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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)

Psychiatric phenotypes associated with hyperprolinemia:A systematic review

Namavar Yasmin, Duineveld Denise Joanne, Both Geertje Ingena Angelique, Fiksinski Ania Maria, Vorstman Jacob Abraham Schrey, Verhoeven-Duif Nanda Margriet, Zinkstok Janneke Rozemarijn 24 Jul 2021, In: American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 186 , p. 289-317 29 p.

Same or different? Language skills of children with 22q11.2 Deletion Syndrome and children with Developmental Language Disorder

Everaert Emma, Selten Iris, Boerma Tessel, Hulshof Merel, Houben ML, Vorstman Jacob, Gerrits Elianne, Wijnen Frank 3 Jun 2021,

Neurodevelopmental Trajectories and Psychiatric Morbidity:Lessons Learned From the 22q11.2 Deletion Syndrome

Fiksinski Ania M, Schneider Maude, Zinkstok Janneke, Baribeau Danielle, Chawner Samuel J R A, Vorstman Jacob A S Mar 2021, In: Current Psychiatry Reports. 23

A normative chart for cognitive development in a genetically selected population

Fiksinski Ania M, Bearden Carrie E, Bassett Anne S, Kahn Rene S, Zinkstok Janneke R, Hooper Stephen R, Tempelaar Wanda, Vorstman Jacob A S, Breetvelt Elemi J, , Houben ML 2021, In: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology. 47 , p. 1379-1386 8 p.

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 2021, In: Psychological medicine. 52 , p. 3184-3192 9 p.

Effect of disease related biases on the subjective assessment of social functioning in Alzheimer's disease and schizophrenia patients

Jongs Niels, Penninx Brenda, Arango Celso, Ayuso-Mateos Jose Luis, van der Wee Nic, Rossum Inge Winter-van, Saris Ilja M J, van Echteld Amber, Koops Sanne, Bilderbeck Amy C, Raslescu Andreea, Dawson Gerard R, Sommer Bernd, Marston Hugh, Vorstman Jacob A, Eijkemans Marinus Jc, Kas Martien J 9 Nov 2020, In: Journal of Psychiatric Research. 145 , p. 302-308 7 p.

The role of rare compound heterozygous events in autism spectrum disorder

Lin Bochao Danae, Colas Fabrice, Nijman Isaac J., Medic Jelena, Brands William, Parr Jeremy R., van Eijk Kristel R., Klauck Sabine M., Chiocchetti Andreas G., Freitag Christine M., Maestrini Elena, Bacchelli Elena, Coon Hilary, Vicente Astrid, Oliveira Guiomar, Pagnamenta Alistair T., Gallagher Louise, Ennis Sean, Anney Richard, Bourgeron Thomas, Luykx Jurjen J., Vorstman Jacob 22 Jun 2020, In: Translational Psychiatry. 10 , p. 1-8

Het taalprofiel van kinderen met het 22q11.2 deletiesyndroom in vergelijking met kinderen met TOS

Boerma Tessel, Selten Iris, Everaert Emma, Duinkerke F., Wijnen Frank, Gerrits Elianne, Houben ML, Vorstman Jacob 6 Mar 2020,

Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins

Vervoort Lisanne, Demaerel Wolfram, Rengifo Laura Y., Odrzywolski Adrian, Vergaelen Elfi, Hestand Matthew S., Breckpot Jeroen, Devriendt Koen, Swillen Ann, McDonald-McGinn Donna M., Fiksinski Ania M., Zinkstok Janneke R., Morrow Bernice E., Heung Tracy, Vorstman Jacob A.S., Bassett Anne S., Chow Eva W.C., Shashi Vandana, Vermeesch Joris R., 15 Nov 2019, In: Human Molecular Genetics. 28 , p. 3724-3733 10 p.

Neurobiological perspective of 22q11.2 deletion syndrome

Zinkstok Janneke R., Boot Erik, Bassett Anne S., Hiroi Noboru, Butcher Nancy J., Vingerhoets Claudia, Vorstman Jacob A.S., van Amelsvoort Therese A.M.J. 1 Nov 2019, In: The Lancet Psychiatry. 6 , p. 951-960 10 p.

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