Profile photo Houben

Houben

Assistant Professor - medical

Strategic program(s):

Biography

Michiel was trained as a medical doctor (2002) and pediatrician (2010) and as a clinical epidemiologist (2009) at the UMC Utrecht. In 2011 he obtained his PhD on his thesis entitled: RSV Bronchiolitis in Healthy Term Infants, Pathogenesis and Prediction. Since 2010 he works as a general pediatrician in the Wilhelmina Children’s Hospital (UMC Utrecht) and since 2014 he is head of the section of general en social pediatrics. He is the pediatrician and coordinator of the 22q11.2 deletion syndrome childhood outward patient clinic and studies the heterogeneity and prognostic factors of this syndrome, in close collaboration with colleagues of other pediatric, surgery, psychiatric, psychology and genetics specialties. He is also involved in several further studies on the healthy term birth (amniotic fluid) cohort from his PhD trajectory.

Recent publications

Identification of a pathogenic deep intronic variant in ATRX ends a diagnostic odyssey Jasper J. van der Smagt, Angeliki P. Lampri, Iris de Lange, Mariëlle Alders, Michiel L. Houben, Marco J. Koudijs, Richard H. van Jaarsveld
European Journal of Medical Genetics, 2024, vol. 69
Bi-allelic variants in NAE1 cause intellectual disability, ischiopubic hypoplasia, stress-mediated lymphopenia and neurodegeneration Irena J.J. Muffels, Imre F. Schene, Holger Rehmann, Maarten P.G. Massink, Maria M. van der Wal, Corinna Bauder, Martha Labeur, Natalia G. Armando, Maarten H. Lequin, Michiel L. Houben, Jaques C. Giltay, Saskia Haitjema, Albert Huisman, Fleur Vansenne, Judith Bluvstein, John Pappas, Lala V. Shailee, Yuri A. Zarate, Michal Mokry, Gijs W. van Haaften, Edward E.S. Nieuwenhuis, Damian Refojo, Femke van Wijk, Sabine A. Fuchs, Peter M. van Hasselt
American Journal of Human Genetics, 2023, vol. 110, p.146-160
Grammatical skills of Dutch children with 22q11.2 Deletion Syndrome in comparison with children with Developmental Language Disorder Tessel Boerma, Emma Everaert, Dinte Vlieger, Maaike Steggink, Iris Selten, Michiel Houben, Jacob Vorstman, Ellen Gerrits, Frank Wijnen
Frontiers in Communication, 2023, vol. 8
Executive functioning in preschoolers with 22q11.2 deletion syndrome and the impact of congenital heart defects Emma Everaert, Jacob A.S. Vorstman, Iris S. Selten, Martijn G. Slieker, Frank Wijnen, Tessel D. Boerma, Michiel L. Houben
Journal of neurodevelopmental disorders, 2023, vol. 15, p.15
Behaviors related to autism spectrum disorder in children with developmental language disorder and children with 22q11.2 deletion syndrome Iris Selten, Tessel Boerma, Emma Everaert, Ellen Gerrits, Michiel Houben, Frank Wijnen, Jacob Vorstman
Autism and Developmental Language Impairments, 2023, vol. 8, p.1-18

Fellowships & Awards

2018: Uitreiking cheque €150.00 aan ML Houben, voor onderzoek naar Predictors van Neurocognitieve Achteruitgang bij Kinderen met 22q11.2 Deletiesyndroom (door Stichting Steun 22q11)

External positions

Bestuurslid NVK-sectie Erfelijke en Aangeboren Aandoeningen (EAA) - Algemeen kinderarts met dit aandachtsgebied - Ned. Ver. Kindergeneeskunde

Member of the Multidisciplinary advisory board of the Dutch patient support group “Steun 22Q11" - Kinderarts & medisch coordinator van 22q11-polikliniek WKZ / UMCU - Dutch patient support group “Steun 22Q11"