Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Jacob A S Vorstman"'
Autor:
Marijn Muurling, Lianne M Reus, Casper de Boer, Sterre C Wessels, Raj R Jagesar, Jacob A S Vorstman, Martien J H Kas, Pieter Jelle Visser
Publikováno v:
JMIR Aging, Vol 5, Iss 2, p e33856 (2022)
BackgroundIn people with cognitive impairment, loss of social interactions has a major impact on well-being. Therefore, patients would benefit from early detection of symptoms of social withdrawal. Current measurement techniques such as questionnaire
Externí odkaz:
https://doaj.org/article/372fda4d04b84f0aabb6612ff4d1ff5c
Autor:
Eske M Derks, Jacob A S Vorstman, Stephan Ripke, Rene S Kahn, Schizophrenia Psychiatric Genomic Consortium, Roel A Ophoff
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e37852 (2012)
The presence of subclinical levels of psychosis in the general population may imply that schizophrenia is the extreme expression of more or less continuously distributed traits in the population. In a previous study, we identified five quantitative m
Externí odkaz:
https://doaj.org/article/8e803611ef2a448791142017a44705d1
Autor:
Maurice J C M Magnée, Victor A F Lamme, Monique G M de Sain-van der Velden, Jacob A S Vorstman, Chantal Kemner
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e25882 (2011)
BACKGROUND: Individuals with the 22q11.2 deletion syndrome (22q11DS) are at increased risk for schizophrenia and Autism Spectrum Disorders (ASDs). Given the prevalence of visual processing deficits in these three disorders, a causal relationship betw
Externí odkaz:
https://doaj.org/article/b3ee62e4db9441fca9efc2d5e327cb82
Autor:
Bert van der Zwaag, Lude Franke, Martin Poot, Ron Hochstenbach, Henk A Spierenburg, Jacob A S Vorstman, Emma van Daalen, Maretha V de Jonge, Nienke E Verbeek, Eva H Brilstra, Ruben van 't Slot, Roel A Ophoff, Michael A van Es, Hylke M Blauw, Jan H Veldink, Jacobine E Buizer-Voskamp, Frits A Beemer, Leonard H van den Berg, Cisca Wijmenga, Hans Kristian Ploos van Amstel, Herman van Engeland, J Peter H Burbach, Wouter G Staal
Publikováno v:
PLoS ONE, Vol 4, Iss 5, p e5324 (2009)
The recent identification of copy-number variation in the human genome has opened up new avenues for the discovery of positional candidate genes underlying complex genetic disorders, especially in the field of psychiatric disease. One major challenge
Externí odkaz:
https://doaj.org/article/115a6726e5774d2e93fc65849cc3a2e9
Autor:
Dorinde Korteling, Marco P. Boks, Ania M. Fiksinski, Ilja N. van Hoek, Jacob A. S. Vorstman, Nanda M. Verhoeven-Duif, Judith J. M. Jans, Janneke R. Zinkstok
Publikováno v:
Translational Psychiatry, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract The 22q11.2 deletion syndrome (22q11.2DS) is characterized by a well-defined microdeletion and is associated with increased risk of neurodevelopmental phenotypes including autism spectrum disorders (ASD) and intellectual impairment. The typi
Externí odkaz:
https://doaj.org/article/813bd39245924393afee3b6cedb922b1
Autor:
Emma Everaert, Jacob A. S. Vorstman, Iris S. Selten, Martijn G. Slieker, Frank Wijnen, Tessel D. Boerma, Michiel L. Houben
Publikováno v:
Journal of Neurodevelopmental Disorders. 15
Background Executive functioning (EF) is an umbrella term for various cognitive functions that play a role in monitoring and planning to effectuate goal-directed behavior. The 22q11.2 deletion syndrome (22q11DS), the most common microdeletion syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::690eafb40036129b7ee01e1f918fd1f5
https://doi.org/10.1186/s11689-023-09484-y
https://doi.org/10.1186/s11689-023-09484-y
Autor:
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edward J Higginbotham, John Wei, Sabah Shaikh, Nicole M Roslin, Jeffrey R MacDonald, Giovanna Pellecchia, Thomas Nalpathamkalam, Sylvia Lamoureux, Roozbeh Manshaei, Jennifer Howe, Brett Trost, Bhooma Thiruvahindrapuram, Christian R Marshall, Ryan K C Yuen, Richard F Wintle, Lisa J Strug, Dimitri J Stavropoulos, Jacob A S Vorstman, Paul Arnold, Daniele Merico, Marc Woodbury-Smith, Jennifer Crosbie, Russell J Schachar, Stephen W Scherer
Publikováno v:
Human Molecular Genetics.
We assessed the relationship of gene copy number variation (CNV) in mental health/neurodevelopmental traits and diagnoses, physical health and cognition in a community sample of 7100 unrelated children and youth of European or East Asian ancestry (Sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f89131ad199bfe0d4fedf77aac2e50d0
https://doi.org/10.1093/hmg/ddad074
https://doi.org/10.1093/hmg/ddad074
Autor:
Sébastien, Jacquemont, Guillaume, Huguet, Marieke, Klein, Samuel J R A, Chawner, Kirsten A, Donald, Marianne B M, van den Bree, Jonathan, Sebat, David H, Ledbetter, John N, Constantino, Rachel K, Earl, Donna M, McDonald-McGinn, Therese, van Amelsvoort, Ann, Swillen, Anne H, O'Donnell-Luria, David C, Glahn, Laura, Almasy, Evan E, Eichler, Stephen W, Scherer, Elise, Robinson, Anne S, Bassett, Christa Lese, Martin, Brenda, Finucane, Jacob A S, Vorstman, Carrie E, Bearden, Raquel E, Gur
Publikováno v:
Am J Psychiatry
Rare genomic disorders (RGDs) confer elevated risk for neurodevelopmental psychiatric disorders. In this era of intense genomics discoveries, the landscape of RGDs is rapidly evolving. However, there has not been comparable progress to date in scalab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b9f5350ab0a288890d5b1876e14e794
https://pubmed.ncbi.nlm.nih.gov/35236119
https://pubmed.ncbi.nlm.nih.gov/35236119
Publikováno v:
Journal of Multilingual and Multicultural Development. :1-17
This exploratory study reports on the implementation of a novel web-based multilingual learning platform. This tool allows content to be delivered in different languages simultaneously, including l...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45a66f9f8e6a44fa92af2beb40200ae9
https://doi.org/10.1080/01434632.2021.1916022
https://doi.org/10.1080/01434632.2021.1916022
Autor:
Anne S. Bassett, Jacob A. S. Vorstman, Maria Corral, Christian R. Marshall, Gregory Costain, René S. Kahn, Tracy Heung, Ania Fiksinski, Elemi J. Breetvelt
Publikováno v:
Psychological Medicine. 52:3184-3192
BackgroundGenotype-first and within-family studies can elucidate factors that contribute to psychiatric illness. Combining these approaches, we investigated the patterns of influence of parental scores, a high-impact variant, and schizophrenia on dim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5d5419f862dc198323fd23efa36fbe4
https://doi.org/10.1017/s0033291720005279
https://doi.org/10.1017/s0033291720005279