Predictive Validity and Accuracy of Oral Reading Fluency for English Learners von Vanderwood, Michael L., Tung, Catherine Y., Checca, C. Jason

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Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways von Jansen, Philip R., Watanabe, Kyoko, Stringer, Sven, Skene, Nathan, Bryois, Julien, Hammerschlag, Anke R., de Leeuw, Christiaan A., Benjamins, Jeroen S., Muñoz-Manchado, Ana B., Nagel, Mats, Savage, Jeanne E., Tiemeier, Henning, White, Tonya, Tung, Joyce Y., Hinds, David A., Vacic, Vladimir, Wang, Xin, Sullivan, Patrick F., van der Sluis, Sophie, Polderman, Tinca J. C., Smit, August B., Hjerling-Leffler, Jens, Van Someren, Eus J. W., Posthuma, Danielle

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Disease risk scores for skin cancers von Fontanillas, Pierre, Alipanahi, Babak, Furlotte, Nicholas A., Johnson, Michaela, Wilson, Catherine H., Pitts, Steven J., Gentleman, Robert, Auton, Adam

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Interactions of PVT1 and CASC11 on Prostate Cancer Risk in African Americans von Lin, Hui-Yi, Callan, Catherine Y, Fang, Zhide, Tung, Heng-Yuan, Park, Jong Y

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Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways von Howard, David M., Adams, Mark J., Shirali, Masoud, Clarke, Toni-Kim, Marioni, Riccardo E., Davies, Gail, Coleman, Jonathan R. I., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Wigmore, Eleanor M., Gibson, Jude, Hagenaars, Saskia P., Lewis, Cathryn M., Ward, Joey, Smith, Daniel J., Sullivan, Patrick F., Haley, Chris S., Breen, Gerome, Deary, Ian J., McIntosh, Andrew M.

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An atlas of genetic influences on osteoporosis in humans and mice von Morris, John A., Kemp, John P., Youlten, Scott E., Laurent, Laetitia, Logan, John G., Chai, Ryan C., Vulpescu, Nicholas A., Forgetta, Vincenzo, Kleinman, Aaron, Mohanty, Sindhu T., Sergio, C. Marcelo, Quinn, Julian, Nguyen-Yamamoto, Loan, Luco, Aimee-Lee, Vijay, Jinchu, Simon, Marie-Michelle, Pramatarova, Albena, Medina-Gomez, Carolina, Trajanoska, Katerina, Ghirardello, Elena J., Butterfield, Natalie C., Curry, Katharine F., Leitch, Victoria D., Sparkes, Penny C., Adoum, Anne-Tounsia, Mannan, Naila S., Komla-Ebri, Davide S. K., Pollard, Andrea S., Dewhurst, Hannah F., Hassall, Thomas A. D., Beltejar, Michael-John G., Adams, Douglas J., Vaillancourt, Suzanne M., Kaptoge, Stephen, Baldock, Paul, Cooper, Cyrus, Reeve, Jonathan, Ntzani, Evangelia E., Evangelou, Evangelos, Ohlsson, Claes, Karasik, David, Rivadeneira, Fernando, Kiel, Douglas P., Tobias, Jonathan H., Gregson, Celia L., Harvey, Nicholas C., Grundberg, Elin, Goltzman, David, Adams, David J., Lelliott, Christopher J., Hinds, David A., Ackert-Bicknell, Cheryl L., Hsu, Yi-Hsiang, Maurano, Matthew T., Croucher, Peter I., Williams, Graham R., Bassett, J. H. Duncan, Evans, David M., Richards, J. Brent

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Incorporating functional priors improves polygenic prediction accuracy in UK Biobank and 23andMe data sets von Márquez-Luna, Carla, Gazal, Steven, Loh, Po-Ru, Kim, Samuel S., Furlotte, Nicholas, Auton, Adam, Price, Alkes L.

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Multi-trait analysis of genome-wide association summary statistics using MTAG von Turley, Patrick, Walters, Raymond K., Maghzian, Omeed, Okbay, Aysu, Lee, James J., Fontana, Mark Alan, Nguyen-Viet, Tuan Anh, Wedow, Robbee, Zacher, Meghan, Furlotte, Nicholas A., Magnusson, Patrik, Oskarsson, Sven, Johannesson, Magnus, Visscher, Peter M., Laibson, David, Cesarini, David, Neale, Benjamin M., Benjamin, Daniel J.

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Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders von Walters, Raymond K., Polimanti, Renato, Adkins, Amy E., Aliev, Fazil, Bertelsen, Sarah, Biernacka, Joanna M., Bigdeli, Tim B., Chen, Li-Shiun, Degenhardt, Franziska, Docherty, Anna R., Foo, Jerome C., Frank, Josef, Gordon, Scott, Hartmann, Annette M., Hartz, Sarah M., Herms, Stefan, Hoffmann, Per, Jan Hottenga, Jouke, Konte, Bettina, Lahti, Jari, Lahti-Pulkkinen, Marius, Ligthart, Lannie, Loukola, Anu, Mbarek, Hamdi, McQueen, Matthew B., Milaneschi, Yuri, Palviainen, Teemu, Pearson, John F., Ripatti, Samuli, Salvatore, Jessica E., Schwandt, Melanie, Sherva, Richard, Webb, Bradley T., Wedow, Robbee, Wetherill, Leah, Wills, Amanda G., Chen, Danfeng, Choi, Doo-Sup, Copeland, William E., Dahmen, Norbert, Degenhardt, Louisa, Domingue, Benjamin W., Elson, Sarah L., Gäbel, Wolfgang, Ising, Marcus, Keyes, Margaret, Kiefer, Falk, Lucae, Susanne, Lynskey, Michael T., Maier, Wolfgang, Männistö, Satu, Nurnberger, John I., Palotie, Aarno, Preuss, Ulrich, Ridinger, Monika, Scherbaum, Norbert, Schuckit, Marc A., Soyka, Michael, Treutlein, Jens, Wodarz, Norbert, Adkins, Daniel E., Boden, Joseph M., Boomsma, Dorret I., Brown, Sandra A., Bucholz, Kathleen K., Cichon, Sven, Costello, E. Jane, Diazgranados, Nancy, Eriksson, Johan G., Foroud, Tatiana M., Gillespie, Nathan A., Hesselbrock, Victor, Hewitt, John K., Horwood, John, Johnson, Eric O., Kaprio, Jaakko A., Kendler, Kenneth S., Krauter, Kenneth, Lichtenstein, Paul, Lind, Penelope A., McGue, Matt, MacKillop, James, Madden, Pamela A. F., Martin, Nicholas G., Medland, Sarah E., Nöthen, Markus M., Palmer, Abraham A., Penninx, Brenda W. J. H., Porjesz, Bernice, Rice, John P., Rietschel, Marcella, Riley, Brien P., Rujescu, Dan, Shen, Pei-Hong, Silberg, Judy, Stallings, Michael C., Tarter, Ralph E., Vrieze, Scott, Wall, Tamara L., Whitfield, John B.

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Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways von Nagel, Mats, Jansen, Philip R., Stringer, Sven, Watanabe, Kyoko, de Leeuw, Christiaan A., Bryois, Julien, Savage, Jeanne E., Hammerschlag, Anke R., Skene, Nathan G., Muñoz-Manchado, Ana B., White, Tonya, Tiemeier, Henning, Linnarsson, Sten, Hjerling-Leffler, Jens, Polderman, Tinca J. C., Sullivan, Patrick F., van der Sluis, Sophie, Posthuma, Danielle

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Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis von Schormair, Barbara, Zhao, Chen, Bell, Steven, Tilch, Erik, Salminen, Aaro V, Pütz, Benno, Dauvilliers, Yves, Stefani, Ambra, Högl, Birgit, Poewe, Werner, Kemlink, David, Sonka, Karel, Bachmann, Cornelius G, Paulus, Walter, Trenkwalder, Claudia, Oertel, Wolfgang H, Hornyak, Magdolna, Teder-Laving, Maris, Metspalu, Andres, Hadjigeorgiou, Georgios M, Polo, Olli, Fietze, Ingo, Ross, Owen A, Wszolek, Zbigniew, Butterworth, Adam S, Soranzo, Nicole, Ouwehand, Willem H, Roberts, David J, Danesh, John, Allen, Richard P, Earley, Christopher J, Ondo, William G, Xiong, Lan, Montplaisir, Jacques, Gan-Or, Ziv, Perola, Markus, Vodicka, Pavel, Dina, Christian, Franke, Andre, Tittmann, Lukas, Stewart, Alexandre F R, Shah, Svati H, Gieger, Christian, Peters, Annette, Rouleau, Guy A, Berger, Klaus, Oexle, Konrad, Di Angelantonio, Emanuele, Hinds, David A, Müller-Myhsok, Bertram, Winkelmann, Juliane, Balkau, B, Ducimetière, P, Eschwège, E, Rancière, F, Alhenc-Gelas, F, Gallois, Y, Girault, A, Fumeron, F, Marre, M, Roussel, R, Bonnet, F, Bonnefond, A, Cauchi, S, Froguel, P, Cogneau, J, Born, C, Caces, E, Cailleau, M, Lantieri, O, Moreau, JG, Rakotozafy, F, Tichet, J, Vol, S, Agee, Michelle, Alipanahi, Babak, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Elson, Sarah L, Fontanillas, Pierre, Furlotte, Nicholas A, Hinds, David A, Hromatka, Bethann S, Huber, Karen E, Kleinman, Aaron, Litterman, Nadia K, McIntyre, Matthew H, Mountain, Joanna L, Northover, Carrie AM, Pitts, Steven J, Sathirapongsasuti, J Fah, Sazonova, Olga V, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Vacic, Vladimir, Wilson, Catherine H

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A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder von Walters, Raymond K., Lee, S. Hong, Brikell, Isabell, Ghirardi, Laura, Larsson, Henrik, Lichtenstein, Paul, Bell, Robert K., Bryc, Katarzyna, Fontanillas, Pierre, Hromatka, Bethann S., Huber, Karen E., Litterman, Nadia K., McIntyre, Matthew H., Mountain, Joanna L., Pitts, Steven J., Vacic, Vladimir, Anney, Richard J.L., Vasquez, Alejandro Arias, Arranz, Maria Jesús, Banaschewski, Tobias, Banaschewski, Tobias J., Mortensen, Preben Bo, Børglum, Anders, Charach, Alice, Crosbie, Jennifer, Dalsgaard, Soeren, Demontis, Ditte, Dempfle, Astrid, Elia, Josephine, Faraone, Stephen V., Franke, Barbara, Freitag, Christine, Gelernter, Joel, Grevet, Eugenio, Haavik, Jan, Hakonarson, Hakon, Hawi, Ziarih, Hinney, Anke, Holmans, Peter, Ickowitz, Abel, Kent, Lindsey, Kittel-Schneider, Sarah, Langley, Kate, Lesch, Klaus-Peter, Loo, Sandra K., Martin, Joanna, Medland, Sarah E., Mulas, Fernando, Mulligan, Aisling, O’Donovan, Michael C., Oades, Robert D., Palmason, Haukur, Rhode, Luis, Roeyers, Herbert, Romanos, Marcel, Romanos, Jasmin, Rothenberger, Aribert, Schäfer, Helmut, Scherag, André, Schimmelmann, Benno G., Sergeant, Joseph, Smalley, Susan L., Sonuga-Barke, Edmund J.S., Steinhausen, Hans-Christoph, Sullivan, Patrick F., Todorov, Alexandre, Waldman, Irwin, Wang, Yufeng, Warnke, Andreas, Williams, Nigel, Witt, Stephanie H., Yang, Li, Agerbo, Esben, Belliveau, Rich, Børglum, Anders D., Chambert, Kimberly, Dalsgaard, Søren, Dumont, Ashley, Goldstein, Jacqueline, Grove, Jakob, Howrigan, Daniel P., Huang, Hailiang, Martin, Alicia R., Mattheisen, Manuel, Moran, Jennifer, Mors, Ole, Pallesen, Jonatan, Poterba, Timothy, Poulsen, Jesper Buchhave, Robinson, Elise B., Satterstrom, F. Kyle, Stevens, Christine, Turley, Patrick, Pedersen, Marianne Giørtz, Mors, Ole, Nordentoft, Merete, Hougaard, David M., Bybjerg-Grauholm, Jonas, Franke, Barbara, Neale, Benjamin M.

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Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use von Liu, Mengzhen, Jiang, Yu, Wedow, Robbee, Li, Yue, Brazel, David M., Chen, Fang, Datta, Gargi, Davila-Velderrain, Jose, Tian, Chao, Zhan, Xiaowei, Choquet, Hélène, Docherty, Anna R., Faul, Jessica D., Foerster, Johanna R., Fritsche, Lars G., Gabrielsen, Maiken Elvestad, Gordon, Scott D., Haessler, Jeffrey, Hottenga, Jouke-Jan, Huang, Hongyan, Jang, Seon-Kyeong, Jansen, Philip R., Ling, Yueh, Matoba, Nana, McMahon, George, Orrù, Valeria, Palviainen, Teemu, Pandit, Anita, Reginsson, Gunnar W., Skogholt, Anne Heidi, Smith, Jennifer A., Taylor, Amy E., Turman, Constance, Willemsen, Gonneke, Young, Hannah, Young, Kendra A., Zhao, Wei, Zhou, Wei, Bjornsdottir, Gyda, Boehnke, Michael, Boomsma, Dorret I., Chen, Chu, Cucca, Francesco, Davies, Gareth E., Eaton, Charles B., Ehringer, Marissa A., Esko, Tõnu, Fiorillo, Edoardo, Gillespie, Nathan A., Heath, Andrew C., Hokanson, John E., Hopfer, Christian J., Iacono, William G., Kamatani, Yoichiro, Kardia, Sharon L. R., Keller, Matthew C., Kellis, Manolis, Kooperberg, Charles, Kraft, Peter, Krauter, Kenneth S., Laakso, Markku, Lind, Penelope A., Loukola, Anu, Lutz, Sharon M., Madden, Pamela A. F., Martin, Nicholas G., McQueen, Matthew B., Medland, Sarah E., Mohlke, Karen L., Nielsen, Jonas B., Okada, Yukinori, Peters, Ulrike, Polderman, Tinca J. C., Rimm, Eric, Rose, Richard J., Runarsdottir, Valgerdur, Stallings, Michael C., Stefansson, Hreinn, Thai, Khanh K., Tindle, Hilary A., Tyrfingsson, Thorarinn, Wall, Tamara L., Weir, David R., Weisner, Constance, Whitfield, John B., Yin, Jie, Zuccolo, Luisa, Bierut, Laura J., Hveem, Kristian, Lee, James J., Munafò, Marcus R., Saccone, Nancy L., David, Sean P., Jorgenson, Eric, Kaprio, Jaakko, Stefansson, Kari, Thorgeirsson, Thorgeir E., Abecasis, Gonçalo, Liu, Dajiang J., Vrieze, Scott

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Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals von Okbay, Aysu, Wu, Yeda, Wang, Nancy, Jayashankar, Hariharan, Bennett, Michael, Nehzati, Seyed Moeen, Sidorenko, Julia, Kweon, Hyeokmoon, Goldman, Grant, Gjorgjieva, Tamara, Jiang, Yunxuan, Hicks, Barry, Tian, Chao, Hinds, David A., Ahlskog, Rafael, Magnusson, Patrik K. E., Oskarsson, Sven, Hayward, Caroline, Campbell, Archie, Porteous, David J., Freese, Jeremy, Herd, Pamela, Watson, Chelsea, Jala, Jonathan, Conley, Dalton, Koellinger, Philipp D., Johannesson, Magnus, Laibson, David, Meyer, Michelle N., Lee, James J., Kong, Augustine, Yengo, Loic, Cesarini, David, Turley, Patrick, Visscher, Peter M., Beauchamp, Jonathan P., Benjamin, Daniel J., Young, Alexander I.

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A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease von Wightman, Douglas P., Jansen, Iris E., Savage, Jeanne E., Shadrin, Alexey A., Bahrami, Shahram, Holland, Dominic, Rongve, Arvid, Børte, Sigrid, Winsvold, Bendik S., Drange, Ole Kristian, Martinsen, Amy E., Skogholt, Anne Heidi, Willer, Cristen, Bråthen, Geir, Bosnes, Ingunn, Nielsen, Jonas Bille, Fritsche, Lars G., Thomas, Laurent F., Pedersen, Linda M., Gabrielsen, Maiken E., Johnsen, Marianne Bakke, Meisingset, Tore Wergeland, Zhou, Wei, Proitsi, Petroula, Hodges, Angela, Dobson, Richard, Velayudhan, Latha, Heilbron, Karl, Auton, Adam, Sealock, Julia M., Davis, Lea K., Pedersen, Nancy L., Reynolds, Chandra A., Karlsson, Ida K., Magnusson, Sigurdur, Stefansson, Hreinn, Thordardottir, Steinunn, Jonsson, Palmi V., Snaedal, Jon, Zettergren, Anna, Skoog, Ingmar, Kern, Silke, Waern, Margda, Zetterberg, Henrik, Blennow, Kaj, Stordal, Eystein, Hveem, Kristian, Zwart, John-Anker, Athanasiu, Lavinia, Selnes, Per, Saltvedt, Ingvild, Sando, Sigrid B., Ulstein, Ingun, Djurovic, Srdjan, Fladby, Tormod, Aarsland, Dag, Selbæk, Geir, Ripke, Stephan, Stefansson, Kari, Andreassen, Ole A., Posthuma, Danielle

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Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heter... von Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Law, Matthew H, Nandakumar, Priyanka, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Olsen, Catherine M, Neale, Rachel E, Fitzgerald, Rebecca, Thrift, Aaron P, Vaughan, Thomas L, Buas, Matthew F, Hinds, David A, Gharahkhani, Puya, Kendall, Bradley J, MacGregor, Stuart, Fitzgerald, Rebecca, Buas, Matt, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Bird, Nigel C, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Whiteman, David C, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Clark, Sarah K, Elson, Sarah L, Fletez-Brant, Kipper, Fontanillas, Pierre, Furlotte, Nicholas A, Gandhi, Pooja M, Heilbron, Karl, Hicks, Barry, Hinds, David A, Huber, Karen E, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, Luff, Marie K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Mozaffari, Sahar V, Nandakumar, Priyanka, Noblin, Elizabeth S, Northover, Carrie AM, O'Connell, Jared, Petrakovitz, Aaron A, Pitts, Steven J, David Poznik, G., Fah Sathirapongsasuti, J, Shastri, Anjali J, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Tunney, Robert J, Vacic, Vladimir, Wang, Xin, Zare, Amir S

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Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum von Fejzo, Marlena S., Sazonova, Olga V., Sathirapongsasuti, J. Fah, Hallgrímsdóttir, Ingileif B., Vacic, Vladimir, MacGibbon, Kimber W., Schoenberg, Frederic P., Mancuso, Nicholas, Slamon, Dennis J., Mullin, Patrick M.

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A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma von Seviiri, Mathias, Law, Matthew H., Ong, Jue-Sheng, Gharahkhani, Puya, Fontanillas, Pierre, Olsen, Catherine M., Whiteman, David C., MacGregor, Stuart

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Insights into the genetic basis of retinal detachment von Boutin, Thibaud S, Charteris, David G, Chandra, Aman, Campbell, Susan, Hayward, Caroline, Campbell, Archie, Nandakumar, Priyanka, Hinds, David, Mitry, Danny, Vitart, Veronique

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Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts von Sanchez-Roige, Sandra, Palmer, Abraham A, Fontanillas, Pierre, Elson, Sarah L, Adams, Mark J, Howard, David M, Edenberg, Howard J, Davies, Gail, Crist, Richard C, Deary, Ian J, McIntosh, Andrew M, Clarke, Toni-Kim

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