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

Assistant Professor - medical

  • Psychiatry

Research Output (99)

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.

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

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 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.