Dual-energy CT in gout patients: Do all colour-coded lesions actually represent monosodium urate crystals? by Christiansen, Sara Nysom, Müller, Felix Christoph, Østergaard, Mikkel, Slot, Ole, Maller, Jakob M, Bargesen, Henrik F, Gosvig, Kasper Kjaerulf, Terslev, Lene

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Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants by Satterstrom, F Kyle, Walters, Raymond K, Singh, Tarjinder, Wigdor, Emilie M, Lescai, Francesco, Demontis, Ditte, Kosmicki, Jack A, Grove, Jakob, Stevens, Christine, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Palmer, Duncan S, Maller, Julian B, Nordentoft, Merete, Mors, Ole, Robinson, Elise B, Hougaard, David M, Werge, Thomas M, Bo Mortensen, Preben, Neale, Benjamin M, Børglum, Anders D, Daly, Mark J

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Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases by Yang, Jialiang, Huang, Tao, Petralia, Francesca, Long, Quan, Zhang, Bin, Argmann, Carmen, Zhao, Yong, Mobbs, Charles V, Schadt, Eric E, Zhu, Jun, Tu, Zhidong

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Elevated polygenic burden for autism is associated with differential DNA methylation at birth by Hannon, Eilis, Schendel, Diana, Ladd-Acosta, Christine, Grove, Jakob, Hansen, Christine Søholm, Andrews, Shan V, Hougaard, David Michael, Bresnahan, Michaeline, Mors, Ole, Hollegaard, Mads Vilhelm, Bækvad-Hansen, Marie, Hornig, Mady, Mortensen, Preben Bo, Børglum, Anders D, Werge, Thomas, Pedersen, Marianne Giørtz, Nordentoft, Merete, Buxbaum, Joseph, Daniele Fallin, M, Bybjerg-Grauholm, Jonas, Reichenberg, Abraham, Mill, Jonathan

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Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language by Verhoef, Ellen, Demontis, Ditte, Burgess, Stephen, Shapland, Chin Yang, Dale, Philip S, Okbay, Aysu, Neale, Benjamin M, Faraone, Stephen V, Stergiakouli, Evie, Davey Smith, George, Fisher, Simon E, Børglum, Anders D, St Pourcain, Beate

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The FIB-PPH trial: fibrinogen concentrate as initial treatment for postpartum haemorrhage: study protocol for a randomised controlled trial by Wikkelsoe, Anne Juul, Afshari, Arash, Stensballe, Jakob, Langhoff-Roos, Jens, Albrechtsen, Charlotte, Ekelund, Kim, Hanke, Gabriele, Sharif, Heidi Fosgrau, Mitchell, Anja U, Svare, Jens, Troelstrup, Ane, Pedersen, Lars Møller, Lauenborg, Jeannet, Madsen, Mette Gøttge, Bødker, Birgit, Møller, Ann M

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Correction: Corrigendum: Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases by Yang, Jialiang, Huang, Tao, Petralia, Francesca, Zhang, Bin, Argmann, Carmen, Mobbs, Charles V., Schadt, Eric E., Zhu, Jun, Deluca, David S., Segrè, Ayellet V., Sullivan, Timothy J., Gelfand, Ellen T., Maller, Julian B., Tukiainen, Taru, Lek, Monkol, Ward, Lucas D., Iriarte, Benjamin, Palmer, Cameron D., Winckler, Wendy, Kellis, Manolis, MacArthur, Daniel G., Shablin, Andrey A., Li, Gen, Zhou, Yi-Hui, Nobel, Andrew B., Rusyn, Ivan, Wright, Fred A., Lappalainen, Tuuli, Ferreira, Pedro G., Rivas, Manuel A., Battle, Alexis, Monlong, Jean, Sammeth, Michael, Reverter, Ferran, Goldmann, Jakob, Koller, Daphne, Guigo, Roderic, McCarthy, Mark I., Dermitzakis, Emmanouil T., Konkashbaev, Anuar, Nicolae, Dan L., Flutre, Timothée, Wen, Xiaoquan, Stephens, Matthew, Pritchard, Jonathan K., Lin, Luan, Liu, Jun, Brown, Amanda, Tidwell, Denee, Lo, Edmund, Salvatore, Mike, Thomas, Jeffrey A., Lonsdale, John T., Choi, Christopher, Karasik, Ellen, Ramsey, Kimberly, Moser, Michael T., Gillard, Bryan M., Syron, John, Fleming, Johnelle, Magazine, Harold, Walters, Gary D., Bridge, Jason P., Miklos, Mark, Sullivan, Susan, Barker, Laura K., Traino, Heather, Mosavel, Magboeba, Valley, Dana R., Rohrer, Daniel C., Jewel, Scott, Branton, Philip, Sobin, Leslie H., Qi, Liqun, Wu, Shenpei, Tabor, David, Smith, Anna M., Buia, Stephen A., Undale, Anita H., Roche, Nancy, Britton, Angela, Burges, Robin, Seleski, John, Korzeniewski, Greg E., Erickson, Kenyon, Marcus, Yvonne, Lu, Chunrong, Mash, Deborah C., Volpi, Simona, Struewing, Jeff, Colantuoni, Deborah, Little, Roger, Koester, Susan, Carithers, NCI Latarsha J., Moore, Helen M., Guan, Ping, Sawyer, Sherilyn J., Demchok, Joanne P., Vaught, Jimmie B., Rabiner, Chana A.

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Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome by Rivas, Manuel A, Pirinen, Matti, Conrad, Donald F, Lek, Monkol, Tsang, Emily K, Karczewski, Konrad J, Maller, Julian B, Kukurba, Kimberly R, DeLuca, David S, Fromer, Menachem, Ferreira, Pedro G, Smith, Kevin S, Zhang, Rui, Zhao, Fengmei, Banks, Eric, Poplin, Ryan, Ruderfer, Douglas M, Purcell, Shaun M, Tukiainen, Taru, Minikel, Eric V, Stenson, Peter D, Cooper, David N, Huang, Katharine H, Sullivan, Timothy J, Nedzel, Jared, Bustamante, Carlos D, Li, Jin Billy, Daly, Mark J, Guigo, Roderic, Donnelly, Peter, Ardlie, Kristin, Sammeth, Michael, Dermitzakis, Emmanouil T, McCarthy, Mark I, Montgomery, Stephen B, Lappalainen, Tuuli, MacArthur, Daniel G

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