Karin Wadt

22PUBLICATIONS
89CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cancer diagnosisGene expression (incl. microarray and other genome-wide approaches)Haematological tumoursCancer genetics
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Publications (22)

|Sep 09, 2026
Phenotypic manifestations and variant reclassification of germline PTEN variants: a nationwide Danish study.

|Aug 27, 2026
Novel Co-Occurrence of Germline EGFR p.V843I and Somatic EGFR Exon 19 Deletion in NSCLC: Insights into Reduced Sensitivity to EGFR-TKIs.

|Jun 09, 2026
Interpreting TP53 variants: somatic mosaicism and ERCC6L2-driven clonal evolution.

|Feb 18, 2026
DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing data.

Mads Cort Nielsen, Christian Munch Hagen, Ulrik Kristoffer Stoltze

|Oct 24, 2025
Exploring the spectrum of central nervous system tumours in carriers of germline POT1 variants.

Emilie Neerup Nielsen, Anne Marie Jelsig, Jon Foss-Skiftesvik

|Aug 15, 2025
Childhood Cancer Predisposition and Evolutionary Constraints: Novel Lessons from Germline Genomes from 1,127 Children with Cancer.

Ulrik Kristoffer Stoltze, Thomas van Overeem Hansen, Jon Foss-Skiftesvik

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Frequent Collaborators

6 joint publications

Kjeld Schmiegelow

5 joint publications

Anna Byrjalsen

5 joint publications

Ulrik Stoltze

4 joint publications

Thomas van Overeem Hansen