Martin A. Rooimans
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 22 publications
CRISPR screens in sister chromatid cohesion defective cells reveal PAXIP1-PAGR1 as regulator of chromatin association of cohesin.
Journal: Nucleic acids research
Published: January 19, 2023
MMS22L-TONSL functions in sister chromatid cohesion in a pathway parallel to DSCC1-RFC.
Journal: Life science alliance
Published: July 11, 2022
Publisher Correction: BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.
Journal: Scientific reports
Published: April 07, 2022
Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation.
Journal: Science advances
Published: January 19, 2022
Genome-wide siRNA screens identify RBBP9 function as a potential target in Fanconi anaemia-deficient head-and-neck squamous cell carcinoma.
Journal: Communications biology
Published: December 01, 2021
BIRC2-BIRC3 amplification: a potentially druggable feature of a subset of head and neck cancers in patients with Fanconi anemia.
Journal: Scientific reports
Published: March 11, 2021
ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients.
Journal: The Journal of experimental medicine
Published: April 03, 2020
Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.
Journal: Nature communications
Published: December 20, 2019
Last Updated: 09/26/2026