| 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 | 168 | 2013 |
| 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 | 144 | 2004 |
| 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 | 141 | 2003 |
| 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 | 136 | 2009 |
| 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 | 105 | 2016 |
| 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 | 92 | 2014 |
| 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 | 82 | 2014 |
| 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 | 58 | 2009 |
| 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 | 37 | 2007 |
| 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 | 35 | 2010 |
| 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, 121-128, 2004 | 35 | 2004 |
| 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 | 34 | 2013 |
| 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 | 31 | 2014 |
| 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 | 24 | 2020 |
| 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 | 23 | 2020 |
| 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 | 23 | 2015 |
| 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 | 21 | 2016 |
| 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 | 18 | 2017 |
| 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 | 9 | 2020 |
| 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), 55, 2021 | 8 | 2021 |
