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2015 Journal Article A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationshipsVisscher, Peter M. and Goddard, Michael E. (2015). A general unified framework to assess the sampling variance of heritability estimates using pedigree or marker-based relationships. Genetics, 199 (1), 223-232. doi: 10.1534/genetics.114.171017 |
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2015 Conference Publication Pleiotropy with educational attainment: results based on a GWAS with 300,000 individualsBeauchamp, 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 . |
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2015 Journal Article New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritisLee, S. Hong, Byrne, Enda M., Hultman, Christina M., Kahler, Anna, Vinkhuyzen, Anna A. E., Ripke, Stephan, Andreassen, Ole A., Frisell, Thomas, Gusev, Alexander, Hu, Xinli, Karlsson, Robert, Mantzioris, Vasilis X., McGrath, John J., Mehta, Divya, Stahl, Eli A., Zhao, Qiongyi, Kendler, Kenneth S., Sullivan, Patrick F., Price, Alkes L., O'Donovan, Michael, Okada, Yukinori, Mowry, Bryan J., Raychaudhuri, Soumya, Wray, Naomi R., Schizophrenia Working Group of the Psychiatric Genomics Consortium, Rheumatoid Arthritis Consortium International and Visscher, Peter M . (2015). New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis. International Journal of Epidemiology, 44 (5) dyv136, 1-16. doi: 10.1093/ije/dyv136 |
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2014 Journal Article Diel fluctuations in solute distributions and biogeochemical cycling in a hypersaline microbial mat from Shark Bay, WAPages, Anais, Welsh, David T., Teasdale, Peter R., Grice, Kliti, Vacher, Michael, Bennett, William W. and Visscher, Pieter T. (2014). Diel fluctuations in solute distributions and biogeochemical cycling in a hypersaline microbial mat from Shark Bay, WA. Marine Chemistry, 167, 102-112. doi: 10.1016/j.marchem.2014.05.003 |
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2014 Journal Article The contribution of genetic variants to disease depends on the rulerWitte, John S., Visscher, Peter M. and Wray, Naomi R. (2014). The contribution of genetic variants to disease depends on the ruler. Nature Reviews Genetics, 15 (11), 765-776. doi: 10.1038/nrg3786 |
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2014 Journal Article Replicability and robustness of genome-wide-association studies for behavioral traitsRietveld, Cornelius A., Conley, Dalton, Eriksson, Nicholas, Esko, Tonu, Medland, Sarah E., Vinkhuyzen, Anna A. E., Yang, Jian, Boardman, Jason D., Chabris, Christopher F., Dawes, Christopher T., Domingue, Benjamin W., Hinds, David A., Johannesson, Magnus, Kiefer, Amy K., Laibson, David, Magnusson, Patrik K. E., Mountain, Joanna L., Oskarsson, Sven, Rostapshova, Olga, Teumer, Alexander, Tung, Joyce Y., Visscher, Peter M., Benjamin, Daniel J., Cesarini, David and Koellinger, Philipp D. (2014). Replicability and robustness of genome-wide-association studies for behavioral traits. Psychological Science, 25 (11), 1975-1986. doi: 10.1177/0956797614545132 |
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2014 Journal Article Benthic protists and fungi of Mediterranean deep hypsersaline anoxic basin redoxcline sedimentsBernhard, Joan M., Kormas, Konstantinos, Pachiadaki, Maria G., Rocke, Emma, Beaudoin, David J., Morrison, Colin, Visscher, Pieter T., Cobban, Alec, Starczak, Victoria R. and Edgcomb, Virginia P. (2014). Benthic protists and fungi of Mediterranean deep hypsersaline anoxic basin redoxcline sediments. Frontiers in Microbiology, 5. doi: 10.3389/fmicb.2014.00605 |
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2014 Journal Article Defining the role of common variation in the genomic and biological architecture of adult human heightWood, Andrew R., Esko, Tonu, Yang, Jian, Vedantam, Sailaja, Pers, Tune H., Gustafsson, Stefan, Chu, Audrey Y., Estrada, Karol, Luan, Jian'an, Kutalik, Zoltan, Amin, Najaf, Buchkovich, Martin L., Croteau-Chonka, Damien C., Day, Felix R., Duan, Yanan, Fall, Tove, Fehrmann, Rudolf, Ferreira, Teresa, Jackson, Anne U., Karjalainen, Juha, Lo, Ken Sin, Locke, Adam E., Magi, Reedik, Mihailov, Evelin, Porcu, Evelin, Randall, Joshua C., Scherag, Andre, Vinkhuyzen, Anne A. E., Westra, Harm-Jan ... Frayling, Timothy M. (2014). Defining the role of common variation in the genomic and biological architecture of adult human height. Nature Genetics, 46 (11), 1173-1186. doi: 10.1038/ng.3097 |
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2014 Journal Article Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common DiseasesGusev, Alexander, Lee, S. Hong, Trynka, Gosia, Finucane, Hilary, Vilhjálmsson, Bjarni J., Xu, Han, Zang, Chongzhi, Ripke, Stephan, Bulik-Sullivan, Brendan, Stahl, Eli, Schizophrenia Working Group of the Psychiatric Genomics Consortium, SWE-SCZ Consortium, Kaehler, Anna K., Hultman, Christina M., Purcell, Shaun M., McCarroll, Steven A., Daly, Mark, Pasaniuc, Bogdan, Sullivan, Patrick F., Neale, Benjamin M., Wray, Naomi R., Raychaudhuri, Soumya, Price, Alkes L., Visscher, Peter M., Mowry, Bryan J., Psychosis Endophenotypes International Consortium and Wellcome Trust Case Control Consortium (2014). Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases. American Journal of Human Genetics, 95 (5), 535-552. doi: 10.1016/j.ajhg.2014.10.004 |
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2014 Journal Article Genetic and environmental exposures constrain epigenetic drift over the human life courseShah, Sonia, McRae, Allan F., Marioni, Riccardo E., Harris, Sarah E., Gibson, Jude, Henders, Anjali K., Redmond, Paul, Cox, Simon R., Pattie, Alison, Corley, Janie, Murphy, Lee, Martin, Nicholas G., Montgomery, Grant W., Starr, John M., Wray, Naomi R., Deary, Ian J. and Visscher, Peter M. (2014). Genetic and environmental exposures constrain epigenetic drift over the human life course. Genome Research, 24 (11), 1725-1733. doi: 10.1101/gr.176933.114 |
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2014 Journal Article Evidence for arsenic metabolism and cycling by microorganisms 2.7 billion years agoSforna, Marie Catherine, Philippot, Pascal, Somogyi, Andrea, van Zuilen, Mark A., Medjoubi, Kadda, Schoepp-Cothenet, Barbara, Nitschke, Wolfgang and Visscher, Pieter T. (2014). Evidence for arsenic metabolism and cycling by microorganisms 2.7 billion years ago. Nature Geoscience, 7 (11), 811-815. doi: 10.1038/NGEO2276 |
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2014 Journal Article Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosisBenyamin, Beben, Esko, Tonu, Ried, Janina S., Radhakrishnan, Aparna, Vermeulen, Sita H., Traglia, Michela, Goegele, Martin, Anderson, Denise, Broer, Linda, Podmore, Clara, Luan, Jian'an, Kutalik, Zoltan, Sanna, Serena, van der Meer, Peter, Tanaka, Toshiko, Wang, Fudi, Westra, Harm-Jan, Franke, Lude, Mihailov, Evelin, Milani, Lili, Haeldin, Jonas, Winkelmann, Juliane, Meitinger, Thomas, Thiery, Joachim, Peters, Annette, Waldenberger, Melanie, Rendon, Augusto, Jolley, Jennifer, Sambrook, Jennifer ... Whitfield, John B. (2014). Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Nature Communications, 5 (1) 5926, 4926.1-4926.10. doi: 10.1038/ncomms5926 |
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2014 Journal Article Another explanation for apparent epistasis: replyHemani, Gibran, Shakhbazov, Konstantin, Westra, Harm-Jan, Esko, Tonu, Henders, Anjali K., McRae, Allan F., Yang, Jian, Gibson, Greg, Martin, Nicholas G., Metspalu, Andres, Franke, Lude, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2014). Another explanation for apparent epistasis: reply. Nature, 514 (7520), E5-E6. doi: 10.1038/nature13692 |
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2014 Journal Article The Effect on Melanoma Risk of Genes Previously Associated With Telomere LengthIles, Mark M., Bishop, D. Timothy, Taylor, John C., Hayward, Nicholas K., Brossard, Myriam, Cust, Anne E., Dunning, Alison M., Lee, Jeffrey E., Moses, Eric K., Akslen, Lars A., AMFS Investigators, Andresen, Per A., Avril, Marie-Francoise, Azizi, Esther, Scarra, Giovanna Bianchi, Brown, Kevin M., Debniak, Tadeusz, Elder, David E., Friedman, Eitan, Ghiorzo, Paola, Gillanders, Elizabeth M., Goldstein, Alisa M., Gruis, Nelleke A., Hansson, Johan, Harland, Mark, Helsing, Per, Hocevar, Marko, Hoiom, Veronica, IBD investigators ... Visscher, Peter (2014). The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length. JNCI Journal of the National Cancer Institute, 106 (10) dju267. doi: 10.1093/jnci/dju267 |
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2014 Journal Article Beyond the Single SNP: Emerging Developments in Mendelian Randomization in the “Omics” EraBrion, Marie-Jo A., Benyamin, Beben, Visscher, Peter M. and Smith, George Davey (2014). Beyond the Single SNP: Emerging Developments in Mendelian Randomization in the “Omics” Era. Current Epidemiology Reports, 1 (4), 228-236. doi: 10.1007/s40471-014-0024-2 |
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2014 Journal Article Common genetic variants associated with cognitive performance identified using the proxy-phenotype methodRietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., De Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, Van Der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, Van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America, 111 (38), 13790-13794. doi: 10.1073/pnas.1404623111 |
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2014 Journal Article Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014)Rietveld, Cornelius A., Esko, Tonu, Davies, Gail, Pers, Tune H., Turley, Patrick, Benyamin, Beben, Chabris, Christopher F., Emilsson, Valur, Johnson, Andrew D., Lee, James J., de Leeuw, Christiaan, Marioni, Riccardo E., Medland, Sarah E., Miller, Michael B., Rostapshova, Olga, van der Lee, Sven J., Vinkhuyzen, Anna A. E., Amin, Najaf, Conley, Dalton, Derringer, Jaime, van Duijn, Cornelia M., Fehrmann, Rudolf, Franke, Lude, Glaeser, Edward L., Hansell, Narelle K., Hayward, Caroline, Iacono, William G., Ibrahim-Verbaas, Carla, Jaddoe, Vincent ... Koellinger, Philipp D. (2014). Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (vol 111, pg 13790, 2014). Proceedings of the National Academy of Sciences of the United States of America, 112 (4), E380-E380. doi: 10.1073/pnas.1424631112 |
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2014 Journal Article A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in EuropeansTimpson, Nicholas J., Walter, Klaudia, Min, Josine L., Tachmazidou, Ioanna, Malerba, Giovanni, Shin, So-Youn, Chen, Lu, Futema, Marta, Southam, Lorraine, Iotchkova, Valentina, Cocca, Massimiliano, Huang, Jie, Memari, Yasin, McCarthy, Shane, Danecek, Petr, Muddyman, Dawn, Mangino, Massimo, Menni, Cristina, Perry, John R. B., Ring, Susan M., Gaye, Amadou, Dedoussis, George, Farmaki, Aliki-Eleni, Burton, Paul, Talmud, Philippa J., Gambaro, Giovanni, Spector, Tim D., Smith, George Davey, Durbin, Richard ... Yang, Jian (2014). A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans. Nature Communications, 5 (1) 4871, 1-10. doi: 10.1038/ncomms5871 |
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2014 Journal Article Motor neuron disease: common genetic variants and the heritability of ALSAl-Chalabi, Ammar and Visscher, Peter M. (2014). Motor neuron disease: common genetic variants and the heritability of ALS. Nature Reviews Neurology, 10 (10), 549-550. doi: 10.1038/nrneurol.2014.166 |
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2014 Journal Article Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip dataChen, Guo-Bo, Lee, Sang Hong, Brion, Marie-Jo A., Montgomery, Grant W., Wray, Naomi R., Radford-Smith, Graham L., Visscher, Peter M., The International IBD Genetics Consortium, Australia and New Zealand IBDGC, Belgium Genetic Consortium, Initiative on Crohn and Colitis, NIDDK IBDGC, United Kingdom IBDGC and Wellcome Trust Case Control Consortium (2014). Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data. Human Molecular Genetics, 23 (17) ddu174, 4710-4720. doi: 10.1093/hmg/ddu174 |
