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

Assistant Professor - medical

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Research Output (102)

Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

Demaerel Wolfram, Hestand Matthew S., Vergaelen Elfi, Swillen Ann, López-Sánchez Marcos, Pérez-Jurado Luis A., McDonald-Mcginn Donna M., Zackai Elaine, Emanuel Beverly S., Morrow Bernice E., Breckpot Jeroen, Devriendt Koenraad, Vermeesch Joris R., Antshel Kevin M., Arango Celso, Armando Marco, Bassett Anne S., Bearden Carrie E., Boot Erik, Bravo-Sanchez Marta, Breetvelt Elemi, Busa Tiffany, Butcher Nancy J., Campbell Linda E., Carmel Miri, Chow Eva W C, Crowley T. Blaine, Cubells Joseph, Cutler David, Demaerel Wolfram, Digilio Maria Cristina, Duijff Sasja, Eliez Stephan, Emanuel Beverly S., Epstein Michael P., Evers Rens, Fernandez Garcia-Moya Luis, Fiksinski Ania, Fraguas David, Fremont Wanda, Fritsch Rosemarie, Garcia-Minaur Sixto, Golden Aaron, Gothelf Doron, Guo Tingwei, Gur Ruben C., Gur Raquel E., Heine-Suner Damian, Hestand Matthew, Vorstman Jacob, 5 okt 2017, In: American Journal of Human Genetics. 101 , p. 616-622 7 p.

Autism genetics:opportunities and challenges for clinical translation

Vorstman Jacob A S, Parr Jeremy R, Moreno-De-Luca Daniel, Anney Richard J L, Nurnberger John I, Hallmayer Joachim F jun 2017, In: Nature Reviews. Genetics. 18 , p. 362-376 15 p.

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

Yuen Ryan K C et al. 29 mrt 2017, In: Nature Neuroscience. 20 , p. 602-611 10 p.

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.

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