Professor Peter Visscher: Program in complex trait genomics
The Visscher laboratory specialises in developing methodology that enables analyses aimed at understanding the genetic basis of differences in risk for disease, and other phenotypes between individuals. This research crosses the boundaries of quantitative and statistical genetics, population genetics and human genetics. Applications are diverse but include the study of cognition, cognitive change, and psychiatric and neurological disorders.
Researcher biography
Visscher joined the University of Queensland in 2011, where he is Professor of Quantitative Genetics. He is a Laureate Fellow of the Australian Research Council. Visscher was elected a Fellow of the Australian Academy of Science in 2010, a Fellow of the Royal Society (London) in 2018 and a Foreign Member of the Royal Netherlands Academy of Arts and Sciences in 2018.
Visscher's research is about genetic variation for complex traits (including quantitative traits and disease) in populations, with the broad aim to understand and quantify the causes and consequences of human trait variation.
Prof Peter Visscher, Prof Naomi Wray and Prof Jian Yang together comprise the Executive Team of the Program in Complex Trait Genomics (PCTG). PCTG comprises a critical mass of more than 30 post-doctoral researchers plus research assistants and students, all supported by external grant funding. Their skills lie in the ability to develop and apply statistical methods within the framework of quantitative, population and statistical genetics and to use theory to understand and predict results from data analyses. They play leading roles in the international research consortia. The focus of current research activities is in the detection and fine-mapping of loci underlying complex traits (including common disease), based upon theoretical studies and applications of methods to large datasets, in population genetics studies using theoretical approaches and high-density genetic marker data, and in systems genomics studies.
Book Chapters
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
Journal Articles
Trastulla, Lucia, Dolgalev, Georgii, Moser, Sylvain, Jiménez-Barrón, Laura T., Andlauer, Till F. M., von Scheidt, Moritz, Ruderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Stahl, Eli A., Domenici, Enrico, Adolfsson, Rolf, 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., Black, Donald W., Blackwood, Douglas H. R., Borglum, Anders D., Bramon, Elvira, Bruggeman, Richard ... Ziller, Michael J. (2024). Distinct genetic liability profiles define clinically relevant patient strata across common diseases. Nature Communications , 15 (1) 5534. doi: 10.1038/s41467-024-49338-2
Davies, Neil M., Hemani, Gibran, Neiderhiser, Jenae M., Martin, Hilary C., Mills, Melinda C., Visscher, Peter M., Yengo, Loïc, Young, Alexander Strudwick and Keller, Matthew C. (2024). The importance of family-based sampling for biobanks. Nature, 634 (8035), 795-803. doi: 10.1038/s41586-024-07721-5
Sidorenko, Julia, Couvy-Duchesne, Baptiste, Kemper, Kathryn E., Moen, Gunn-Helen, Bhatta, Laxmi, Åsvold, Bjørn Olav, Mägi, Reedik, Estonian Biobank Research Team, Ani, Alireza, Wang, Rujia, Nolte, Ilja M., Lifelines Cohort Study, Nolte, Ilja M., Gordon, Scott, Hayward, Caroline, Campbell, Archie, Benjamin, Daniel J., Cesarini, David, Evans, David M., Goddard, Michael E., Haley, Chris S., Porteous, David, Medland, Sarah E., Martin, Nicholas G., Snieder, Harold, Metspalu, Andres, Hveem, Kristian, Brumpton, Ben, Visscher, Peter M. and Yengo, Loic (2024). Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics, 56 (11), 2352-2360. doi: 10.1038/s41588-024-01940-2
Kemper, Kathryn E., Sidorenko, Julia, Wang, Huanwei, Hayes, Ben J., Wray, Naomi R., Yengo, Loic, Keller, Matthew C., Goddard, Michael and Visscher, Peter M. (2024). Genetic influence on within-person longitudinal change in anthropometric traits in the UK Biobank. Nature Communications, 15 (1) 3776, 3776. doi: 10.1038/s41467-024-47802-7
Keaton, Jacob M., Kamali, Zoha, Xie, Tian, Vaez, Ahmad, Williams, Ariel, Goleva, Slavina B., Ani, Alireza, Evangelou, Evangelos, Hellwege, Jacklyn N., Yengo, Loic, Young, William J., Traylor, Matthew, Giri, Ayush, Zheng, Zhili, Zeng, Jian, Chasman, Daniel I., Morris, Andrew P., Caulfield, Mark J., Hwang, Shih-Jen, Kooner, Jaspal S., Conen, David, Attia, John R., Morrison, Alanna C., Loos, Ruth J. F., Kristiansson, Kati, Schmidt, Reinhold, Hicks, Andrew A., Pramstaller, Peter P., Nelson, Christopher P. ... ICBP Consortium (2024). Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits. Nature Genetics, 56 (5), 1-14. doi: 10.1038/s41588-024-01714-w
Zheng, Zhili, Liu, Shouye, Sidorenko, Julia, Wang, Ying, Lin, Tian, Yengo, Loic, Turley, Patrick, Ani, Alireza, Wang, Rujia, Nolte, Ilja M., Snieder, Harold, Aguirre-Gamboa, Raul, Deelen, Patrick, Franke, Lude, Kuivenhoven, Jan A., Lopera Maya, Esteban A., Sanna, Serena, Swertz, Morris A., Vonk, Judith M., Wijmenga, Cisca, Yang, Jian, Wray, Naomi R., Goddard, Michael E., Visscher, Peter M., Zeng, Jian and LifeLines Cohort Study (2024). Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries. Nature Genetics, 56 (5), 1-11. doi: 10.1038/s41588-024-01704-y
Li, Yanni, Van Den Berg, Eline H., Kurilshikov, Alexander, Zhernakova, Dasha V., Gacesa, Ranko, Hu, Shixian, Lopera-Maya, Esteban A., Zhernakova, Alexandra, Aguirre-Gamboa, Raul, Deelen, Patrick, Franke, Lude, Kuivenhoven, Jan A., Lopera-Maya, Esteban A., Nolte, Ilja M., Sanna, Serena, Snieder, Harold, Swertz, Morris A., Visscher, Peter M., Vonk, Judith M., Wijmenga, Cisca, De Meijer, Vincent E., Sanna, Serena, Dullaart, Robin P. F., Blokzijl, Hans, Festen, Eleonora A. M., Fu, Jingyuan and Weersma, Rinse K. (2024). Genome-wide Studies Reveal Genetic Risk Factors for Hepatic Fat Content. Genomics, Proteomics and Bioinformatics, 22 (2) qzae031. doi: 10.1093/gpbjnl/qzae031
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
Xue, Angli, Zhu, Zhihong, Wang, Huanwei, Jiang, Longda, Visscher, Peter M., Zeng, Jian and Yang, Jian (2024). Unravelling the complex causal effects of substance use behaviours on common diseases. Communications Medicine, 4 (1) ARTN 43, 43. doi: 10.1038/s43856-024-00473-3
Zhernakova, Daria V., Wang, Daoming, Liu, Lei, Andreu-Sánchez, Sergio, Zhang, Yue, Ruiz-Moreno, Angel J., Peng, Haoran, Plomp, Niels, Del Castillo-Izquierdo, Ángela, Gacesa, Ranko, Lopera-Maya, Esteban A., Temba, Godfrey S., Kullaya, Vesla I., van Leeuwen, Sander S., Aguirre-Gamboa, Raul, Deelen, Patrick, Franke, Lude, Kuivenhoven, Jan A., Nolte, Ilja M., Sanna, Serena, Snieder, Harold, Swertz, Morris A., Visscher, Peter M., Vonk, Judith M., Xavier, Ramnik J., de Mast, Quirijn, Joosten, Leo A. B., Riksen, Niels P., Rutten, Joost H. W. ... Fu, Jingyuan (2024). Host genetic regulation of human gut microbial structural variation. Nature, 625 (7996), 813-821. doi: 10.1038/s41586-023-06893-w
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 (2024). Erratum: Autism-related dietary preferences mediate autism-gut microbiome associations (Cell (2021) 184(24) (5916–5931.e17), (S0092867421012319), (10.1016/j.cell.2021.10.015)). Cell, 187 (2), 495-510. doi: 10.1016/j.cell.2023.12.001
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
Maury, Eduardo A., Sherman, Maxwell A., Genovese, Giulio, Gilgenast, Thomas G., Kamath, Tushar, Burris, S. J., Rajarajan, Prashanth, Flaherty, Erin, Akbarian, Schahram, Chess, Andrew, McCarroll, Steven A., Loh, Po-Ru, Phillips-Cremins, Jennifer E., Brennand, Kristen J., Macosko, Evan Z., Walters, James T.R., O'Donovan, Michael, Sullivan, Patrick, Marshall, Christian R., Merico, Daniele, Thiruvahindrapuram, Bhooma, Wang, Zhouzhi, Scherer, Stephen W., Howrigan, Daniel P, Ripke, Stephan, Bulik-Sullivan, Brendan, Farh, Kai-How, Fromer, Menachem, Goldstein, Jacqueline I. ... Walsh, Christopher A. (2023). Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell Genomics, 3 (8) 100356, 1-21. doi: 10.1016/j.xgen.2023.100356
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
Hsu, Yu-Han H., Pintacuda, Greta, Liu, Ruize, Nacu, Eugeniu, Kim, April, Tsafou, Kalliopi, Petrossian, Natalie, Crotty, William, Suh, Jung Min, Riseman, Jackson, Martin, Jacqueline M., Biagini, Julia C., Mena, Daya, Ching, Joshua K.T., Malolepsza, Edyta, Li, Taibo, Singh, Tarjinder, Ge, Tian, Egri, Shawn B., Tanenbaum, Benjamin, Stanclift, Caroline R., Apffel, Annie M., Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T.R., Farh, Kai-How, Holmans, Peter A., Lee, Phil ... Lage, Kasper (2023). Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia. iScience, 26 (5) 106701, 1-28. doi: 10.1016/j.isci.2023.106701
Yap, Chloe X., Henders, Anjali K., Alvares, Gail A., Giles, Corey, Huynh, Kevin, Nguyen, Anh, Wallace, Leanne, McLaren, Tiana, Yang, Yuanhao, Hernandez, Leanna M., Gandal, Michael J., Hansell, Narelle K., Cleary, Dominique, Grove, Rachel, Hafekost, Claire, Harun, Alexis, Holdsworth, Helen, Jellett, Rachel, Khan, Feroza, Lawson, Lauren P., Leslie, Jodie, Levis Frenk, Mira, Masi, Anne, Mathew, Nisha E., Muniandy, Melanie, Nothard, Michaela, Miller, Jessica L., Nunn, Lorelle, Strike, Lachlan T. ... The Busselton Health Study Investigators (2023). Interactions between the lipidome and genetic and environmental factors in autism. Nature Medicine, 29 (4), 936-949. doi: 10.1038/s41591-023-02271-1
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
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. ... Lifelines Cohort Study (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
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
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
Trubetskoy, Vassily, Pardiñas, Antonio F, Qi, Ting, Panagiotaropoulou, Georgia, Awasthi, Swapnil, Bigdeli, Tim B, Bryois, Julien, Chen, Chia-Yen, Dennison, Charlotte A, Hall, Lynsey S, Lam, Max, Watanabe, Kyoko, Frei, Oleksandr, Ge, Tian, Harwood, Janet C, Koopmans, Frank, Magnusson, Sigurdur, Richards, Alexander L, Sidorenko, Julia, Wu, Yang, Zeng, Jian, Grove, Jakob, Kim, Minsoo, Li, Zhiqiang, Voloudakis, Georgios, Zhang, Wen, Adams, Mark, Agartz, Ingrid, Atkinson, Elizabeth G ... Schizophrenia Working Group of the Psychiatric Genomics Consortium (2022). Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature, 604 (7906), 502-508. doi: 10.1038/s41586-022-04434-5
Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K E, Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N. ... Social Science Genetic Association Consortium (2022). Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Nature Genetics, 54 (4), 437-449. doi: 10.1038/s41588-022-01016-z
Wainschtein, Pierrick, Jain, Deepti, Zheng, Zhili, Aslibekyan, Stella, Becker, Diane, Bi, Wenjian, Brody, Jennifer, Carlson, Jenna C., Correa, Adolfo, Du, Margaret Mengmeng, Fernandez-Rhodes, Lindsay, Ferrier, Kendra R., Graff, Misa, Guo, Xiuqing, He, Jiang, Heard-Costa, Nancy L., Highland, Heather M., Hirschhorn, Joel N., Howard-Claudio, Candace M., Isasi, Carmen R., Jackson, Rebecca, Jiang, Jicai, Joehanes, Roby, Justice, Anne E., Kalyani, Rita R., Kardia, Sharon, Lange, Ethan, LeBoff, Meryl, Lee, Seunggeun ... NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium (2022). Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data. Nature Genetics, 54 (3), 263-273. doi: 10.1038/s41588-021-00997-7
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
Gadd, Danni A., Hillary, Robert F., McCartney, Daniel L., Zaghlool, Shaza B., Stevenson, Anna J., Cheng, Yipeng, Fawns-Ritchie, Chloe, Nangle, Cliff, Campbell, Archie, Flaig, Robin, Harris, Sarah E., Walker, Rosie M., Shi, Liu, Tucker-Drob, Elliot M., Gieger, Christian, Peters, Annette, Waldenberger, Melanie, Graumann, Johannes, McRae, Allan F., Deary, Ian J., Porteous, David J., Hayward, Caroline, Visscher, Peter M., Cox, Simon R., Evans, Kathryn L., McIntosh, Andrew M., Suhre, Karsten and Marioni, Riccardo E. (2022). Epigenetic scores for the circulating proteome as tools for disease prediction. eLife, 11 e71802, 1-24. doi: 10.7554/eLife.71802
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
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Chen, Jingchun, Lee, Grace, Fanous, Ayman H., Zhao, Zhongming, Jia, Peilin, O'neill, Anthony, Walsh, Dermot, Kendler, Kenneth S., Chen, Xiangning, O’Donovan, Michael C., Kirov, George K, Craddock, Nick J, Holmans, Peter A, Williams, Nigel M, Georgieva, Lyudmila, Nikolov, Ivan, Norton, N., Williams, H., Toncheva, Draga, Milanova, Vihra, Owen, Michael J, Hultman, Christina M, Lichtenstein, Paul, Thelander, Emma F, Sullivan, Patrick, Morris, Derek W, O’Dushlaine, Colm T., Kenny, Elaine, Quinn, Emma M ... Scolnick, Edward M (2011). Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia Research, 131 (1-3), 43-51. doi: 10.1016/j.schres.2011.06.023
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
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
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, 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
O'Dushlaine, C., Kenny, Elaine, Heron, E., Donohoe, G., Gill, Michael, Morris, Derek W., Corvin, Aiden, O'Dushlaine, Colm T., Quinn, Emma M., 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, Choudhury, Khalid, Datta, Susmita, Pimm, Jonathan ... The International Schizophrenia Consortium (2011). Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Molecular Psychiatry, 16 (3), 286-292. doi: 10.1038/mp.2010.7
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
Frank, Rene A. W., McRae, Allan F., Pocklington, Andrew J., van de Lagemaat, Louie N., Navarro, Pau, Croning, Mike D. R., Komiyama, Noboru H., Bradley, Sophie J., Challiss, R. A. John, Armstrong, J. Douglas, Finn, Robert D., Malloy, Mary P., MacLean, Alan W., Harris, Sarah E., Starr, John M., Bhaskar, Sanjeev S., Howard, Eleanor K., Hunt, Sarah E., Coffey, Alison J., Ranganath, Venkatesh, Deloukas, Panos, Rogers, Jane, Muir, Walter J., Deary, Ian J., Blackwood, Douglas H., Visscher, Peter M. and Grant, Seth G. N. (2011). Clustered coding variants in the glutamate receptor complexes of individuals with schizophrenia and bipolar disorder. PLoS One, 6 (4) e19011, e19011.1-e19011.9. doi: 10.1371/journal.pone.0019011
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
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
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
Heid, Iris M., Jackson, Anne U., Randall, Joshua C., Winkler, Thomas W., Qi, Lu, Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, Zillikens, M. Carola, Speliotes, Elizabeth K., Maegi, Reedik, Workalemahu, Tsegaselassie, White, Charles C., Bouatia-Naji, Nabila, Harris, Tamara B., Berndt, Sonja I., Ingelsson, Erik, Willer, Cristen J., Weedon, Michael N., Luan, Jianan, Vedantam, Sailaja, Esko, Tonu, Kilpelaeinen, Tuomas O., Kutalik, Zoltan, Li, Shengxu, Monda, Keri L., Dixon, Anna L., Holmes, Christopher C., Kaplan, Lee M., Liang, Liming ... Lindgren, Cecilia M. (2010). Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Nature Genetics, 42 (11), 949-962. doi: 10.1038/ng.685
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
Elizabeth K Speliotes, Cristen J Willer, Sonja I Berndt, Keri L Monda, Gudmar Thorleifsson, Anne U Jackson, Hana Lango Allen, Cecilia M Lindgren, Jian'an Luan, Reedik Magi, Joshua C Randall, Sailaja Vedantam, Thomas W Winkler, Lu Qi, Tsegaselassie Workalemahu, Iris M Heid, Valgerdur Steinthorsdottir, Heather M Stringham, Michael N Weedon, Eleanor Wheeler, Andrew R Wood, Teresa Ferreira, Robert J Weyant, Ayellet V Segre, Karol Estrada, Liming Liang, James Nemesh, Ju-Hyun Park, Stefan Gustafsson ... Ruth J F Loos (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nature Genetics, 42 (11), 937-948. doi: 10.1038/ng.686
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Stone, Jennifer L., O'Donovan, Michael C., Gurling, Hugh, Kirov, George K., Blackwood, Douglas H. R., Corvin, Aiden, Craddock, Nick J., Gill, Michael, Hultman, Christina M., Lichtenstein, Paul, McQuillin, Andrew, Pato, Carlos N., Ruderfer, Douglas M., Owen, Michael J., St Clair, David, Sullivan, Patrick F., Sklar, Pamela, Purcell, Shaun M., Scolnick, E. M., Holmans, P. A., Georgieva, L., Nikolov, I., Norton, N., Williams, H., Williams, N. M., Toncheva, D., Milanova, V., Thelander, E. F., Morris, D. W. ... Sklar, P. (2008). Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature, 455 (7210), 237-241. doi: 10.1038/nature07239
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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 (S1) 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
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
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.
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.
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.
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
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.
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
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, 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
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, PM (1998). On the sampling variance of intraclass correlations and genetic correlations. Genetics, 149 (3), 1605-1614.
Visscher, P M (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
VISSCHER, PT, NIJBURG, JW and VANGEMERDEN, H (1990). POLYSULFIDE UTILIZATION BY THIOCAPSA-ROSEOPERSICINA. Archives of Microbiology, 155 (1), 75-81. doi: 10.1007/BF00291278
STEUDEL, R, HOLDT, G, VISSCHER, PT and VANGEMERDEN, H (1990). SEARCH FOR POLYTHIONATES IN CULTURES OF CHROMATIUM-VINOSUM AFTER SULFIDE INCUBATION. Archives of Microbiology, 153 (5), 432-437. doi: 10.1007/BF00248423
Conference Papers
Zeng, Jian, Wu, Yang, Zheng, Zhili, Thibaut, Loic, Goddard, Michael, Wray, Naomi and Visscher, Peter (2024). Genome-wide Fine-mapping Improves Identification Of Causal Variants. World Congress of Psychiatric Genetics WCPG 2024, Singapore, 15-19 October 2024. Amsterdam, Netherlands: Elsevier. doi: 10.1016/j.euroneuro.2024.08.037
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
Becker, Joel, Burik, Casper A. P., Goldman, Grant, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Belsky, Daniel W., Linner, Richard Karlsson, Ahlskog, Rafael, Kleinman, Aaron, Hinds, David A., Caspi, Avshalom, Corcoran, David L., Moffitt, Terrie E., Poulton, Richie, Sugden, Karen, Williams, Benjamin S., Harris, Kathleen Mullan, Steptoe, Andrew, Ajnakina, Olesya, Milani, Lili, Esko, Tonu, Iacono, William G., McGue, Matt, Magnusson, Patrik K. E., Mallard, Travis T., Harden, K. Paige, Tucker-Drob, Elliot M., Herd, Pamela ... Okbay, Aysu (2021). Resource Profile and User Guide of the Polygenic Index Repository. 51st Annual Meeting of the Behavior-Genetics-Association (BGA), Electr Network, Jun 29, 2021. NEW YORK: SPRINGER.
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
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
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
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
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.
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
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.
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
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.
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.
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.
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
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
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.
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.
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.
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 .
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
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
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.
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.
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