Volatilization and Mineralization of [3-14C]Fluoranthene After Soil Incorporation and Soil Surface Application von Ophoff, H., Stork, A., Veerkamp, W., Führ, F.

Volltext

Photodegradation and Volatility of Pesticides: Chamber Experiments von Kromer, Thomas, Ophoff, Holger, Stork, Andreas, Fuehr, Fritz

Volltext

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.

Volltext

Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci von Børglum, A D, Demontis, D, Grove, J, Pallesen, J, Hollegaard, M V, Pedersen, C B, Hedemand, A, Mattheisen, M, Uitterlinden, A, Nyegaard, M, Ørntoft, T, Wiuf, C, Didriksen, M, Nordentoft, M, Nöthen, M M, Rietschel, M, Ophoff, R A, Cichon, S, Yolken, R H, Hougaard, D M, Mortensen, P B, Mors, O

Volltext

Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects von van Eijk, Kristel R, de Jong, Simone, Boks, Marco P M, Langeveld, Terry, Colas, Fabrice, Veldink, Jan H, de Kovel, Carolien G F, Janson, Esther, Strengman, Eric, Langfelder, Peter, Kahn, René S, van den Berg, Leonard H, Horvath, Steve, Ophoff, Roel A

Volltext

Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients von Saris, Christiaan G J, Horvath, Steve, van Vught, Paul W J, van Es, Michael A, Blauw, Hylke M, Fuller, Tova F, Langfelder, Peter, DeYoung, Joseph, Wokke, John H J, Veldink, Jan H, van den Berg, Leonard H, Ophoff, Roel A

Volltext

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

Volltext

A double hit implicates DIAPH3 as an autism risk gene von Vorstman, J A S, van Daalen, E, Jalali, G R, Schmidt, E R E, Pasterkamp, R J, de Jonge, M, Hennekam, E A M, Janson, E, Staal, W G, van der Zwaag, B, Burbach, J P H, Kahn, R S, Emanuel, B S, van Engeland, H, Ophoff, R A

Volltext

Is human blood a good surrogate for brain tissue in transcriptional studies? von Cai, Chaochao, Langfelder, Peter, Fuller, Tova F, Oldham, Michael C, Luo, Rui, van den Berg, Leonard H, Ophoff, Roel A, Horvath, Steve

Volltext

Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients von Vrijenhoek, Terry, Buizer-Voskamp, Jacobine E., van der Stelt, Inge, Strengman, Eric, Sabatti, Chiara, Geurts van Kessel, Ad, Brunner, Han G., Ophoff, Roel A., Veltman, Joris A.

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Aging effects on DNA methylation modules in human brain and blood tissue von Horvath, Steve, Zhang, Yafeng, Langfelder, Peter, Kahn, René S, Boks, Marco PM, van Eijk, Kristel, van den Berg, Leonard H, Ophoff, Roel A

Volltext

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

Volltext

Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner von de Jong, Simone, Chepelev, Iouri, Janson, Esther, Strengman, Eric, van den Berg, Leonard H, Veldink, Jan H, Ophoff, Roel A

Volltext

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

Volltext

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study von van Es, Michael A, MD, Van Vught, Paul W, MSc, Blauw, Hylke M, MD, Franke, Lude, MSc, Saris, Christiaan G, MD, Andersen, Peter M, MD, Van Den Bosch, Ludo, PhD, de Jong, Sonja W, MD, van 't Slot, Ruben, BSc, Birve, Anna, PhD, Lemmens, Robin, MD, de Jong, Vianney, MD, Baas, Frank, PhD, Schelhaas, Helenius J, MD, Sleegers, Kristel, MD, Van Broeckhoven, Christine, PhD, Wokke, John HJ, MD, Wijmenga, Cisca, PhD, Robberecht, Wim, MD, Veldink, Jan H, MD, Ophoff, Roel A, PhD, van den Berg, Leonard H, MD

Volltext

High educational performance is a distinctive feature of bipolar disorder: a study on cognition in bipolar disorder, schizophrenia patients, relatives and controls von Vreeker, A., Boks, M. P. M., Abramovic, L., Verkooijen, S., van Bergen, A. H., Hillegers, M. H. J., Spijker, A. T., Hoencamp, E., Regeer, E. J., Riemersma-Van der Lek, R. F., Stevens, A. W. M. M., Schulte, P. F. J., Vonk, R., Hoekstra, R., van Beveren, N. J. M., Kupka, R. W., Brouwer, R. M., Bearden, C. E., MacCabe, J. H., Ophoff, R. A.

Volltext