y bi a mä troy in grassen Nöthen“. Zur kritischen Edition eines Paradestücks des Wandertheaters von Neuhuber, Christian

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Talmud torah bʼOdessa; maʼamor yakar wʼnisgav, mʼsapper tʼhilloth beth ha-sefer ha-hu, umafli mʼʼod tʼkhunath bʼne Israel unʼtoth ruham lilmod ulʼlammed. Nothen imre shefer ʼal darkhe ha-hin-nukh ugʼmilluth hasadim bikhlal, meʼeth ... N. Pirogof ... Neʼetak millʼshon Russian lissʼfath ʼever ʼim Parshegen ha-nishtʼwan meʼeth Aleksander Zederbaum von Pirogov, Nikolaĭ Ivanovich, 1810-1881

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Juliane Noth, Transmedial Landscapes and Modern Chinese Painting von John Clark

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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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Zur Poetik und Medienpraxis von Rudolf Zacharias Beckers ,,Noth- und Hilfsbüchlein" (1788/98) von Penke, Niels

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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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Emmy Noether - Mathematician Extraordinaire von Rowe, David E

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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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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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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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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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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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