Kathleen Claes

Miscellaneous
open access

EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer (vol 32, pg 479, 2024)

Trudi McDevitt, Miranda Durkie, Norbert Arnold, George J. Burghel, Samantha Butler, Kathleen Claes (UGent) , Peter Logan, Rachel Robinson, Katie Sheils, Nicola Wolstenholme, et al.

(2026) EUROPEAN JOURNAL OF HUMAN GENETICS.

ACTH-secreting atypical carcinoid lung tumour expanding the Lynch syndrome spectrum

Kevin Van Compernolle, Jacques Van Huysse, Kathleen Claes (UGent) , Ellen Denayer, Marie Bex and Annick Van den Bruel

(2026) JOURNAL OF MEDICAL GENETICS. 63(2). p.136-139

Unmasking NF1 mosaicism : optical genome mapping identifies a novel t(15;17) translocation in melanocytes

Joséphine Blancke, Suzanne Vanhauwaert (UGent) , Stijn Van de Sompele (UGent) , Kathleen Claes (UGent) , Bert Callewaert (UGent) , Lien Depaepe, Sandra Janssens (UGent) , Sofie De Schepper (UGent) , Siebe Loontiens (UGent) , Lore Pottie (UGent) , et al.

(2026) JOURNAL OF MEDICAL GENETICS.

Miscellaneous

Myhre syndrome in adulthood : clinical variability and emerging genotype-phenotype correlations ( vol 32, pg 1086, 2024)

Eva Vanbelleghem (UGent) , Tim Van Damme (UGent) , Aude Beyens (UGent) , Sofie Symoens (UGent) , Kathleen Claes (UGent) , Julie De Backer (UGent) , Ilse Meerschaut, Floris Vanommeslaeghe (UGent) , Sigurd Delanghe (UGent) , Jenneke van den Ende, et al.

(2026) EUROPEAN JOURNAL OF HUMAN GENETICS.

Evaluation of the AmplideX® SMA Plus Kit for comprehensive SMN1/SMN2 analysis in Spinal Muscular Atrophy

Liesbeth Claeys (UGent) , Annelies De Jaegher (UGent) , Jennifer Anckaert (UGent) , Xenia Leroy (UGent) , Tjoïlina Reyniers (UGent) , Melek Yoruk (UGent) , Elfride De Baere (UGent) and Kathleen Claes (UGent)

(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.316-317

Exploring cfDNA copy number profiles to monitor tumor dynamics in pancreatic adenocarcinoma

Nele Vandenbussche (UGent) , LUIS ABREU DE CARVALHO (UGent) , Greet Wieme (UGent) , Bram Parton (UGent) , Béatrice Lintermans (UGent) , Suzane Moura Ribeiro (UGent) , Anne Hoorens (UGent) , Karen Geboes (UGent) , Frederik Berrevoet (UGent) and Kathleen Claes (UGent)

(2025) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 33(Supplement 1). p.531-531

Miscellaneous

Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

Michiel Vanhooydonck (UGent) , Elyne De Neef (UGent) , Hanna De Saffel (UGent) , Annekatrien Boel (UGent) , Andy Willaert (UGent) , Bert Callewaert (UGent) and Kathleen Claes (UGent)

(2025) BioRxiv.

Journal Article
A1
open access

EMT‐associated bias in the Parsortix® system observed with pancreatic cancer cell lines

Nele Vandenbussche (UGent) , Renske Imschoot (UGent) , Béatrice Lintermans (UGent) , Lode Denolf (UGent) , Joachim Taminau (UGent) , Charlotte Fieuws, Geert Berx (UGent) , Kris Gevaert (UGent) and Kathleen Claes (UGent)

(2025) MOLECULAR ONCOLOGY. 19. p.3360-3375

Clinical characteristics and outcome of patients with atypical Hemolytic Uremic Syndrome : Belgian cohort of the global aHUS registry

Johan Vande Walle (UGent) , Laurent Weekers, Kathleen Claes, Broeders Nilufer, Evelien Snauwaert (UGent) , Djalila Mekahli, Eric Goffin, Laure Collard, Nathalie Godefroid, Brigitte Adams, et al.

(2025) PEDIATRIC NEPHROLOGY. In Pediatric Nephrology 40. p.1324-1324

Journal Article
A1
open access

Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

Michiel Vanhooydonck (UGent) , Elyne De Neef (UGent) , Hanna De Saffel (UGent) , Annekatrien Boel (UGent) , Andy Willaert (UGent) , Bert Callewaert (UGent) and Kathleen Claes (UGent)

(2025) LAB ANIMAL. 54(6). p.165-172

Academic Bibliography

Kathleen Claes

Public URL

EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer (vol 32, pg 479, 2024)

ACTH-secreting atypical carcinoid lung tumour expanding the Lynch syndrome spectrum

Unmasking NF1 mosaicism : optical genome mapping identifies a novel t(15;17) translocation in melanocytes

Myhre syndrome in adulthood : clinical variability and emerging genotype-phenotype correlations ( vol 32, pg 1086, 2024)

Evaluation of the AmplideX® SMA Plus Kit for comprehensive SMN1/SMN2 analysis in Spinal Muscular Atrophy

Exploring cfDNA copy number profiles to monitor tumor dynamics in pancreatic adenocarcinoma

Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

EMT‐associated bias in the Parsortix® system observed with pancreatic cancer cell lines

Clinical characteristics and outcome of patients with atypical Hemolytic Uremic Syndrome : Belgian cohort of the global aHUS registry

Prime editing outperforms homology-directed repair as a tool for CRISPR-mediated variant knock-in in zebrafish

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