C. elegans mitotic cyclins have distinct as well as overlapping functions in chromosome segregation

Por van der Voet, Monique, Lorson, Monique A., Srinivasan, Dayalan G., Bennett, Karen L., van den Heuvel, Sander
Publicado em 2009

Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders

Por Lotan, Amit, Fenckova, Michaela, Bralten, Janita, Alttoa, Aet, Dixson, Luanna, Williams, Robert W., van der Voet, Monique
Publicado no Front Neurosci (2014)

The EBAX-type Cullin-RING E3 Ligase and Hsp90 Guard the Protein Quality of the SAX-3/Robo Receptor in Developing Neurons

Por Wang, Zhiping, Hou, Yanli, Guo, Xing, van der Voet, Monique, Boxem, Mike, Dixon, Jack E., Chisholm, Andrew D., Jin, Yishi
Publicado em 2013

A combined binary interaction and phenotypic map of C. elegans cell polarity proteins

Por Koorman, Thijs, Klompstra, Diana, van der Voet, Monique, Lemmens, Irma, Ramalho, João J., Nieuwenhuize, Susan, van den Heuvel, Sander, Tavernier, Jan, Nance, Jeremy, Boxem, Mike
Publicado no Nat Cell Biol (2016)

Intracranial Aneurysms in Finnish Families: Confirmation of Linkage and Refinement of the Interval to Chromosome 19q13.3

Por van der Voet, Monique, Olson, Jane M., Kuivaniemi, Helena, Dudek, Doreen M., Skunca, Magdalena, Ronkainen, Antti, Niemelä, Mika, Jääskeläinen, Juha, Hernesniemi, Juha, Helin, Katariina, Leinonen, Eira, Biswas, Moumita, Tromp, Gerard
Publicado em 2004

APC16 is a conserved subunit of the anaphase-promoting complex/cyclosome

Por Kops, Geert J. P. L., van der Voet, Monique, Manak, Michael S., van Osch, Maria H. J., Naini, Said M., Brear, Andrea, McLeod, Ian X., Hentschel, Dirk M., Yates, John R., van den Heuvel, Sander, Shah, Jagesh V.
Publicado em 2010

PC16 is a conserved subunit of the anaphase-promoting complex/cyclosome

Por Kops, Geert J. P. L., van der Voet, Monique, Manak, Michael S., van Osch, Maria H. J., Naini, Said M., Brear, Andrea, McLeod, Ian X., Hentschel, Dirk M., Yates, John R., van den Heuvel, Sander, Shah, Jagesh V.
Publicado em 2010

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy

Por Zazo Seco, Celia, Castells-Nobau, Anna, Joo, Seol-hee, Schraders, Margit, Foo, Jia Nee, van der Voet, Monique, Velan, S. Sendhil, Nijhof, Bonnie, Oostrik, Jaap, de Vrieze, Erik, Katana, Radoslaw, Mansoor, Atika, Huynen, Martijn, Szklarczyk, Radek, Oti, Martin, Tranebjærg, Lisbeth, van Wijk, Erwin, Scheffer-de Gooyert, Jolanda M., Siddique, Saadat, Baets, Jonathan, de Jonghe, Peter, Kazmi, Syed Ali Raza, Sadananthan, Suresh Anand, van de Warrenburg, Bart P., Khor, Chiea Chuen, Göpfert, Martin C., Qamar, Raheel, Schenck, Annette, Kremer, Hannie, Siddiqi, Saima
Publicado no Dis Model Mech (2017)