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dr. J.A.S. (Jacob) Vorstman

dr. J.A.S. (Jacob) Vorstman

Associate Professor

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Research Output (119)

Intellectual functioning in relation to autism and ADHD symptomatology in children and adolescents with 22q11.2 deletion syndrome

Hidding E., Swaab H., de Sonneville L. M. J., van Engeland H., Sijmens-Morcus M. E. J., Klaassen P. W. J., Duijff S. N., Vorstman J. A. S. Sep 2015, In: Journal of Intellectual Disability Research. 59 , p. 803-815 13 p.

Cognitieve achteruitgang meetbaar jaren voor de eerste psychotische episode

Vorstman Jacob 1 Aug 2015, In: Tijdschrift voor Psychiatrie. 57 , p. 613-614 2 p.

Genome-wide burden of deleterious coding variants increased in schizophrenia

Loohuis Loes M. Olde, Vorstman Jacob A. S., Ori Anil P., Staats Kim A., Wang Tina, Richards Alexander L., Leonenko Ganna, Walters James T., DeYoung Joseph, Cantor Rita M., Ophoff Roel A., Jul 2015, In: Nature Communications [E]. 6 6 p.

Pharmacological Treatment of 22q112 Deletion Syndrome-related Psychoses

Boot E., Butcher N. J., Vorstman J. A S, Van Amelsvoort T. A M J, Fung W. L A, Bassett A. S. 19 Jun 2015, In: Pharmacopsychiatry. 48 , p. 219-220 2 p.

Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma

Luykx J. J., Bakker S. C., Visser W. F., Verhoeven-Duif N., Buizer-Voskamp J. E., den Heijer J. M., Boks M. P M, Sul J. H., Eskin E., Ori A. P., Cantor R. M., Vorstman J., Strengman E., DeYoung J., Kappen T. H., Pariama E., van Dongen E. P A, Borgdorff P., Bruins P., de Koning T. J., Kahn R. S., Ophoff R. A. 10 Feb 2015, In: Molecular Psychiatry. 20 , p. 1557-1564 8 p.

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., Emanuel Beverly S., Zackai Elaine H., Kushan Leila, Fremont Wanda, Schoch Kelly, Stoddard Joel, Cubells Joseph, Fu Fiona, Campbell Linda E., Fritsch Rosemarie, Vergaelen Elfi, Neeleman Marjolein, Boot Erik, Debbané Martin, Philip Nicole, Green Tamar, Van DenBree Marianne B M, Murphy Declan, Canyelles Jaume Morey, Arango Celso, Murphy Kieran C., Pontillo Maria 1 Jan 2015, In: JAMA Psychiatry. 72 , p. 377-385 9 p.

Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11.2 deletion syndrome

Mlynarski Elisabeth E., Sheridan Molly B., Xie Michael, Guo Tingwei, Racedo Silvia E., McDonald-Mcginn Donna M., Gai Xiaowu, Chow Eva W C, Vorstman Jacob, Swillen Ann, Devriendt Koen, Breckpot Jeroen, Digilio Maria Cristina, Marino Bruno, Dallapiccola Bruno, Philip Nicole, Simon Tony J., Roberts Amy E., Piotrowicz Małgorzata, Bearden Carrie E., Eliez Stephan, Gothelf Doron, Coleman Karlene, Kates Wendy R., Devoto Marcella, Zackai Elaine, Heine-Suñer Damian, Shaikh Tamim H., Bassett Anne S., Goldmuntz Elizabeth, Morrow Bernice E., Emanuel Beverly S. 1 Jan 2015, In: American Journal of Human Genetics. 96 , p. 753-764 12 p.

Behavioral phenotype in children with 22q11Ds:Agreement between parents and teachers

Klaassen Petra W J, Duijff Sasja N., Sinnema Gerben, Beemer Frits A., Swanenburg de Veye Henriëtte F N, Vorstman Jacob A S 1 Jan 2015, In: Psychological Assessment. 27 , p. 272-279 8 p.

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

Schneider M., Debbane M., Bassett A.S., Chow E.W., Fung W.L., de Bree M., Owen M., Murphy K., Niarchou M., Kates W., Antshel K.M., Fremont W., McDonald-McGinn D.M., Gur R.E., et al X, Duijff S.N., Vorstman J.A.S., Klaassen P.W.J., Eliez S. 2014, In: American Journal of Psychiatry. 171 , p. 627-639 13 p.

Using genetic findings in autism for the development of new pharmaceutical compounds

Vorstman J.A.S., Spooren W., Persico M., Collier D.A., Aigner S., Jagasia R., Glennon J., Buitelaar J.K. 2014, In: Psychopharmacology. 231 , p. 1063-1078 16 p.

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