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2013 Journal Article Meta-analysis of gene-level associations for rare variants based on single-variant statisticsHu, Yi-Juan, Berndt, Sonja I., Gustafsson, Stefan, Ganna, Andrea, Hirschhorn, Joel, North, Kari E., Ingelsson, Erik, Lin, Dan-Yu, Collins, Francis S., Berndt, Sonja I., Gustafsson, Stefan, Ma¨gi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, To˜nu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian’an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W. ... Ingelsson, Erik (2013). Meta-analysis of gene-level associations for rare variants based on single-variant statistics. American Journal of Human Genetics, 93 (2), 236-248. doi: 10.1016/j.ajhg.2013.06.011 |
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2013 Journal Article Introgression and the fate of domesticated genes in a wild mammal populationFeulner, Philine G. D., Gratten, Jacob, Kijas, James W., Visscher, Peter M., Pemberton, Josephine M. and Slate, Jon (2013). Introgression and the fate of domesticated genes in a wild mammal population. Molecular Ecology, 22 (16), 4210-4221. doi: 10.1111/mec.12378 |
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2013 Journal Article Commentary: height and Mendel's theory: the long and the short of itVisscher, Peter M. (2013). Commentary: height and Mendel's theory: the long and the short of it. International Journal of Epidemiology, 42 (4) dyt069, 944-945. doi: 10.1093/ije/dyt069 |
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2013 Journal Article From personalized to public health genomicsGibson, Greg and Visscher, Peter M. (2013). From personalized to public health genomics. Genome Medicine, 5 (60) 60, 1-2. doi: 10.1186/gm464 |
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2013 Journal Article Pitfalls of predicting complex traits from SNPsWray, Naomi R., Yang, Jian, Hayes, Ben J., Price, Alkes L., Goddard, Michael E. and Visscher, Peter M. (2013). Pitfalls of predicting complex traits from SNPs. Nature Reviews Genetics, 14 (7), 507-515. doi: 10.1038/nrg3457 |
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2013 Journal Article DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilitiesTrzaskowski, Maciej, Davis, Oliver S. P., DeFries, John C., Yang, Jian, Visscher, Peter M. and Plomin, Robert (2013). DNA evidence for strong genome-wide pleiotropy of cognitive and learning abilities. Behavior Genetics, 43 (4), 267-273. doi: 10.1007/s10519-013-9594-x |
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2013 Journal Article Insights into foraminiferal influences on microfabrics of microbialites at Highborne Cay, BahamasBernhard, Joan M., Edgcomb, Virginia P., Visscher, Pieter T., McIntyre-Wressnig, Anna, Summons, Roger E., Bouxsein, Mary L., Louis, Leeann and Jeglinski, Marleen (2013). Insights into foraminiferal influences on microfabrics of microbialites at Highborne Cay, Bahamas. Proceedings of the National Academy of Sciences of the United States of America, 110 (24), 9830-9834. doi: 10.1073/pnas.1221721110 |
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2013 Journal Article 708 common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traitsThomson, P. A., Parla, J. S., McRae, A. F., Kramer, M., Ramakrushnan, K., Yao, J., Soares, D. C., McCarthy, S., Morris, S. W., Cardone, L., Cass, S., Ghiban, E., Hennah, W., Evans, K. L., Rebolini, D., Millar, J. K., Harris, S. E., Starr, J. M., MacIntyre, J., Generation Scotland, McIntosh, A. M., Watson, J. D., Deary, I. J., Visscher, P. M., Blackwood, D. H., McCombie, W. R. and Porteous, D. J. (2013). 708 common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. Molecular Psychiatry, Advance online publication (6), 1-8. doi: 10.1038/mp.2013.68 |
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2013 Journal Article Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel diseaseWei, Zhi, Wang, Wei, Bradfield, Jonathan, Li, Jin, Cardinale, Christopher, Frackelton, Edward, Kim, Cecilia, Mentch, Frank, Van Steen, Kristel, Visscher, Peter M., Baldassano, Robert N., Hakonarson, Hakon and International IBD Genetics Consortium (2013). Large sample size, wide variant spectrum, and advanced machine-learning technique boost risk prediction for inflammatory bowel disease. American Journal of Human Genetics, 92 (6), 1008-1012. doi: 10.1016/j.ajhg.2013.05.002 |
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2013 Journal Article GWAS of 126,559 individuals identifies genetic variants associated with educational attainmentRietveld, Cornelius A., Medland, Sarah E., Derringer, Jaime, Yang, Jian, Esko, Tonu, Martin, Nicolas W., Westra, Harm-Jan, Shakhbazov, Konstantin, Abdellaoui, Abdel, Agrawal, Arpana, Albrecht, Eva, Alizadeh, Behrooz Z., Amin, Najaf, Bamard, John, Baumeister, Sebastian E., Benke, Kelly S., Bielak, Lawrence F., Boatman, Jeffrey A., Boyle, Patricia A., Davies, Gail, De Leeuw, Christiaan, Eklund, Niina, Evans, Daniel S., Ferhmann, Rudolf, Fischer, Krista, Gieger, Christian, Gjessing, Hakon K., Haegg, Sara, Harris, Jennifer R. ... Koellinger, Philipp D. (2013). GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science, 340 (6139), 1467-1471. doi: 10.1126/science.1235488 |
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2013 Journal Article Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disordersden Hoed, Marcel, Eijgelsheim, Mark, Esko, Tonu, Brundel, Bianca J. J. M., Peal, David S., Evans, David M., Nolte, Ilja M., Segre, Ayellet V., Holm, Hilma, Handsaker, Robert E., Westra, Harm-Jan, Johnson, Toby, Isaacs, Aaron, Yang, Jian, Lundby, Alicia, Zhao, Jing Hua, Kim, Young Jin, Go, Min Jin, Almgren, Peter, Bochud, Murielle, Boucher, Gabrielle, Cornelis, Marilyn C., Gudbjartsson, Daniel, Hadley, David, van der Harst, Pim, Hayward, Caroline, den Heijer, Martin, Igl, Wilmar, Jackson, Anne U. ... Loos, Ruth J. F. (2013). Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nature Genetics, 45 (6), 621-634. doi: 10.1038/ng.2610 |
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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 Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012)Verweij, K. J. H., Yang, J., Lahti, J., Veijola, J., Hintsanen, M., Pulkki-Raback, L., Heinonen, K., Pouta, A., Pesonen, A. -K., Widen, E., Taanila, A., Isohanni, M., Miettunen, J., Palotie, A., Penke, L., Service, S. K., Heath, A. C., Montgomery, G. W., Raitakari, O., Kaehoenen, M., Viikari, J., Raeikkoenen, K., Eriksson, J. G., Keltikangas-Jaervinen, L., Lehtimaeki, T., Martin, N. G., Jaervelin, M. -R., Visscher, P. M., Keller, M. C. and Zietsch, B. P. (2013). Correction: Maintenance of variation in human personality: testing evolutionary models by estimating heritability due to common causal variants and investigating the effect of distant inbreeding (vol 66, pg 3238, 2012). Evolution, 67 (5), 1537-1537. doi: 10.1111/evo.12095 |
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2013 Journal Article Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP dataPowell, Joseph E., Henders, Anjali K., McRae, Allan F., Kim, Jinhee, Hemani, Gibran, Martin, Nicholas G., Dermitzakis, Emmanouil T., Gibson, Greg, Montgomery, Grant W. and Visscher, Peter M. (2013). Congruence of additive and non-additive effects on gene expression estimated from pedigree and SNP data. PLoS Genetics, 9 (5) e1003502, e1003502.1-e1003502.10. doi: 10.1371/journal.pgen.1003502 |
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2013 Journal Article Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureBerndt, Sonja I., Gustafsson, Stefan, Maegi, Reedik, Ganna, Andrea, Wheeler, Eleanor, Feitosa, Mary F., Justice, Anne E., Monda, Keri L., Croteau-Chonka, Damien C., Day, Felix R., Esko, Tonu, Fall, Tove, Ferreira, Teresa, Gentilini, Davide, Jackson, Anne U., Luan, Jian'an, Randall, Joshua C., Vedantam, Sailaja, Willer, Cristen J., Winkler, Thomas W., Wood, Andrew R., Workalemahu, Tsegaselassie, Hu, Yi-Juan, Lee, Sang Hong, Liang, Liming, Lin, Dan-Yu, Min, Josine L., Neale, Benjamin M., Thorleifsson, Gudmar ... Ingelsson, Erik (2013). Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nature Genetics, 45 (5), 501-U69. doi: 10.1038/ng.2606 |
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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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Featured 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 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 |
