prof. dr. ir. Kathleen Claes
- ORCID iD
- 0000-0003-0841-7372
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Towards improved Parsortix® efficiency for circulating tumor cell enrichment in pancreatic cancer
(2024) -
- Journal Article
- open access
EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer
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- Journal Article
- open access
The clinical use of exome sequencing to diagnose PCD patients
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Advances in CRISPR-mediated knock-in of disease-related variants in zebrafish
(2024) -
Advances in CRISPR-mediated knock-in of disease- and cancer-related variants in zebrafish
(2024) -
- Journal Article
- A1
- open access
Identification of potentially actionable genetic variants in epithelial ovarian cancer : a retrospective cohort study
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The psychological impact of genetic testing in childhood cancer : a systematic review
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Assessing recovery rates of mesenchymal and epithelial pancreatic tumor cells using the Parsortix system
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- Journal Article
- A1
- open access
A preclinical platform for assessing long-term drug efficacy exploiting mechanically tunable scaffolds colonized by a three-dimensional tumor microenvironment
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- Journal Article
- A1
- open access
ENIGMA CHEK2gether Project : a comprehensive study identifies functionally impaired CHEK2 germline missense variants associated with increased breast cancer risk
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- Journal Article
- A1
- open access
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2
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- Journal Article
- A1
- open access
Implementation of dihydropyrimidine dehydrogenase deficiency testing in Europe
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HRAS-related epidermal nevus syndromes : expansion of the spectrum with first branchial arch defects
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- Journal Article
- A2
- open access
Clinical presentation of sporadic and hereditary pheochromocytoma/paraganglioma
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- Miscellaneous
- open access
Atm deficient zebrafish model reveals conservation of the tumour suppressor function and a role in fertility
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Liquid biopsies to predict surgical resectability after FOLFIRINOX chemotherapy in patients with locally advanced and borderline resectable pancreatic ductal adenocarcinoma
(2022) -
Belgian guidelines for the frequency of participation of the Medical Centers of Human Genetics to external quality assessment schemes for analyses focused on rare diseases
(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(Supplement 1). p.472-472 -
- Journal Article
- A1
- open access
Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants : application of a points-based ACMG/AMP approach
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- Journal Article
- A1
- open access
Noncoding aberrations in mismatch repair genes underlie a substantial part of the missing heritability in Lynch syndrome
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- Journal Article
- A1
- open access
Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort
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- Journal Article
- A1
- open access
PRECISION : the Belgian molecular profiling program of metastatic cancer for clinical decision and treatment assignment
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- Journal Article
- A1
- open access
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
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- Journal Article
- A1
- open access
Application of an ultrasensitive NGS-based blood test for the diagnosis of early-stage lung cancer : sensitivity, a hurdle still difficult to overcome
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- Journal Article
- A1
- open access
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
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- Journal Article
- A1
- open access
Breast and prostate cancer risks for male BRCA1 and BRCA2 pathogenic variant carriers using polygenic risk scores
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- Journal Article
- A1
- open access
TIM3+ TRBV11-2 T cells and IFNγ signature in patrolling monocytes and CD16+ NK cells delineate MIS-C
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Joint Belgian recommendation on screening for DPD-deficiency in patients treated with 5-FU, capecitabine (and tegafur)
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- Journal Article
- A1
- open access
Shallow-depth sequencing of cell-free DNA for Hodgkin and diffuse large B-cell lymphoma (differential) diagnosis : a standardized approach with underappreciated potential
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Genetic testing in prostate cancer in clinical practice
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- Journal Article
- A1
- open access
Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
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Somatic mosaics in hereditary tumor predisposition syndromes
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- Journal Article
- A1
- open access
Comparison of microsatellite instability detection by immunohistochemistry and molecular techniques in colorectal and endometrial cancer
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- Journal Article
- A1
- open access
Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients
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- Journal Article
- A1
- open access
Frequency of participation in external quality assessment programs focused on rare diseases : Belgian guidelines for human genetics centers
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Integration of genomics and transcriptomics allows the identification of rare DNA damage defects in PID patients with a cancer predisposition
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Integration of genomics and transcriptomics to identify DNA damage defects in PID patients prone to cancer
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Prevalence of germline pathogenic variants in cancer predisposing genes in Czech and Belgian pancreatic cancer patients
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Dealing with pseudogenes in in the next generation sequencing era
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- Journal Article
- A1
- open access
Enhanced MCP-1 release in early autosomal dominant polycystic kidney disease
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- Journal Article
- A1
- open access
The predictive ability of the 313 variant-based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
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- Journal Article
- A1
- open access
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
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Hereditary syndromes and pancreatic cancer
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Zebrafish as an in vivo screening tool to establish PARP inhibitor efficacy
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Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene
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Integration of genomics and transcriptomics to identify DNAdamage defects in PID patients with a cancer predisposition
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Timing of blood sampling for butyrylcholinesterase phenotyping in patients with prolonged neuromuscular block after mivacurium or suxamethonium
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Missing heritability in Bloom syndrome : first report of a deep intronic variant leading to pseudo‐exon activation in the BLM gene
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- Journal Article
- A1
- open access
Myxoid hepatocellular adenoma, a rare variant of hepatocellular adenoma with distinct imaging features : a case report with immunohistochemical and molecular analysis and literature review
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Shallow whole-genome sequencing of cell-free DNA for B-cell lymphoma diagnosis and disease monitoring: a standardized approach with underappreciated potential
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Shallow whole-genome sequencing of cell-free DNA for B-cell lymphoma diagnosis and disease monitoring : a standardized approach with underappreciated potential
(2020)