ADuLT: An efficient and robust time-to-event GWAS by Pedersen, Emil M, Agerbo, Esben, Plana-Ripoll, Oleguer, Steinbach, Jette, Krebs, Morten D, Hougaard, David M, Werge, Thomas, Nordentoft, Merete, Børglum, Anders D, Musliner, Katherine L, Ganna, Andrea, Schork, Andrew J, Mortensen, Preben B, McGrath, John J, Privé, Florian, Vilhjálmsson, Bjarni J

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The genetic architecture of sporadic and multiple consecutive miscarriage by Laisk, Triin, Soares, Ana Luiza G, Ferreira, Teresa, Painter, Jodie N, Censin, Jenny C, Laber, Samantha, Bacelis, Jonas, Chen, Chia-Yen, Lepamets, Maarja, Lin, Kuang, Liu, Siyang, Millwood, Iona Y, Ramu, Avinash, Southcombe, Jennifer, Andersen, Marianne S, Yang, Ling, Becker, Christian M, Børglum, Anders D, Gordon, Scott D, Bybjerg-Grauholm, Jonas, Helgeland, Øyvind, Hougaard, David M, Jin, Xin, Johansson, Stefan, Juodakis, Julius, Kartsonaki, Christiana, Kukushkina, Viktorija, Lind, Penelope A, Metspalu, Andres, Montgomery, Grant W, Morris, Andrew P, Mors, Ole, Mortensen, Preben B, Njølstad, Pål R, Nordentoft, Merete, Nyholt, Dale R, Lippincott, Margaret, Seminara, Stephanie, Salumets, Andres, Snieder, Harold, Zondervan, Krina, Werge, Thomas, Chen, Zhengming, Conrad, Donald F, Jacobsson, Bo, Li, Liming, Martin, Nicholas G, Neale, Benjamin M, Nielsen, Rasmus, Walters, Robin G, Granne, Ingrid, Medland, Sarah E, Mägi, Reedik, Lawlor, Deborah A, Lindgren, Cecilia M

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Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci by Fadista, João, Skotte, Line, Karjalainen, Juha, Abner, Erik, Sørensen, Erik, Ullum, Henrik, Werge, Thomas, Esko, Tõnu, Milani, Lili, Palotie, Aarno, Daly, Mark, Melbye, Mads, Feenstra, Bjarke, Geller, Frank

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The Wave2 scaffold Hem-1 is required for transition of fetal liver hematopoiesis to bone marrow by Shao, Lijian, Chang, Jianhui, Feng, Wei, Wang, Xiaoyan, Williamson, Elizabeth A, Li, Ying, Schajnovitz, Amir, Scadden, David, Mortensen, Luke J, Lin, Charles P, Li, Linheng, Paulson, Ariel, Downing, James, Zhou, Daohong, Hromas, Robert A

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Uncovering the heritable components of multimorbidities and disease trajectories using a nationwide cohort by Westergaard, David, Jørgensen, Frederik Hytting, Waaben, Jens, Jung, Alexander Wolfgang, Lademann, Mette, Hansen, Thomas Folkmann, Cremers, Jolien, Ostrowski, Sisse Rye, Pedersen, Ole Birger Vesterager, Reguant, Roc, Jørgensen, Isabella Friis, Fitzgerald, Tom, Birney, Ewan, Banasik, Karina, Mortensen, Laust, Brunak, Søren

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FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses by Ahluwalia, Tarunveer S, Eliasen, Anders U, Sevelsted, Astrid, Pedersen, Casper-Emil T, Stokholm, Jakob, Chawes, Bo, Bork-Jensen, Jette, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Linneberg, Allan, Sharma, Amitabh, Weiss, Scott T, Evans, Michael D, Jackson, Daniel J, Morin, Andreanne, Krogfelt, Karen A, Schjørring, Susanne, Mortensen, Preben B, Hougaard, David M, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Mors, Ole, Nordentoft, Merete, Børglum, Anders D, Werge, Thomas, Agerbo, Esben, Gern, James E, Lemanske, Jr, Robert F, Ober, Carole, Pedersen, Anders G, Bisgaard, Hans, Bønnelykke, Klaus

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High-resolution epidemiological landscape from ~290,000 SARS-CoV-2 genomes from Denmark by Khurana, Mark P, Curran-Sebastian, Jacob, Scheidwasser, Neil, Morgenstern, Christian, Rasmussen, Morten, Fonager, Jannik, Stegger, Marc, Tang, Man-Hung Eric, Juul, Jonas L, Escobar-Herrera, Leandro Andrés, Møller, Frederik Trier, Byberg-Grauholm, Jonas, Aasbjerg, Gitte Nygaard, Ring, Aleksander, Sieber, Raphael, Hansen, Tobias Nikolaj Gress, Gunalan, Vithiagaran, Nielsen, Claus, Ellegaard, Kirsten, Larsen, Nicolai Balle, Hartmann, Esben Mørk, Jensen, Anders, Sørensen, Karina Meden, Østergaard, Stine K, Sørensen, Emil A, Jensen, Thomas B. N, Fuster-Collados, Emilio, Chiche-Lapierre, Clarisse, Andersen, Kasper S, Michaelsen, Thomas Y, Petersen, Celine, Hansen, Susan H, Krarup, Henrik Bygum, Schønning, Kristian, Paulsen, Sarah Juel, Schneider, Uffe Vest, Pedersen, Martin Schou, Castruita, Jose Alfredo Samaniego, Thomsen, Marianne Kragh, Ellermann-Eriksen, Svend, Thomsen, Karina Gravgaard, Andersen, Dorte Terp, Steinke, Kat, Skov, Marianne Nielsine, Larsen, Sanne Løkkegaard, Hoppe, Morten, Nielsen, Lene, Sundelin, Thomas, Coia, John E, Laugesen, Asta Lili, Johansen, Rikke Lykke, Nielsen, Xiaohui, Albertsen, Mads, Kraemer, Moritz U. G, du Plessis, Louis, Jokelainen, Pikka, Lehmann, Sune, Krause, Tyra G, Ullum, Henrik, Duchêne, David A, Mortensen, Laust H, Bhatt, Samir

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Associations between patterns in comorbid diagnostic trajectories of individuals with schizophrenia and etiological factors by Krebs, Morten Dybdahl, Themudo, Gonçalo Espregueira, Benros, Michael Eriksen, Mors, Ole, Børglum, Anders D, Hougaard, David, Mortensen, Preben Bo, Nordentoft, Merete, Gandal, Michael J, Fan, Chun Chieh, Geschwind, Daniel H, Schork, Andrew J, Werge, Thomas, Thompson, Wesley K

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Distinct genetic liability profiles define clinically relevant patient strata across common diseases by von Scheidt, Moritz, Ripke, Stephan, Stahl, Eli A., Domenici, Enrico, Agartz, Ingrid, Alexander, Madeline, Belliveau, Richard A., Bene, Judit, Bevilacqua, Elizabeth, Black, Donald W., Cahn, Wiepke, Chen, Eric Y. H., Chen, Ronald Y. L., Cheng, Wei, Cheung, Eric F. C., Cichon, Sven, Cohen, Nadine, Davis, Kenneth L., Del Favero, Jurgen, Dikeos, Dimitris, Dinan, Timothy, Escott-Price, Valentina, Farrell, Martilias S., Frank, Josef, Freimer, Nelson B., Friedman, Joseph I., Gejman, Pablo V., Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Gratten, Jacob, Gurling, Hugh, de Haan, Lieuwe, Hamshere, Marian L., Hansen, Thomas, Haroutunian, Vahram, Hirschhorn, Joel N., Hofman, Andrea, Karachanak-Yankova, Sena, Kennedy, James L., Kim, Yunjung, Kirov, George, Kuzelova-Ptackova, Hana, Leboyer, Marion, Lee, Phil H., Lencz, Todd, Lerer, Bernard, Li, Qingqin S., Mattheisen, Manuel, McCarroll, Steven A., Meijer, Carin J., Metspalu, Andres, Mokrab, Younes, Mowry, Bryan J., Nicodemus, Kristin K., O’Callaghan, Eadbhard, O’Neill, F. Anthony, Olincy, Ann, Pantelis, Christos, Papadimitriou, George N., Perkins, Diana O., Pers, Tune H., Pocklington, Andrew J., Powell, John, Quested, Digby, Rasmussen, Henrik B., Richards, Alexander L., Dan Rujescu, Salomaa, Veikko, Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Shi, Jianxin, Sigurdsson, Engilbert, Silverman, Jeremy M., Sim, Kang, Slominsky, Petr, Smoller, Jordan W., Spencer, Chris C. A., Clair, David St, Stefansson, Kari, Stogmann, Elisabeth, Stroup, T. Scott, Suvisaari, Jaana, Svrakic, Dragan M., Tosato, Sarah, Treutlein, Jens, Walsh, Dermot, Webb, Bradley T., Wildenauer, Dieter B., Williams, Stephanie, Wolen, Aaron R., Wong, Emily H. M., Sullivan, Patrick F., Sklar, Pamela, Kendler, Kenneth S., Heilbronner, Urs, Homuth, Georg, Iorio, Francesco, Ziller, Michael J.

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Multi-PGS enhances polygenic prediction by combining 937 polygenic scores by Albiñana, Clara, Zhu, Zhihong, Schork, Andrew J, Ingason, Andrés, Aschard, Hugues, Brikell, Isabell, Bulik, Cynthia M, Petersen, Liselotte V, Agerbo, Esben, Grove, Jakob, Nordentoft, Merete, Hougaard, David M, Werge, Thomas, Børglum, Anders D, Mortensen, Preben Bo, McGrath, John J, Neale, Benjamin M, Privé, Florian, Vilhjálmsson, Bjarni J

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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia by McLaughlin, Russell L, Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R, O'Brien, Margaret, Kahn, René S, Ophoff, Roel A, Goris, An, Bradley, Daniel G, Al-Chalabi, Ammar, van den Berg, Leonard H, Luykx, Jurjen J, Hardiman, Orla, Veldink, Jan H

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Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots by Albiñana, Clara, Zhu, Zhihong, Borbye-Lorenzen, Nis, Boelt, Sanne Grundvad, Cohen, Arieh S, Skogstrand, Kristin, Wray, Naomi R, Revez, Joana A, Privé, Florian, Petersen, Liselotte V, Bulik, Cynthia M, Plana-Ripoll, Oleguer, Musliner, Katherine L, Agerbo, Esben, Børglum, Anders D, Hougaard, David M, Nordentoft, Merete, Werge, Thomas, Mortensen, Preben Bo, Vilhjálmsson, Bjarni J, McGrath, John J

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Publisher Correction: Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots by Albiñana, Clara, Zhu, Zhihong, Borbye-Lorenzen, Nis, Boelt, Sanne Grundvad, Cohen, Arieh S, Skogstrand, Kristin, Wray, Naomi R, Revez, Joana A, Privé, Florian, Petersen, Liselotte V, Bulik, Cynthia M, Plana-Ripoll, Oleguer, Musliner, Katherine L, Agerbo, Esben, Børglum, Anders D, Hougaard, David M, Nordentoft, Merete, Werge, Thomas, Mortensen, Preben Bo, Vilhjálmsson, Bjarni J, McGrath, John J

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Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition by Anstee, Quentin M, Knapp, Susanne, Maguire, Edward P, Hosie, Alastair M, Thomas, Philip, Mortensen, Martin, Bhome, Rohan, Martinez, Alonso, Walker, Sophie E, Dixon, Claire I, Ruparelia, Kush, Montagnese, Sara, Kuo, Yu-Ting, Herlihy, Amy, Bell, Jimmy D, Robinson, Iain, Guerrini, Irene, McQuillin, Andrew, Fisher, Elizabeth M C, Ungless, Mark A, Gurling, Hugh M D, Morgan, Marsha Y, Brown, Steve D M, Stephens, David N, Belelli, Delia, Lambert, Jeremy J, Smart, Trevor G, Thomas, Howard C

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