Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients von Buizer-Voskamp, Jacobine E, Muntjewerff, Jan-Willem, Strengman, Eric, Sabatti, Chiara, Stefansson, Hreinn, Vorstman, Jacob A.S, Ophoff, Roel A

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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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Using genetic findings in autism for the development of new pharmaceutical compounds von Vorstman, Jacob A. S., Spooren, Will, Persico, Antonio M., Collier, David A., Aigner, Stefan, Jagasia, Ravi, Glennon, Jeffrey C., Buitelaar, Jan K.

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TWENTY YEARS OF RESEARCH ON THE 22Q11.2 DELETION SYNDROME AND SCHIZOPHRENIA: WHAT HAVE WE LEARNED SO FAR? von Vorstman, Jacob A.S, Kahn, René

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THE 22Q11.2 DELETION SYNDROME AS A MODEL FOR DEMENTIA PRAECOX von Vorstman, Jacob A.S, Breetvelt, Elemi, Duijff, Sasja, Kahn, René

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Increased paternal age and the influence on burden of genomic copy number variation in the general population von Buizer-Voskamp, Jacobine E., Blauw, Hylke M., Boks, Marco P. M., van Eijk, Kristel R., Veldink, Jan H., Hennekam, Eric A. M., Vorstman, Jacob A. S., Mulder, Flip, Tiemeier, Henning, Uitterlinden, André G., Kiemeney, Lambertus A., van den Berg, Leonard H., Kahn, René S., Sabatti, Chiara, Ophoff, Roel A.

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Autism genetics: opportunities and challenges for clinical translation von Vorstman, Jacob A. S., Parr, Jeremy R., Moreno-De-Luca, Daniel, Anney, Richard J. L., Nurnberger Jr, John I., Hallmayer, Joachim F.

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Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia von Hoogendoorn, Mechteld L.C, Vorstman, Jacob A.S, Jalali, Gholam R, Selten, Jean-Paul, Sinke, Richard J, Emanuel, Beverly S, Kahn, René S

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A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome von Fiksinski, Ania M., Hoftman, Gil D., Vorstman, Jacob A. S., Bearden, Carrie E.

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

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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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Selective Serotonin Reuptake Inhibitor Treatment Post Gene Therapy for an Ultrarare Neurometabolic Disorder (AADC Deficiency) von Baribeau, Danielle A., Vorstman, Jacob A.S., Pearson, Toni S.

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Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model von Fiksinski, Ania M., Heung, Tracy, Corral, Maria, Breetvelt, Elemi J., Costain, Gregory, Marshall, Christian R., Kahn, Rene S., Vorstman, Jacob A.S., Bassett, Anne S.

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A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome von Fiksinski, Ania M, Hoftman, Gil D, Vorstman, Jacob A.S, Bearden, Carrie E

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Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome von Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.

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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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Neurobiological perspective of 22q11.2 deletion syndrome von Zinkstok, Janneke R, Boot, Erik, Bassett, Anne S, Hiroi, Noboru, Butcher, Nancy J, Vingerhoets, Claudia, Vorstman, Jacob A S, van Amelsvoort, Therese A M J

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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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Genetic causes of developmental disorders von Vorstman, Jacob A S, Ophoff, Roel A

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Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome von Fiksinski, Ania M., Schneider, Maude, Murphy, Clodagh M., Armando, Marco, Vicari, Stefano, Canyelles, Jaume M., Gothelf, Doron, Eliez, Stephan, Breetvelt, Elemi J., Arango, Celso, Vorstman, Jacob A. S.

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