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2013 Journal Article Polygenic risk for schizophrenia is associated with cognitive change between childhood and old ageMcIntosh, Andrew M., Gow, Alan, Luciano, Michelle, Davies, Gail, Liewald, David C., Harris, Sarah E., Corley, Janie, Hall, Jeremy, Starr, John M., Porteous, David J., Tenesa, Albert, Visscher, Peter M. and Deary, Ian J. (2013). Polygenic risk for schizophrenia is associated with cognitive change between childhood and old age. Biological Psychiatry, 73 (10), 938-943. doi: 10.1016/j.biopsych.2013.01.011 |
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2013 Journal Article All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPsSchork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael C., Furberg, Helena, The Tobacco and Genetics Consortium, The Bipolar Disorder Psychiatric Genomics Consortium, The Schizophrenia Psychiatric Genomics Consortium, Schork, Nicholas J., Andreassen, Ole A., Dale, Anders M., McGrath, John J., Mowry, Bryan and Visscher, Peter (2013). All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PloS Genetics, 9 (4) e1003449, e1003449. doi: 10.1371/journal.pgen.1003449 |
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2013 Journal Article Interpreting the role of de novo protein-coding mutations in neuropsychiatric diseaseGratten, Jacob, Visscher, Peter M., Mowry, Bryan J. and Wray, Naomi R. (2013). Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease. Nature Genetics, 45 (3), 234-238. doi: 10.1038/ng.2555 |
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2013 Journal Article Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohortsVimaleswaran, Karani S., Berry, Diane J., Lu, Chen, Tikkanen, Emmi, Pilz, Stefan, Hiraki, Linda T., Cooper, Jason D., Dastani, Zari, Li, Rui, Houston, Denise K., Wood, Andrew R., Michaëlsson, Karl, Vandenput, Liesbeth, Zgaga, Lina, Yerges-Armstrong, Laura M., McCarthy, Mark I., Dupuis, Josée, Kaakinen, Marika, Kleber, Marcus E., Jameson, Karen, Arden, Nigel, Raitakari, Olli, Viikari, Jorma, Lohman, Kurt K., Ferrucci, Luigi, Melhus, Håkan, Ingelsson, Erik, Byberg, Liisa, Lind, Lars ... Hirschhorn, J. N. (2013). Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts. PLoS Medicine, 10 (2) e1001383, e1001383. doi: 10.1371/journal.pmed.1001383 |
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2013 Journal Article Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosisLee, S. Hong, Harold, Denise, Nyholt, Dale R., ANZGene Consortium, International Endogene Consortium, Genetic and Environmental Risk for Alzheimer’s disease (GERAD1) Consortium, Goddard, Michael E., Zondervan, Krina T., Williams, Julie, Montgomery, Grant W., Wray, Naomi R. and Visscher, Peter M. (2013). Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Human Molecular Genetics, 22 (4) dds491, 832-841. doi: 10.1093/hmg/dds491 |
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2013 Journal Article Calculating statistical power in Mendelian randomization studiesBrion, Marie-Jo A., Shakhbazov, Konstantin and Visscher, Peter M. (2013). Calculating statistical power in Mendelian randomization studies. International Journal of Epidemiology, 42 (5) dyt179, 1497-1501. doi: 10.1093/ije/dyt179 |
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2013 Journal Article Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by seasonParnell, Grant P., Gatt, Prudence N., McKay, Fiona C., Schibeci, Stephen, Krupa, Malgorzata, Powell, Joseph E., Visscher, Peter M., Montgomery, Grant W., Lechner-Scott, Jeannette, Broadley, Simon, Liddle, Christopher, Slee, Mark, Vucic, Steve, Stewart, Graeme J. and Booth, David R. (2013). Ribosomal protein S6 mRNA is a biomarker upregulated in multiple sclerosis, downregulated by interferon treatment, and affected by season. Multiple Sclerosis, 20 (6), 675-685. doi: 10.1177/1352458513507819 |
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2013 Journal Article Genetic and nongenetic variation revealed for the principal components of human gene expressionGoldinger, Anita, Henders, Anjali K., McRae, Allan F., Martin, Nicholas G., Gibson, Greg, Montgomery, Grant W., Visscher, Peter M. and Powell, Joseph E. (2013). Genetic and nongenetic variation revealed for the principal components of human gene expression. Genetics, 195 (3), 1117-1128. doi: 10.1534/genetics.113.153221 |
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2013 Journal Article Estimation of SNP heritability from dense genotype dataLee, S. Hong, Yang, Jian, Chen, Guo-Bo, Ripke, Stephan, Stahl, Eli A., Hultman, Christina M., Sklar, Pamela, Visscher, Peter M., Sullivan, Patrick F., Goddard, Michael E. and Wray, Naomi (2013). Estimation of SNP heritability from dense genotype data. American Journal Of Human Genetics, 93 (6), 1151-1155. doi: 10.1016/j.ajhg.2013.10.015 |
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2013 Journal Article PHOSPHATE-RELATED ARTIFACTS IN CARBONATE MINERALIZATION EXPERIMENTSGallagher, Kimberley L., Braissant, Olivier, Kading, Tristan J., Dupraz, Christophe and Visscher, Pieter T. (2013). PHOSPHATE-RELATED ARTIFACTS IN CARBONATE MINERALIZATION EXPERIMENTS. Journal of Sedimentary Research, 83 (1-2), 39-51. doi: 10.2110/jsr.2013.9 |
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2012 Journal Article A genome-wide association study implicates the APOE locus in nonpathological cognitive ageingDavies, G., Harris, S. E., Reynolds, C. A., Payton, A., Knight, H. M., Liewald, D. C., Lopez, L. M., Luciano, M., Gow, A. J., Corley, J., Henderson, R., Murray, C., Pattie, A., Fox, H. C., Redmond, P., Lutz, M. W., Chiba-Falek, O., Linnertz, C., Saith, S., Haggarty, P., McNeill, G., Ke, X., Ollier, W., Horan, M., Roses, A. D., Ponting, C. P., Porteous, D. J., Tenesa, A., Pickles, A. ... Deary, I. J. (2012). A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. Molecular Psychiatry, 19 (1), 76-87. doi: 10.1038/mp.2012.159 |
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2012 Journal Article Seventy-five genetic loci influencing the human red blood cellvan der Harst, Pim, Zhang, Weihua, Leach, Irene Mateo, Rendon, Augusto, Verweij, Niek, Sehmi, Joban, Paul, Dirk S., Elling, Ulrich, Allayee, Hooman, Li, Xinzhong, Radhakrishnan, Aparna, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Albers, Cornelis A., Al-Hussani, Abtehale, Asselbergs, Folkert W., Ciullo, Marina, Danjou, Fabrice, Dina, Christian, Esko, Tonu, Evans, David M., Franke, Lude, Goegele, Martin, Hartiala, Jaana, Hersch, Micha, Holm, Hilma, Hottenga, Jouke-Jan, Kanoni, Stavroula ... Chambers, John C. (2012). Seventy-five genetic loci influencing the human red blood cell. Nature, 492 (7429), 369-375. doi: 10.1038/nature11677 |
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2012 Journal Article Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteriaGallagher, K. L., Kading, T. J., Braissant, O., Dupraz, C. and Visscher, P. T. (2012). Inside the alkalinity engine: the role of electron donors in the organomineralization potential of sulfate-reducing bacteria. Geobiology, 10 (6), 518-530. doi: 10.1111/j.1472-4669.2012.00342.x |
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2012 Journal Article Reclassify controls at your own riskWitte, John S. and Visscher, Peter M. (2012). Reclassify controls at your own risk. Epidemiology, 23 (6), 910-911. doi: 10.1097/EDE.0b013e31826cc118 |
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2012 Journal Article Functional gene group analysis identifies synaptic gene groups as risk factor for schizophreniaLips, E. S., Cornelisse, L. N., Toonen, R. F., Min, J. L., Hultman, C. M., International Schizophrenia Consortium, Holmans, P. A., O'Donovan, M. C., Purcell, S. M., Smit, A. B., Verhage, M., Sullivan, P. F., Visscher, P. M. and Posthuma, D. (2012). Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Molecular Psychiatry, 17 (10), 996-1006. doi: 10.1038/mp.2011.117 |
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2012 Journal Article Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihoodLee, S. H., Yang, J., Goddard, M. E., Visscher, P. M. and Wray, N. R. (2012). Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood. Bioinformatics, 28 (19) bts474, 2540-2542. doi: 10.1093/bioinformatics/bts474 |
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2012 Journal Article Effect of Inorganic and Organic Ligands on the Bioavailability of Methylmercury as Determined by Using a <i>mer-lux</i> BioreporterNdu, Udonna, Mason, Robert P., Zhang, Huan, Lin, Senjie and Visscher, Pieter T. (2012). Effect of Inorganic and Organic Ligands on the Bioavailability of Methylmercury as Determined by Using a mer-lux Bioreporter. Applied and Environmental Microbiology, 78 (20), 7276-7282. doi: 10.1128/AEM.00362-12 |
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2012 Journal Article A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterolSurakka, Ida, Whitfield, John B., Perola, Markus, Visscher, Peter M., Montgomery, Grant W., Falchi, Mario, Willemsen, Gonneke, de Geus, Eco J. C., Magnusson, Patrik K. E., Christensen, Kaare, Sorensen, Thorild I. A., Pietilainen, Kirsi H., Rantanen, Taina, Silander, Kaisa, Widen, Elisabeth, Muilu, Juhu, Rahman, Iffat, Liljedahl, Ulrika, Syvanen, Ann-Christine, Palotie, Aarno, Kaprio, Jaakko, Kyvik, Kirsten O., Pedersen, Nancy L., Boomsma, Dorret I., Spector, Tim, Martin, Nicolas G., Ripatti, Samuli and Peltonen, Leena (2012). A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Twin Research and Human Genetics, 15 (6), 691-699. doi: 10.1017/thg.2012.63 |
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2012 Journal Article Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreedingVerweij, Karin J. H., Yang, Jian, Lahti, Jari, Veijola, Juha, Hintsanen, Mirka, Pulkki-Raback, Laura, Heinonen, Kati, Pouta, Anneli, Pesonen, Anu-Katriina, Widen, Elisabeth, Taanila, Anja, Isohanni, Matti, Miettunen, Jouko, Palotie, Aarno, Penke, Lars, Service, Susan K., Heath, Andrew C., Montgomery, Grant W., Raitakari, Olli, Kahonen, Mika, Viikari, Jorma, Raikkonen, Katri, Eriksson, Johan G., Keltikangas-Jarvinen, Liisa, Lehtimaki, Terho, Martin, Nicholas G., Jarvelin, Marjo-Riitta, Visscher, Peter M., Keller, Matthew C. and Zietsch, Brendan P. (2012). Maintenance of genetic variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding. Evolution, 66 (10), 3238-3251. doi: 10.1111/j.1558-5646.2012.01679.x |
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2012 Journal Article FTO genotype is associated with phenotypic variability of body mass indexYang, Jian, Loos, Ruth J., Powell, Joseph E., Medland, Sarah E, Speliotes, Elizabeth K., Chasman, Daniel I., Rose, Lynda M., Thorleifsson, Gudmar, Steinthorsdottir, Valgerdur, Magi, Reedik, Waite, Lindsay, Vernon Smith, Albert, Yerges-Armstrong, Laura M., Monda, Keri L., Hadley, David, Mahajan, Anubha, Li, Guo, Kapur, Karen, Vitart, Veronique, Huffman, Jennifer E., Wang, Sophie R., Palmer, Cameron, Esko, To˜nu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayse, Isaacs, Aaron, Feitosa, Mary F., Luan, Jian’an ... Visscher, Peter (2012). FTO genotype is associated with phenotypic variability of body mass index. Nature, 490 (7419), 267-272. doi: 10.1038/nature11401 |
