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

Assistant Professor - medical

  • Psychiatry

Research Output (99)

Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder

Lipstein Noa, Verhoeven-Duif Nanda M., Michelassi Francesco E., Calloway Nathaniel, Van Hasselt Peter M., Pienkowska Katarzyna, Van Haaften Gijs, Van Haelst Mieke M., van Empelen R., Cuppen Inge, Van Teeseling Heleen C., Evelein Annemieke M V, Vorstman Jacob A., Thoms Sven, Jahn Olaf, Duran KJ, Monroe Glen R., Ryan Timothy A., Taschenberger Holger, Dittman Jeremy S., Rhee Jeong Seop, Visser Gepke, Jans Judith J., Brose Nils 1 mrt 2017, In: Journal of Clinical Investigation. 127 , p. 1005-1018 14 p.

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome

Hidding E., Swaab H., de Sonneville L. M J, van Engeland H., Vorstman J. A S 1 nov 2016, In: Clinical Genetics. 90 , p. 420-427 8 p.

Explaining the variable penetrance of CNVs:Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion

Klaassen Petra, Duijff Sasja, Swanenburg de Veye Henriëtte, Beemer Frits, Sinnema Gerben, Breetvelt Elemi, Schappin Renske, Vorstman Jacob sep 2016, In: American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 171 , p. 790–796

The sociability score:App-based social profiling from a healthcare perspective

Eskes Paul, Spruit Marco, Brinkkemper Sjaak, Vorstman Jacob, Kas Martien J. 1 jun 2016, In: Computers in Human Behavior. 59 , p. 39-48 10 p.

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Mlynarski Elisabeth E., Xie Michael, Taylor Deanne, Sheridan Molly B., Guo Tingwei, Racedo Silvia E., McDonald-McGinn Donna M., 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, Goldmuntz Elizabeth, Bassett Anne S., Morrow Bernice E., Emanuel Beverly S., The International Chromosome 22Q11 2 Consortium mrt 2016, In: Human Genetics. 135 , p. 273–285 13 p.

Early interventions in risk groups for schizophrenia:what are we waiting for?

Sommer Iris E, Bearden Carrie E, van Dellen Edwin, Breetvelt Elemi J, Duijff Sasja N, Maijer Kim, van Amelsvoort Therese, de Haan Lieuwe, Gur Raquel E, Arango Celso, Díaz-Caneja Covadonga M, Vinkers Christiaan H, Vorstman Jacob As 2016, In: npj Schizophrenia. 2

Psychose:Symptomen en stoornissen onderscheiden bij kinderen en adolescenten

Vorstman J. A., Breetvelt E. J., Hillegers M. H., Scheepers F. E. 1 dec 2015, In: Tijdschrift voor Psychiatrie. 57 , p. 928-932 5 p.

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. 19 nov 2015, In: Nature Reviews Disease Primers. 1

Unmet needs in paediatric psychopharmacology:Present scenario and future perspectives

Persico Antonio M., Arango Celso, Buitelaar Jan K., Correll Christoph U., Glennon Jeffrey C., Hoekstra Pieter J., Moreno Carmen, Vitiello Benedetto, Vorstman Jacob, Zuddas Alessandro, okt 2015, In: European Neuropsychopharmacology. 25 , p. 1513-1531 19 p.

AUTISM SPECTRUM AND PSYCHOSIS RISK IN THE 22Q11.2 DELETION SYNDROME. FINDINGS FROM A PROSPECTIVE LONGITUDINAL STUDY

Fiksinski A. M., Breetvelt E. J., Duijff S. N., Bassett A. S., Vorstman J. A. S. sep 2015, In: Journal of Intellectual Disability Research. 59 , p. 789-790 2 p.