Requirements and Operational Guidelines for Secure and Sustainable Digital Phenotyping: Design and Development Study

por Jagesar, Raj R, Vorstman, Jacob A, Kas, Martien J
Publicado 2021

Developing Gene-Based Personalised Interventions in Autism Spectrum Disorders

por Freitag, Christine M., Persico, Antonio M., Vorstman, Jacob A. S.
Publicado 2022

From Genes to Therapy in Autism Spectrum Disorder

por Vorstman, Jacob A. S., Freitag, Christine M., Persico, Antonio M.
Publicado 2022

A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome

por Fiksinski, Ania M., Hoftman, Gil D., Vorstman, Jacob A. S., Bearden, Carrie E.
Publicado 2022

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 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 2013

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

por Fiksinski, Ania M., Schneider, Maude, Zinkstok, Janneke, Baribeau, Danielle, Chawner, Samuel J. R. A., Vorstman, Jacob A. S.
Publicado 2021

Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects

por Everaert, Emma, Vorstman, Jacob A. S., Selten, Iris S., Slieker, Martijn G., Wijnen, Frank, Boerma, Tessel D., Houben, Michiel L.
Publicado 2023

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 2011

Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model

por 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.
Publicado 2022

Assessment of Social Behavior Using a Passive Monitoring App in Cognitively Normal and Cognitively Impaired Older Adults: Observational Study

por Muurling, Marijn, Reus, Lianne M, de Boer, Casper, Wessels, Sterre C, Jagesar, Raj R, Vorstman, Jacob A S, Kas, Martien J H, Visser, Pieter Jelle
Publicado 2022

Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome

por Korteling, Dorinde, Boks, Marco P., Fiksinski, Ania M., van Hoek, Ilja N., Vorstman, Jacob A. S., Verhoeven-Duif, Nanda M., Jans, Judith J. M., Zinkstok, Janneke R.
Publicado 2022

Affective and psychotic reactivity to daily-life stress in adults with 22q11DS: a study using the experience sampling method

por Schneider, Maude, Vaessen, Thomas, van Duin, Esther D. A., Kasanova, Zuzana, Viechtbauer, Wolfgang, Reininghaus, Ulrich, Vingerhoets, Claudia, Booij, Jan, Swillen, Ann, Vorstman, Jacob A. S., van Amelsvoort, Thérèse, Myin-Germeys, Inez
Publicado 2020

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 2015

Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

por Costain, Gregory, Walker, Susan, Argiropoulos, Bob, Baribeau, Danielle A., Bassett, Anne S., Boot, Erik, Devriendt, Koen, Kellam, Barbara, Marshall, Christian R., Prasad, Aparna, Serrano, Moises A., Stavropoulos, D. James, Twede, Hope, Vermeesch, Joris R., Vorstman, Jacob A. S., Scherer, Stephen W.
Publicado 2019

A framework for assessing neuropsychiatric phenotypes by using smartphone-based location data

por Jongs, Niels, Jagesar, Raj, van Haren, Neeltje E. M., Penninx, Brenda W. J. H., Reus, Lianne, Visser, Pieter J., van der Wee, Nic J. A., Koning, Ina M., Arango, Celso, Sommer, Iris E. C., Eijkemans, Marinus J. C., Vorstman, Jacob A., Kas, Martien J.
Publicado 2020

Social responsiveness scale-aided analysis of the clinical impact of copy number variations in autism

por van Daalen, Emma, Kemner, Chantal, Verbeek, Nienke E., van der Zwaag, Bert, Dijkhuizen, Trijnie, Rump, Patrick, Houben, Renske, van ‘t Slot, Ruben, de Jonge, Maretha V., Staal, Wouter G., Beemer, Frits A., Vorstman, Jacob A. S., Burbach, J. Peter H., van Amstel, Hans Kristian Ploos, Hochstenbach, Ron, Brilstra, Eva H., Poot, Martin
Publicado 2011

Attention deficit hyperactivity disorder symptoms as antecedents of later psychotic outcomes in 22q11.2 deletion syndrome

por Niarchou, Maria, Chawner, Samuel J.R.A., Fiksinski, Ania, Vorstman, Jacob A.S., Maeder, Johanna, Schneider, Maude, Eliez, Stephan, Armando, Marco, Pontillo, Maria, Vicari, Stefano, McDonald-McGinn, Donna M., Emanuel, Beverly S., Zackai, Elaine H., Bearden, Carrie E., Shashi, Vandana, Hooper, Stephen R., Owen, Michael J., Gur, Raquel E., Wray, Naomi R., van den Bree, Marianne B.M., Thapar, Anita
Publicado 2019

Gene copy number variation and pediatric mental health/neurodevelopment in a general population

por Zarrei, Mehdi, Burton, Christie L, Engchuan, Worrawat, Higginbotham, Edward J, Wei, John, Shaikh, Sabah, Roslin, Nicole M, MacDonald, Jeffrey R, Pellecchia, Giovanna, Nalpathamkalam, Thomas, Lamoureux, Sylvia, Manshaei, Roozbeh, Howe, Jennifer, Trost, Brett, Thiruvahindrapuram, Bhooma, Marshall, Christian R, Yuen, Ryan K C, Wintle, Richard F, Strug, Lisa J, Stavropoulos, Dimitri J, Vorstman, Jacob A S, Arnold, Paul, Merico, Daniele, Woodbury-Smith, Marc, Crosbie, Jennifer, Schachar, Russell J, Scherer, Stephen W
Publicado 2023

Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism

por van der Zwaag, Bert, Franke, Lude, Poot, Martin, Hochstenbach, Ron, Spierenburg, Henk A., Vorstman, Jacob A. S., van Daalen, Emma, de Jonge, Maretha V., Verbeek, Nienke E., Brilstra, Eva H., van 't Slot, Ruben, Ophoff, Roel A., van Es, Michael A., Blauw, Hylke M., Veldink, Jan H., Buizer-Voskamp, Jacobine E., Beemer, Frits A., van den Berg, Leonard H., Wijmenga, Cisca, van Amstel, Hans Kristian Ploos, van Engeland, Herman, Burbach, J. Peter H., Staal, Wouter G.
Publicado 2009