Sotabase

Career

· Assistant Professor, Université de Namur2021–2022
· Assistant Professor, Université catholique de Louvain2019–2020
· Cabinet Advisor Digital Inclusion, Vlaamse overheid2019–2022
· Senior Researcher, imec2018–
· Assistant Professor Senior Researcher, Thomas More University of Applied Sciences2017–2019
· Senior Research Lead On Digital Inclusion Citizen Engagement, imec-SMIT, Vrije Universiteit Brussel2016–
· Assistant Professor, Vrije Universiteit Brussel2016–
· PhD, Communication and Media Studies, Vrije Universiteit Brussel2008–2016
· PhD Researcher Teaching Assistant, Vrije Universiteit Brussel2007–2016
· MSc, Communication Sciences, Information Society and Globalization, magna cum laude, Vrije Universiteit Brussel2003–2007
· Bachelor of Applied Science - BASc, Photography, LUCA School of Arts1993–1996

Publications (72)

Guidelines for diagnostic next-generation sequencing
European Journal of Human Genetics · 2015
495
cited
A Post‐Hoc Comparison of the Utility of Sanger Sequencing and Exome Sequencing for the Diagnosis of Heterogeneous Diseases
Human Mutation · 2013
345
cited
Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6.
American Journal of Human Genetics · 2012
318
cited
TRIDENT-2: National Implementation of Genome-Wide Non-Invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
American Journal of Human Genetics · 2019
309
cited
Globozoospermia revisited.
Human Reproduction Update · 2007
192
cited
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP
Biological Psychiatry · 2019
138
cited
Genotype–phenotype mapping of chromosome 18q deletions by high‐resolution array CGH: An update of the phenotypic map
American Journal of Medical Genetics. Part A · 2007
129
cited
The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands
European Journal of Human Genetics · 2016
112
cited
Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study
Genetics in Medicine · 2017
111
cited
TRIO loss of function is associated with mild intellectual disability and affects dendritic branching and synapse function.
Human Molecular Genetics · 2016
98
cited
European Cytogeneticists Association Register of Unbalanced Chromosome Aberrations (ECARUCA); an online database for rare chromosome abnormalities.
European Journal of Medical Genetics · 2006
95
cited
Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging
Prenatal Diagnosis · 2020
93
cited
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins
Human Genetics · 2016
92
cited
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study
American Journal of Human Genetics · 2022
86
cited
Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt–Hopkins syndrome
American Journal of Medical Genetics. Part A · 2008
77
cited
The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial
European Journal of Human Genetics · 2016
68
cited
1 in 38 individuals at risk of a dominant medically actionable disease
European Journal of Human Genetics · 2018
64
cited
The consequences of implementing non-invasive prenatal testing in Dutch national health care: a cost-effectiveness analysis.
European Journal of Obstetrics, Gynecology, and Reproductive Biology · 2014
62
cited
Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment
Prenatal Diagnosis · 2015
50
cited
Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis
European Journal of Human Genetics · 2011
49
cited
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Ilse Feenstra | Researcher Profile | Sotabase | Sotabase