Publications by authors named "Wouter Koole"

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Prevalence of germline pathogenic variants in 779 patients with metastatic prostate cancer.
Michiel Vlaming, Wouter Koole, R Jeroen A van Moorselaar, Eveline M A Bleiker, Ellen van de Geer

BJU Int· December 2025

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Evidence for pathogenicity of c.8351G>A p.(Arg2784Gln) and the challenges in classification of pathogenic variants with reduced penetrance.
Setareh Moghadasi, Maria Zanti, Fonnet Bleeker, Marinus Blok, Merel E Braspenning, Wouter Koole

J Med Genet· December 2025

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An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2.
Koen C Demaegd, Aoife Kernan, Johnathan Cooper-Knock, Joke J F A van Vugt, Calum Harvey, Wouter Koole

Eur J Hum Genet· September 2025

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Familial Occurrence of Adult Granulosa Cell Tumors: Analysis of Whole-Genome Germline Variants.
Joline F Roze, Joachim Kutzera, Wouter Koole, Margreet G E M Ausems, Kristi Engelstad

Cancers (Basel)· May 2021

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Parents' Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands.
Maartje Blom, Robbert G M Bredius, Marleen E Jansen, Gert Weijman, Evelien A Kemper, Wouter Koole

J Clin Immunol· January 2021

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A in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss.
Suzanne E de Bruijn, Jeroen J Smits, Chang Liu, Cornelis P Lanting, Andy J Beynon, Wouter Koole

J Med Genet· July 2020

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MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization.
Evelien G G Sprenkeler, Stefanie S V Henriet, Anton T J Tool, Iris C Kreft, Ivo van der Bijl, Wouter Koole

Blood· June 2020

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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment.
Jeroen J Smits, Jaap Oostrik, Andy J Beynon, Sarina G Kant, Pia A M de Koning Gans, Wouter Koole

Hum Genet· January 2019

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A Polymerase Theta-dependent repair pathway suppresses extensive genomic instability at endogenous G4 DNA sites.
Wouter Koole, Robin van Schendel, Andrea E Karambelas, Jane T van Heteren, Kristy L Okihara

Nat Commun· October 2015

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FANCJ promotes DNA synthesis through G-quadruplex structures.
Pau Castillo Bosch, Sandra Segura-Bayona, Wouter Koole, Jane T van Heteren, James M Dewar

EMBO J· November 2014

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Mosaic analysis and tumor induction in zebrafish by microsatellite instability-mediated stochastic gene expression.
Wouter Koole, Marcel Tijsterman

Dis Model Mech· July 2014

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A versatile microsatellite instability reporter system in human cells.
Wouter Koole, Henning S Schäfer, Reuven Agami, Gijs van Haaften, Marcel Tijsterman

Nucleic Acids Res· September 2013

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A broad requirement for TLS polymerases η and κ, and interacting sumoylation and nuclear pore proteins, in lesion bypass during C. elegans embryogenesis.
Sophie F Roerink, Wouter Koole, L Carine Stapel, Ron J Romeijn, Marcel Tijsterman

PLoS Genet· June 2012

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Embryonic stem cells require Wnt proteins to prevent differentiation to epiblast stem cells.
Derk ten Berge, Dorota Kurek, Tim Blauwkamp, Wouter Koole, Alex Maas

Nat Cell Biol· August 2011

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Wnt signaling mediates self-organization and axis formation in embryoid bodies.
Derk ten Berge, Wouter Koole, Christophe Fuerer, Matt Fish, Elif Eroglu

Cell Stem Cell· November 2008

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Identification of conserved pathways of DNA-damage response and radiation protection by genome-wide RNAi.
Gijs van Haaften, Ron Romeijn, Joris Pothof, Wouter Koole, Leon H F Mullenders

Curr Biol· July 2006

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