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Neurotoxicity Research|December 17, 2008
Clinical perspectives on the genetics of schizophrenia: a bottom-up orientationWillem M A Verhoeven, Siegfried TuinierInternational Review of Neurobiology|May 16, 2006
Prader-Willi syndrome: atypical psychoses and motor dysfunctionsWillem M A Verhoeven, Siegfried TuinierBMJ Case Reports|June 13, 2012
Schizotypy: key feature of Klinefelter's syndrome?Willem M A Verhoeven, Jos I M EggerHandbook of Clinical Neurology|August 26, 2023
Forensically relevant challenging behaviors and the genetics domainJos I M Egger, Willem M A VerhoevenAmerican Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 31, 2009
Behavioral phenotype in the 9q subtelomeric deletion syndrome: a report about two adult patientsWillem M A Verhoeven, Tjitske Kleefstra, Jos I M EggerEuropean Journal of Medical Genetics|August 30, 2019
A longitudinal perspective on the pharmacotherapy of 24 adult patients with Phelan McDermid syndromeWillem M A Verhoeven, Jos I M Egger, Nicole de LeeuwBMJ Case Reports|January 19, 2013
Kallmann syndrome and paranoid schizophrenia: a rare combinationWillem M A Verhoeven, Jos I M Egger, Johannes E Hovens, et al.European Journal of Medical Genetics|December 6, 2011
A de novo 3.57 Mb microdeletion in 8q12.3q13.2 in a patient with mild intellectual disability and epilepsyWillem M A Verhoeven, Jos I M Egger, Ilse Feenstra, et al.Neuropsychiatric Disease and Treatment|April 8, 2014
Neuropsychological phenotype of a patient with a de novo 970 kb interstitial deletion in the distal 16p11.2 regionJos I M Egger, Willem M A Verhoeven, Wim Verbeeck, et al.BMJ Case Reports|October 1, 2017
Phelan-McDermid syndrome due to <i>SHANK3</i> mutation in an intellectually disabled adult male: successful treatment with lithiumJos I M Egger, Willem M A Verhoeven, Renske Groenendijk-Reijenga, et al.Pageof 4