Anna Byrjalsen

13PUBLICATIONS
54CO-AUTHORS
Cancer diagnosisCancer geneticsInfant and child healthGenomicsGene expression (incl. microarray and other genome-wide approaches)
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Publications (13)

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

|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

|Nov 18, 2024
Rare germline chromosome 1 duplication identified in young male with colon cancer: a case report investigating causality.

Anna Byrjalsen, Sara L Garcia, Line Borgwardt

|Sep 24, 2024
Novel germline TP53 variant (p.(Phe109Ile)) confers high risk of cancer.

Anna Byrjalsen, Ulrik Kristoffer Stoltze, Charlotte Lautrup

|Jul 11, 2023
The effect of a single SMARCA4 exon deletion on RNA splicing: Implications for variant classification.

Anna Byrjalsen, Ulrik Stoltze, Mana Mehrjouy

|Mar 02, 2023
Perception and management of cancer predisposition in pediatric cancer centers: A European-wide questionnaire-based survey.

Jelena Lazic, Oskar A Haas, Ugur Özbek

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Frequent Collaborators

5 joint publications

Karin Wadt

3 joint publications

Ulrik Kristoffer Stoltze

2 joint publications

Thomas van Overeem Hansen

2 joint publications

Lisa L Hjalgrim