Successful Electroconvulsive Therapy in a Young Woman With Chronic Catatonia

Por Ozgen, Heval, Wijkstra, Jaap, Vorstman, Jacob
Publicado em 2012

The genetic overlap of attention deficit hyperactivity disorder and autistic spectrum disorder

Por Stam, Arie J, Schothorst, Patricia F, Vorstman, Jacob AS, Staal, Wouter G
Publicado em 2009

Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis

Por Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A.
Publicado em 2012

Correction: Investigation of the Genetic Association between Quantitative Measures of Psychosis and Schizophrenia: A Polygenic Risk Score Analysis

Por Derks, Eske M., Vorstman, Jacob A. S., Ripke, Stephan, Kahn, Rene S., Ophoff, Roel A.
Publicado em 2013

Self-Reported Speech Problems in Adolescents and Young Adults with 22q11.2 Deletion Syndrome: A Cross-Sectional Cohort Study

Por Spruijt, Nicole E, Vorstman, Jacob AS, Kon, Moshe, Mink van der Molen, Aebele B
Publicado em 2014

Behavioral signatures related to genetic disorders in autism

Por Bruining, Hilgo, Eijkemans, Marinus JC, Kas, Martien JH, Curran, Sarah R, Vorstman, Jacob AS, Bolton, Patrick F
Publicado em 2014

Dissecting the Clinical Heterogeneity of Autism Spectrum Disorders through Defined Genotypes

Por Bruining, Hilgo, de Sonneville, Leo, Swaab, Hanna, de Jonge, Maretha, Kas, Martien, van Engeland, Herman, Vorstman, Jacob
Publicado em 2010

Genome-wide analysis shows increased frequency of CNV deletions in Dutch schizophrenia patients

Por Buizer-Voskamp, Jacobine E, Muntjewerff, Jan-Willem, Strengman, Eric, Sabatti, Chiara, Stefansson, Hreinn, Vorstman, Jacob AS, Ophoff, Roel A
Publicado em 2011

Prevalence of 22q11.2 deletions in 311 Dutch patients with schizophrenia

Por Hoogendoorn, Mechteld L.C., Vorstman, Jacob A.S., Jalali, Gholam R., Selten, Jean-Paul, Sinke, Richard J., Emanuel, Beverly S., Kahn, René S.
Publicado em 2007

A palindrome-driven complex rearrangement of 22q11.2 and 8q24.1 elucidated using novel technologies

Por Gotter, Anthony L., Nimmakayalu, Manjunath A., Jalali, G. Reza, Hacker, April M., Vorstman, Jacob, Conforto Duffy, Danielle, Medne, Livija, Emanuel, Beverly S.
Publicado em 2007

Association of the PIK4CA Schizophrenia-Susceptibility Gene in Adults With the 22q11.2 Deletion Syndrome

Por Vorstman, Jacob A.S., Chow, Eva W., Ophoff, Roel A., van Engeland, Herman, Beemer, Frits A., Kahn, René S., Sinke, Richard J., Bassett, Anne S.
Publicado em 2009

Proline and COMT Status Affect Visual Connectivity in Children with 22q11.2 Deletion Syndrome

Por Magnée, Maurice J. C. M., Lamme, Victor A. F., de Sain-van der Velden, Monique G. M., Vorstman, Jacob A. S., Kemner, Chantal
Publicado em 2011

Systematic genotype–phenotype analysis of autism susceptibility loci implicates additional symptoms to co-occur with autism

Por Buizer-Voskamp, Jacobine E, Franke, Lude, Staal, Wouter G, van Daalen, Emma, Kemner, Chantal, Ophoff, Roel A, Vorstman, Jacob AS, van Engeland, Herman, Wijmenga, Cisca
Publicado em 2010

Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome

Por da Silva Alves, Fabiana, Boot, Erik, Schmitz, Nicole, Nederveen, Aart, Vorstman, Jacob, Lavini, Christina, Pouwels, Petra, de Haan, Lieuwe, Linszen, Don, van Amelsvoort, Therese
Publicado em 2011

Correction: Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome

Por da Silva Alves, Fabiana, Boot, Erik, Schmitz, Nicole, Nederveen, Aart, Vorstman, Jacob, Lavini, Christina, Pouwels, Petra, de Haan, Lieuwe, Linszen, Don, van Amelsvoort, Therese
Publicado em 2011

Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

Por Bassett, Anne S., McDonald-McGinn, Donna M., Devriendt, Koen, Digilio, Maria Cristina, Goldenberg, Paula, Habel, Alex, Marino, Bruno, Oskarsdottir, Solveig, Philip, Nicole, Sullivan, Kathleen, Swillen, Ann, Vorstman, Jacob
Publicado em 2011

Genome-wide burden of deleterious coding variants increased in schizophrenia

Por Loohuis, Loes M. Olde, Vorstman, Jacob A. S., Ori, Anil P., Staats, Kim A., Wang, Tina, Richards, Alexander L., Leonenko, Ganna, Walters, James T., DeYoung, Joseph, Cantor, Rita M., Ophoff, Roel A.
Publicado no Nat Commun (2015)

Proline Affects Brain Function in 22q11DS Children with the Low Activity COMT(158) Allele

Por Vorstman, Jacob AS, Turetsky, Bruce I, Sijmens-Morcus, Monique EJ, de Sain, Monique G, Dorland, Bert, Sprong, Mirjam, Rappaport, Eric F, Beemer, Frits A, Emanuel, Beverly S, Kahn, René S, van Engeland, Herman, Kemner, Chantal
Publicado em 2008

22q11.2 deletion syndrome

Por 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.
Publicado no Nat Rev Dis Primers (2015)

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

Por 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
Publicado no NPJ Schizophr (2016)