Body fatness and physical activity at young ages and the risk of breast cancer in premenopausal women von Magnusson, C M K, Roddam, A W, Pike, M C, Chilvers, C, Crossley, B, Hermon, C, McPherson, K, Peto, J, Vessey, M, Beral, V

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Large-scale metabolomic profiling identifies novel biomarkers for incident coronary heart disease von Ganna, Andrea, Salihovic, Samira, Sundström, Johan, Broeckling, Corey D, Hedman, Asa K, Magnusson, Patrik K E, Pedersen, Nancy L, Larsson, Anders, Siegbahn, Agneta, Zilmer, Mihkel, Prenni, Jessica, Arnlöv, Johan, Lind, Lars, Fall, Tove, Ingelsson, Erik

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Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index von Yang, Jian, Bakshi, Andrew, Zhu, Zhihong, Hemani, Gibran, Vinkhuyzen, Anna A E, Lee, Sang Hong, Robinson, Matthew R, Perry, John R B, Nolte, Ilja M, van Vliet-Ostaptchouk, Jana V, Snieder, Harold, Esko, Tonu, Milani, Lili, Mägi, Reedik, Metspalu, Andres, Hamsten, Anders, Magnusson, Patrik K E, Pedersen, Nancy L, Ingelsson, Erik, Soranzo, Nicole, Keller, Matthew C, Wray, Naomi R, Goddard, Michael E, Visscher, Peter M

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Copy number variation in schizophrenia in Sweden von Szatkiewicz, J P, O'Dushlaine, C, Chen, G, Chambert, K, Moran, J L, Neale, B M, Fromer, M, Ruderfer, D, Akterin, S, Bergen, S E, Kähler, A, Magnusson, P K E, Kim, Y, Crowley, J J, Rees, E, Kirov, G, O'Donovan, M C, Owen, M J, Walters, J, Scolnick, E, Sklar, P, Purcell, S, Hultman, C M, McCarroll, S A, Sullivan, P F

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Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder von Bergen, S E, O'Dushlaine, C T, Ripke, S, Lee, P H, Ruderfer, D M, Akterin, S, Moran, J L, Chambert, K D, Handsaker, R E, Backlund, L, Ösby, U, McCarroll, S, Landen, M, Scolnick, E M, Magnusson, P K E, Lichtenstein, P, Hultman, C M, Purcell, S M, Sklar, P, Sullivan, P F

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Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct von Ferreira, Manuel A.R., Mathur, Riddhima, Vonk, Judith M., Szwajda, Agnieszka, Brumpton, Ben, Granell, Raquel, Brew, Bronwyn K., Ullemar, Vilhelmina, Lu, Yi, Jiang, Yunxuan, Magnusson, Patrik K.E., Karlsson, Robert, Hinds, David A., Paternoster, Lavinia, Koppelman, Gerard H., Almqvist, Catarina

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A genome-wide association study of kynurenic acid in cerebrospinal fluid: implications for psychosis and cognitive impairment in bipolar disorder von Sellgren, C M, Kegel, M E, Bergen, S E, Ekman, C J, Olsson, S, Larsson, M, Vawter, M P, Backlund, L, Sullivan, P F, Sklar, P, Smoller, J W, Magnusson, P K E, Hultman, C M, Walther-Jallow, L, Svensson, C I, Lichtenstein, P, Schalling, M, Engberg, G, Erhardt, S, Landén, M

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The Risk of Treatment-Emergent Mania With Methylphenidate in Bipolar Disorder von Viktorin, Alexander, Rydén, Eleonore, Thase, Michael E, Chang, Zheng, Lundholm, Cecilia, D’Onofrio, Brian M, Almqvist, Catarina, Magnusson, Patrik K.E, Lichtenstein, Paul, Larsson, Henrik, Landén, Mikael

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High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction von McClay, Joseph L, Shabalin, Andrey A, Dozmorov, Mikhail G, Adkins, Daniel E, Kumar, Gaurav, Nerella, Srilaxmi, Clark, Shaunna L, Bergen, Sarah E, Hultman, Christina M, Magnusson, Patrik K E, Sullivan, Patrick F, Aberg, Karolina A, van den Oord, Edwin J C G

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Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia von Halvorsen, Matthew, Huh, Ruth, Oskolkov, Nikolay, Wen, Jia, Netotea, Sergiu, Giusti-Rodriguez, Paola, Karlsson, Robert, Bryois, Julien, Nystedt, Björn, Ameur, Adam, Kähler, Anna K., Ancalade, NaEshia, Farrell, Martilias, Crowley, James J., Li, Yun, Magnusson, Patrik K. E., Gyllensten, Ulf, Hultman, Christina M., Sullivan, Patrick F., Szatkiewicz, Jin P.

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A polygenic burden of rare disruptive mutations in schizophrenia von Purcell, Shaun M., Moran, Jennifer L., Fromer, Menachem, Ruderfer, Douglas, Solovieff, Nadia, Roussos, Panos, O’Dushlaine, Colm, Chambert, Kimberly, Bergen, Sarah E., Kähler, Anna, Duncan, Laramie, Stahl, Eli, Genovese, Giulio, Fernández, Esperanza, Collins, Mark O., Komiyama, Noboru H., Choudhary, Jyoti S., Magnusson, Patrik K. E., Banks, Eric, Shakir, Khalid, Garimella, Kiran, Fennell, Tim, DePristo, Mark, Grant, Seth G. N., Haggarty, Stephen J., Gabriel, Stacey, Scolnick, Edward M., Lander, Eric S., Hultman, Christina M., Sullivan, Patrick F., McCarroll, Steven A., Sklar, Pamela

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Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia von Wen, Jia, Trost, Brett, Engchuan, Worrawat, Halvorsen, Matthew, Pallotto, Linda M., Mitina, Aleksandra, Ancalade, NaEshia, Farrell, Martilias, Backstrom, Ian, Guo, Keyi, Pellecchia, Giovanna, Thiruvahindrapuram, Bhooma, Giusti-Rodriguez, Paola, Rosen, Jonathan David, Li, Yun, Won, Hyejung, Magnusson, Patrik K. E., Gyllensten, Ulf, Bassett, Anne S., Hultman, Christina M., Sullivan, Patrick F., Yuen, Ryan K. C., Szatkiewicz, Jin P.

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The Risk of Switch to Mania in Patients With Bipolar Disorder During Treatment With an Antidepressant Alone and in Combination With a Mood Stabilizer von Viktorin, Alexander, Lichtenstein, Paul, Thase, Michael E., Larsson, Henrik, Lundholm, Cecilia, Magnusson, Patrik K.E., Landén, Mikael

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A methylome-wide study of aging using massively parallel sequencing of the methyl-CpG-enriched genomic fraction from blood in over 700 subjects von McClay, Joseph L, Aberg, Karolina A, Clark, Shaunna L, Nerella, Srilaxmi, Kumar, Gaurav, Xie, Lin Y, Hudson, Alexandra D, Harada, Aki, Hultman, Christina M, Magnusson, Patrik K E, Sullivan, Patrick F, Van Den Oord, Edwin J C G

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A latent neurogenic program in astrocytes regulated by Notch signaling in the mouse von Magnusson, Jens P., Göritz, Christian, Tatarishvili, Jemal, Dias, David O., Smith, Emma M. K., Lindvall, Olle, Kokaia, Zaal, Frisén, Jonas

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Methylome-Wide Association Study of Schizophrenia: Identifying Blood Biomarker Signatures of Environmental Insults von Aberg, Karolina A, McClay, Joseph L, Nerella, Srilaxmi, Clark, Shaunna, Kumar, Gaurav, Chen, Wenan, Khachane, Amit N, Xie, Linying, Hudson, Alexandra, Gao, Guimin, Harada, Aki, Hultman, Christina M, Sullivan, Patrick F, Magnusson, Patrik K. E, van den Oord, Edwin J. C. G

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Smoking is associated with mosaic loss of chromosome Y von Dumanski, Jan P., Rasi, Chiara, Lönn, Mikael, Davies, Hanna, Ingelsson, Martin, Giedraitis, Vilmantas, Lannfelt, Lars, Magnusson, Patrik K. E., Lindgren, Cecilia M., Morris, Andrew P., Cesarini, David, Johannesson, Magnus, Janson, Eva Tiensuu, Lind, Lars, Pedersen, Nancy L., Ingelsson, Erik, Forsberg, Lars A.

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Meta-GWAS Accuracy and Power (MetaGAP) Calculator Shows that Hiding Heritability Is Partially Due to Imperfect Genetic Correlations across Studies von de Vlaming, Ronald, Okbay, Aysu, Rietveld, Cornelius A, Johannesson, Magnus, Magnusson, Patrik K E, Uitterlinden, André G, van Rooij, Frank J A, Hofman, Albert, Groenen, Patrick J F, Thurik, A Roy, Koellinger, Philipp D

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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects von Howe, Laurence J., Nivard, Michel G., Morris, Tim T., Hansen, Ailin F., Rasheed, Humaira, Cho, Yoonsu, Chittoor, Geetha, Ahlskog, Rafael, Lind, Penelope A., Palviainen, Teemu, van der Zee, Matthijs D., Cheesman, Rosa, Mangino, Massimo, Wang, Yunzhang, Li, Shuai, Klaric, Lucija, Ratliff, Scott M., Bielak, Lawrence F., Nygaard, Marianne, Giannelis, Alexandros, Willoughby, Emily A., Reynolds, Chandra A., Balbona, Jared V., Andreassen, Ole A., Ask, Helga, Baras, Aris, Bauer, Christopher R., Boomsma, Dorret I., Campbell, Archie, Campbell, Harry, Chen, Zhengming, Christofidou, Paraskevi, Corfield, Elizabeth, Dahm, Christina C., Dokuru, Deepika R., Evans, Luke M., de Geus, Eco J. C., Giddaluru, Sudheer, Gordon, Scott D., Harden, K. Paige, Hill, W. David, Hughes, Amanda, Kerr, Shona M., Kim, Yongkang, Kweon, Hyeokmoon, Latvala, Antti, Lawlor, Deborah A., Li, Liming, Lin, Kuang, Magnus, Per, Magnusson, Patrik K. E., Mallard, Travis T., Martikainen, Pekka, Mills, Melinda C., Njølstad, Pål Rasmus, Overton, John D., Pedersen, Nancy L., Porteous, David J., Reid, Jeffrey, Silventoinen, Karri, Southey, Melissa C., Stoltenberg, Camilla, Tucker-Drob, Elliot M., Wright, Margaret J., Hewitt, John K., Keller, Matthew C., Stallings, Michael C., Lee, James J., Christensen, Kaare, Kardia, Sharon L. R., Peyser, Patricia A., Smith, Jennifer A., Wilson, James F., Hopper, John L., Hägg, Sara, Spector, Tim D., Pingault, Jean-Baptiste, Plomin, Robert, Havdahl, Alexandra, Bartels, Meike, Martin, Nicholas G., Oskarsson, Sven, Justice, Anne E., Millwood, Iona Y., Hveem, Kristian, Naess, Øyvind, Willer, Cristen J., Åsvold, Bjørn Olav, Koellinger, Philipp D., Kaprio, Jaakko, Medland, Sarah E., Walters, Robin G., Benjamin, Daniel J., Turley, Patrick, Evans, David M., Davey Smith, George, Hayward, Caroline, Brumpton, Ben, Hemani, Gibran, Davies, Neil M.

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Most Reported Genetic Associations With General Intelligence Are Probably False Positives von Chabris, Christopher F., Hebert, Benjamin M., Benjamin, Daniel J., Beauchamp, Jonathan, Cesarini, David, van der Loos, Matthijs, Johannesson, Magnus, Magnusson, Patrik K. E., Lichtenstein, Paul, Atwood, Craig S., Freese, Jeremy, Hauser, Taissa S., Hauser, Robert M., Christakis, Nicholas, Laibson, David

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