Characterization of the sulfate-reducing and syntrophic population in granular sludge from a full-scale anaerobic reactor treating papermill wastewater von Elferink, S.J.W.H.O, Vorstman, W.J.C, Sopjes, A, Stams, A.J.M

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The influence of oxygen and carbon dioxide on the growth of prevalent enterobacteriaceae and Pseudomonas species isolated from fresh and controlled-atmosphere-stored vegetables von BENNIK, M. H. J, VORSTMAN, W, SMID, E. J, GORRIS, L. G. M

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The influence of oxygen and carbon dioxide on the growth of prevalent Enterobacteriaceae andPseudomonasspecies isolated from fresh and controlled-atmosphere-stored vegetables von Bennik, M.H, Vorstman, W, Smid, E.J, Gorris, L.G

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High induction of cytochrome p4501a activity without changes in retinoid and thyroid hormone levels in flounder (Platichthys flesus) exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin von Besselink, H. T., van Santen, E., Vorstman, W., Vethaak, A. D., Koeman, J. H., Brouwer, A.

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HIGH INDUCTION OF CYTOCHROME P4501A ACTIVITY WITHOUT CHANGES IN RETINOID AND THYROID HORMONE LEVELS IN FLOUNDER (PLATICHTHYS FLESUS) EXPOSED TO 2,3,7,8-TETRACHLORODIBENZO-p-DIOXIN von Besselink, H.T., van Santen, E., Vorstman, W., Vethaak, A.D., Koeman, J.H., Brouwer, A.

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A framework for an evidence-based gene list relevant to autism spectrum disorder von Schaaf, Christian P., Betancur, Catalina, Yuen, Ryan K. C., Parr, Jeremy R., Skuse, David H., Gallagher, Louise, Bernier, Raphael A., Buchanan, Janet A., Buxbaum, Joseph D., Chen, Chun-An, Dies, Kira A., Elsabbagh, Mayada, Firth, Helen V., Frazier, Thomas, Hoang, Ny, Howe, Jennifer, Marshall, Christian R., Michaud, Jacques L., Rennie, Olivia, Szatmari, Peter, Chung, Wendy K., Bolton, Patrick F., Cook, Edwin H., Scherer, Stephen W., Vorstman, Jacob A. S.

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Contemplating syndromic autism von Vorstman, Jacob A.S., Scherer, Stephen W.

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Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion von Vorstman, Jacob A.S, Breetvelt, Elemi J, Thode, Kirstin I, Chow, Eva W.C, Bassett, Anne S

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What a finding of gene copy number variation can add to the diagnosis of developmental neuropsychiatric disorders von Vorstman, Jacob, Scherer, Stephen W

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Cognitive Decline Preceding the Onset of Psychosis in Patients With 22q11.2 Deletion Syndrome von Vorstman, Jacob A. S, Breetvelt, Elemi J, Duijff, Sasja N, Eliez, Stephan, Schneider, Maude, Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Shashi, Vandana, Hooper, Stephen R, Chow, Eva W. C, Fung, Wai Lun Alan, Butcher, Nancy J, Young, Donald A, McDonald-McGinn, Donna M, Vogels, Annick, van Amelsvoort, Therese, Gothelf, Doron, Weinberger, Ronnie, Weizman, Abraham, Klaassen, Petra W. J, Koops, Sanne, Kates, Wendy R, Antshel, Kevin M, Simon, Tony J, Ousley, Opal Y, Swillen, Ann, Gur, Raquel E, Bearden, Carrie E, Kahn, René S, Bassett, Anne S

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Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia von Lin, Jhih-Rong, Zhao, Yingjie, Jabalameli, M. Reza, Nguyen, Nha, Mitra, Joydeep, Swillen, Ann, Vorstman, Jacob A. S., Chow, Eva W. C., van den Bree, Marianne, Emanuel, Beverly S., Vermeesch, Joris R., Owen, Michael J., Williams, Nigel M., Bassett, Anne S., McDonald-McGinn, Donna M., Gur, Raquel E., Bearden, Carrie E., Morrow, Bernice E., Lachman, Herbert M., Zhang, Zhengdong D.

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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

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The 22Q11.2 Deletion in Children: High Rate of Autistic Disorders and Early Onset of Psychotic Symptoms von Vorstman, Jacob A. S, Morcus, Monique E. J, Duijff, Sasja N, Klaassen, Petra W. J, Heineman-de, Josien A, Beemer, Frits A, Swaab, Hanna, Kahn, Rene S, van Engeland, Herman

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Gene copy number variation and pediatric mental health/neurodevelopment in a general population von Zarrei, Mehdi, Burton, Christie L, Engchuan, Worrawat, Higginbotham, Edward J, Wei, John, Shaikh, Sabah, Roslin, Nicole M, MacDonald, Jeffrey R, Pellecchia, Giovanna, Nalpathamkalam, Thomas, Lamoureux, Sylvia, Manshaei, Roozbeh, Howe, Jennifer, Trost, Brett, Thiruvahindrapuram, Bhooma, Marshall, Christian R, Yuen, Ryan K C, Wintle, Richard F, Strug, Lisa J, Stavropoulos, Dimitri J, Vorstman, Jacob A S, Arnold, Paul, Merico, Daniele, Woodbury-Smith, Marc, Crosbie, Jennifer, Schachar, Russell J, Scherer, Stephen W

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Digital phenotyping and the COVID-19 pandemic: Capturing behavioral change in patients with psychiatric disorders von Jagesar, Raj R., Roozen, Mila C., van der Heijden, Inge, Ikani, Nessa, Tyborowska, Anna, Penninx, Brenda W.J.H., Ruhe, Henricus G., Sommer, Iris E.C., Kas, Martien J., Vorstman, Jacob A.S.

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Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia von de Vrij, Femke M., Bouwkamp, Christian G., Gunhanlar, Nilhan, Shpak, Guy, Lendemeijer, Bas, Baghdadi, Maarouf, Gopalakrishna, Shreekara, Ghazvini, Mehrnaz, Li, Tracy M., Quadri, Marialuisa, Olgiati, Simone, Breedveld, Guido J., Coesmans, Michiel, Mientjes, Edwin, de Wit, Ton, Verheijen, Frans W., Beverloo, H. Berna, Cohen, Dan, Kok, Rob M., Bakker, P. Roberto, Nijburg, Aviva, Spijker, Annet T., Haffmans, P. M. Judith, Hoencamp, Erik, Bergink, Veerle, Vorstman, Jacob A., Wu, Timothy, Olde Loohuis, Loes M., Amin, Najaf, Langen, Carolyn D., Hofman, Albert, Hoogendijk, Witte J., van Duijn, Cornelia M., Ikram, M. Arfan, Vernooij, Meike W., Tiemeier, Henning, Uitterlinden, André G., Elgersma, Ype, Distel, Ben, Gribnau, Joost, White, Tonya, Bonifati, Vincenzo, Kushner, Steven A.

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Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome von Schneider, Maude, Debbané, Martin, Bassett, Anne S., Chow, Eva W.C., Fung, Wai Lun Alan, van den Bree, Marianne B.M., Owen, Michael, Murphy, Kieran C., Niarchou, Maria, Kates, Wendy R., Antshel, Kevin M., Fremont, Wanda, McDonald-McGinn, Donna M., Gur, Raquel E., Zackai, Elaine H., Vorstman, Jacob, Duijff, Sasja N., Klaassen, Petra W.J., Swillen, Ann, Gothelf, Doron, Green, Tamar, Weizman, Abraham, Van Amelsvoort, Therese, Evers, Laurens, Boot, Erik, Shashi, Vandana, Hooper, Stephen R., Bearden, Carrie E., Jalbrzikowski, Maria, Armando, Marco, Vicari, Stefano, Murphy, Declan G., Ousley, Opal, Campbell, Linda E., Simon, Tony J., Eliez, Stephan

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A Regional Burden of Sequence-Level Variation in the 22q11.2 Region Influences Schizophrenia Risk and Educational Attainment von Breetvelt, Elemi J., Smit, Karel C., van Setten, Jessica, Merico, Daniele, Wang, Xiao, Vaartjes, Ilonca, Bassett, Anne S., Boks, Marco P.M., Szatmari, Peter, Scherer, Stephen W., Kahn, René S., Vorstman, Jacob A.S.

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Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders von Pinto, Dalila, Delaby, Elsa, Merico, Daniele, Barbosa, Mafalda, Merikangas, Alison, Klei, Lambertus, Thiruvahindrapuram, Bhooma, Xu, Xiao, Ziman, Robert, Vorstman, Jacob A.S., Thompson, Ann, Regan, Regina, Pilorge, Marion, Pellecchia, Giovanna, Pagnamenta, Alistair T., Oliveira, Bárbara, Magalhaes, Tiago R., Lowe, Jennifer K., Howe, Jennifer L., Gilbert, John, Duketis, Eftichia, Dombroski, Beth A., Cuccaro, Michael, Crawford, Emily L., Correia, Catarina T., Conroy, Judith, Conceição, Inês C., Chiocchetti, Andreas G., Casey, Jillian P., Cai, Guiqing, Cabrol, Christelle, Bacchelli, Elena, Gallinger, Steven, Cotterchio, Michelle, Zwaigenbaum, Lonnie, Wittemeyer, Kerstin, Wing, Kirsty, van Engeland, Herman, Tryfon, Ana, Thomson, Susanne, Rogé, Bernadette, Roberts, Wendy, Poustka, Fritz, Mouga, Susana, Minshew, Nancy, McInnes, L. Alison, McGrew, Susan G., Lord, Catherine, Leboyer, Marion, Le Couteur, Ann S., Kolevzon, Alexander, Jiménez González, Patricia, Jacob, Suma, Holt, Richard, Guter, Stephen, Green, Jonathan, Green, Andrew, Gillberg, Christopher, Duque, Frederico, Delorme, Richard, Dawson, Geraldine, Chaste, Pauline, Café, Cátia, Brennan, Sean, Bourgeron, Thomas, Bolton, Patrick F., Bernier, Raphael, Baird, Gillian, Bailey, Anthony J., Almeida, Joana, Wijsman, Ellen M., Vieland, Veronica J., Vicente, Astrid M., Schellenberg, Gerard D., Pericak-Vance, Margaret, Paterson, Andrew D., Parr, Jeremy R., Oliveira, Guiomar, Nurnberger, John I., Monaco, Anthony P., Maestrini, Elena, Klauck, Sabine M., Hakonarson, Hakon, Haines, Jonathan L., Geschwind, Daniel H., Freitag, Christine M., Folstein, Susan E., Ennis, Sean, Coon, Hilary, Battaglia, Agatino, Szatmari, Peter, Sutcliffe, James S., Hallmayer, Joachim, Gill, Michael, Cook, Edwin H., Buxbaum, Joseph D., Devlin, Bernie, Gallagher, Louise, Betancur, Catalina, Scherer, Stephen W.

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Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia von Fiksinski, A. M., Breetvelt, E. J., Lee, Y. J., Boot, E., Butcher, N., Palmer, L., Chow, E. W. C., Kahn, R. S., Vorstman, J. A. S., Bassett, A. S.

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