Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Esther D.A. van Duin"'
Autor:
Esther D.A. van Duin, Johannes G. Ramaekers, Jacobus F.A. Jansen, Mathilde van Oudenaren, Janneke Zinkstok, Claudia Vingerhoets, Therese van Amelsvoort, Desmond H. Y. Tse, Grainne M. McAlonan, Dennis Hernaus
Publikováno v:
Journal of Psychopharmacology, 34(8):0269881120922977, 856-863. SAGE Publications Ltd
Journal of Psychopharmacology (Oxford, England)
Journal of Psychopharmacology (Oxford, England)
Aims: 22q11.2 deletion syndrome (22q11.2DS) is associated with impaired cognitive functioning. Glutamatergic pathways have been linked with cognition and are hypothesized to be disrupted in 22q11.2DS patients, possibly ‘shifting’ the excitatory (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6ef202858a40a941741923c6a92015
https://doi.org/10.1177/0269881120922977
https://doi.org/10.1177/0269881120922977
Autor:
Therese van Amelsvoort, Lisa D. Palmer, Jacob Vorstman, Annick Vogels, Jan Booij, Ania M Fiksinski, Liewe de Haan, Esther D.A. van Duin, L. J. M. Evers, Claudia Vingerhoets, Elfi Vergaelen, Genetic Risk, Ann Swillen, Anne S. Bassett, Carin J. Meijer, Oswald J.N. Bloemen, Elemi J. Breetvelt, Mathilde van Oudenaren, Erik Boot
Publikováno v:
British Journal of Psychiatry, 215(5), 661-667. Cambridge University Press
British journal of psychiatry, 215(5), 661-667. Royal College of Psychiatrists
British journal of psychiatry, 215(5), 661-667. Royal College of Psychiatrists
Background22q11.2 deletion syndrome (22q11DS), one of the most common recurrent copy number variant disorders, is associated with dopaminergic abnormalities and increased risk for psychotic disorders.AimsGiven the elevated prevalence of substance use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec552744ade0af4d960439651ad9c0a
https://doi.org/10.1192/bjp.2018.258
https://doi.org/10.1192/bjp.2018.258
Autor:
Claudia Vingerhoets, Jan Booij, Jenny Ceccarini, Zuzana Kasanova, Oliver Winz, Esther D.A. van Duin, Inez Myin-Germeys, Alexander Heinzel, Siamak Mohammadkhani-Shali, Therese van Amelsvoort, Jytte van Huijstee, Felix M. Mottaghy
Publikováno v:
Psychological Medicine, 50(5):003329171900062, 799-807. Cambridge University Press
Psychological medicine, 50(5), 799-807. Cambridge University Press
Psychological medicine, 50(5), 799-807. Cambridge University Press
BackgroundThe 22q11.2 deletion syndrome (22q11DS) is caused by a deletion on chromosome 22 locus q11.2. This copy number variant results in haplo-insufficiency of the catechol-O-methyltransferase (COMT) gene, and is associated with a significant incr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::788b79d74abf630c89200fa66ec9012f
https://cris.maastrichtuniversity.nl/en/publications/7993e39e-41f1-43f2-b88a-45834ba3ce31
https://cris.maastrichtuniversity.nl/en/publications/7993e39e-41f1-43f2-b88a-45834ba3ce31
Autor:
Richard Duncan, Tao Wang, Carrie E. Bearden, David J. Cutler, Stephen T. Warren, Maria Pontillo, Robert Sean Gallagher, Elemi J. Breetvelt, Tingwei Guo, Nancy J. Butcher, Jennifer G. Mulle, Claudia Ornstein, Claudia Vingerhoets, Clodagh M. Murphy, Ehud Mekori-Domachevsky, Wendy R. Kates, Jacob A. S. Vorstman, Tracy Heung, Joris Vermeesch, Maria Gudbrandsen, Ann Swillen, H. Richard Johnston, Oanh Tran, Marco Armando, Joseph F. Cubells, Raoul Belzeaux, Jeroen Breckpot, Bruno Marino, Tony J. Simon, Harold I. Salmons, Maria Jalbrzikowski, Wanda Fremont, Anna J. Voss, Worrawat Engchuan, Opal Y. Ousley, Stefano Vicari, Jordi Rosell, Sixto García-Miñaur, Declan G. Murphy, Alexander Diacou, Ania Fiksinski, Abraham Weizman, Edward Moss, Stephan Eliez, Miri Carmel, Vandana Shashi, Anne S. Bassett, Ronnie Weinberger, Hayley Moss, Marianne Bernadette van den Bree, Kelly Schoch, Maude Schneider, Linda E. Campbell, Sasja N. Duijff, Eileen Daly, Annick Vogels, Stephen R. Hooper, David Fraguas, Sarah E. Prasad, Chelsea Lowther, Michael John Owen, Frédérique Béna, Gabriela M. Repetto, Eva W.C. Chow, Bernice E. Morrow, Robert J. Sharkus, Celso Arango, Christian R. Marshall, Jasna Raventos-Simic, Jaume Morey-Canyelles, Tiffany Busa, Andrea Jin, James T.R. Walters, Leila Kushan, Wolfram Demaerel, Monica E. Calkins, Jhih Rong Lin, Elaine H. Zackai, Esther D.A. van Duin, Antonio Buzzanca, Corrado Sandini, Kieran C. Murphy, Beverly S. Emanuel, Erik Boot, Maria Niarchou, Nigel Williams, Elfi Vergaelen, Maria Cristina Digilio, Daniele Merico, Karlene Coleman, Gregory A. Costain, Matthew S. Hestand, Peter Holmans, Michael E. Zwick, Michael P. Epstein, Damià H. Suñer, Yingjie Zhao, Marta Unolt, Kathryn McCabe, Aaron M. Holleman, Zhengdong Zhang, Rosemarie Fritsch, Alex V. Kotlar, Elena Michaelovsky, T. Blaine Crowley, Brenna Lilley, Sunny X. Tang, Rens Evers, Ruben C. Gur, Isabelle Cleynen, Flora Tassone, Nicole Philip, Kevin M. Antshel, Koen Devriendt, Antonio F. Pardiñas, Pankaj Chopra, Thomas Monfeuga, Fabio Di Fabio, Therese van Amelsvoort, Aaron Golden, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Daniel E. McGinn
Publikováno v:
Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group
Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c91788310dcf6c66ef3ac3973170b9
http://hdl.handle.net/20.500.12278/33344
http://hdl.handle.net/20.500.12278/33344
Autor:
Merrit C.H. Beck, Felix M. Mottaghy, Therese van Amelsvoort, Alexander Heinzel, Inez Myin-Germeys, Jenny Ceccarini, Zuzana Kasanova, Michael J. Frank, Esther D.A. van Duin, Siamak Mohammadkhani-Shali, Jan Booij, Oliver Winz, Dennis Hernaus
Publikováno v:
European neuropsychopharmacology, 28(6), 732-742. Elsevier
European Neuropsychopharmacology, 28(6), 732-742. Elsevier
European Neuropsychopharmacology, 28(6), 732-742. Elsevier
22q11.2 deletion syndrome (22q11DS) is a genetic disorder caused by a microdeletion on chromosome 22q11.2 and associated with an increased risk for developing psychosis. The catechol-O-methyltransferase (COMT) gene is located in the deleted region an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::141afd52a5baca5628d56464ad37e2d2
https://doi.org/10.1016/j.euroneuro.2018.03.005
https://doi.org/10.1016/j.euroneuro.2018.03.005
Autor:
Therese van Amelsvoort, Zuzana Kasanova, Alexander Heinzel, Jan Booij, Jenny Ceccarini, Michael J. Frank, Esther D.A. van Duin, Felix M. Mottaghy, Thomas Vaessen, Inez Myin-Germeys, Henrietta Steinhart
Publikováno v:
Psychological Medicine, 48(11), 1909-1914. Cambridge University Press
Psychological medicine, 48(11), 1909-1914. Cambridge University Press
Psychological medicine, 48(11), 1909-1914. Cambridge University Press
BackgroundAbnormalities in reward learning in psychotic disorders have been proposed to be linked to dysregulated subcortical dopaminergic (DA) neurotransmission, which in turn is a suspected mechanism for predisposition to psychosis. We therefore ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1ee721a5b329370c83e1e0fd1466b5b
https://doi.org/10.1017/s0033291717003476
https://doi.org/10.1017/s0033291717003476
Autor:
Janita Bralten, Catharina A. Hartman, Marina Hakobjan, Jaap Oosterlaan, Pieter J. Hoekstra, Hanneke van Ewijk, Martine Hoogman, Barbara Franke, Jan K. Buitelaar, Esther D.A. van Duin, Dirk J. Heslenfeld
Publikováno v:
Journal of Child Psychology and Psychiatry and Allied Disciplines, 58, 958-966
van Ewijk, H, Bralten, J, van Duin, E D A, Hakobjan, M, Buitelaar, J K, Heslenfeld, D J, Hoekstra, P J, Hartman, C, Hoogman, M, Oosterlaan, J & Franke, B 2017, ' Female-specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls ', Journal of Child Psychology and Psychiatry, vol. 58, no. 8, pp. 958-966 . https://doi.org/10.1111/jcpp.12742
Journal of Child Psychology and Psychiatry and Allied Disciplines, 58, 8, pp. 958-966
Journal of Child Psychology and Psychiatry, 58(8), 958-966. Wiley
Journal of Child Psychology and Psychiatry, 58(8), 958-966. Wiley-Blackwell
van Ewijk, H, Bralten, J, van Duin, E D A, Hakobjan, M, Buitelaar, J K, Heslenfeld, D J, Hoekstra, P J, Hartman, C, Hoogman, M, Oosterlaan, J & Franke, B 2017, ' Female-specific association of NOS1 genotype with white matter microstructure in ADHD patients and controls ', Journal of Child Psychology and Psychiatry, vol. 58, no. 8, pp. 958-966 . https://doi.org/10.1111/jcpp.12742
Journal of Child Psychology and Psychiatry and Allied Disciplines, 58, 8, pp. 958-966
Journal of Child Psychology and Psychiatry, 58(8), 958-966. Wiley
Journal of Child Psychology and Psychiatry, 58(8), 958-966. Wiley-Blackwell
Contains fulltext : 177347pre.pdf (Author’s version preprint ) (Open Access) BACKGROUND: The nitric oxide synthase gene (NOS1) exon 1f (ex1f) VNTR is a known genetic risk factor for Attention-Deficit/Hyperactivity Disorder (ADHD), particularly in f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a50391f417d6417bc1cea6fb273381b
https://hdl.handle.net/1871.1/aca851fa-452b-459c-80c6-f5ccc1a5c1cb
https://hdl.handle.net/1871.1/aca851fa-452b-459c-80c6-f5ccc1a5c1cb
Autor:
Jan Booij, Zuzana Kasanova, Therese van Amelsvoort, Wolfgang Viechtbauer, Claudia Vingerhoets, Thomas Vaessen, Ann Swillen, Esther D.A. van Duin, Dennis Hernaus, Inez Myin-Germeys, Peter Saalbrink, Jacob A. S. Vorstman, Ulrich Reininghaus
Publikováno v:
Psychoneuroendocrinology, 106, 85-94. Elsevier Science
Psychoneuroendocrinology, 106, 85-94. Elsevier Limited
Psychoneuroendocrinology, 106, 85-94. Elsevier Limited
BACKGROUND: 22q11.2 deletion syndrome (22q11DS) is a genetic disorder associated with neurodevelopmental, anxiety and mood disorders, as well as an increased risk for developing psychosis. Cortisol levels and stress reactivity reflect hypothalamic-pi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2799b84e21d8b8bd182547325f85c93
https://pubmed.ncbi.nlm.nih.gov/30959234
https://pubmed.ncbi.nlm.nih.gov/30959234
Autor:
Therese van Amelsvoort, Mathilde van Oudenaren, Dennis Hernaus, Jaap Janssen, Grainne M. McAlonan, Claudia Vingerhoets, Esther D.A. van Duin, J.G. Ramaekers, Desmond H. Y. Tse, Oswald J.N. Bloemen
Publikováno v:
Schizophrenia Bulletin
Background 22q11.2 deletion syndrome (22q11DS) is characterized by a microdeletion on the long arm of chromosome 22. The clinical phenotype of this syndrome is highly variable but symptoms include cognitive impairment, heart malformations, auto-immun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3034ed28c57b80202ac83e0474f75e1
http://europepmc.org/articles/PMC5888583
http://europepmc.org/articles/PMC5888583
Autor:
Fabiana da Silva Alves, Koen Schruers, Nicole Schmitz, Dennis Hernaus, Liesbet Goossens, Therese van Amelsvoort, Esther D.A. van Duin
Publikováno v:
Journal of Neurodevelopmental Disorders, 8. Springer Verlag
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders, 8. Springer New York
Journal of Neurodevelopmental Disorders
Journal of neurodevelopmental disorders, 8. Springer New York
Background: 22q11.2 deletion syndrome (22q11DS) is caused by a microdeletion on chromosome 22q11.2 and associated with an increased risk to develop psychosis. The gene coding for catechol-O-methyl-transferase (COMT) is located at the deleted region,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a694a225e60d2bb227dd7537658290f7
https://doi.org/10.1186/s11689-016-9158-5
https://doi.org/10.1186/s11689-016-9158-5