma, Dorret I. (2008). Vitamin D receptor gene polymorphisms have negligible effect on human height. Twin Research and Human Genetics, 11 (5), 488-494. doi: 10.1375/twin.11.5.488

Anderson, Carl A., Zhu, Gu, Falchi, Mario, van den Berg, Stéphanie M., Treloar, Susan A., Spector, Timothy D., Martin, Nicholas G., Boomsma, Dorret I., Visscher, Peter M. and Montgomery, Grant W. (2008). A genome-wide linkage scan for age at menarche in three populations of European descent. Journal of Clinical Endocrinology and Metabolism., 93 (10), 3965-3970. doi: 10.1210/jc.2007-2568

Keith, Jonathan M., McRae, Allan, Duffy, David, Mengersen, Kerrie and Visscher, Peter M. (2008). Calculation of IBD probabilities with dense SNP or sequence data. Genetic Epidemiology, 32 (6), 513-519. doi: 10.1002/gepi.20324

Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J.C., Davis, Oliver S.P., Wright, Margaret J., Starr, John M., de Geus, Eco J.C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Erratum: Testing replication of a 5-SNP set for general cognitive ability in six population samples (European Journal of Human Genetics (2008) 10.1038/ejhg.2008.100). European Journal of Human Genetics, 16 (8), 1025-1025. doi: 10.1038/ejhg.2008.124

Oldmeadow, Chris, Wood, Ian, Mengersen, Kerrie, Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2008). Investigation of the relationship between smoking and appendicitis in Australian twins. Annals of Epidemiology, 18 (8), 631-636. doi: 10.1016/j.annepidem.2008.04.004

Webbink, Dinand, Martin, Nicholas G. and Visscher, Peter M. (2008). Does teenage childbearing increase smoking, drinking and body size?. Journal of Health Economics, 27 (4), 888-903. doi: 10.1016/j.jhealeco.2008.02.005

Dolezal, M., Schwarzenbacher, H., Soller, M., Soelkner, J. and Visscher, P. M. (2008). Multiple-marker mapping for selective DNA pooling within large families. Journal of Dairy Science, 91 (7), 2864-2873. doi: 10.3168/jds.2007-0397

McRae, Allan F., Byrne, Enda M., Zhao, Zhen Zhen, Montgomery, Grant W. and Visscher, Peter M. (2008). Power and SNP tagging in whole mitochondrial genome association studies. Genome Research, 18 (6), 911-917. doi: 10.1101/gr.074872.107

Visscher, Peter M. (2008). Sizing up human height variation. Nature Genetics, 40 (5), 489-490. doi: 10.1038/ng0508-489

Edmonds, Caroline J., Isaacs, Elizabeth B., Visscher, Peter M., Rogers, Mary, Lanigan, Julie, Singhal, Atul, Lucas, Alan, Gringras, Paul, Denton, Jane and Deary, Ian J. (2008). Inspection time and cognitive abilities in twins aged 7 to 17 years: age-related changes, heritability and genetic covariance. Intelligence, 36 (3), 210-225. doi: 10.1016/j.intell.2007.05.004

Anderson, Carl A., Maclean, Alan, Dunnigan, Matthew G., Pelosi, Anthony J., Murray, Valerie, Mckee, Irene, McDonald, George, Burt, David W., Morrice, David R., Muir, Walter J., Visscher, Peter M. and Blackwood, Douglas H. R. (2008). A genome-wide linkage study in families with major depression and co-morbid unexplained swelling. American Journal of Medical Genetics Part B-Neuropsychiatric Genetics, 147 (3), 356-362. doi: 10.1002/ajmg.b.30615

Benyamin, Beben, Perola, Markus, Cornes, Belinda K., Madden, Pamela A. F., Palotie, Aarno, Nyholt, Dale R., Montgomery, Grant W., Peltonen, Leena, Martin, Nicholas G. and Visscher, Peter M. (2008). Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs. European Journal of Human Genetics, 16 (4), 516-524. doi: 10.1038/sj.ejhg.5201992

Nagamine, Yoshitaka, Nirasawa, Keijiro, Takahashi, Hideaki, Sasaki, Osamu, Ishii, Kazuo, Minezawa, Mitsuru, Oda, Senichi, Visscher, Peter M. and Furukawa, Tsutomu (2008). Estimation of the time of divergence between Japanese Mishima island cattle and other cattle populations using microsatellite DNA markers. Journal of Heredity, 99 (2), 202-207. doi: 10.1093/jhered/esm129

Visscher, Peter M., Andrew, Toby and Nyholt, Dale R. (2008). Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained. European Journal of Human Genetics, 16 (3), 387-390. doi: 10.1038/sj.ejhg.5201990

Avendano, S., Visscher, P. M. and Villanueva, B. (2008). Response to selection from using identified genes and quadratic indices in two-traits breeding goals. Spanish Journal of Agricultural Research, 6 (SPEC. ISS.), 88-97. doi: 10.5424/sjar/200806S1-377

Hill, William G., Goddard, Michael E. and Visscher, Peter M. (2008). Data and theory point to mainly additive genetic variance for complex traits. PLoS Genetics, 4 (2), e1000008. doi: 10.1371/journal.pgen.1000008

Gratten, J., Wilson, A. J., McRae, A. F., Beraldi, D., Visscher, P. M., Pemberton, J. M. and Slate, J. (2008). A localized negative genetic correlation constrains microevolution of coat color in wild sheep. Science, 319 (5861), 318-320. doi: 10.1126/science.1151182

Wray, Naomi R., Middeldorp, Christel M., Birley, Andrew J., Gordon, Scott D., Sullivan, Patrick F., Visscher, Peter M., Nyholt, Dale R, Willemsen, Gonneke, de Geus, Eco J.C., Slagboom, P. Eline, Montgomery, Grant W., Martin, Nicholas G. and Boomsma, Dorret I. (2008). Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands. Archives of General Psychiatry, 65 (6), 649-658. doi: 10.1001/archpsyc.65.6.649

Luciano, Michelle, Lind, Penelope A., Deary, Ian J., Payton, Antony, Posthuma, Danielle, Butcher, Lee M., Bochdanovits, Zoltan, Whalley, Lawrence J., Visscher, Peter M., Harris, Sarah E., Polderman, Tinca J. C., Davis, Oliver S. P., Wright, Margaret J., Starr, John M., de Geus, Eco J. C., Bates, Timothy C., Montgomery, Grant W., Boomsma, Dorret I., Martin, Nicholas G. and Plomin, Robert (2008). Testing replication of a 5-SNP set for general cognitive ability in six population samples. European Journal of Human Genetics, 16 (11), 1388-1395. doi: 10.1038/ejhg.2008.100

Wray, Naomi, Goddard, Michael E. and Visscher, Peter (2008). Prediction of individual genetic risk of complex disease. Current Opinion in Genetics and Development, 18 (3), 257-263. doi: 10.1016/j.gde.2008.07.006

Visscher, Peter, Hill, William G. and Wray, Naomi (2008). Heritability in the genomics era — concepts and misconceptions. Nature Reviews Genetics, 9 (4), 255-266. doi: 10.1038/nrg2322

Ayub, Muhammad, Irfan, Muhammad, Maclean, Alan, Naeem, Farooq, MacGregor, Stuart, Visscher, Peter M., Muir, Walter and Blackwood, Douglas (2008). Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages. Human Heredity, 66 (3), 190-198. doi: 10.1159/000135265

Macgregor, Stuart, Zhao, Zhen Zhen, Henders, Anjali, Martin, Nicholas G., Montgomery, Grant W. and Visscher, Peter M. (2008). Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays. Nucleic Acids Research, 36 (6) e35, 291-296. doi: 10.1093/nar/gkm1060

Deary, Ian J., Gow, Alan J., Taylor, Michelle D., Corley, Janie, Brett, Caroline, Wilson, Valerie, Campbell, Harry, Whalley, Lawrence J., Visscher, Peter M., Porteous, David J. and Starr, John M. (2007). The Lothian Birth Cohort 1936: A study to examine influences on cognitive ageing from age 11 to age 70 and beyond. BMC Geriatrics, 7 (1) 28. doi: 10.1186/1471-2318-7-28

Thornblad, Tobias A., Elliott, Kate S., Jowett, Jeremy and Visscher, Peter M. (2007). Prioritization of positional candidate genes using multiple web-based software tools. Twin Research and Human Genetics, 10 (6), 861-870. doi: 10.1375/twin.10.6.861

Visscher, Peter M. and Duffy, David L. (2007). The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits (vol 30, pg 30, 2006). Genetic Epidemiology, 31 (7), 801-801. doi: 10.1002/gepi.20268

Visscher, Peter M., Macgregor, Stuart, Benyamin, Beben, Zhu, Gu, Gordon, Scott, Medland, Sarah, Hill, William G., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Liu, Yao-Zhong, Deng, Hong-Wen, Montgomery, Grant W. and Martin, Nicholas G. (2007). Genome partitioning of genetic variation for height from 11,214 sibling pairs. American Journal of Human Genetics, 81 (5), 1104-1110. doi: 10.1086/522934

Benyamin, B., Sorensen, T. I. A., Schousboe, K., Fenger, M., Visscher, P. M. and Kyvik, K. O. (2007). Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome?. Diabetologia, 50 (9), 1880-1888. doi: 10.1007/s00125-007-0758-1

Anderson, Carl A., Duffy, David L., Martin, Nicholas G. and Visscher, Peter M. (2007). Estimation of variance components for age at menarche in twin families. Behavior Genetics, 37 (5), 668-677. doi: 10.1007/s10519-007-9163-2

Webbink, Dinand, Hay, David and Visscher, Peter M. (2007). Does sharing the same class in school improve cognitive abilities of twins?. Twin Research and Human Genetics, 10 (4), 573-580. doi: 10.1375/twin.10.4.573

Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G., Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R., Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Karre, Kyvik, Kirsten Ohm, Sorensen, Thorkild I., Pedersen, Nancy L., Magnusson, Patrik K., Spector, Tim D., Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena and GenomEUtwin Project (2007). Combined genome scans for body stature in 6,602 European twins: Evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick, Visscher, Peter M., Montgomery, Grant W., Benyamin, Beben, Harris, Jennifer R, Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Kaare, Ohm Kyvik, Kirsten, Sørensen, Thorkild I. A., Pedersen, Nancy L., Magnusson, Patrik K.E., Spector, Tim D, Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno and Peltonen, Leena (2007). Combined genome scans for body stature in 6602 European twins: evidence for common Caucasian loci. PLoS Genetics, 3 (6), 1019-1028. doi: 10.1371/journal.pgen.0030097

Beraldi, Dario, McRae, Allan F., Gratten, Jacob, Slate, Jon, Visscher, Peter M. and Pemberton, Josephine M. (2007). Mapping quantitative trait loci underlying fitness-related traits in a free-living sheep population. Evolution, 61 (6), 1403-1416. doi: 10.1111/j.1558-5646.2007.00106.x

Gratten, J., Beraldi, D., Lowder, B. V., McRae, A. F., Visscher, P. M., Pemberton, J. M. and Slate, J. (2007). Compelling evidence that a single nucleotide substitution in TYRP1 is responsible for coat-colour polymorphism in a free-living population of Soay sheep. Proceedings of the Royal Society of London: Biological Sciences, 274 (1610), 619-626. doi: 10.1098/rspb.2006.3762

Gordon, Scott and Visscher, Peter M. (2007). Residual linkage: why do linkage peaks not disappear after an association study?. Human Genetics, 121 (1), 77-82. doi: 10.1007/s00439-006-0278-y

McRae, A. F., Matigian, N. A., Vadlamudi, L., Mulley, J. C., Mowry, B., Martin, N. G., Berkovic, S. F., Hayward, N. K. and Visscher, P. M. (2007). Replicated effects of sex and genotype on gene expression in human lymphoblastoid cell lines. Human Molecular Genetics, 16 (4), 364-373. doi: 10.1093/hmg/ddl456

Wray, N. R., Birley, A. J., Sullivan, P. F., Visscher, P. M. and Martin, N. G. (2007). Genetic and phenotypic stability of measures of neuroticism over 22 years. Twin Research & Human Genetics, 10 (5), 695-702. doi: 10.1375/twin.10.5.695

Benyamin, Beben, Martin, Ian C. A., Cheung, Carol C., Buckley, Michael F., Thomson, Peter C., Visscher, Peter M. and Moran, Chris (2007). Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: regression v. maximum likelihood. Australian Journal of Experimental Agriculture, 47 (6), 677-682. doi: 10.1071/EA06123

Wray, Naomi R., Goddard, Michael E. and Visscher, Peter M. (2007). Prediction of individual genetic risk to disease from genome-wide association studies. Genome Research, 17 (10), 1520-1528. doi: 10.1101/gr.6665407

Tenesa, Albert, Navarro, Pau, Hayes, Ben J., Duffy, David L., Clarke, Geraldine M., Goddard, Mike E. and Visscher, Peter M. (2007). Recent human effective population size estimated from linkage disequilibrium. Genome Research, 17 (4), 520-526. doi: 10.1101/gr.6023607

Wood, I. A., Visscher, P. M. and Mengersen, K. L. (2007). Classification based upon gene expression data: bias and precision of error rates. Bioinformatics, 23 (11), 1363-1370. doi: 10.1093/bioinformatics/btm117

Beraldi, Dario, McRae, Allan F., Gratten, Jacob, Slate, Jon, Visscher, Peter M., Pemberton, Josephine M. and Pilkington, Jill G. (2007). Quantitative trait loci (QTL) mapping of resistance to strongyles and coccidia in the free-living Soay sheep (Ovis aries). Journal of Parasitology, 37 (1), 121-129. doi: 10.1016/j.ijpara.2006.09.007

Visscher, P. M. (2007). Variation of estimates of SNP and haplotype diversity and linkage disequilibrium in samples from the same population due to experimental and evolutionary sample size. Annals of Human Genetics, 71 (1), 119-126. doi: 10.1111/j.1469-1809.2006.00305.x

Mcgee, TR (2007). Introduction to social research: Quantitative and qualitative approaches. Journal of Sociology, 43 (3), 324-326. doi: 10.1177/14407833070110030604

Ivkovic, Vladimir, Vitart, Veronique, Rudan, Igor, Janicijevic, Branka, Smolej-Narancic, Nina, Skaric-Juric, Tatjana, Barbalic, Maja, Polasek, Ozren, Kolcic, Ivana, Biloglav, Zrinka, Visscher, Peter M., Hayward, Caroline, Hastie, Nicholas D., Anderson, Niall, Campbell, Harry, Wright, Alan F., Rudan, Pavao and Deary, Ian J. (2007). The Eysenck personality factors: Psychometric structure, reliability, heritability and phenotypic and genetic correlations with psychological distress in an isolated Croatian population. Personality and Individual Differences, 42 (1), 123-133. doi: 10.1016/j.paid.2006.06.025

Navarro, P., Visscher, P. M., Chatziplis, D., Koerhuis, A. N. M. and Haley, C. S. (2006). Segregation analysis of blood oxygen saturation in broilers suggests a major gene influence on ascites. British Poultry Science, 47 (6), 671-684. doi: 10.1080/00071660601077931

Navarro, P., Visscher, P. M., Chatziplis, D., Koerhuis, A. N. M. and Haley, C. S. (2006). Genetic parameters for blood oxygen saturation, body weight and breast conformation in 4 meat-type chicken lines. British Poultry Science, 47 (6), 659-670. doi: 10.1080/00071660601042372

Benyamin, Beben, Deary, Ian J. and Visscher, Peter M. (2006). Precision and bias of a normal finite mixture distribution model to analyze twin data when zygosity is unknown: simulations and application to IQ phenotypes on a large sample of twin pairs. Behavior Genetics, 36 (6), 935-946. doi: 10.1007/s10519-006-9086-3

Visscher, Peter M. (2006). A note on the asymptotic distribution of likelihood ratio tests to test variance components. Twin Research and Human Genetics, 9 (4), 490-495. doi: 10.1375/183242706778024928

Webbink, Dinand, Roeleveld, Jaap and Visscher, Peter M. (2006). Identification of twin pairs from large population-based samples. Twin Research and Human Genetics, 9 (4), 496-500. doi: 10.1375/183242706778024892

Ferreira, Manuel A. R., Visscher, Peter M., Martin, Nicholas G. and Duffy, David L. (2006). A simple method to localise pleiotropic susceptibility loci using univariate linkage analyses of correlated traits. European Journal of Human Genetics, 14 (8), 953-962. doi: 10.1038/sj.ejhg.5201646

Visscher, Peter M. and Hill, William G. (2006). Estimation of recombination rate and detection of recombination hotspots from dense single-nucleotide polymorphism trio data. Genetics, 173 (4), 2415-2417. doi: 10.1534/genetics.106.056531

Beraldi, Dario, McRae, Allan F., Gratten, Jacob, Slate, Jon, Visscher, Peter M. and Pemberton, Josephine M. (2006). Development of a linkage map and mapping of phenotypic polymorphisms in a free-living population of Soay sheep (Ovis aries). Genetics, 173 (3), 1521-1537. doi: 10.1534/genetics.106.057141

Anderson, Carl A., McRae, Allan F. and Visscher, Peter M. (2006). A simple linear regression method for quantitative trait loci linkage analysis with censored observations. Genetics, 173 (3), 1735-1745. doi: 10.1534/genetics.106.055921

Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A. R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. Plos Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

Visscher, Peter M., Medland, Sarah E., Ferreira, Manuel A.R., Morley, Katherine I., Zhu, Gu, Cornes, Belinda K., Montgomery, Grant W. and Martin, Nicholas G. (2006). Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings. PLoS Genetics, 2 (3), 316-325. doi: 10.1371/journal.pgen.0020041

Macgregor, S, Knott, SA and Visscher, PM (2006). False disease region identification from identity-by-descent haplotype sharing in the presence of phenocopies. Twin Research and Human Genetics, 9 (1), 9-16. doi: 10.1375/183242706776403000

Visscher, PM and Duffy, DL (2006). The value of relatives with phenotypes but missing genotypes in association studies for quantitative traits. Genetic Epidemiology, 30 (1), 30-36. doi: 10.1002/gepi.20124

Macgregor, Stuart, Cornes, Belinda K., Martin, Nicholas G. and Visscher, Peter M. (2006). Bias, precision and heritability of self-reported and clinically measured height in Australian twins. Human Genetics, 120 (4), 571-580. doi: 10.1007/s00439-006-0240-z

Macgregor, S., Visscher, P. M. and Montgomery, G. (2006). Analysis of pooled DNA samples on high density arrays without prior knowledge of differential hybridization rates. Nucleic Acids Research, 34 (7) e55. doi: 10.1093/nar/gkl136

Posthuma, D., Visscher, P. M., Willemsen, G., Zhu, G., Martin, N. G., Slagboom, P. E., de Geus, E. J. C. and Boomsma, D. I. (2006). Replicated linkage for eye color on 15q using comparative ratings of sibling pairs. Behavior Genetics, 36 (1), 12-17. doi: 10.1007/s10519-005-9007-x

Montgomery, Grant W., Zhu, Gu, Hottenga, Jouke J., Duffy, David L., Heath, Andrew C., Boomsma, Dorret I., Martin, Nicholas G. and Visscher, Peter M. (2006). HLA and Genomewide Allele Sharing in Dizygotic Twins. American Journal of Human Genetics, 79 (6), 1052-1058. doi: 10.1086/510136

Ferreira, MAR, O'Gorman, L, Le Souef, P, Burton, PR, Toelle, BG, Robertson, CF, Visscher, PM, Martin, NG and Duffy, DL (2005). Robust estimation of experimentwise P values applied to a genome scan of multiple asthma traits identifies a new region of significant linkage on chromosome 20q13. American Journal of Human Genetics, 77 (6), 1075-1085. doi: 10.1086/497997

Macgregor, S, Knott, SA, White, and Visscher, PM (2005). Quantitative trait locus analysis of longitudinal quantitative trait data in complex pedigrees. Genetics, 171 (3), 1365-1376. doi: 10.1534/genetics.105.043828

Benyamin, Beben, Wilson, Valerie, Whalley, Lawrence J., Visscher, Peter M. and Deary, Ian J. (2005). Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish mental surveys of 1932 and 1947. Behavior Genetics, 35 (5), 525-534. doi: 10.1007/s10519-005-3556-x

Thomas, Stuart, Porteous, David and Visscher, Peter M. (2005). Erratum: (Genetic Epidemiology (2004) 26 (116-124)). Genetic Epidemiology, 29 (2). doi: 10.1002/gepi.20083

McRae, AF, Pemberton, JM and Visscher, PM (2005). Modeling linkage disequilibrium in natural populations: The example of the Soay sheep population of St. Kilda, Scotland. Genetics, 171 (1), 251-258. doi: 10.1534/genetics.105.040972

Navarro, P, Visscher, PM, Knott, SA, Burt, DW, Hocking, PM and Haley, CS (2005). Mapping of quantitative trait loci affecting organ weights and blood variables in a broiler layer cross. British Poultry Science, 46 (4), 430-442. doi: 10.1080/00071660500158055

Charlesworth, B, Keightley, P and Visscher, P (2005). Introduction: Population genetics, quantitative genetics and animal improvement: papers in honour of William (Bill) Hill. Philosophical Transactions of the Royal Society B-Biological Sciences, 360 (1459), 1365-1366. doi: 10.1098/rstb.2005.1678

Uimari, P, Kontkanen, O, Visscher, PM, Pirskanen, M, Fuentes, R and Salonen, JT (2005). Genome-wide linkage disequilibrium from 100,000 SNPs in the East Finland founder population. Twin Research and Human Genetics, 8 (3), 185-197. doi: 10.1375/1832427054253086

Wall, E, Visscher, PM, Hospital, F and Woolliams, JA (2005). Genomic contributions in livestock gene introgression programmes. Genetics Selection Evolution, 37 (3), 291-313. doi: 10.1051/gse:2005003

McRae, AF, Bishop, SC, Walling, GA, Wilson, AD and Visscher, PM (2005). Mapping of multiple quantitative trait loci for growth and carcass traits in a complex commercial sheep pedigree. Animal Science, 80 (8), 135-141. doi: 10.1079/ASC41040135

Tenesa, A, Visscher, PM, Carothers, AD and Knott, SA (2005). Mapping quantitative trait loci using linkage disequilibrium: Marker- versus trait-based methods. Behavior Genetics, 35 (2), 219-228. doi: 10.1007/s10519-004-0811-5

Montgomery, GW, Campbell, MJ, Dickson, P, Herbert, S, Siemering, K, Ewen-White, KR, Visscher, PM and Martin, NG (2005). Estimation of the rate of SNP genotyping errors from DNA extracted from different tissues. Twin Research and Human Genetics, 8 (4), 346-352. doi: 10.1375/1832427054936673

Visscher, Peter M., Benyamin, Beben and White, Ian (2004). The use of linear mixed models to estimate variance components from data on twin pairs by maximum likelihood. Twin Research, 7 (6), 670-674. doi: 10.1375/1369052042663742

Macgregor, S, Visscher, PM, Knott, SA, Thomson, P, Porteous, DJ, Millar, JK, Devon, RS, Blackwood, D and Muir, WJ (2004). A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Molecular Psychiatry, 9 (12), 1083-1090. doi: 10.1038/sj.mp.4001544

Visscher, Peter M. (2004). Power of the classical twin design revisited. Twin Research, 7 (5), 505-512. doi: 10.1375/1369052042335250

Visscher, Peter M. and Wray, Naomi R. (2004). Conventional multipoint nonparametric linkage analysis is not necessarily inherently biased. American Journal of Human Genetics, 75 (4), 718-720. doi: 10.1086/424755

Walling, GA, Visscher, PM, Wilson, AD, McTeir, BL, Simm, G and Bishop, SC (2004). Mapping of quantitative trait loci for growth and carcass traits in commercial sheep populations. Journal of Animal Science, 82 (8), 2234-2245.

Yu, XJ, Knott, SA and Visscher, PM (2004). Theoretical and empirical power of regression and maximum-likelihood methods to map quantitative trait loci in general pedigrees. American Journal of Human Genetics, 75 (1), 17-26. doi: 10.1086/421845

Visscher, PM and Goddard, ME (2004). Prediction of the confidence interval of quantitative trait loci location. Behavior Genetics, 34 (4), 477-482. doi: 10.1023/B:BEGE.0000023652.93162.e8

Deary, IJ, Whiteman, MC, Pattie, A, Starr, JM, Hayward, C, Wright, AF, Visscher, PM, Tynan, MC and Whalley, LJ (2004). Apolipoprotein E gene variability and cognitive functions at age 79: A follow-up of the Scottish Mental Survey of 1932. Psychology and Aging, 19 (2), 367-371. doi: 10.1037/0882-7974.19.2.367

Nsengimana, J, Baret, P, Haley, CS and Visscher, PM (2004). Linkage disequilibrium in the domesticated pig. Genetics, 166 (3), 1395-1404. doi: 10.1534/genetics.166.3.1395

Thomas, S, Porteous, D and Visscher, PM (2004). Power of direct vs. indirect haplotyping in association studies. Genetic Epidemiology, 26 (2), 116-124. doi: 10.1002/gepi.10300

Nagamine, Y, Visscher, PM and Haley, CS (2004). QTL detection and allelic effects for growth and fat traits in outbred pig populations. Genetics Selection Evolution, 36 (1), 83-96. doi: 10.1051/gse:2003052

Schousboe, K, Visscher, PM, Erbas, B, Kyvik, KO, Hopper, JL, Henriksen, JE, Heitmann, BL and Sorensen, TIA (2004). Twin study of genetic and environmental influences on adult body size, shape, and composition. International Journal of Obesity, 28 (1), 39-48. doi: 10.1038/sj.ijo.0802524

Tenesa, A, Wright, AF, Knott, SA, Carothers, AD, Hayward, C, Angius, A, Persico, , Maestrale, G, Hastie, ND, Pirastu, M and Visscher, PM (2004). Extent of linkage disequilibrium in a Sardinian sub-isolate: sampling and methodological considerations. Human Molecular Genetics, 13 (1), 25-33. doi: 10.1093/hmg/ddh001

Macgregor, Stuart, Knott, Sara A, White, Ian, Visscher, Peter M and Framingham Heart Study, (2003). Longitudinal variance-components analysis of the Framingham Heart Study data. BMC genetics, 4 Suppl 1 S22, S22. doi: 10.1186/1471-2156-4-S1-S22

Tenesa, A, Knott, SA, Carothers, AD and Visscher, PM (2003). Power of linkage disequilibrium mapping to detect a quantitative trait locus (QTL) in selected samples of unrelated individuals. Annals of Human Genetics, 67 (6), 557-566. doi: 10.1046/j.1529-8817.2003.00058.x

Schousboe, K, Visscher, PM, Henriksen, JE, Hopper, JL, Sorensen, TIA and Kyvik, KO (2003). Twin study of genetic and environmental influences on glucose tolerance and indices of insulin sensitivity and secretion. Diabetologia, 46 (9), 1276-1283. doi: 10.1007/s00125-003-1165-x

Visscher, PM, Tynan, M, Whiteman, MC, Pattie, A, White, , Hayward, C, Wright, AF, Starr, JM, Whalley, LJ and Deary, IJ (2003). Lack of association between polymorphisms in angiotensin-converting-enzyme and methylenetetrahydrofolate reductase genes and normal cognitive ageing in humans. Neuroscience Letters, 347 (3), 175-178. doi: 10.1016/S0304-3940(03)00691-8

Segurado, R, Detera-Wadleigh, SD, Levinson, DF, Lewis, CM, Gill, M, Nurnberg, JI, Craddock, N, DePaulo, , Baron, M, Gershon, ES, Ekholm, J, Cichon, S, Turecki, G, Claes, S, Kelsoe, , Schofield, PR, Badenhop, RF, Morissette, J, Coon, H, Blackwood, D, McInnes, LA, Foroud, T, Edenberg, HJ, Reich, T, Rice, JP, Goate, A, McInnis, MG, McMahon, FJ, Badner, JA ... Akarsu, N (2003). Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. American Journal of Human Genetics, 73 (1), 49-62. doi: 10.1086/376547

Hernandez-Sanchez, J, Visscher, P, Plastow, G and Haley, C (2003). Candidate gene analysis for quantitative traits using the transmission disequilibrium test: The example of the melanocortin 4-receptor in pigs. Genetics, 164 (2), 637-644.

Visscher, PM and Le Hellard, S (2003). Simple method to analyze SNP-based association studies using DNA pools. Genetic Epidemiology, 24 (4), 291-296. doi: 10.1002/gepi.10240

Hayes, Ben J., Visscher, Peter M., McPartlan, Helen C. and Goddard, Mike E. (2003). Novel multilocus measure of linkage disequilibrium to estimate past effective population size. Genome Research, 13 (4), 635-643. doi: 10.1101/gr.387103

Argente, MJ, Blasco, A, Ortega, JA, Haley, CS and Visscher, PM (2003). Analyses for the presence of a major gene affecting uterine capacity in unilaterally ovariectomized rabbits. Genetics, 163 (3), 1061-1068.

Tenesa, A, Knott, SA, Ward, D, Smith, D, Williams, JL and Visscher, PM (2003). Estimation of linkage disequilibrium in a sample of the United Kingdom dairy cattle population using unphased genotypes. Journal of Animal Science, 81 (3), 617-623.

Porteous, DJ, Evans, KL, Millar, JK, Pickard, BS, Thomson, PA, James, R, MacGregor, S, Wray, NR, Visscher, PM, Muir, WJ and Blackwood, DH (2003). Genetics of schizophrenia and bipolar affective disorder: Strategies to identify candidate. Cold Spring Harbor Symposia On Quantitative Biology, 68, 383-394. doi: 10.1101/sqb.2003.68.383

Macgregor, S, Visscher, PM, Knott, S, Porteous, D, Muir, W, Millar, K and Blackwood, D (2002). Is schizophrenia linked to chromosome 1q?. Science, 298 (5602), 2277-2277.

Slate, J, Visscher, PM, MacGregor, S, Stevens, D, Tate, ML and Pemberton, JM (2002). A genome scan for quantitative trait loci in a wild population of red deer (Cervus elaphus). Genetics, 162 (4), 1863-1873.

Nagamine, Y, Knott, SA, Visscher, PM and Haley, CS (2002). Simple deterministic identity-by-descent coefficients and estimation of QTL allelic effects in full and half sibs. Genetical Research, 80 (3), 237-243. doi: 10.1017/S0016672302005918

Visscher, Peter (2002). Erratum: Increased rate of twins among affected sib pairs (American Journal of Human Genetics (October 2002) 71 (995-996)). American Journal of Human Genetics, 71 (5). doi: 10.1086/344211

Visscher, PM, Woolliams, JA, Smith, D and Williams, JL (2002). Estimation of pedigree errors in the UK dairy population using microsatellite markers and the impact on selection. Journal of Dairy Science, 85 (9), 2368-2375. doi: 10.3168/jds.S0022-0302(02)74317-8

Le Hellard, Stéphanie, Ballereau, Stéphane J, Visscher, Peter M, Torrance, Helen S, Pinson, Jeni, Morris, Stewart W, Thomson, Marian L, Semple, Colin A M, Muir, Walter J, Blackwood, Douglas H R, Porteous, David J and Evans, Kathryn L (2002). SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. Nucleic acids research, 30 (15)

Le Hellard, Stéphanie, Ballereau, Stéphane J, Visscher, Peter M, Torrance, Helen S, Pinson, Jeni, Morris, Stewart W, Thomson, Marian L, Semple, Colin A M, Muir, Walter J, Blackwood, Douglas H R, Porteous, David J and Evans, Kathryn L (2002). SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. Nucleic acids research, 30 (15). doi: 10.1093/nar/gnf070

Yazdi, MH, Visscher, PM, Ducrocq, and Thompson, R (2002). Heritability, reliability of genetic evaluations and response to selection in proportional hazard models. Journal of Dairy Science, 85 (6), 1563-1577. doi: 10.3168/jds.S0022-0302(02)74226-4

Villanueva, B, Verspoor, E and Visscher, PM (2002). Parental assignment in fish using microsatellite genetic markers with finite numbers of parents and offspring. Animal Genetics, 33 (1), 33-41. doi: 10.1046/j.1365-2052.2002.00804.x

Seaton, G, Haley, CS, Knott, SA, Kearsey, M and Visscher, PM (2002). QTL Express: mapping quantitative trait loci in of simple and complex pedigrees. Bioinformatics, 18 (2), 339-340. doi: 10.1093/bioinformatics/18.2.339

Walling, GA, Haley, CS, Perez-Enciso, M, Thompson, R and Visscher, PM (2002). On the mapping of quantitative trait loci at marker and non-marker locations. Genetical Research, 79 (1), 97-106. doi: 10.1017/S0016672301005420

Visscher, P. M. and Hopper, J. L. (2002). Erratum: Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin data (Annals of Human Genetics (2001) vol. 65 (6)). Annals of Human Genetics, 66 (1) S0003480002009417, ii-ii. doi: 10.1017/S0003480002009417

Balding, David J., Carothers, Andrew D., Marchini, Jonathan L., Cardon, Lon R., Vetta, Atam, Griffiths, Bob, Weir, B. S., Hill, W. G., Goldstein, Darlene, Strimmer, Korbinian, Myers, Simon, Beaumont, Mark A., Glasbey, C. A., Mayer, C. D., Richardson, Sylvia, Marshall, Clare, Durrett, Richard, Nielsen, Rasmus, Visscher, P. M., Knott, S. A., Haley, C. S., Ball, Roderick D., Hackett, Christine A., Holmes, Susan, Husmeier, Dirk, Jansen, Ritsert C., Ter Braak, Cajo J.F., Maliepaard, Chris A., Boer, Martin P. ... Gabrielson, Edward (2002). Discussion on the meeting on 'statistical modelling and analysis of genetic data'. Journal of the Royal Statistical Society. Series B: Statistical Methodology, 64 (4), 737-775. doi: 10.1111/1467-9868.00359

Visscher, Peter M (2002). Increased rate of twins among affected sib pairs. American journal of human genetics, 71 (4). doi: 10.1086/342991

Balding, DJ, Carothers, AD, Marchini, JL, Cardon, LR, Vetta, A, Griffiths, B, Weir, BS, Hill, WG, Goldstein, D, Strimmer, K, Myers, S, Beaumont, MA, Glasbey, CA, Mayer, CD, Richardson, S, Marshall, C, Durrett, R, Nielsen, R, Visscher, PM, Knott, SA, Haley, CS, Ball, RD, Hackett, CA, Holmes, S, Husmeier, D, Jansen, RC, ter Braak, CJF, Maliepaard, CA, Boer, MP ... Gabrielson, E (2002). Discussion on the meeting on 'Statistical modelling and analysis of genetic data'. Journal of the Royal Statistical Society Series B-Statistical Methodology, 64, 737-775.

Visscher, PM and Hopper, JL (2001). Power of regression and maximum likelihood methods to map QTL from sib-pair and DZ twin data. Annals of Human Genetics, 65 (6), 583-601. doi: 10.1046/j.1469-1809.2001.6560583.x

Visscher, PM, Yazdi, MH, Jackson, AD, Schalling, M, Lindblad, K, Yuan, QP, Porteous, D, Muir, WJ and Blackwood, DHR (2001). Genetic survival analysis of age-at-onset of bipolar disorder: evidence for anticipation or cohort effect in families. Psychiatric Genetics, 11 (3), 129-137. doi: 10.1097/00041444-200109000-00004

Blackwood, Douglas H.R., Visscher, Peter M. and Muir, Walter J. (2001). Genetic studies of bipolar affective disorder in large families. The British journal of psychiatry : the journal of mental science, 178 (Suppl 41), S134-S136. doi: 10.1192/bjp.178.41.s134

Visscher, P and Haley, C (2001). True and false positive peaks in genomewide scans: The long and the short of it. Genetic Epidemiology, 20 (4), 409-414. doi: 10.1002/gepi.1010

Roughsedge, T, Brotherstone, S and Visscher, PM (2001). Bias and power in the estimation of a maternal family variance component in the presence of incomplete and incorrect pedigree information. Journal of Dairy Science, 84 (4), 944-950. doi: 10.3168/jds.S0022-0302(01)74552-3

Visscher, P.M. (2001). erratum: A viable herd of genetically uniform cattle. Nature, 410 (6824), 36-36. doi: 10.1038/35065164

Visscher, PM, Smith, D, Hall, SJG and Williams, JA (2001). A viable herd of genetically uniform cattle - Deleterious alleles seem to have been purged in a feral strain of inbred cows.. Nature, 409 (6818), 303-303. doi: 10.1038/35053160

Blackwood, D. H., Visscher, P. M. and Muir, W. J. (2001). Genetic studies of bipolar affective disorder in large families. British Journal of Psychiatry, 178 (Suppl. 141), s134-s136.

George, AW, Visscher, PM and Haley, CS (2000). Mapping quantitative trait loci in complex pedigrees: A two-step variance component approach. Genetics, 156 (4), 2081-2092.

Visscher, P., Yazdi, H., Jackson, A., Schalling, M., Porteous, D., Muir, W. and Blackwood, D. (2000). Genetic survival analysis of age-at-onset of bipolar disorder: Evidence for anticipation and a year-of-birth effect in families. American Journal of Medical Genetics - Neuropsychiatric Genetics, 96 (4)

Roughsedge, T, Visscher, PM and Brotherstone, S (2000). Effects of cow families on production traits in dairy cattle. Animal Science, 71 (1), 49-57. doi: 10.1017/S1357729800054886

Walling, G. A., Visscher, P. M., Andersson, L., Rothschild, M. F., Wang, L. Z., Moser, G., Groenen, M. A. M., Bidanel, J. P., Cepica, S., Archibald, A. L., Geldermann, H., de Koning, D. J., Milan, D. and Haley, C. S. (2000). Combined analyses of data from quantitative trait loci mapping studies: Chromosome 4 effects on porcine growth and fatness. Genetics, 155 (3), 1369-1378.

Roughsedge, T, Brotherstone, S and Visscher, PM (2000). Effects of cow families on type traits in dairy cattle. Animal Science, 70 (3), 391-398. doi: 10.1017/S1357729800051730

Lubbers, R, Brotherstone, S, Ducrocq, VP and Visscher, PM (2000). A comparison of a linear and proportional hazards approach to analyse discrete longevity data in dairy cows. Animal Science, 70 (2), 197-206. doi: 10.1017/S1357729800054667

Visscher, P, Whittaker, J and Jansen, R (2000). Mapping multiple QTL of different effects: comparison of a simple sequential testing strategy and multiple QTL mapping. Molecular Breeding, 6 (1), 11-24. doi: 10.1023/A:1009612308004

Slate, J, Pemberton, JM and Visscher, PM (1999). Power to detect QTL in a free-living polygynous population. Heredity, 83 (3), 327-336. doi: 10.1038/sj.hdy.6885830

Visscher, PM (1999). Speed congenics: accelerated genome recovery using genetic markers. Genetical Research, 74 (1), 81-85. doi: 10.1017/S0016672399003857

Roughsedge, T, Brotherstone, S and Visscher, PM (1999). Quantifying genetic contributions to a dairy cattle population using pedigree analysis. Livestock Production Science, 60 (2-3), 359-369. doi: 10.1016/S0301-6226(99)00106-2

Visscher, PM, Haley, CS, Heath, SC, Muir, WJ and Blackwood, DHR (1999). Detecting QTLs for uni- and bipolar disorder using a variance component method. Psychiatric Genetics, 9 (2), 75-84. doi: 10.1097/00041444-199906000-00005

Roughsedge, T, Brotherstone, S and Visscher, PM (1999). Estimation of variance of maternal lineage effects at the Langhill dairy herd. Animal Science, 68 (1), 79-86.

Visscher, PM and Haley, CS (1999). On the efficiency of marker-assisted introgression. Animal Science, 68 (1), 59-68.

Walling, GA, Archibald, AL, Cattermole, JA, Downing, AC, Finlayson, HA, Nicholson, D, Visscher, PM, Walker, CA and Haley, CS (1998). Mapping of quantitative trait loci on porcine chromosome 4. Animal Genetics, 29 (6), 415-424. doi: 10.1046/j.1365-2052.1998.296360.x

Visscher, P. M., Haley, C. S., Heath, S. C., Muir, W. J. and Blackwood, D. H.R. (1998). Detecting QTLS for uni and bipolar disorder using a variance component method. American Journal of Medical Genetics - Neuropsychiatric Genetics, 81 (6)

Lebreton, CH, Visscher, PM, Haley, CS, Semikhodskii, A and Quarrie, SA (1998). A nonparametric bootstrap method for testing close linkage vs. pleiotrophy of coincident quantitative trait loci. Genetics, 150 (2), 931-943.

de Koning, DJ, Visscher, PM, Knott, SA and Haley, CS (1998). A strategy for QTL detection in half-sib populations. Animal Science, 67 (2), 257-268. doi: 10.1017/S1357729800010018

Baret, PV, Knott, SA and Visscher, PM (1998). On the use of linear regression and maximum likelihood for QTL mapping in half-sib designs. Genetical Research, 72 (2), 149-158. doi: 10.1017/S0016672398003450

Visscher, PM and Haley, CS (1998). Power of a chromosomal test to detect genetic variation using genetic markers. Heredity, 81 (3), 317-326. doi: 10.1046/j.1365-2540.1998.00398.x

Haley, CS and Visscher, PM (1998). Strategies to utilize marker-quantitative trait loci associations. Journal of Dairy Science, 81, 85-97. doi: 10.3168/jds.S0022-0302(98)70157-2

Visscher, P M (1998). On the sampling variance of intraclass correlations and genetic correlations. Genetics, 149 (3), 1605-1614.

Visscher, PM (1998). On the sampling variance of intraclass correlations and genetic correlations. Genetics, 149 (3), 1605-1614.

Walling, GA, Visscher, PM and Haley, CS (1998). A comparison of bootstrap methods to construct confidence intervals in QTL mapping. Genetical Research, 71 (2), 171-180. doi: 10.1017/S0016672398003164

Lebreton, CM and Visscher, PM (1998). Empirical nonparametric bootstrap strategies in quantitative trait loci mapping: Conditioning on the genetic model. Genetics, 148 (1), 525-535.

vanHeelsum, AM, Visscher, PM and Haley, CS (1997). Marker-assisted introgression using non-unique marker alleles .1. Selection on the presence of linked marker alleles. Animal Genetics, 28 (3), 181-187. doi: 10.1111/j.1365-2052.1997.00112.x

vanHeelsum, AM, Haley, CS and Visscher, PM (1997). Marker-assisted introgression using non-unique marker alleles .2. Selection on probability of presence of the introgressed allele. Animal Genetics, 28 (3), 188-194. doi: 10.1111/j.1365-2052.1997.00113.x

Visscher, PM, Haley, CS and Thompson, R (1996). Marker-assisted introgression in backcross breeding programs. Genetics, 144 (4), 1923-1932.

Visscher, PM and Haley, CS (1996). Detection of putative quantitative trait loci in line crosses under infinitesimal genetic models. Theoretical and Applied Genetics, 93 (5-6), 691-702. doi: 10.1007/BF00224064

Visscher, PM, Haley, CS and Knott, SA (1996). Mapping QTLs for binary traits in backcross and F-2 populations. Genetical Research, 68 (1), 55-63. doi: 10.1017/S0016672300033887

Whittaker, JC, Thompson, R and Visscher, PM (1996). On the mapping of QTL by regression of phenotype on marker-type. Heredity, 77 (1), 23-32. doi: 10.1038/hdy.1996.104

Bowman, PJ, Visscher, PM and Goddard, ME (1996). Customized selection indices for dairy bulls in Australia. Animal Science, 62 (3), 393-403. doi: 10.1017/S1357729800014946

Visscher, PM, Thompson, R and Haley, CS (1996). Confidence intervals in QTL mapping by bootstrapping. Genetics, 143 (2), 1013-1020.

Visscher, PM (1996). Proportion of the variation in genetic composition in backcrossing programs explained by genetic markers. Journal of Heredity, 87 (2), 136-138. doi: 10.1093/oxfordjournals.jhered.a022969

Visscher, PM and Thompson, R (1995). Haplotype frequencies of linked loci in backcross populations derived from inbred lines. Heredity, 75 (6), 644-649. doi: 10.1038/hdy.1995.184

VISSCHER, PM and GODDARD, ME (1995). GENETIC ANALYSES OF PROFIT FOR AUSTRALIAN DAIRY-CATTLE. Animal Science, 61 (1), 9-18. doi: 10.1017/S1357729800013461

VISSCHER, PM and GODDARD, ME (1995). GENETIC-PARAMETERS FOR MILK-YIELD, SURVIVAL WORKABILITY, AND TYPE TRAITS FOR AUSTRALIAN DAIRY-CATTLE. Journal of Dairy Science, 78 (1), 205-220. doi: 10.3168/jds.S0022-0302(95)76630-9

VISSCHER, PM, BOWMAN, PJ and GODDARD, ME (1994). BREEDING OBJECTIVES FOR PASTURE BASED DAIRY PRODUCTION SYSTEMS. Livestock Production Science, 40 (2), 123-137. doi: 10.1016/0301-6226(94)90042-6

VISSCHER, PM and THOMPSON, R (1992). COMPARISONS BETWEEN GENETIC VARIANCES ESTIMATED FROM DIFFERENT TYPES OF RELATIVES IN DAIRY-CATTLE. Animal Production, 55 (3), 315-320. doi: 10.1017/S0003356100021000

VISSCHER, PM and HILL, WG (1992). HETEROGENEITY OF VARIANCE AND DAIRY-CATTLE BREEDING. Animal Production, 55 (3), 321-329. doi: 10.1017/S0003356100021012

VISSCHER, PM (1992). POWER OF LIKELIHOOD RATIO TESTS FOR HETEROGENEITY OF INTRACLASS CORRELATION AND VARIANCE IN BALANCED HALF-SIB DESIGNS. Journal of Dairy Science, 75 (5), 1320-1330. doi: 10.3168/jds.S0022-0302(92)77883-7

VISSCHER, PM, THOMPSON, R and HILL, WG (1991). ESTIMATION OF GENETIC AND ENVIRONMENTAL VARIANCES FOR FAT YIELD IN INDIVIDUAL HERDS AND AN INVESTIGATION INTO HETEROGENEITY OF VARIANCE BETWEEN HERDS. Livestock Production Science, 28 (4), 273-290. doi: 10.1016/0301-6226(91)90010-N

VISSCHER, PM (1991). ON THE ESTIMATION OF VARIANCES WITHIN HERD-MEAN PRODUCTION GROUPS. Journal of Dairy Science, 74 (6), 1987-1992. doi: 10.3168/jds.S0022-0302(91)78367-7

Zeng, Jian, Zheng, Zhili, Liu, Shouye, Sidorenko, Julia, Yengo, Loic, Turley, Patrick, Ani, Alireza, Wang, Rujia, Nolte, Ilja, Snieder, Harold, Yang, Jian, Wray, Naomi, Goddard, Michael and Visscher, Peter (2023). Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. World Congress of Psychiatric Genetics (WCPG), Montreal, ON, Canada, 10 - 14 October 2023. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/j.euroneuro.2023.08.063

Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hermon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Tian, Chao, Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David, Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton C., Koellinger, Philipp D., Johannesson, Magnus, Laibson, David I., Meyer, Michelle N., Lee, James J., Kong, Augustine ... Young, Alexander I. (2021). Polygenic prediction within and between families from a 3-million-person GWAS of educational attainment. Behavior Genetics Association 51st Annual Meeting, Online, 2021. New York, NY United States: Springer. doi: 10.1007/s10519-021-10087-3

Couvy-Duchesne, Baptiste, Zhang, Futao, Kemper, Kathryn E., Sidorenko, Julia, Wray, Naomi R., Visscher, Peter M., Yang, Jian and Colliot, Olivier (2021). Association and prediction of phenotypic traits from neuroimaging data using a multi-component mixed model excluding the target vertex. Conference on Medical Imaging - Image Processing, Online, 15-19 February, 2021. Bellingham, WA, United States: SPIE. doi: 10.1117/12.2581022

Couvy-Duchesne, Baptiste, Zhang, Futao, Kemper, Kathryn E., Sidorenko, Julia, Wray, Naomi R., Visscher, Peter M., Colliot, Olivier and Yang, Jian (2020). Linear mixed models minimise false positive rate and enhance precision of mass univariate vertex-wise analyses of grey-matter. 17th International Symposium on Biomedical Imaging (ISBI), Iowa City, IA, United States, 3-7 April, 2020 . Piscataway, NJ, United States: IEEE Computer Society. doi: 10.1109/ISBI45749.2020.9098719

Evans, Luke, Border, Richard, du Pont, Alta, Friedman, Naomi, Johnson, Emma, Yang, Jian, Visscher, Peter and Keller, Matthew (2019). Exploring the genetic architecture of psychiatric disorders using partitioned heritability approaches. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October 2018. AMSTERDAM: ELSEVIER. doi: 10.1016/j.euroneuro.2018.08.032

Gratten, Jacob, Yang, Yuanhao, Trzaskowski, Maciej, Kemper, Kathryn, Yengo, Loic, Zheng, Zhili, Zhang, Futao, Zhu, Zhihong, Mcrae, Allan, Yang, Jian, Wray, Naomi and Visscher, Peter (2019). Common genetic variation explains a high proportion of the elevated risk of psychiatric disorders in children of younger mothers. 26th World Congress of Psychiatric Genetics (WCPG), Glasgow, Scotland, 11-15 October, 2018. Amsterdam, Netherlands: Elsevier BV. doi: 10.1016/j.euroneuro.2018.08.167

Keller, Matthew, de Candia, Teresa, Jones, Matt, Tahmasbi, Rasool, Evans, Luke, Evans, David, Eaves, Lindon, Yang, Jian, Visscher, Peter and Goddard, Mike (2019). Effects of assortative mating on estimates of SNP heritability. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.08.016

de Vlaming, R., Johannesson, M., Magnusson, P. K. E., Ikram, M. A. and Visscher, P. M. (2019). Equivalence of LD-score regression and individual-level-data methods. 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG), Milan, Italy, 16-19 June 2018 . London, United Kingdom: Nature Publishing Group.

Couvy-Duchesne, Baptiste, Strike, Lachlan, Zhang, Futao, Wray, Naomi, Wright, Margaret, Visscher, Peter and Yang, Jian (2019). Inter-individual cortical and subcortical similarity is associated with differences in psychiatric, cognition and socio-economic traits. 25th World Congress of Psychiatric Genetics (WCPG), Orlando, FL, United States, 13-17 October 2017. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2017.08.140

Ghaemmaghami, P., Muto, V., Jaspar, M., Meyer, C., Elansary, M., Van Egroo, M., Berthomier, C., Lambot, E., Brandewinder, M., Luxen, A., Degueldre, C., Salmon, E., Archer, S., Phillips, C., Dijk, D. -J., Visscher, P., Posthuma, D., Van Someren, E., Collette, F., Georges, M., Maquet, P. and Vandewalle, G. (2018). The genetic liability for insomnia is associated with the number of awakenings during sleep in young and healthy individuals. 24th Congress of the European-Sleep-Research-Society (ESRS), Basel Switzerland, Sep 25-28, 2018. HOBOKEN: WILEY.

Zeng, Jian, de Vlaming, Ronald, Wu, Yang, Robinson, Matthew R., Lloyd-Jones, Luke R., Yengo, Loic, Yap, Chloe X., Xue, Angli, Sidorenko, Julia, Mcrae, Allan F., Powell, Joseph E., Montgomery, Grant W., Metspalu, Andres, Esko, Tonu, Gibson, Greg, Wray, Naomi R., Visscher, Peter M. and Yang, Jian (2018). Signatures of negative selection in the genetic architecture of human complex traits. 48th Annual Meeting of the Behavior-Genetics-Association (BGA), Boston MA, United States, 20-23 June 2018. New York, NY United States: Springer New York.

Visscher, Peter M., Wray, Naomi R. and Yang, Jian (2018). Invited abstract: Leveraging big GWAS data to address question about selection, pleiotropy, assortative mating and epidemiology. 27th Annual Meeting of the International Genetic Epidemiology Society (IGES), San Diego, CA, United States, 14-16 October 2018. Hoboken, NJ, United States: John Wiley & Sons.

Tucci, Serena, McCoy, Rajiv, Vernot, Benjamin, Vohr, Sam, Robinson, Matthew R., Barbieri, Chiara, Fu, Wenqing, Sudoyo, Herawati, Visscher, Peter M., Barbujani, Guido, Akey, Joshua M. and Green, Richard E. (2018). Evolutionary history and adaptation from high-coverage whole-genome sequences of the pygmy population of Flores, Indonesia. 87th Annual Meeting of the American-Association-of-Physical-Anthropologists (AAPA), Austin, TX, United States, 11-14 April 2018. Hoboken, NJ, United States: John Wiley & Sons.

Chundru, V. Kartik, Marioni, Riccardo E., Deary, Ian J., Wray, Naomi R., Visscher, Peter M. and McRae, Allan F. (2018). Fine-mapping reveals complex genetic architecture underlying DNA methylation. Human Genome Meeting, Yokohama, Japan, 12-15 March 2018. London, United Kingdom: Henry Stewart Publications. doi: 10.1186/s40246-018-0138-6

Okbay, Aysu, Wedow, Robbee, Kong, Edward, Turley, Patrick, Lee, James, Zacher, Meghan, Thom, Kevin, Anh Tuan Nguyen, , Maghzian, Omeed, Linner, Richard Karlsson, Robinson, Matthew, Visscher, Peter, Benjamin, Daniel and Cesarini, David (2017). GWAS of educational attainment: phase 3-main results. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo Norway, Jun 28-Jul 01, 2017. NEW YORK: SPRINGER.

de Vlaming, Ronald, Johannesson, Magnus, Magnusson, Patrik K. E., Ikram, M. Arfan and Visscher, Peter M. (2017). Equivalence of LD-score regression and individual-level-data methods. 47th Behavior Genetics Annual Meeting, Oslo, Norway, 28 June - 29 September 2017. New York, NY, United States: Springer . doi: 10.1007/s10519-017-9879-6

Kassam, Irfahan, Wu, Yang, Visscher, Peter M. and McRae, Allan F. (2017). Tissue-specific sexual dimorphism in autosomal gene expression. Annual Meeting of the International-Genetic-Epidemiology-Society (IGES), Cambridge, England, 9-11 September 2017. Hoboken, NJ, United States: John Wiley & Sons. doi: 10.1002/gepi.22062

Mehta, Divya, Tropf, Felix, Gratten, Jacob, Bacanu, Silviu, Bakshi, Andrew, Mowry, Bryan, Kendler, Kenneth, Yang, Jian, Visscher, Peter, McGrath, John, Mills, Melinda, Wray, Naomi and Lee, Sang Hong (2017). Evidence for genetic overlap between schizophrenia and maternal age at first birth. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto, ON, Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2015.09.010

Wedow, Robbee, Okbay, Aysu, Kong, Edward, Turley, Patrick, Lee, James, Zacher, Meghan, Thom, Kevin, Anh Tuan Nguyen,, Maghzian, Omeed, Linner, Richard Karlsson, Robinson, Matthew, Visscher, Peter, Cesarini, David and Benjamin, Daniel (2017). GWAS of educational attainment, phase 3: prediction. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo Norway, June 28 - July 1 2017. New York, NY, United States: Springer.

Posthuma, Danielle, Benyamin, Beben, de Leeuw, Christiaan, Sullivan, Patrick, van Bochoven, Arjen, Polderman, Tinca and Visscher, Peter (2017). Fifty Years of Twin Studies On Psychiatric Traits Show That for the Majority of Traits Genetic Variation Is Mostly Additive. 23rd Annual World Congress of Psychiatric Genetics (WCPG), Toronto Canada, 16-20 October 2015. Amsterdam, Netherlands: Elsevier.

Walters, Raymond, Turley, Patrick, Maghzian, Omeed, Okbay, Aysu, Lee, James, Fontana, Mark, Tuan Anh Nguyen-Viet,, Furlotte, Nicholas, Magnusson, Patrik K. E., Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter, Laibson, David, Cesarini, David, Neale, Benjamin and Benjamin, Daniel (2017). MTAG: multi-trait analysis of GWAS implicates novel loci for depressive symptoms, neuroticism, and subjective well-being. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo, Norway, 28 June - 1 July 2017. New York, NY, United States: Springer.

Lee, James, Okbay, Aysu, Wedow, Robbee, Kong, Edward, Turley, Patrick, Zacher, Meghan, Thom, Kevin, Anh Tuan Nguyen Viet,, Maghzian, Omeed, Linner, Richard Karlsson, Robinson, Matthew, Visscher, Peter, Benjamin, Daniel and Cesarini, David (2017). GWAS of educational attainment, phase 3: biological findings. 47th Annual Meeting of the Behavior-Genetics-Association (BGA), Oslo, Norway, 28 June - 1 July 2017. New York, NY, United States: Springer.

Maier, Robert, Robinson, Matt, Wray, Naomi and Visscher, Peter (2016). Multivariate Genetic Risk Scores Can Increase Risk Prediction Accuracy for a wide Range of Traits. Annual Meeting of the International-Genetic-Epidemiology-Society, Toronto Canada, 24-26 October 2016. United States: John Wiley & Sons.

Beauchamp, Jonathan, Turley, Patrick, Fontana, Mark, Okbay, Aysu, Lee, James, Rietveld, Cornelius, de Vlaming, Ronald, Visscher, Peter, Esko, Tonu, Koellinger, Philipp, Cesarini, David and Benjamin, Daniel (2015). Pleiotropy with educational attainment: results based on a GWAS with 300,000 individuals. 45th Annual Meeting of the Behavior-Genetics-Association, San Diego, CA, United States, 20 June 2015. New York, NY, United States: Springer .

Okada, Yukinori, Wu, Di, Terao, Chikashi, Ikari, Katsunori, Kochi, Yuta, Ohmura, Koichiro, Suzuki, Akari, Yamanaka, Hisashi, Denny, Joshua C., Greenberg, Jeffrey D., Graham, Robert R., Brown, Matthew A., Bae, Sang-Cheol, Worthington, Jane, Padyukov, Leonid, Klareskog, Lars, Gregersen, Peter K., Visscher, Peter M., Siminovitch, Katherine A. and Plenge, Robert M. (2013). Biological Insights From Genetics Of Rheumatoid Arthritis Contribute To Drug Discovery. 77th Annual Meeting of the American College of Rheumatology / 48th Annual Meeting of the Association of Rheumatology Health Professionals, San Diego CA, United States, 25-30 October 2013. Hoboken, NJ United States: John Wiley and Sons. doi: 10.1002/art.38216

Justice, Anne, North, Kari, Loos, Ruth, Vedantam, Sailaja, Day, Felix, Berndt, Sonja, Gustafsson, Stefan, Locke, Adam, Powell, Corey, Bratati, Kahali, Croteau-Chonka, Damien, Winkler, Thomas, Scherag, Andre, Barroso, Ines, Beckmann, Jacqui, Lindgren, Cecilia, Pers, Tune, Visscher, Peter, Willer, Cristen, Yang, Jian, Mohlke, Karen, Hirschorn, Joel, Ingelsson, Erik, Boehnke, Michael and Speliotes, Elizabeth (2013). Meta-analysis of Genetic Associations in up to 339,224 Individuals Identify 66 New Loci for Bmi, Confirming a Neuronal Contribution to Body Weight Regulation and Implicating Several Novel Pathways. Scientific Sessions of the American-Heart-Association on Epidemiology and Prevention/Physical Activity, Nutrition and Metabolism, New Orleans La, 19 - 22 March 2013. Baltimore, MD United States: Lippincott Williams & Wilkins.

Rietveld, Cornelius, Koellinger, Philipp, Benjamin, Daniel, Cesarini, David, Davey-Smith, George, Davies, Gail, Deary, Ian, Johannesson, Magnus, Plomin, Robert, Posthuma, D. and Visscher, Peter (2013). Are SNPs associated with educational attainment also associated with cognitive function?. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9

Ebejer, Jane, Medland, Sarah, Martin, Nick G., Wright, Margaret, Montgomery, Grant, Powell, Joseph, Visscher, Peter and Duffy, David (2013). Clarification of varying genetic expression and structure within adolescent monozygotic and dizygotic twins discordant for high and low attention and activity. 43rd Annual Meeting of the Behavior-Genetics-Association, Marseille France, 28 June-02 July 2013. New York, NY United States: Springer New York LLC. doi: 10.1007/s10519-013-9623-9

de Candia, Teresa, Lee, Hong, Yang, Jian, Browning, Brian, Gejman, Pablo, Levinson, Douglas, Hewitt, John, Visscher, Peter, Wray, Naomi and Keller, Matthew (2012). Additive genetic variation in risk to schizophrenia across African American and European American populations. 42nd Annual Meeting of the Behavior-Genetics-Association, Edinburgh Scotland, Jun 22-25, 2012.

Benjamin, Daniel, Cesarini, David, van der Loos, Matthijs, Dawes, Chris, Koellinger, Philipp, Magnusson, Patrik, Chabris, Chris, Conley, Dalton, Laibson, David, Johannesson, Magnus and Visscher, Peter (2012). The genetic architecture of economic and political preferences. 42nd Annual Meeting of the Behavior Genetics Association, Edinburgh Scotland, 22-25 June 2012. New York, NY United States: Springer New York LLC.

Visscher, Peter M. (2009). Whole genome approaches to quantitative genetics. 3rd International Conference of Quantitative Genetics, Hangzhou Peoples R China, Aug 18-24, 2007. DORDRECHT: SPRINGER. doi: 10.1007/s10709-008-9301-7

Benyamin, Beben, Deary, Ian J. and Visscher, Peter M. (2006). Precision and bias of a mixture distribution model to analyse twin data when zygosity is unknown: Simulations and application to IQ phenotypes on a large sample of twin pairs. 36th Annual Meeting of the Behavior-Genetics-Association, Storrs, CT, United States, 24 June 2006. New York, United States: Springer New York LLC.

Kyvik, KO, Benyamin, B, Schousboe, K, Fenger, M, Sorensen, TIA and Visscher, P (2005). Multivariate genetic analyses of phenotypes related to the metabolic syndrome. 41st Annual Meeting of the European-Association-for-the-Study-of-Diabetes, Athens Greece, Sep 10-15, 2005. SPRINGER.

Blackwood, D. H.R., Visscher, P. M. and Muir, W. J. (2001). Genetic studies of bipolar affective disorder in large families.

Visscher, P, Pong-Wong, R, Whittemore, C and Haley, C (2000). Impact of biotechnology on (cross)breeding programmes in pigs. 49th EAAP Meeting, Warsaw Poland, Aug, 1998. AMSTERDAM: ELSEVIER SCIENCE BV. doi: 10.1016/S0301-6226(99)00180-3

Visscher, PM, Mackinnon, M and Haley, CS (1997). Efficiency of marker assisted selection. Allerton II Conference on Genetic Analysis of Economically Important Traits in Livestock, Monticello Il, Nov 06-09, 1996. NEW YORK: MARCEL DEKKER INC. doi: 10.1080/10495399709525872

Professor Peter Visscher

Professor Peter Visscher: Program in complex trait genomics

Researcher biography

Professor Peter Visscher

Professor Peter Visscher: Program in complex trait genomics

Researcher biography

Publications

Book Chapters

Journal Articles

Conference Papers