A functional IL-6 receptor ( IL6R ) variant is a risk factor for persistent atopic dermatitis von Esparza-Gordillo, Jorge, PhD, Schaarschmidt, Heidi, ME, Liang, Liming, PhD, Cookson, William, MD, DPhil, Bauerfeind, Anja, PhD, Lee-Kirsch, Min-Ae, MD, Nemat, Katja, MD, Henderson, John, MD, Paternoster, Lavinia, PhD, Harper, John I., MD, Mangold, Elisabeth, MD, Nothen, Markus M., MD, Rüschendorf, Franz, PhD, Kerscher, Tamara, PhD, Marenholz, Ingo, PhD, Matanovic, Anja, MSc, Lau, Susanne, MD, Keil, Thomas, MD, MSc, Bauer, Carl-Peter, MD, Kurek, Michael, MD, Ciechanowicz, Andrzej, MD, Macek, Milan, MD, DSc, Franke, Andre, PhD, Kabesch, Michael, MD, Hubner, Norbert, MD, Abecasis, Gonçalo, PhD, Weidinger, Stephan, MD, Moffatt, Miriam, DPhil, Lee, Young-Ae, MD

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Identification and functional characterization of rare SHANK2 variants in schizophrenia von Peykov, S, Berkel, S, Schoen, M, Weiss, K, Degenhardt, F, Strohmaier, J, Weiss, B, Proepper, C, Schratt, G, Nöthen, M M, Boeckers, T M, Rietschel, M, Rappold, G A

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Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder von Chen, D T, Jiang, X, Akula, N, Shugart, Y Y, Wendland, J R, Steele, C J M, Kassem, L, Park, J-H, Chatterjee, N, Jamain, S, Cheng, A, Leboyer, M, Muglia, P, Schulze, T G, Cichon, S, Nöthen, M M, Rietschel, M, McMahon, F J

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Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations von Weidinger, Stephan, Illig, Thomas, Baurecht, Hansjörg, Irvine, Alan D., Rodriguez, Elke, Diaz-Lacava, Amalia, Klopp, Norman, Wagenpfeil, Stefan, Zhao, Yiwei, Liao, Haihui, Lee, Simon P., Palmer, Colin N.A., Jenneck, Claudia, Maintz, Laura, Hagemann, Tobias, Behrendt, Heidrun, Ring, Johannes, Nothen, Markus M., McLean, W. H. Irwin, Novak, Natalija

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Cortical surface area alterations shaped by genetic load for neuroticism von Opel, Nils, Amare, Azmeraw T., Redlich, Ronny, Repple, Jonathan, Kaehler, Claas, Grotegerd, Dominik, Dohm, Katharina, Zaremba, Dario, Leehr, Elisabeth J., Böhnlein, Joscha, Förster, Katharina, Bürger, Christian, Meinert, Susanne, Enneking, Verena, Emden, Daniel, Leenings, Ramona, Winter, Nils, Hahn, Tim, Heindel, Walter, Bauer, Jochen, Wilhelms, David, Schmitt, Simon, Jansen, Andreas, Krug, Axel, Nenadic, Igor, Rietschel, Marcella, Witt, Stephanie, Forstner, Andreas J., Nöthen, Markus M., Kircher, Tilo, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von Dekker, Annelot M., Diekstra, Frank P., van der Spek, Rick A. A., Võsa, Urmo, Yang, Jian, Vajda, Alice, Lin, Kuang, Vrabec, Katarina, Koritnik, Blaž, Zidar, Janez, de Visser, Marianne, Leonardis, Lea, Millecamps, Stéphanie, Meininger, Vincent, Mora, Jesus S., Colville, Shuna, Morrison, Karen E., Shaw, Pamela J., Hardy, John, Pittman, Alan, Sidle, Katie, Malaspina, Andrea, Petri, Susanne, Drepper, Carsten, Meyer, Thomas, Ophoff, Roel A., Staats, Kim A., Van Deerlin, Vivianna M., Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Basak, A Nazli, Hamzeiy, Hamid, Parman, Yesim, Meitinger, Thomas, Smith, Bradley N., Lichtner, Peter, Radivojkov-Blagojevic, Milena, Andres, Christian R., Maurel, Cindy, Landwehrmeyer, Bernhard, Brice, Alexis, Payan, Christine A. M., Saker-Delye, Safaa, Tittmann, Lukas, Rietschel, Marcella, Cichon, Sven, Nöthen, Markus M., Tzourio, Christophe, Dartigues, Jean-François, Cereda, Cristina, Uitterlinden, Andre G., Estrada, Karol, Hofman, Albert, Curtis, Charles, Comi, Giacomo P., D'Alfonso, Sandra, Fogh, Isabella, Bertolin, Cinzia, Sorarù, Gianni, Tiloca, Cinzia, Ratti, Antonia, Calvo, Andrea, Brunetti, Maura, van Doormaal, Perry T. C., Arcuti, Simona, Capozzo, Rosa, Lunetta, Christian, Riva, Nilo, Filosto, Massimiliano, Muller, Bernard, Tazelaar, Gijs H. P., Zhang, Katharine, McCann, Emily P., Rowe, Dominic B., Grosskreutz, Julian, Ringer, Thomas, Prell, Tino, Stubendorff, Beatrice, Beghi, Ettore, Pupillo, Elisabetta, Blokhuis, Anna M., Tortelli, Rosanna, Powell, John, Ludolph, Albert C., Van Damme, Philip, Franke, Lude, Brown, Robert H., Sproviero, William, Andersen, Peter M., Silani, Vincenzo, Jones, Ashley R., Pasterkamp, R Jeroen, Breen, Gerome, Al-Chalabi, Ammar, Veldink, Jan H., Kenna, Kevin P., Harschnitz, Oliver, Schellevis, Raymond D., Brands, William J.

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Biological insights from 108 schizophrenia-associated genetic loci von Neale, Benjamin M, Pers, Tune H, Agartz, Ingrid, Agerbo, Esben, Amin, Farooq, Bergen, Sarah E, Bigdeli, Tim B, Buckner, Randy L, Cai, Guiqing, Catts, Stanley V, Chan, Raymond C. K, Chen, Eric Y. H, Cheng, Wei, Cheung, Eric F. C, Ann Chong, Siow, Robert Cloninger, C, Cohen, Nadine, Crowley, James J, Davidson, Michael, Davis, Kenneth L, Del Favero, Jurgen, Demontis, Ditte, Dinan, Timothy, Djurovic, Srdjan, Drapeau, Elodie, Eriksson, Johan, Escott-Price, Valentina, Friedl, Marion, Fromer, Menachem, Genovese, Giulio, Georgieva, Lyudmila, Giusti-Rodriguez, Paola, Gopal, Srihari, Gratten, Jacob, Hammer, Christian, Hofman, Andrea, Hougaard, David M, Julia, Antonio, Klovins, Janis, Ausrele Kucinskiene, Zita, Hong Lee, S, Lerer, Bernard, Limborska, Svetlana, Lubinski, Jan, Macek Jr, Milan, Magnusson, Patrik K. E, Mattheisen, Manuel, McDonald, Colm, Michie, Patricia T, Milanova, Vihra, Mokrab, Younes, Muller-Myhsok, Bertram, Nenadic, Igor, Nordin, Annelie, Van Os, Jim, Endophenotypes International Consortium, Psychosis, Parkhomenko, Elena, Pejovic-Milovancevic, Milica, Pimm, Jonathan, Price, Alkes, Purcell, Shaun M, Quested, Digby, Rasmussen, Henrik B, Roffman, Joshua L, Schubert, Christian R, Schwab, Sibylle G, Scott, Rodney J, Seidman, Larry J, Silverman, Jeremy M, Smoller, Jordan W, Steinberg, Stacy, Strengman, Eric, Strohmaier, Jana, Svrakic, Dragan M, Soderman, Erik, Thirumalai, Srinivas, Toncheva, Draga, Tosato, Sarah, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Wolen, Aaron R, Zheng, Xuebin, Wray, Naomi R, Visscher, Peter M, Trust Case-Control Consortium, Wellcome, Andreassen, Ole A, Blackwood, Douglas H. R, Esko, Tonu, Gill, Michael, Jablensky, Assen V, McCarroll, Steven A, Mowry, Bryan J, Owen, Michael J, Pato, Carlos N, Posthuma, Danielle, Rujescu, Dan, Sham, Pak C, Sklar, Pamela, St Clair, David

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A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder von Baum, A E, Akula, N, Cabanero, M, Cardona, I, Corona, W, Klemens, B, Schulze, T G, Cichon, S, Rietschel, M, Nöthen, M M, Georgi, A, Schumacher, J, Schwarz, M, Abou Jamra, R, Höfels, S, Propping, P, Satagopan, J, Detera-Wadleigh, S D, Hardy, J, McMahon, F J

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Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection von Pardiñas, Antonio F., Holmans, Peter, Pocklington, Andrew J., Escott-Price, Valentina, Ripke, Stephan, Carrera, Noa, Legge, Sophie E., Bishop, Sophie, Cameron, Darren, Hamshere, Marian L., Han, Jun, Hubbard, Leon, Lynham, Amy, Mantripragada, Kiran, Rees, Elliott, MacCabe, James H., McCarroll, Steven A., Baune, Bernhard T., Breen, Gerome, Byrne, Enda M., Dannlowski, Udo, Eley, Thalia C., Hayward, Caroline, Martin, Nicholas G., McIntosh, Andrew M., Plomin, Robert, Porteous, David J., Wray, Naomi R., Caballero, Armando, Geschwind, Daniel H., Huckins, Laura M., Ruderfer, Douglas M., Santiago, Enrique, Sklar, Pamela, Stahl, Eli A., Won, Hyejung, Agerbo, Esben, Als, Thomas D., Andreassen, Ole A., Bækvad-Hansen, Marie, Mortensen, Preben Bo, Pedersen, Carsten Bøcker, Børglum, Anders D., Bybjerg-Grauholm, Jonas, Djurovic, Srdjan, Durmishi, Naser, Pedersen, Marianne Giørtz, Golimbet, Vera, Grove, Jakob, Hougaard, David M., Mattheisen, Manuel, Molden, Espen, Mors, Ole, Nordentoft, Merete, Pejovic-Milovancevic, Milica, Sigurdsson, Engilbert, Silagadze, Teimuraz, Hansen, Christine Søholm, Stefansson, Kari, Stefansson, Hreinn, Steinberg, Stacy, Tosato, Sarah, Werge, Thomas, Collier, David A., Rujescu, Dan, Kirov, George, Owen, Michael J., O’Donovan, Michael C., Walters, James T. R.

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Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells von Thier, Marc, Wörsdörfer, Philipp, Lakes, Yenal B., Gorris, Raphaela, Herms, Stefan, Opitz, Thoralf, Seiferling, Dominic, Quandel, Tamara, Hoffmann, Per, Nöthen, Markus M., Brüstle, Oliver, Edenhofer, Frank

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A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis von Buch, Stephan, Stickel, Felix, Trépo, Eric, Way, Michael, Herrmann, Alexander, Nischalke, Hans Dieter, Brosch, Mario, Rosendahl, Jonas, Berg, Thomas, Ridinger, Monika, Rietschel, Marcella, McQuillin, Andrew, Frank, Josef, Kiefer, Falk, Schreiber, Stefan, Lieb, Wolfgang, Soyka, Michael, Semmo, Nasser, Aigner, Elmar, Datz, Christian, Schmelz, Renate, Brückner, Stefan, Zeissig, Sebastian, Stephan, Anna-Magdalena, Wodarz, Norbert, Devière, Jacques, Clumeck, Nicolas, Sarrazin, Christoph, Lammert, Frank, Gustot, Thierry, Deltenre, Pierre, Völzke, Henry, Lerch, Markus M, Mayerle, Julia, Eyer, Florian, Schafmayer, Clemens, Cichon, Sven, Nöthen, Markus M, Nothnagel, Michael, Ellinghaus, David, Huse, Klaus, Franke, Andre, Zopf, Steffen, Hellerbrand, Claus, Moreno, Christophe, Franchimont, Denis, Morgan, Marsha Y, Hampe, Jochen

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High loading of polygenic risk in cases with chronic schizophrenia von Meier, S M, Agerbo, E, Maier, R, Pedersen, C B, Lang, M, Grove, J, Hollegaard, M V, Demontis, D, Trabjerg, B B, Hjorthøj, C, Ripke, S, Degenhardt, F, Nöthen, M M, Rujescu, D, Maier, W, Werge, T, Mors, O, Hougaard, D M, Børglum, A D, Wray, N R, Rietschel, M, Nordentoft, M, Mortensen, P B, Mattheisen, M

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Brazilian guidelines for the management of brain-dead potential organ donors. The task force of the AMIB, ABTO, BRICNet, and the General Coordination of the National Transplant Sys... von Westphal, Glauco Adrieno, Robinson, Caroline Cabral, Cavalcanti, Alexandre Biasi, Gonçalves, Anderson Ricardo Roman, Guterres, Cátia Moreira, Teixeira, Cassiano, Stein, Cinara, Franke, Cristiano Augusto, da Silva, Daiana Barbosa, Pontes, Daniela Ferreira Salomão, Nunes, Diego Silva Leite, Abdala, Edson, Dal-Pizzol, Felipe, Bozza, Fernando Augusto, Machado, Flávia Ribeiro, de Andrade, Joel, Cruz, Luciane Nascimento, de Azevedo, Luciano Cesar Pontes, Machado, Miriam Cristine Vahl, Rosa, Regis Goulart, Manfro, Roberto Ceratti, Nothen, Rosana Reis, Lobo, Suzana Margareth, Rech, Tatiana Helena, Lisboa, Thiago, Colpani, Verônica, Falavigna, Maicon

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Reconstructing changes in seep activity by means of pore water and solid phase Sr/Ca and Mg/Ca ratios in pockmark sediments of the Northern Congo Fan von Nöthen, K., Kasten, S.

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Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III von Björkqvist, Jenny, de Maat, Steven, Lewandrowski, Urs, Di Gennaro, Antonio, Oschatz, Chris, Schönig, Kai, Nöthen, Markus M, Drouet, Christian, Braley, Hal, Nolte, Marc W, Sickmann, Albert, Panousis, Con, Maas, Coen, Renné, Thomas

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Breakthroughs in the genetics of orofacial clefting von Mangold, Elisabeth, Ludwig, Kerstin U, Nöthen, Markus M

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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder von Jarick, I, Volckmar, A-L, Pütter, C, Pechlivanis, S, Nguyen, T T, Dauvermann, M R, Beck, S, Albayrak, Ö, Scherag, S, Gilsbach, S, Cichon, S, Hoffmann, P, Degenhardt, F, Nöthen, M M, Schreiber, S, Wichmann, H-E, Jöckel, K-H, Heinrich, J, Tiesler, C M T, Faraone, S V, Walitza, S, Sinzig, J, Freitag, C, Meyer, J, Herpertz-Dahlmann, B, Lehmkuhl, G, Renner, T J, Warnke, A, Romanos, M, Lesch, K-P, Reif, A, Schimmelmann, B G, Hebebrand, J, Scherag, A, Hinney, A

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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness von Hochfeld, Lara M, Bertolini, Marta, Broadley, David, Botchkareva, Natalia V, Betz, Regina C, Schoch, Susanne, Nöthen, Markus M, Heilmann-Heimbach, Stefanie

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Impact of depositional and biogeochemical processes on small scale variations in nodule abundance in the Clarion‐Clipperton Fracture Zone von Mewes, K., Mogollón, J.M., Picard, A., Rühlemann, C., Kuhn, T., Nöthen, K., Kasten, S.

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High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia von Malhotra, Dheeraj, McCarthy, Shane, Michaelson, Jacob J., Vacic, Vladimir, Burdick, Katherine E., Yoon, Seungtai, Cichon, Sven, Corvin, Aiden, Gary, Sydney, Gershon, Elliot S., Gill, Michael, Karayiorgou, Maria, Kelsoe, John R., Krastoshevsky, Olga, Krause, Verena, Leibenluft, Ellen, Levy, Deborah L., Makarov, Vladimir, Bhandari, Abhishek, Malhotra, Anil K., McMahon, Francis J., Nöthen, Markus M., Potash, James B., Rietschel, Marcella, Schulze, Thomas G., Sebat, Jonathan

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