Willem M.A. Verhoeven, M.D., Ph.D.
Affiliations: | 1999-2014 | Psychiatry | Erasmus Medical Center Rotterdam, Rotterdam, Netherlands |
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Parents
Sign in to add mentor| David de Wied | grad student | 1983 | |
| Herman M. van Praag | grad student | 1983 | UMC Utrecht |
Children
Sign in to add trainee| Thomas Linka | grad student | 2009 | Erasmus MC |
| Marc Schneider | grad student | 2012 | Erasmus MC |
| Ellen Wingbermühle | grad student | 2013 | Erasmus MC |
| Amir Ahmed | grad student | 2016 | Erasmus MC |
| Nora A.W. van de Kerkhof | grad student | 2017 | Erasmus Medical Center Rotterdam, Psychiatry |
| Ingrid M. Lens-Daey Ouwens | grad student | 2019 | Erasmus MC |
Collaborators
Sign in to add collaborator| Siegfried Tuinier | collaborator | 2008 | |
| Jos I.M. Egger | collaborator | 2004-2014 | Erasmus MC |
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Publications
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| Egger J, Verhoeven W, Verbeeck W, et al. (2023) A Novel Distal 22Q11.21 Microduplication in a 43-Year-Old Male Patient with Mild Intellectual Disability, Social Cognitive Dysfunctions, and Anxiety. Clinical Neuropsychiatry. 20: 424-428 |
| Verhoeven W, Zuijdam J, Scheick A, et al. (2022) Myoclonic-Atonic Epilepsy Caused by a Novel de Novo Heterozygous Missense Variant in the Gene: Brief Discussion of the Literature and Detailed Case Description of a Severely Intellectually Disabled Adult Male Patient. International Medical Case Reports Journal. 15: 753-759 |
| Verhoeven W, Houwink E, de Leeuw N, et al. (2021) Hoe herkent u het zeldzame Phelan-McDermidsyndroom? Huisarts En Wetenschap. 1-3 |
| Verhoeven W, Egger J, Kipp J, et al. (2019) A novel MBD5 mutation in an intellectually disabled adult female patient with epilepsy: Suggestive of early onset dementia? Molecular Genetics & Genomic Medicine. 7 |
| Verhoeven W, Egger J, Räkers E, et al. (2018) Phenotypic characterization of an older adult male with late-onset epilepsy and a novel mutation in ASXL3 shows overlap with the associated Bainbridge-Ropers syndrome Neuropsychiatric Disease and Treatment. 14: 867-870 |
| van de Kerkhof NW, Fekkes D, van der Heijden FM, et al. (2016) Cycloid psychoses in the psychosis spectrum: evidence for biochemical differences with schizophrenia. Neuropsychiatric Disease and Treatment. 12: 1927-33 |
| Verhoeven WM, Egger JI, Knegt AC, et al. (2016) Absence epilepsy and the CHD2 gene: an adolescent male with moderate intellectual disability, short-lasting psychoses, and an interstitial deletion in 15q26.1-q26.2. Neuropsychiatric Disease and Treatment. 12: 1135-1139 |
| Verhoeven WM, Tuinier S, Curfs LM. (2016) Prader-Willi syndrome: cycloid psychosis in a genetic subtype? Acta Neuropsychiatrica. 15: 32-7 |
| Verhoeven WM. (2016) Chronicity, genes en behavior. Acta Neuropsychiatrica. 12: 193-7 |
| Verhoeven WM, Tuinier S, Curfs LM. (2016) Psychopathologie en Pathogenese van enkele behavioural phenotypes. Acta Neuropsychiatrica. 10: 87-9 |