Kathleen Claes

Statistics Belgium — Belgium

Biochemistry, Genetics and Molecular Biology · Life Sciences

68h-index14.1kcitations452works1.92yr avg
OpenAlex↗ORCID↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

BRCA gene mutations in cancer(149), Cancer Genomics and Diagnostics(47), CRISPR and Genetic Engineering(45), DNA Repair Mechanisms(43), Ovarian cancer diagnosis and treatment(43)

Publications393 total

Navigating market access after conditional reimbursement: a communication roadmap for disinvesting orphan drugs
International Journal of Technology Assessment in Health Care·2026Open Access
ACTH-secreting atypical carcinoid lung tumour expanding the Lynch syndrome spectrum
Journal of Medical Genetics·2025
Genome-wide association study of 398,238 women unveils seven loci associated with high-grade serous ovarian cancer
npj Genomic Medicine·2025Open Access
Exploring cfDNA copy number profiles to characterize disease stages in pancreatic adenocarcinoma
Pancreatology·2025
REN p.L16del Mutation Is Associated with a Milder In Vitro and Clinical Phenotype Compared with Other Signal Peptide Mutations
Journal of the American Society of Nephrology·2025
#1876 Time to diagnosis in patients with rare kidney diseases: findings form the European Rare Kidney Disease Registry
Nephrology Dialysis Transplantation·2025Open Access
#3242 Long-term outcomes in IgA nephropathy: findings from the ERKNet patient registry (ERKReg)
Nephrology Dialysis Transplantation·2025Open Access
Author Correction: Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus
Nature Communications·2025Open Access
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
UNC Libraries·2025Open Access
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation
2025Open Access
<scp>EMT</scp> ‐associated bias in the Parsortix® system observed with pancreatic cancer cell lines
Molecular Oncology·2025· 1 citedOpen Access
P-804 Improving CRISPR/Cas9 gene correction in early mouse embryos using RNase-resistant crRNA XT
Human Reproduction·2025Open Access
Cracking rare disorders: a new minimally invasive RNA-seq protocol
npj Genomic Medicine·2025· 4 citedOpen Access
Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish
Lab Animal·2025· 7 citedOpen Access
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C&gt;T;701G&gt;A];[806_810del] variants in the RDH12 gene
Stem Cell Research·2025· 1 citedOpen Access
Prediction of surgical resectability after FOLFIRINOX chemotherapy for borderline resectable and locally advanced pancreatic cancer (PeRFormanCe): a multicenter prospective trial - trial protocol
BMC Surgery·2025· 1 citedOpen Access
Author response for "EMT-associated bias in the Parsortix® system observed with pancreatic cancer cell lines"
2025
Replication stress, microcephalic primordial dwarfism, and compromised immunity in ATRIP deficient patients
The Journal of Experimental Medicine·2025· 3 citedOpen Access
Investigating Chromosomal Radiosensitivity in Inborn Errors of Immunity: Insights from DNA Repair Disorders and Beyond
Journal of Clinical Immunology·2025Open Access
Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish
2025· 1 cited
page 1 of 20Next →

Frequent Co-authors

Daniel Barrowdale(15), Irene L. Andrulis(15), D. Gareth Evans(15), Javier Benı́tez(14), Maria A. Caligo(14), Kristiina Aittomäki(13), Saundra S. Buys(11), Orland Dı́ez(11), Judith Balmañà(11), Rósa B. Barkardóttir(11), Susan M. Domchek(10), Fergus J. Couch(10), Joe Dennis(10), Bernardo Bonanni(10), Trinidad Caldés(10), Peter Devilee(10), Debra Frost(10), Julian Adlard(10), Ian Campbell(10), Bruce Poppe(9)