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2018 Journal Article Oligo-Miocene lacustrine microbial and metazoan buildups from the Limagne Basin (French Massif Central)Roche, Adeline, Vennin, Emmanuelle, Bouton, Anthony, Olivier, Nicolas, Wattinne, Aurelia, Bundeleva, Irina, Deconinck, Jean-Francois, Virgone, Aurelien, Gaucher, Eric C. and Visscher, Pieter T. (2018). Oligo-Miocene lacustrine microbial and metazoan buildups from the Limagne Basin (French Massif Central). Palaeogeography Palaeoclimatology Palaeoecology, 504, 34-59. doi: 10.1016/j.palaeo.2018.05.001 |
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2018 Journal Article Evolutionary history and adaptation of a human pygmy population of Flores Island, IndonesiaTucci, Serena, Vohr, Samuel H., McCoy, Rajiv C., Vernot, Benjamin, Robinson, Matthew R., Barbieri, Chiara, Nelson, Brad J., Fu, Wenqing, Purnomo, Gludhug A., Sudoyo, Herawati, Eichler, Evan E., Barbujani, Guido, Visscher, Peter M., Akey, Joshua M. and Green, Richard E. (2018). Evolutionary history and adaptation of a human pygmy population of Flores Island, Indonesia. Science, 361 (6401), 511-515. doi: 10.1126/science.aar8486 |
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2018 Journal Article Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetesXue, Angli, Wu, Yang, Zhu, Zhihong, Zhang, Futao, Kemper, Kathryn E., Zheng, Zhili, Yengo, Loic, Lloyd-Jones, Luke R., Sidorenko, Julia, Wu, Yeda, eQTLGen Consortium, McRae, Allan F., Visscher, Peter M., Zeng, Jian and Yang, Jian (2018). Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Nature Communications, 9 (1) 2941, 2941. doi: 10.1038/s41467-018-04951-w |
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2018 Journal Article Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individualsLee, James J., Wedow, Robbee, Okbay, Aysu, Kong, Edward, Maghzian, Omeed, Zacher, Meghan, Nguyen-Viet, Tuan Anh, Bowers, Peter, Sidorenko, Julia, Karlsson Linnér, Richard, Fontana, Mark Alan, Kundu, Tushar, Lee, Chanwook, Li, Hui, Li, Ruoxi, Royer, Rebecca, Timshel, Pascal N., Walters, Raymond K., Willoughby, Emily A., Yengo, Loïc, 23andMe Research Team, COGENT (Cognitive Genomics Consortium), Social Science Genetic Association Consortium, Alver, Maris, Bao, Yanchun, Clark, David W., Day, Felix R., Furlotte, Nicholas A., Joshi, Peter K. ... Cesarini, David (2018). Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Nature Genetics, 50 (8), 1112-1121. doi: 10.1038/s41588-018-0147-3 |
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2018 Journal Article Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesisPace, A., Bourillot, R., Bouton, A., Vennin, E., Braissant, O., Dupraz, C., Duteil, T., Bundeleva, I., Patrier, P., Galaup, S., Yokoyama, Y., Franceschi, M., Virgone, A. and Visscher, P. T. (2018). Formation of stromatolite lamina at the interface of oxygenic-anoxygenic photosynthesis. Geobiology, 16 (4), 378-398. doi: 10.1111/gbi.12281 |
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2018 Journal Article Misestimation of heritability and prediction accuracy of male-pattern baldnessYap, Chloe X., Sirodenko, Julia, Marioni, Riccardo E., Yengo, Loic, Wray, Naomi R. and Visscher, Peter M. (2018). Misestimation of heritability and prediction accuracy of male-pattern baldness. Nature Communications, 9 (1) 2537, 2537. doi: 10.1038/s41467-018-04807-3 |
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2018 Journal Article Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de AtacamaSancho-Tomas, Maria, Somogyi, Andrea, Medjoubi, Kadda, Bergamaschi, Antoine, Visscher, Pieter T., Van Driessche, Alexander E. S., Gerard, Emmanuelle, Farias, Maria E., Contreras, Manuel and Philippot, Pascal (2018). Distribution, redox state and (bio)geochemical implications of arsenic in present day microbialites of Laguna Brava, Salar de Atacama. Chemical Geology, 490, 13-21. doi: 10.1016/j.chemgeo.2018.04.029 |
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2018 Journal Article A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed frameworkLeBlanc, Marissa, Zuber, Verena, Thompson, Wesley K., Andreassen, Ole A., Frigessi, Arnoldo, Andreassen, Bettina Kulle, Ripke, Stephan, Neale, Benjamin M., Corvin, Aiden, Walters, James T. R., Farh, Kai-How, Lee, Phil, Bulik-Sullivan, Brendan, Collier, David, Huang, Hailiang, Pers, Tune, Agartz, Ingrid, Agerbo, Esben, Albus, Margot, Alexander, Madeline, Amin, Farooq, Bacanu, Silviu A., Begemann, Martin, Belliveau, Richard A., Bene, Judit, Bevilacqua, Elizabeth, Bigdeli, Tim B., Black, Donald W., Bruggeman, Richard ... Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium (2018). A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework. BMC Genomics, 19 (1) 494. doi: 10.1186/s12864-018-4859-7 |
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2018 Journal Article Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypesRuderfer, Douglas M., Ripke, Stephan, McQuillin, Andrew, Boocock, James, Stahl, Eli A., Pavlides, Jennifer M. Whitehead, Mullins, Niamh, Charney, Alexander W., Ori, Anil P.S., Loohuis, Loes M. Olde, Domenici, Enrico, Di Florio, Arianna, Papiol, Sergi, Kalman, Janos L., Trubetskoy, Vassily, Adolfsson, Rolf, Agartz, Ingrid, Agerbo, Esben, Akil, Huda, Albani, Diego, Albus, Margot, Alda, Martin, Alexander, Madeline, Alliey-Rodriguez, Ney, Als, Thomas D., Amin, Farooq, Anjorin, Adebayo, Arranz, Maria J., Awasthi, Swapnil ... Kendler, Kenneth S. (2018). Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes. Cell, 173 (7), 1705-1715.e16. doi: 10.1016/j.cell.2018.05.046 |
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2018 Journal Article Common disease is more complex than implied by the core gene omnigenic modelWray, Naomi R., Wijmenga, Cisca, Sullivan, Patrick F., Yang, Jian and Visscher, Peter M. (2018). Common disease is more complex than implied by the core gene omnigenic model. Cell, 173 (7), 1573-1580. doi: 10.1016/j.cell.2018.05.051 |
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2018 Journal Article Identifying gene targets for brain-related traits using transcriptomic and methylomic data from bloodQi, Ting, Wu, Yang, Zeng, Jian, Zhang, Futao, Xue, Angli, Jiang, Longda, Zhu, Zhihong, Kemper, Kathryn, Yengo, Loic, Zheng, Zhili, eQTLGen Consortium, Marioni, Riccardo E., Montgomery, Grant W., Deary, Ian J., Wray, Naomi R., Visscher, Peter M., McRae, Allan F. and Yang, Jian (2018). Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood. Nature Communications, 9 (1) 2282, 2282. doi: 10.1038/s41467-018-04558-1 |
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2018 Journal Article Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humansCuellar Partida, Gabriel, Laurin, Charles, Ring, Susan M., Gaunt, Tom R., McRae, Allan, Visscher, Peter M., Montgomery, Grant W., Martin, Nicholas G., Hemani, Gibran, Suderman, Matthew, Relton, Caroline L., Davey Smith, George and Evans, David M. (2018). Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans. Human Molecular Genetics, 27 (16), 2927-2939. doi: 10.1093/hmg/ddy206 |
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2018 Journal Article GWAS on family history of Alzheimer's diseaseMarioni, Riccardo E., Harris, Sarah E., Zhang, Qian, McRae, Allan F., Hagenaars, Saskia P., Hill, W. David, Davies, Gail, Ritchie, Craig W., Gale, Catharine R., Starr, John M., Goate, Alison M., Porteous, David J., Yang, Jian, Evans, Kathryn L., Deary, Ian J., Wray, Naomi R. and Visscher, Peter M. (2018). GWAS on family history of Alzheimer's disease. Translational Psychiatry, 8 (1) 99, 99. doi: 10.1038/s41398-018-0150-6 |
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2018 Journal Article Erratum: evidence of directional and stabilizing selection in contemporary humans (Proceedings of the National Academy of Sciences of the United States of America (2017) 115 (151–156) DOI: 10.1073/pnas.1707227114)Sanjak, Jaleal S., Sidorenko, Julia, Robinson, Matthew R., Thornton, Kevin R. and Visscher, Peter M. (2018). Erratum: evidence of directional and stabilizing selection in contemporary humans (Proceedings of the National Academy of Sciences of the United States of America (2017) 115 (151–156) DOI: 10.1073/pnas.1707227114). Proceedings of the National Academy of Sciences of the United States of America, 115 (20). doi: 10.1073/pnas.1806837115 |
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2018 Journal Article Global genetic differentiation of complex traits shaped by natural selection in humansGuo, Jing, Wu, Yang, Zhu, Zhihong, Zheng, Zhili, Trzaskowski, Maciej, Zeng, Jian, Robinson, Matthew R., Visscher, Peter M. and Yang, Jian (2018). Global genetic differentiation of complex traits shaped by natural selection in humans. Nature Communications, 9 (1) 1865, 1865. doi: 10.1038/s41467-018-04191-y |
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2018 Journal Article Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depressionWray, Naomi R., Ripke, Stephan, Mattheisen, Manuel, Trzaskowski, Maciej, Byrne, Enda M., Abdellaoui, Abdel, Adams, Mark J., Agerbo, Esben, Air, Tracy M., Andlauer, Till M. F., Bacanu, Silviu-Alin, Baekvad-Hansen, Marie, Beekman, Aartjan F. T., Bigdeli, Tim B., Binder, Elisabeth B., Blackwood, Douglas R. H., Bryois, Julien, Buttenschon, Henriette N., Bybjerg-Grauholm, Jonas, Cai, Na, Castelao, Enrique, Christensen, Jane Hvarregaard, Clarke, Toni-Kim, Coleman, Jonathan I. R., Colodro-Conde, Lucia, Couvy-Duchesne, Baptiste, Craddock, Nick, Crawford, Gregory E., Crowley, Cheynna A. ... Sullivan, Patrick F. (2018). Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Nature Genetics, 50 (5), 668-+. doi: 10.1038/s41588-018-0090-3 |
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2018 Journal Article Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traitsEvans, Luke M., Tahmasbi, Rasool, Vrieze, Scott I., Abecasis, Gonçalo R., Das, Sayantan, Gazal, Steven, Bjelland, Douglas W., de Candia, Teresa R., Haplotype Reference Consortium, Goddard, Michael E., Neale, Benjamin M., Yang, Jian, Visscher, Peter M. and Keller, Matthew C. (2018). Comparison of methods that use whole genome data to estimate the heritability and genetic architecture of complex traits. Nature genetics, 50 (5), 737-745. doi: 10.1038/s41588-018-0108-x |
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2018 Journal Article Signatures of negative selection in the genetic architecture of human complex traitsZeng, 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. Nature Genetics, 50 (5), 746-753. doi: 10.1038/s41588-018-0101-4 |
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2018 Journal Article Cohort Profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS)Hebert, Harry L., Shepherd, Bridget, Milburn, Keith, Veluchamy, Abirami, Meng, Weihua, Carr, Fiona, Donnelly, Louise A., Tavendale, Roger, Leese, Graham, Colhoun, Helen M., Dow, Ellie, Morris, Andrew D., Doney, Alexander S., Lang, Chim C., Pearson, Ewan R., Smith, Blair H. and Palmer, Colin N. A. (2018). Cohort Profile: Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS). International Journal of Epidemiology, 47 (2), 380-+. doi: 10.1093/ije/dyx140 |
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2018 Journal Article Narrow-sense heritability estimation of complex traits using identity-by-descent informationEvans, Luke M., Tahmasbi, Rasool, Jones, Matt, Vrieze, Scott I., Abecasis, Gonçalo R., Das, Sayantan, Bjelland, Douglas W., de Candia, Teresa R., Yang, Jian, Goddard, Michael E., Visscher, Peter M., Keller, Matthew C. and Haplotype Reference Consortium (2018). Narrow-sense heritability estimation of complex traits using identity-by-descent information. Heredity, 121 (6), 1-15. doi: 10.1038/s41437-018-0067-0 |
