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Nature|April 30, 2015
Sequential cancer mutations in cultured human intestinal stem cellsJarno Drost, Richard H van Jaarsveld, Bas Ponsioen, et al.Clinical Genetics|November 1, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variantsEva Z Jacobs, Kathleen Brown, Melissa C Byler, et al.The Journal of Clinical Investigation|June 1, 2022
Impaired activity of the fusogenic micropeptide Myomixer causes myopathy resembling Carey-Fineman-Ziter syndromeAndres Ramirez-Martinez, Yichi Zhang, Marie-Jose van den Boogaard, et al.Nature|July 13, 2022
Nuclear chromosome locations dictate segregation error frequenciesSjoerd J Klaasen, My Anh Truong, Richard H van Jaarsveld, et al.Clinical Genetics|April 27, 2020
HNRNPH1-related syndromic intellectual disability: Seven additional cases suggestive of a distinct syndromic neurodevelopmental syndromeSara C Reichert, Rachel Li, Scott A Turner, et al.Human Mutation|July 29, 2022
De novo putative loss-of-function variants in TAF4 are associated with a neuro-developmental disorderBeau D E Janssen, Marie-Jose H van den Boogaard, Klaske Lichtenbelt, et al.Nature Genetics|May 1, 2019
Ongoing chromosomal instability and karyotype evolution in human colorectal cancer organoidsAna C F Bolhaqueiro, Bas Ponsioen, Bjorn Bakker, et al.Cancer Discovery|May 5, 2019
Oral Mucosal Organoids as a Potential Platform for Personalized Cancer TherapyElse Driehuis, Sigrid Kolders, Sacha Spelier, et al.Cell Death & Disease|May 30, 2024
Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformationsElizabeth A Werren, Emily R Peirent, Henna Jantti, et al.Human Molecular Genetics|May 27, 2025
KDM2B variants in the CxxC domain impair its DNA-binding ability and cause a distinct neurodevelopmental syndromeAmber S E van Oirsouw, Michael A Hadders, Martijn Koetsier, et al.Pageof 4