Back

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

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

Associate Professor

Show full profile

Research Output (119)

The 22q11.2 deletion syndrome as a model for idiopathic scoliosis - A hypothesis

Homans Jelle F, de Reuver Steven, Breetvelt Elemi J, Vorstman Jacob A S, Deeney Vincent F X, Flynn John M, McDonald-McGinn Donna M, Kruyt Moyo C, Castelein René M Jun 2019, In: Medical Hypotheses. 127 , p. 57-62 6 p.

Neurocognition and adaptive functioning in a genetic high risk model of schizophrenia

Fiksinski A. M., Breetvelt E. J., Lee Y. J., Boot E., Butcher N., Palmer L., Chow E. W.C., Kahn R. S., Vorstman J. A.S., Bassett A. S. 1 Apr 2019, In: Psychological Medicine. 49 , p. 1047-1054 8 p.

Double hits in schizophrenia

Vorstman Jacob A S, Olde Loohuis Loes M, Kahn René S, Ophoff Roel A, 1 Aug 2018, In: Human Molecular Genetics. 27 , p. 2755-2761 7 p.

Preventive strategies for mental health

Arango Celso, Díaz-Caneja Covadonga M., McGorry Patrick D., Rapoport Judith, Sommer Iris E., Vorstman Jacob A., McDaid David, Marín Oscar, Serrano-Drozdowskyj Elena, Freedman Robert, Carpenter William 1 Jul 2018, In: The Lancet Psychiatry. 5 , p. 591-604 14 p.

Analysis of shared heritability in common disorders of the brain

Anttila Verneri, Bulik-Sullivan Brendan, Finucane Hilary K, Walters Raymond K, Bras Jose, Duncan Laramie, Escott-Price Valentina, Falcone Guido J, Gormley Padhraig, Malik Rainer, Patsopoulos Nikolaos A, Ripke Stephan, Wei Zhi, Yu Dongmei, Lee Phil H, Turley Patrick, Grenier-Boley Benjamin, Chouraki Vincent, Kamatani Yoichiro, Berr Claudine, Letenneur Luc, Hannequin Didier, Amouyel Philippe, Boland Anne, Deleuze Jean-François, Duron Emmanuelle, Vardarajan Badri N, Reitz Christiane, Goate Alison M, Huentelman Matthew J, Kamboh M Ilyas, Larson Eric B, Rogaeva Ekaterina, St George-Hyslop Peter, Hakonarson Hakon, Kukull Walter A, Farrer Lindsay A, Barnes Lisa L, Beach Thomas G, Demirci F Yesim, Head Elizabeth, Hulette Christine M, Jicha Gregory A, Lindhout Dick, Pulit Sara, Vorstman Jacob, Ophoff Roel, Cahn Wiepke, van Os Jim, Koeleman Bobby, 22 Jun 2018, In: Science. 360

White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline

Nuninga Jasper Olivier, Bohlken Marc Marijn, Koops Sanne, Fiksinski Ania M., Mandl René C.W., Breetvelt Elemi J., Duijff Sasja N., Kahn René S., Sommer Iris E.C., Vorstman Jacob A.S. 16 Nov 2017, In: Psychological Medicine. 48 , p. 1655-1663 9 p.

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

Bassett Anne S., Lowther Chelsea, Merico Daniele, Costain Gregory, Chow Eva W C, Van Amelsvoort Therese, McDonald-Mcginn Donna M., Gur Raquel E., Swillen Ann, van den Bree Marianne B M, Murphy Kieran C., Gothelf Doron, Bearden Carrie E., Eliez Stephan, Kates Wendy R., Philip Nicole, Sashi Vandana, Campbell Linda E., Vorstman Jacob, Cubells Joseph, Repetto Gabriela M., Simon Tony J., Boot Erik, Heung Tracy, Evers Rens, Vingerhoets Claudia, Van Duin Esther, Zackai Elaine, Vergaelen Elfi, Devriendt Koen, Vermeesch Joris R., Owen Michael J, Murphy Clodagh M., Michaelovosky Elena, Kushan Leila, Schneider Maude, Fremont Wanda, Busa Tiffany, Hooper Stephen R., McCabe Kathryn, Duijff Sasja, Isaev Karin, Pellecchia Giovanna, Wei John, Gazzellone Matthew J., Scherer Stephen W., Emanuel Beverly S., Guo Tingwei, Morrow Bernice E., Marshall Christian R. 1 Nov 2017, In: American Journal of Psychiatry. 174 , p. 1054-1063 10 p.

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 Oct 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. Apr 2017, In: Nature Neuroscience. 20 , p. 602-611 10 p.

Thank you for your review!

Has this information helped you?

Please tell us why, so that we can improve our website.

Working at UMC Utrecht

Contact

Emergency?

Directions

Appointments

Practical

umcutrecht.nl uses cookies

This website uses cookies This website displays videos from, among others, YouTube. Such parties place cookies (third-party cookies). If you do not want these cookies, you can indicate that here. We also place cookies ourselves to improve our site.

Read more about the cookie policy

Agree No, rather not