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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 |
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2014 Journal Article Erratum: Incorrect Institutional Affiliations of Authors in the Article by Jiang et al (Arthritis Rheumatol (2014))Jiang, Lei, Yin, Jian, Ye, Lingying, Yang, Jian, Hemani, Gibran, Liu, Ai-Jun, Zou, Hejian, He, Dongyi, Sun, Lingyun, Zeng, Xiaofeng, Li, Zhanguo, Zheng, Yi, Lin, Yiping, Liu, Yi, Fang, Yongfei, Xu, Jianhua, Li, Yinong, Dai, Shengming, Guan, Jianlong, Jiang, Lindi, Wei, Qianghua, Wang, Yi, Li, Yang, Huang, Cibo, Zuo, Xiaoxia, Liu, Yu, Wu, Xin, Zhang, Libin, Zhou, Ling ... Xu, Huji (2014). Erratum: Incorrect Institutional Affiliations of Authors in the Article by Jiang et al (Arthritis Rheumatol (2014)). Arthritis and Rheumatology, 66 (7), 1881-1881. doi: 10.1002/art.38728 |
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2014 Journal Article Contribution of genetic variation to transgenerational inheritance of DNA methylationMcRae, Allan F., Powell, Joseph E., Henders, Anjali K., Bowdler, Lisa, Hemani, Gibran, Shah, Sonia, Painter, Jodie N., Martin, Nicholas G., Visscher, Peter M. and Montgomery, Grant W. (2014). Contribution of genetic variation to transgenerational inheritance of DNA methylation. Genome Biology, 15 (5) R73, 1-10. doi: 10.1186/gb-2014-15-5-r73 |
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2014 Journal Article Explaining additional genetic variation in complex traitsRobinson, Matthew R., Wray, Naomi R. and Visscher, Peter M. (2014). Explaining additional genetic variation in complex traits. Trends in Genetics, 30 (4), 124-132. doi: 10.1016/j.tig.2014.02.003 |
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2014 Journal Article DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12Trzaskowski, M., Yang, J., Visscher, P. M. and Plomin, R. (2014). DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12. Molecular Psychiatry, 19 (3), 380-384. doi: 10.1038/mp.2012.191 |
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2014 Journal Article Effects of Elevated Carbon Dioxide and Salinity on the Microbial Diversity in Lithifying Microbial MatsAhrendt, Steven R., Mobberley, Jennifer M., Visscher, Pieter T., Koss, Lawrence L. and Foster, Jamie S. (2014). Effects of Elevated Carbon Dioxide and Salinity on the Microbial Diversity in Lithifying Microbial Mats. Minerals, 4 (1), 145-169. doi: 10.3390/min4010145 |
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2014 Journal Article Childhood intelligence is heritable, highly polygenic and associated with FNBP1LBenyamin, B., St Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franic, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J., Harris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., de Geus, E. J. C., Wellcome Trust Case Control Consortium 2 (WTCCC2), Jaddoe, V. W. V., Starr, J. M. ... Visscher, P. M. (2014). Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry, 19 (2), 253-258. doi: 10.1038/mp.2012.184 |
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2014 Journal Article Active eukaryotes in microbialites from Highborne Cay, Bahamas, and Hamelin Pool (Shark Bay), AustraliaEdgcomb, Virginia P., Bernhard, Joan M., Summons, Roger E., Orsi, William, Beaudoin, David and Visscher, Pieter T. (2014). Active eukaryotes in microbialites from Highborne Cay, Bahamas, and Hamelin Pool (Shark Bay), Australia. Isme Journal, 8 (2), 418-429. doi: 10.1038/ismej.2013.130 |
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2014 Journal Article Advantages and pitfalls in the application of mixed-model association methodsYang, Jian, Zaitlen, Noah A., Goddard, Michael E., Visscher, Peter M. and Price, Alkes L. (2014). Advantages and pitfalls in the application of mixed-model association methods. Nature Genetics, 46 (2), 100-106. doi: 10.1038/ng.2876 |
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2014 Journal Article Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated SamplesVisscher, Peter M., Hemani, Gibran, Vinkhuyzen, Anna A. E., Chen, Guo-Bo, Lee, Sang Hong, Wray, Naomi R., Goddard, Michael E. and Yang, Jian (2014). Statistical Power to Detect Genetic (Co)Variance of Complex Traits Using SNP Data in Unrelated Samples. PLoS Genetics, 10 (4) e1004269, e1004269.1-e1004269.10. doi: 10.1371/journal.pgen.1004269 |
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2014 Journal Article Biological insights from 108 schizophrenia-associated genetic lociSchizophrenia Working Group of the Psychiatric Genomics Consortium, Catts, Stanley V., Gratten, Jacob, Lee, S. Hong, Wray, Naomi R., Visscher, Peter M., Mowry, Bryan J., Nertney, Deborah A., Psychosis Endophenotypes International Consortium and Wellcome Trust Case-Control Consortium 2 (2014). Biological insights from 108 schizophrenia-associated genetic loci. Nature, 511 (7510), 421-427. doi: 10.1038/nature13595 |
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2014 Journal Article Molecular genetic contributions to socioeconomic status and intelligenceMarioni, Riccardo E., Davies, Gail, Hayward, Caroline, Liewald, Dave, Kerr, Shona M., Campbell, Archie, Luciano, Michelle, Smith, Blair H., Padmanabhan, Sandosh, Hocking, Lynne J., Hastie, Nicholas D., Wright, Alan F., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014). Molecular genetic contributions to socioeconomic status and intelligence. Intelligence (Kidlington), 44 (1), 26-32. doi: 10.1016/j.intell.2014.02.006 |
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2014 Journal Article Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass IndexHoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J.H., Teumer, A., Winkler, T. W., Tsernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Mace, A., Rueger, S., Bochud, P.-Y., Barcella, M., Dauvilliers, Y., Benyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S. ... Kutalik Z. (2014). Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index. PLoS Genetics, 10 (7) e1004508, 1-12. doi: 10.1371/journal.pgen.1004508 |
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2014 Journal Article Changing Microspatial Patterns of SulfateReducing Microorganisms (SRM) during Cycling of Marine Stromatolite MatsPetrisor, Alexandru I., Szyjka, Sandra, Kawaguchi, Tomohiro, Visscher, Pieter T., Norman, Robert Sean and Decho, Alan W. (2014). Changing Microspatial Patterns of SulfateReducing Microorganisms (SRM) during Cycling of Marine Stromatolite Mats. International Journal of Molecular Sciences, 15 (1), 850-877. doi: 10.3390/ijms15010850 |
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2014 Journal Article Large-scale genomics unveils the genetic architecture of psychiatric disordersGratten, Jacob, Wray, Naomi R., Keller, Matthew C. and Visscher, Peter M. (2014). Large-scale genomics unveils the genetic architecture of psychiatric disorders. Nature Neuroscience, 17 (6), 782-790. doi: 10.1038/nn.3708 |
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2014 Journal Article Genetics of rheumatoid arthritis contributes to biology and drug discoveryOkada, Yukinori, Wu, Di, Trynka, Gosia, Raj, Towfique, Terao, Chikashi, Ikari, Katsunori, Kochi, Yuta, Ohmura, Koichiro, Suzuki, Akari, Yoshida, Shinji, Graham, Robert R., Manoharan, Arun, Ortmann, Ward, Bhangale, Tushar, Denny, Joshua C., Carroll, Robert J., Eyler, Anne E., Greenberg, Jeffrey D., Kremer, Joel M., Pappas, Dimitrios A., Jiang, Lei, Yin, Jian, Ye, Lingying, Su, Ding-Feng, Yang, Jian, Xie, Gang, Keystone, Ed, Westra, Harm-Jan, Esko, Tonu ... Brown, Matthew A. (2014). Genetics of rheumatoid arthritis contributes to biology and drug discovery. Nature, 506 (7488), 376-381. doi: 10.1038/nature12873 |
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2014 Journal Article Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland studyMarioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M. and Deary, Ian J. (2014). Common genetic variants explain the majority of the correlation between height and intelligence: The generation scotland study. Behavior Genetics, 44 (2), 91-96. doi: 10.1007/s10519-014-9644-z |
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2014 Journal Article Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeansJiang, Lei, Yin, Jian, Ye, Lingying, Yang, Jian, Hemani, Gibran, Liu, Ai-Jun, Zou, Hejian, He, Dongyi, Sun, Lingyun, Zeng, Xiaofeng, Li, Zhanguo, Zheng Yi, Lin, Yiping, Liu, Yi, Fang, Yongfei, Xu, Jianhua, Li, Yinong, Dai, Shengming, Guan, Jianlong, Jiang, Lindi, Wei, Qianghua, Wang, Yi, Li, Yang, Huang, Cibo, Zuo, Xiaoxia, Liu, Yu, Wu, Xin, Zhang, Libin, Zhou, Ling ... Xu, Huji (2014). Novel risk loci for rheumatoid arthritis in han chinese and congruence with risk variants in europeans. Arthritis and Rheumatology, 66 (5), 1121-1132. doi: 10.1002/art.38353 |
