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Monique van der Voet
Monique van der Voet
Morphogenics
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Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders
Z Iqbal, G Vandeweyer, M van der Voet, AM Waryah, MY Zahoor, ...
Human molecular genetics 22 (10), 1960-1970, 2013
1572013
Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13. 3
M van der Voet, JM Olson, H Kuivaniemi, DM Dudek, M Skunca, ...
The American Journal of Human Genetics 74 (3), 564-571, 2004
1432004
Familial intracranial aneurysms: an analysis of 346 multiplex Finnish families
S Wills, A Ronkainen, M van der Voet, H Kuivaniemi, K Helin, E Leinonen, ...
Stroke 34 (6), 1370-1374, 2003
1372003
NuMA-related LIN-5, ASPM-1, calmodulin and dynein promote meiotic spindle rotation independently of cortical LIN-5/GPR/Gα
M Van Der Voet, CWH Berends, A Perreault, T Nguyen-Ngoc, P Gönczy, ...
Nature cell biology 11 (3), 269-277, 2009
1262009
ADHD-associated dopamine transporter, latrophilin and neurofibromin share a dopamine-related locomotor signature in Drosophila
M van der Voet, B Harich, B Franke, A Schenck
Molecular psychiatry 21 (4), 565-573, 2016
932016
Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders
A Lotan, M Fenckova, J Bralten, A Alttoa, L Dixson, RW Williams, ...
Frontiers in neuroscience 8, 331, 2014
832014
Drosophila models of early onset cognitive disorders and their clinical applications
M van der Voet, B Nijhof, MAW Oortveld, A Schenck
Neuroscience & Biobehavioral Reviews, 2014
742014
C. elegans mitotic cyclins have distinct as well as overlapping functions in chromosome segregation
M van der Voet, M Lorson, DG Srinivasan, KL Bennett, S van den Heuvel
Cell cycle 8 (24), 4091-4102, 2009
512009
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer disease
KAB Goddard, JM Olson, H Payami, M van der Voet, H Kuivaniemi, ...
Neurogenetics 5 (2), 121-128, 2004
382004
APC16 is a conserved subunit of the anaphase-promoting complex/cyclosome
GJPL Kops, M van der Voet, MS Manak, MHJ van Osch, SM Naini, ...
Journal of cell science 123 (10), 1623-1633, 2010
352010
Integration of expression profiles and genetic mapping data to identify candidate genes in intracranial aneurysm
S Weinsheimer, GM Lenk, M Van der Voet, S Land, A Ronkainen, ...
Physiological Genomics 32 (1), 45-57, 2007
342007
Altered GPM6A/M6 Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human and Drosophila
A Gregor, JM Kramer, M van der Voet, I Schanze, S Uebe, R Donders, ...
Human mutation 35 (12), 1495-1505, 2014
272014
The EBAX-type Cullin-RING E3 ligase and Hsp90 guard the protein quality of the SAX-3/Robo receptor in developing neurons
Z Wang, Y Hou, X Guo, M van der Voet, M Boxem, JE Dixon, AD Chisholm, ...
Neuron 79 (5), 903-916, 2013
272013
Converging evidence does not support GIT1 as an ADHD risk gene
M Klein, M van der Voet, B Harich, KJE Van Hulzen, AMH Onnink, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015
222015
A combined binary interaction and phenotypic map of C. elegans cell polarity proteins
T Koorman, D Klompstra, M Van Der Voet, I Lemmens, JJ Ramalho, ...
Nature cell biology 18 (3), 337-346, 2016
202016
Contribution of Intellectual Disability–Related Genes to ADHD Risk and to Locomotor Activity in Drosophila
M Klein, EL Singgih, A van Rens, D Demontis, AD Břrglum, NR Mota, ...
American Journal of Psychiatry 177 (6), 526-536, 2020
172020
A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy
C Zazo Seco, A Castells-Nobau, S Joo, M Schraders, JN Foo, ...
Disease models & mechanisms 10 (2), 105-118, 2017
152017
From rare copy number variants to biological processes in ADHD
B Harich, M van der Voet, M Klein, P Čížek, M Fenckova, A Schenck, ...
American Journal of Psychiatry 177 (9), 855-866, 2020
132020
From man to fly – convergent evidence links FBXO25 to ADHD and comorbid psychiatric phenotypes
B Harich, M Klein, CW Ockeloen, M van der Voet, M Schimmel‐Naber, ...
Journal of Child Psychology and Psychiatry 61 (5), 545-555, 2020
52020
Investigating cytosolic 5′-nucleotidase II family genes as candidates for neuropsychiatric disorders in Drosophila (114/150 chr)
EL Singgih, M van der Voet, M Schimmel-Naber, EL Brinkmann, ...
Translational psychiatry 11 (1), 1-10, 2021
42021
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Artikelen 1–20