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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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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Discovery of RXFP2 genetic association in resistant hypertensive men and RXFP2 antagonists for the treatment of resistant hypertension von Zhang, Shan-Shan, Larrabee, Lance, Chang, Andrew H., Desai, Sapna, Sloan, Lisa, Wang, Xin, Wu, Yixuan, Parvez, Nazia, Amaratunga, Karen, Hartman, Allison C., Whitnall, Abby, Mason, Joseph, Barton, Nicholas P., Chu, Audrey Y., Davitte, Jonathan M., Csakai, Adam J., Tibbetts, Caitlin Vestal, Tolbert, Audrey E., O’Keefe, Heather, Polanco, Jessie, Foley, Joseph, Kmett, Casey, Kehler, Jonathan, Kozejova, Gabriela, Wang, Feng, Mayer, Andrew P., Koenig, Patrick, Foletti, Davide, Pitts, Steven J., Schnackenberg, Christine G.

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Genome-wide association studies of antidepressant class response and treatment-resistant depression von Li, Qingqin S., Tian, Chao, Hinds, David

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Effect of genome and environment on metabolic and inflammatory profiles von Sirota, Marina, Willemsen, Gonneke, Sundar, Purnima, Pitts, Steven J, Potluri, Shobha, Prifti, Edi, Kennedy, Sean, Ehrlich, S Dusko, Neuteboom, Jacoline, Kluft, Cornelis, Malone, Karen E, Cox, David R, de Geus, Eco J C, Boomsma, Dorret I

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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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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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Genetic analyses identify widespread sex-differential participation bias von Pirastu, Nicola, Cordioli, Mattia, Nandakumar, Priyanka, Mignogna, Gianmarco, Abdellaoui, Abdel, Hollis, Benjamin, Kanai, Masahiro, Rajagopal, Veera M., Parolo, Pietro Della Briotta, Baya, Nikolas, Carey, Caitlin E., Karjalainen, Juha, Als, Thomas D., Van der Zee, Matthijs D., Day, Felix R., Ong, Ken K., Morisaki, Takayuki, de Geus, Eco, Bellocco, Rino, Okada, Yukinori, Børglum, Anders D., Joshi, Peter, Auton, Adam, Hinds, David, Neale, Benjamin M., Walters, Raymond K., Nivard, Michel G., Perry, John R. B., Ganna, Andrea

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Whole-genome sequence variation, population structure and demographic history of the Dutch population von Francioli, Laurent C, Menelaou, Androniki, Pulit, Sara L, van Dijk, Feerk, Palamara, Pier Francesco, Elbers, Clara C, Neerincx, Pieter B T, Ye, Kai, Guryev, Victor, Kloosterman, Wigard P, Deelen, Patrick, Abdellaoui, Abdel, van Leeuwen, Elisabeth M, van Oven, Mannis, Vermaat, Martijn, Li, Mingkun, Laros, Jeroen F J, Karssen, Lennart C, Kanterakis, Alexandros, Amin, Najaf, Hottenga, Jouke Jan, Lameijer, Eric-Wubbo, Kattenberg, Mathijs, Dijkstra, Martijn, Byelas, Heorhiy, van Setten, Jessica, van Schaik, Barbera D C, Bot, Jan, Nijman, Isaäc J, Renkens, Ivo, Marschall, Tobias, Schönhuth, Alexander, Hehir-Kwa, Jayne Y, Handsaker, Robert E, Polak, Paz, Sohail, Mashaal, Vuzman, Dana, Hormozdiari, Fereydoun, van Enckevort, David, Mei, Hailiang, Koval, Vyacheslav, Moed, Matthijs H, van der Velde, K Joeri, Rivadeneira, Fernando, Estrada, Karol, Medina-Gomez, Carolina, Isaacs, Aaron, McCarroll, Steven A, Beekman, Marian, de Craen, Anton J M, Suchiman, H Eka D, Hofman, Albert, Oostra, Ben, Uitterlinden, André G, Willemsen, Gonneke, Platteel, Mathieu, Veldink, Jan H, van den Berg, Leonard H, Pitts, Steven J, Potluri, Shobha, Sundar, Purnima, Cox, David R, Sunyaev, Shamil R, den Dunnen, Johan T, Stoneking, Mark, de Knijff, Peter, Kayser, Manfred, Li, Qibin, Li, Yingrui, Du, Yuanping, Chen, Ruoyan, Cao, Hongzhi, Li, Ning, Cao, Sujie, Wang, Jun, Bovenberg, Jasper A, Pe'er, Itsik, Slagboom, P Eline, van Duijn, Cornelia M, Boomsma, Dorret I, van Ommen, Gert-Jan B, de Bakker, Paul I W, Swertz, Morris A, Wijmenga, Cisca

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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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Genetic determinants of daytime napping and effects on cardiometabolic health von Dashti, Hassan S., Daghlas, Iyas, Lane, Jacqueline M., Huang, Yunru, Udler, Miriam S., Wang, Heming, Ollila, Hanna M., Jones, Samuel E., Kim, Jaegil, Wood, Andrew R., Weedon, Michael N., Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa

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Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis von Gallagher, C. S., Mäkinen, N., Harris, H. R., Rahmioglu, N., Uimari, O., Cook, J. P., Shigesi, N., Ferreira, T., Velez-Edwards, D. R., Edwards, T. L., Mortlock, S., Ruhioglu, Z., Day, F., Becker, C. M., Karhunen, V., Martikainen, H., Järvelin, M.-R., Cantor, R. M., Ridker, P. M., Terry, K. L., Buring, J. E., Gordon, S. D., Medland, S. E., Montgomery, G. W., Nyholt, D. R., Hinds, D. A., Tung, J. Y., Perry, J. R. B., Lind, P. A., Painter, J. N., Martin, N. G., Morris, A. P., Chasman, D. I., Missmer, S. A., Zondervan, K. T., Morton, C. C.

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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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Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population von Nakka, Priyanka, Pattillo Smith, Samuel, O’Donnell-Luria, Anne H., McManus, Kimberly F., Agee, Michelle, Auton, Adam, Bell, Robert K., Bryc, Katarzyna, Elson, Sarah L., Fontanillas, Pierre, Furlotte, Nicholas A., Hicks, Barry, Hinds, David A., Jewett, Ethan M., Jiang, Yunxuan, Lin, Keng-Han, McCreight, Jennifer C., Huber, Karen E., Kleinman, Aaron, Litterman, Nadia K., McIntyre, Matthew H., Noblin, Elizabeth S., Northover, Carrie A.M., Pitts, Steven J., Poznik, G. David, Shelton, Janie F., Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y., Vacic, Vladimir, Wang, Xin, Mountain, Joanna L., Ramachandran, Sohini, Sathirapongsasuti, J. Fah

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Aging as Accelerated Accumulation of Somatic Variants: Whole-Genome Sequencing of Centenarian and Middle-Aged Monozygotic Twin Pairs von Ye, Kai, Beekman, Marian, Lameijer, Eric-Wubbo, Zhang, Yanju, Moed, Matthijs H., van den Akker, Erik B., Deelen, Joris, Houwing-Duistermaat, Jeanine J., Kremer, Dennis, Anvar, Seyed Yahya, Laros, Jeroen F. J., Jones, David, Raine, Keiran, Blackburne, Ben, Potluri, Shobha, Long, Quan, Guryev, Victor, van der Breggen, Ruud, Westendorp, Rudi G. J., ‘t Hoen, Peter A. C., den Dunnen, Johan, van Ommen, Gert Jan B., Willemsen, Gonneke, Pitts, Steven J., Cox, David R., Ning, Zemin, Boomsma, Dorret I., Slagboom, P. Eline

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Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci von Dudding, Tom, Haworth, Simon, Lind, Penelope A., Sathirapongsasuti, J. Fah, Tung, Joyce Y., Mitchell, Ruth, Colodro-Conde, Lucía, Medland, Sarah E., Gordon, Scott, Elsworth, Benjamin, Paternoster, Lavinia, Franks, Paul W., Thomas, Steven J., Martin, Nicholas G., Timpson, Nicholas J.

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Advancing drug discovery using the power of the human genome von Heilbron, Karl, Mozaffari, Sahar V, Vacic, Vladimir, Yue, Peng, Wang, Wei, Shi, Jingchunzi, Jubb, Adrian M, Pitts, Steven J, Wang, Xin

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Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure von Arvanitis, Marios, Tampakakis, Emmanouil, Zhang, Yanxiao, Wang, Wei, Auton, Adam, Dutta, Diptavo, Glavaris, Stephanie, Keramati, Ali, Chatterjee, Nilanjan, Chi, Neil C., Ren, Bing, Post, Wendy S., Battle, Alexis

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Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality von Adewuyi, Emmanuel O., Mehta, Divya, Sapkota, Yadav, Auta, Asa, Yoshihara, Kosuke, Nyegaard, Mette, Griffiths, Lyn R., Montgomery, Grant W., Chasman, Daniel I., Nyholt, Dale R.

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Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry von Sanchez-Roige, Sandra, Fontanillas, Pierre, Jennings, Mariela V., Bianchi, Sevim B., Huang, Yuye, Hatoum, Alexander S., Sealock, Julia, Davis, Lea K., Elson, Sarah L., Palmer, Abraham A.

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