Operative Treatment of a Congenital Pancreatic Pseudocyst: A Case Report von Büchin-Emunds, Petra, Steinau, G., Riesener, K.-P., Ophoff, K., Kentrup, H., Schumpelick, V.

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Femoral hernia in childhood: evaluation of sonography as a diagnostic aid von Büchin, P., Steinau, G., Ophoff, K., Dreuw, B., Truong, S. N., Schumpelick, V.

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Microvasculature of the human esophagus: A study on 25 autopsy specimens von Treutner, Karl H., Ophoff, Kerstin, Klosterhalfen, Bernd, Winkeltau, Gerd, Schumpelick, Volker

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Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights von Gusev, Alexander, Mancuso, Nicholas, Won, Hyejung, Kousi, Maria, Finucane, Hilary K., Reshef, Yakir, Song, Lingyun, Safi, Alexias, McCarroll, Steven, Neale, Benjamin M., Ophoff, Roel A., O’Donovan, Michael C., Crawford, Gregory E., Geschwind, Daniel H., Katsanis, Nicholas, Sullivan, Patrick F., Pasaniuc, Bogdan, Price, Alkes L.

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Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression von Fu, Jingyuan, Wolfs, Marcel G M, Deelen, Patrick, Westra, Harm-Jan, Fehrmann, Rudolf S N, Te Meerman, Gerard J, Buurman, Wim A, Rensen, Sander S M, Groen, Harry J M, Weersma, Rinse K, van den Berg, Leonard H, Veldink, Jan, Ophoff, Roel A, Snieder, Harold, van Heel, David, Jansen, Ritsert C, Hofker, Marten H, Wijmenga, Cisca, Franke, Lude

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Cortical abnormalities in bipolar disorder: an MRI analysis of 6503 individuals from the ENIGMA Bipolar Disorder Working Group von Westlye, L T, Jahanshad, N, Cheung, J W, Ching, C R K, Versace, A, Bilderbeck, A C, Uhlmann, A, Overs, B, Dima, D, Grotegerd, D, Sprooten, E, Bøen, E, Jimenez, E, Howells, F M, Delvecchio, G, Starke, J, Goikolea, J M, Houenou, J, Beard, L M, Rauer, L, Abramovic, L, Bonnin, M, Ponteduro, M F, Keil, M, Rive, M M, Yao, N, Rosa, P G, Redlich, R, Trost, S, Fears, S C, van Erp, T G M, Nickson, T, Chaim-Avancini, T M, Elvsåshagen, T, Haukvik, U K, Lee, W H, Schene, A H, Lloyd, A J, Young, A H, Nugent, A, Dale, A M, Pfennig, A, Lafer, B, Baune, B T, Ekman, C J, Zarate, C A, Bearden, C E, Henry, C, Simhandl, C, McDonald, C, Bourne, C, Stein, D J, Wolf, D H, Cannon, D M, Glahn, D C, Veltman, D J, Vieta, E, Canales-Rodriguez, E J, Nery, F G, Duran, F L S, Busatto, G F, Roberts, G, Pearlson, G D, Goodwin, G M, Ruhe, H G, Soares, J C, Fullerton, J M, Rybakowski, J K, Chaim, K T, Fatjó-Vilas, M, Soeiro-de-Souza, M G, Boks, M P, Zanetti, M V, Otaduy, M C G, Schaufelberger, M S, Ingvar, M, Phillips, M L, Bauer, M, Landén, M, Lawrence, N S, van Haren, N E M, Horn, N R, Freimer, N B, Schofield, P R, Mitchell, P B, Kahn, R S, Lenroot, R, Machado-Vieira, R, Ophoff, R A, Sarró, S, Frangou, S, Satterthwaite, T D, Hajek, T, Dannlowski, U, Arolt, V, Gattaz, W F, Drevets, W C, Agartz, I, Thompson, P M, Andreassen, O A

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Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid von Luykx, J J, Bakker, S C, Lentjes, E, Neeleman, M, Strengman, E, Mentink, L, DeYoung, J, de Jong, S, Sul, J H, Eskin, E, van Eijk, K, van Setten, J, Buizer-Voskamp, J E, Cantor, R M, Lu, A, van Amerongen, M, van Dongen, E P A, Keijzers, P, Kappen, T, Borgdorff, P, Bruins, P, Derks, E M, Kahn, R S, Ophoff, R A

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Pharmacogenetic Associations of Antipsychotic Drug-Related Weight Gain: A Systematic Review and Meta-analysis von Zhang, Jian-Ping, Lencz, Todd, Zhang, Ryan X, Nitta, Masahiro, Maayan, Lawrence, John, Majnu, Robinson, Delbert G, Fleischhacker, W Wolfgang, Kahn, Rene S, Ophoff, Roel A, Kane, John M, Malhotra, Anil K, Correll, Christoph U

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Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium von van Erp, T G M, Hibar, D P, Rasmussen, J M, Glahn, D C, Pearlson, G D, Andreassen, O A, Agartz, I, Westlye, L T, Haukvik, U K, Dale, A M, Melle, I, Hartberg, C B, Gruber, O, Kraemer, B, Zilles, D, Donohoe, G, Kelly, S, McDonald, C, Morris, D W, Cannon, D M, Corvin, A, Machielsen, M W J, Koenders, L, de Haan, L, Veltman, D J, Satterthwaite, T D, Wolf, D H, Gur, R C, Gur, R E, Potkin, S G, Mathalon, D H, Mueller, B A, Preda, A, Macciardi, F, Ehrlich, S, Walton, E, Hass, J, Calhoun, V D, Bockholt, H J, Sponheim, S R, Shoemaker, J M, van Haren, N E M, Hulshoff Pol, H E, Ophoff, R A, Kahn, R S, Roiz-Santiañez, R, Crespo-Facorro, B, Wang, L, Alpert, K I, Jönsson, E G, Dimitrova, R, Bois, C, Whalley, H C, McIntosh, A M, Lawrie, S M, Hashimoto, R, Thompson, P M, Turner, J A

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CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy von Friedman, J I, Vrijenhoek, T, Markx, S, Janssen, I M, van der Vliet, W A, Faas, B H W, Knoers, N V, Cahn, W, Kahn, R S, Edelmann, L, Davis, K L, Silverman, J M, Brunner, H G, van Kessel, A Geurts, Wijmenga, C, Ophoff, R A, Veltman, J A

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Subcortical volumetric abnormalities in bipolar disorder von Hibar, D P, Westlye, L T, van Erp, T G M, Rasmussen, J, Leonardo, C D, Faskowitz, J, Haukvik, U K, Hartberg, C B, Doan, N T, Agartz, I, Dale, A M, Gruber, O, Krämer, B, Trost, S, Liberg, B, Abé, C, Ekman, C J, Ingvar, M, Landén, M, Fears, S C, Freimer, N B, Bearden, C E, Sprooten, E, Glahn, D C, Pearlson, G D, Emsell, L, Kenney, J, Scanlon, C, McDonald, C, Cannon, D M, Almeida, J, Versace, A, Caseras, X, Lawrence, N S, Phillips, M L, Dima, D, Delvecchio, G, Frangou, S, Satterthwaite, T D, Wolf, D, Houenou, J, Henry, C, Malt, U F, Bøen, E, Elvsåshagen, T, Young, A H, Lloyd, A J, Goodwin, G M, Mackay, C E, Bourne, C, Bilderbeck, A, Abramovic, L, Boks, M P, van Haren, N E M, Ophoff, R A, Kahn, R S, Bauer, M, Pfennig, A, Alda, M, Hajek, T, Mwangi, B, Soares, J C, Nickson, T, Dimitrova, R, Sussmann, J E, Hagenaars, S, Whalley, H C, McIntosh, A M, Thompson, P M, Andreassen, O A

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Sleep disorders during childhood: a practical review von Ophoff, D., Slaats, M. A., Boudewyns, A., Glazemakers, I., Van Hoorenbeeck, K., Verhulst, S. L.

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Copy number variations of chromosome 16p13.1 region associated with schizophrenia von Ingason, A, Rujescu, D, Cichon, S, Sigurdsson, E, Sigmundsson, T, Pietiläinen, O P H, Buizer-Voskamp, J E, Strengman, E, Francks, C, Muglia, P, Gylfason, A, Gustafsson, O, Olason, P I, Steinberg, S, Hansen, T, Jakobsen, K D, Rasmussen, H B, Giegling, I, Möller, H-J, Hartmann, A, Crombie, C, Fraser, G, Walker, N, Lonnqvist, J, Suvisaari, J, Tuulio-Henriksson, A, Bramon, E, Kiemeney, L A, Franke, B, Murray, R, Vassos, E, Toulopoulou, T, Mühleisen, T W, Tosato, S, Ruggeri, M, Djurovic, S, Andreassen, O A, Zhang, Z, Werge, T, Ophoff, R A, Rietschel, M, Nöthen, M M, Petursson, H, Stefansson, H, Peltonen, L, Collier, D, Stefansson, K, Clair, D M St

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Survival prediction in patients undergoing radionuclide therapy based on intratumoral somatostatin-receptor heterogeneity von Werner, Rudolf A, Lapa, Constantin, Ilhan, Harun, Higuchi, Takahiro, Buck, Andreas K, Lehner, Sebastian, Bartenstein, Peter, Bengel, Frank, Schatka, Imke, Muegge, Dirk O, Papp, László, Zsótér, Norbert, Große-Ophoff, Tobias, Essler, Markus, Bundschuh, Ralph A

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Genome-wide association study of obsessive-compulsive disorder von Stewart, S E, Yu, D, Scharf, J M, Neale, B M, Fagerness, J A, Arnold, P D, Evans, P D, Gamazon, E R, McGrath, L, Haddad, S, Crane, J, Hezel, D, Illman, C, Mayerfeld, C, Konkashbaev, A, Liu, C, Pluzhnikov, A, Tikhomirov, A, Rauch, S L, Maier, W, Ruhrmann, S, Grabe, H-J, Lennertz, L, Wagner, M, Bellodi, L, Cavallini, M C, Richter, M A, Cook, E H, Kennedy, J L, Rosenberg, D, Stein, D J, Hemmings, S M J, Azzam, A, Chavira, D A, Fournier, E, Garrido, H, Sheppard, B, Umaña, P, Murphy, D L, Wendland, J R, Veenstra-VanderWeele, J, Denys, D, Blom, R, Deforce, D, Van Nieuwerburgh, F, Walitza, S, Egberts, K, Renner, T, Miguel, E C, Cappi, C, Hounie, A G, Conceição do Rosário, M, Sampaio, A S, Vallada, H, Lanzagorta, N, Camarena, B, Delorme, R, Leboyer, M, Pato, C N, Pato, M T, Voyiaziakis, E, Heutink, P, Cath, D C, Posthuma, D, Smit, J H, Samuels, J, Bienvenu, O J, Cullen, B, Fyer, A J, Grados, M A, Greenberg, B D, McCracken, J T, Riddle, M A, Wang, Y, Coric, V, Leckman, J F, Pittenger, C, Eapen, V, Black, D W, Ophoff, R A, Strengman, E, Cusi, D, Turiel, M, Frau, F, Macciardi, F, Gibbs, J R, Cookson, M R, Singleton, A, Hardy, J, Crenshaw, A T, Parkin, M A, Mirel, D B, Conti, D V, Purcell, S, Nestadt, G, Hanna, G L, Jenike, M A, Knowles, J A, Cox, N, Pauls, D L

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Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralization von Somers, Metten, Ophoff, Roel A, Aukes, Maartje F, Cantor, Rita M, Boks, Marco P, Dauwan, Meenakshi, de Visser, Kees L, Kahn, René S, Sommer, Iris E

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The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia von Richards, Alexander L, Pardiñas, Antonio F, Frizzati, Aura, Tansey, Katherine E, Lynham, Amy J, Holmans, Peter, Legge, Sophie E, Savage, Jeanne E, Agartz, Ingrid, Andreassen, Ole A, Blokland, Gabriella A M, Corvin, Aiden, Cosgrove, Donna, Degenhardt, Franziska, Djurovic, Srdjan, Espeseth, Thomas, Ferraro, Laura, Gayer-Anderson, Charlotte, Giegling, Ina, van Haren, Neeltje E, Hartmann, Annette M, Hubert, John J, Jönsson, Erik G, Konte, Bettina, Lennertz, Leonhard, Olde Loohuis, Loes M, Melle, Ingrid, Morgan, Craig, Morris, Derek W, Murray, Robin M, Nyman, Håkan, Ophoff, Roel A, van Os, Jim, Petryshen, Tracey L, Quattrone, Diego, Rietschel, Marcella, Rujescu, Dan, Rutten, Bart P F, Streit, Fabian, Strohmaier, Jana, Sullivan, Patrick F, Sundet, Kjetil, Wagner, Michael, Escott-Price, Valentina, Owen, Michael J, Donohoe, Gary, O'Donovan, Michael C, Walters, James T R

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Integrative analysis of Dupuytren's disease identifies novel risk locus and reveals a shared genetic etiology with BMI von Major, Megan, Freund, Malika K., Burch, Kathryn S., Mancuso, Nicholas, Ng, Michael, Furniss, Dominic, Pasaniuc, Bogdan, Ophoff, Roel A.

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Three ulcerative colitis susceptibility loci are associated with primary sclerosing cholangitis and indicate a role for IL2, REL, and CARD9 von Janse, Marcel, Lamberts, Laetitia E., Franke, Lude, Raychaudhuri, Soumya, Ellinghaus, Eva, Muri Boberg, Kirsten, Melum, Espen, Folseraas, Trine, Schrumpf, Erik, Bergquist, Annika, Björnsson, Einar, Fu, Jingyuan, Jan Westra, Harm, Groen, Harry J.M., Fehrmann, Rudolf S.N., Smolonska, Joanna, van den Berg, Leonard H., Ophoff, Roel A., Porte, Robert J., Weismüller, Tobias J., Wedemeyer, Jochen, Schramm, Christoph, Sterneck, Martina, Günther, Rainer, Braun, Felix, Vermeire, Severine, Henckaerts, Liesbet, Wijmenga, Cisca, Ponsioen, Cyriel Y., Schreiber, Stefan, Karlsen, Tom H., Franke, Andre, Weersma, Rinse K.

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies von Bulik-Sullivan, Brendan K, Loh, Po-Ru, Finucane, Hilary K, Ripke, Stephan, Yang, Jian, Patterson, Nick, Daly, Mark J, Price, Alkes L, Neale, Benjamin M

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