Ulrik Stoltze

15PUBLICATIONS
65CO-AUTHORS
Haematological tumoursGene expression (incl. microarray and other genome-wide approaches)Cancer geneticsEnvironmental epidemiologyMedical biotechnology diagnostics (incl. biosensors)
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Publications (15)

|Aug 08, 2026
Concurrent Germline RB1 & Mosaic TP53 in a Child With Multiple Childhood Cancers.

|Dec 09, 2025
Role of common host genome variants in Childhood Acute Lymphoblastic Leukemia.

Theis Mikkelsen, Marianne Helenius, Mirella Ampatzidou

|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

|Mar 25, 2025
Overt and covert genetic causes of pediatric acute lymphoblastic leukemia.

Ulrik Stoltze, Stefanie V Junk, Anna Byrjalsen

|Oct 23, 2024
Evolutionary evidence precludes ELP1 as a high-penetrance pediatric cancer predisposition syndrome gene.

Kasper Amund Henriksen, Thomas Van Overeem Hansen, Karin Wadt

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

Anna Byrjalsen, Ulrik Kristoffer Stoltze, Charlotte Lautrup

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Frequent Collaborators

6 joint publications

Kjeld Schmiegelow

5 joint publications

Karin Wadt

4 joint publications

Jon Foss-Skiftesvik

3 joint publications

Anna Byrjalsen