Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients
Buizer-Voskamp, Jacobine E, Muntjewerff, Jan-Willem, Strengman, Eric, Sabatti, Chiara, Stefansson, Hreinn, Vorstman, Jacob A.S, Ophoff, Roel A
Published in Biological psychiatry (1969) (01.10.2011)
Published in Biological psychiatry (1969) (01.10.2011)
Get full text
Journal Article
Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion
Vorstman, Jacob A.S, Breetvelt, Elemi J, Thode, Kirstin I, Chow, Eva W.C, Bassett, Anne S
Published in Schizophrenia research (01.01.2013)
Published in Schizophrenia research (01.01.2013)
Get full text
Journal Article
THE 22Q11.2 DELETION SYNDROME AS A MODEL FOR DEMENTIA PRAECOX
Vorstman, Jacob A.S, Breetvelt, Elemi, Duijff, Sasja, Kahn, René
Published in Schizophrenia research (01.04.2014)
Published in Schizophrenia research (01.04.2014)
Get full text
Journal Article
Using genetic findings in autism for the development of new pharmaceutical compounds
Vorstman, Jacob A. S., Spooren, Will, Persico, Antonio M., Collier, David A., Aigner, Stefan, Jagasia, Ravi, Glennon, Jeffrey C., Buitelaar, Jan K.
Published in Psychopharmacology (01.03.2014)
Published in Psychopharmacology (01.03.2014)
Get full text
Journal Article
Increased paternal age and the influence on burden of genomic copy number variation in the general population
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.
Published in Human genetics (01.04.2013)
Published in Human genetics (01.04.2013)
Get full text
Journal Article
Selective Serotonin Reuptake Inhibitor Treatment Post Gene Therapy for an Ultrarare Neurometabolic Disorder (AADC Deficiency)
Baribeau, Danielle A., Vorstman, Jacob A.S., Pearson, Toni S.
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.06.2024)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.06.2024)
Get full text
Journal Article
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
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.
Published in American journal of human genetics (01.05.2014)
Published in American journal of human genetics (01.05.2014)
Get full text
Journal Article
22q11.2 deletion syndrome
McDonald-McGinn, Donna M., Sullivan, Kathleen E., Marino, Bruno, Philip, Nicole, Swillen, Ann, Vorstman, Jacob A. S., Zackai, Elaine H., Emanuel, Beverly S., Vermeesch, Joris R., Morrow, Bernice E., Scambler, Peter J., Bassett, Anne S.
Published in Nature reviews. Disease primers (19.11.2015)
Published in Nature reviews. Disease primers (19.11.2015)
Get full text
Journal Article
A framework for an evidence-based gene list relevant to autism spectrum disorder
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.
Published in Nature reviews. Genetics (01.06.2020)
Published in Nature reviews. Genetics (01.06.2020)
Get full text
Journal Article
Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology
Jacquemont, Sébastien, Huguet, Guillaume, Klein, Marieke, Chawner, Samuel J.R.A, Donald, Kirsten A, van den Bree, Marianne B.M, Sebat, Jonathan, Ledbetter, David H, Constantino, John N, Earl, Rachel K, McDonald-McGinn, Donna M, van Amelsvoort, Therese, Swillen, Ann, O’Donnell-Luria, Anne H, Glahn, David C, Almasy, Laura, Eichler, Evan E, Scherer, Stephen W, Robinson, Elise, Bassett, Anne S, Martin, Christa Lese, Finucane, Brenda, Vorstman, Jacob A.S, Bearden, Carrie E, Gur, Raquel E
Published in The American journal of psychiatry (01.03.2022)
Published in The American journal of psychiatry (01.03.2022)
Get full text
Journal Article
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome
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
Published in JAMA psychiatry (Chicago, Ill.) (01.04.2015)
Published in JAMA psychiatry (Chicago, Ill.) (01.04.2015)
Get more information
Journal Article
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model
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.
Published in Psychological medicine (01.10.2022)
Published in Psychological medicine (01.10.2022)
Get full text
Journal Article
Digital phenotyping and the COVID-19 pandemic: Capturing behavioral change in patients with psychiatric disorders
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.
Published in European neuropsychopharmacology (01.01.2021)
Published in European neuropsychopharmacology (01.01.2021)
Get full text
Journal Article