Meta-analysis of the heritability of human traits based on fifty years of twin studies von Polderman, Tinca J C, Benyamin, Beben, de Leeuw, Christiaan A, Sullivan, Patrick F, van Bochoven, Arjen, Visscher, Peter M, Posthuma, Danielle

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Common SNPs explain a large proportion of the heritability for human height von Heath, Andrew C, Benyamin, Beben, Nyholt, Dale R, Goddard, Michael E, Gordon, Scott, Martin, Nicholas G, Henders, Anjali K, Madden, Pamela A, Visscher, Peter M, McEvoy, Brian P, Yang, Jian, Montgomery, Grant W

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A method for an unbiased estimate of cross-ancestry genetic correlation using individual-level data von Momin, Md. Moksedul, Shin, Jisu, Lee, Soohyun, Truong, Buu, Benyamin, Beben, Lee, S. Hong

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Integrative multi-omics analysis to gain new insights into COVID-19 von Eshetie, Setegn, Choi, Karmel W., Hyppönen, Elina, Benyamin, Beben, Lee, S. Hong

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Moderate intensity aerobic exercise may enhance neuroplasticity of the contralesional hemisphere after stroke: a randomised controlled study von Hill, Gabrielle, Johnson, Finn, Uy, Jeric, Serrada, Ines, Benyamin, Beben, Van Den Berg, Maayken, Hordacre, Brenton

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Associations of genetically determined iron status across the phenome: A mendelian randomization study von Gill, Dipender, Benyamin, Beben, Moore, Luke S P, Monori, Grace, Zhou, Ang, Koskeridis, Fotios, Evangelou, Evangelos, Laffan, Mike, Walker, Ann P, Tsilidis, Konstantinos K, Dehghan, Abbas, Elliott, Paul, Hyppönen, Elina, Tzoulaki, Ioanna

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Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression von Tarr, Ingrid S., McCann, Emily P., Benyamin, Beben, Peters, Timothy J., Twine, Natalie A., Zhang, Katharine Y., Zhao, Qiongyi, Zhang, Zong-Hong, Rowe, Dominic B., Nicholson, Garth A., Bauer, Denis, Clark, Susan J., Blair, Ian P., Williams, Kelly L.

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Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia von Restuadi, Restuadi, Garton, Fleur C, Benyamin, Beben, Lin, Tian, Williams, Kelly L, Vinkhuyzen, Anna, van Rheenen, Wouter, Zhu, Zhihong, Laing, Nigel G, Mather, Karen A, Sachdev, Perminder S, Ngo, Shyuan T, Steyn, Frederik J, Wallace, Leanne, Henders, Anjali K, Visscher, Peter M, Needham, Merrilee, Mathers, Susan, Nicholson, Garth, Rowe, Dominic B, Henderson, Robert D, McCombe, Pamela A, Pamphlett, Roger, Blair, Ian P, Wray, Naomi R, McRae, Allan F

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Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study von Pichler, Irene, Del Greco M, Fabiola, Gögele, Martin, Lill, Christina M, Bertram, Lars, Do, Chuong B, Eriksson, Nicholas, Foroud, Tatiana, Myers, Richard H, Nalls, Michael, Keller, Margaux F, Benyamin, Beben, Whitfield, John B, Pramstaller, Peter P, Hicks, Andrew A, Thompson, John R, Minelli, Cosetta

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Lifestyle Modifies the Diabetes-Related Metabolic Risk, Conditional on Individual Genetic Differences von Shin, Jisu, Zhou, Xuan, Tan, Joanne T M, Hyppönen, Elina, Benyamin, Beben, Lee, S Hong

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Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels von Benyamin, Beben, McRae, Allan F., Zhu, Gu, Gordon, Scott, Henders, Anjali K., Palotie, Aarno, Peltonen, Leena, Martin, Nicholas G., Montgomery, Grant W., Whitfield, John B., Visscher, Peter M.

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Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study von Tielbeek, Jorim J, Medland, Sarah E, Benyamin, Beben, Byrne, Enda M, Heath, Andrew C, Madden, Pamela A F, Martin, Nicholas G, Wray, Naomi R, Verweij, Karin J H

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Genome Partitioning of Genetic Variation for Height from 11,214 Sibling Pairs von Visscher, Peter M., Macgregor, Stuart, Benyamin, Beben, Zhu, Gu, Gordon, Scott, Medland, Sarah, Hill, William G., Hottenga, Jouke-Jan, Willemsen, Gonneke, Boomsma, Dorret I., Liu, Yao-Zhong, Deng, Hong-Wen, Montgomery, Grant W., Martin, Nicholas G.

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Combined genome scans for body stature in 6,602 European twins: evidence for common Caucasian loci von Perola, Markus, Sammalisto, Sampo, Hiekkalinna, Tero, Martin, Nick G, Visscher, Peter M, Montgomery, Grant W, Benyamin, Beben, Harris, Jennifer R, Boomsma, Dorret, Willemsen, Gonneke, Hottenga, Jouke-Jan, Christensen, Kaare, Kyvik, Kirsten Ohm, Sørensen, Thorkild I A, Pedersen, Nancy L, Magnusson, Patrik K E, Spector, Tim D, Widen, Elisabeth, Silventoinen, Karri, Kaprio, Jaakko, Palotie, Aarno, Peltonen, Leena

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Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese von Gratten, Jacob, Zhao, Qiongyi, Benyamin, Beben, Garton, Fleur, He, Ji, Leo, Paul J, Mangelsdorf, Marie, Anderson, Lisa, Zhang, Zong-Hong, Chen, Lu, Chen, Xiang-Ding, Cremin, Katie, Deng, Hong-Weng, Edson, Janette, Han, Ying-Ying, Harris, Jessica, Henders, Anjali K, Jin, Zi-Bing, Li, Zhongshan, Lin, Yong, Liu, Xiaolu, Marshall, Mhairi, Mowry, Bryan J, Ran, Shu, Reutens, David C, Song, Sharon, Tan, Li-Jun, Tang, Lu, Wallace, Robyn H, Wheeler, Lawrie, Wu, Jinyu, Yang, Jian, Xu, Huji, Visscher, Peter M, Bartlett, Perry F, Brown, Matthew A, Wray, Naomi R, Fan, Dongsheng

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Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis von Nabais, Marta F., Lin, Tian, Benyamin, Beben, Williams, Kelly L., Garton, Fleur C., Vinkhuyzen, Anna A. E., Zhang, Futao, Vallerga, Costanza L., Restuadi, Restuadi, Freydenzon, Anna, Zwamborn, Ramona A. J., Hop, Paul J., Robinson, Matthew R., Gratten, Jacob, Visscher, Peter M., Hannon, Eilis, Mill, Jonathan, Brown, Matthew A., Laing, Nigel G., Mather, Karen A., Sachdev, Perminder S., Ngo, Shyuan T., Steyn, Frederik J., Wallace, Leanne, Henders, Anjali K., Needham, Merrilee, Veldink, Jan H., Mathers, Susan, Nicholson, Garth, Rowe, Dominic B., Henderson, Robert D., McCombe, Pamela A., Pamphlett, Roger, Yang, Jian, Blair, Ian P., McRae, Allan F., Wray, Naomi R.

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Genome-wide association study identifies two loci strongly affecting transferrin glycosylation von KUTALIK, Zoltán, BENYAMIN, Beben, VOLLENWEIDER, Peter, MARQUES-VIDAL, Pedro, WHITFIELD, John B, BERGMANN, Sven, MOOSER, Vincent, WAEBER, Gérard, MONTGOMERY, Grant W, MARTIN, Nicholas G, MADDEN, Pamela A. F, HEATH, Andrew C, BECKMANN, Jacques S

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Cognitive Function in Adolescence: Testing for Interactions Between Breast-Feeding and FADS2 Polymorphisms von Martin, Nicolas W., M.Sc, Benyamin, Beben, Ph.D, Hansell, Narelle K., Ph.D, Montgomery, Grant W., Ph.D, Martin, Nicholas G., Ph.D, Wright, Margaret J., Ph.D, Bates, Timothy C., Ph.D

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Lifestyle, genetic risk and incidence of cancer: a prospective cohort study of 13 cancer types von Byrne, Stephanie, Boyle, Terry, Ahmed, Muktar, Lee, Sang Hong, Benyamin, Beben, Hyppönen, Elina

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Optimal harvesting policy of predator-prey model with free fishing and reserve zones von Toaha, Syamsuddin, Rustam

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