Kathleen B. Claes
Gent, VLG, Belgium
Last Updated: 09/26/2026
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Found 8 publications
Unmasking NF1 mosaicism: optical genome mapping identifies a novel t(15;17) translocation in melanocytes.
Journal: Journal of medical genetics
Published: January 23, 2026
Cracking rare disorders: a new minimally invasive RNA-seq protocol.
Journal: NPJ genomic medicine
Published: November 18, 2024
Somatic mosaics in hereditary tumor predisposition syndromes.
Journal: European journal of medical genetics
Published: April 15, 2021
Comparison of microsatellite instability detection by immunohistochemistry and molecular techniques in colorectal and endometrial cancer.
Journal: Scientific reports
Published: December 17, 2020
Germline Genetic Findings Which May Impact Therapeutic Decisions in Families with a Presumed Predisposition for Hereditary Breast and Ovarian Cancer.
Journal: Cancers
Published: June 24, 2020
The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium.
Journal: Journal of medical genetics
Published: January 24, 2017
PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
Journal: Journal of medical genetics
Published: March 29, 2016
Showing 1-8 of 8
Last Updated: 09/26/2026