Irma Van De Beek
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 38 publications
Later age of natural menopause among women with the pathogenic CHEK2 c.1100delC variant: a validation study.
Journal: Journal of medical genetics
Published: October 30, 2025
Contralateral breast cancer risks for BRCA1, BRCA2, PALB2, CHEK2, and ATM pathogenic variant carriers in two large cohort studies.
Journal: BJC reports
Published: September 25, 2025
Eligibility for bilateral prophylactic mastectomy: An expert opinion study in the Netherlands.
Journal: Breast (Edinburgh, Scotland)
Published: September 09, 2025
Outcomes for ER-positive CHEK2 c.1100delC breast cancer patients compared with breast cancer patients without the variant.
Journal: Breast (Edinburgh, Scotland)
Published: June 26, 2025
Clinical syndromes linked to biallelic germline variants in MCM8 and MCM9.
Journal: HGG advances
Published: December 16, 2024
Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction.
Journal: Breast cancer research : BCR
Published: August 12, 2024
Metastatic disease after removal of a renal cell carcinoma smaller than 3 cm in a patient with Birt-Hogg-Dubé syndrome, a case report.
Journal: Familial cancer
Published: April 12, 2024
Co-observation of germline pathogenic variants in breast cancer predisposition genes: Results from analysis of the BRIDGES sequencing dataset.
Journal: American journal of human genetics
Published: March 29, 2024
Cancer risks for other sites in addition to breast in CHEK2 c.1100delC families.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 29, 2024
Differences in polygenic score distributions in European ancestry populations: implications for breast cancer risk prediction.
Journal: medRxiv : the preprint server for health sciences
Published: February 27, 2024
Recommendations on scuba diving in Birt-Hogg-Dubé syndrome.
Journal: Expert review of respiratory medicine
Published: November 22, 2023
MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset.
Journal: Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation
Published: July 04, 2023
Last Updated: 09/26/2026