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Acta Neurochirurgica|June 6, 2022
Genetic predisposition to central nervous system tumors in children - what the neurosurgeon should knowJon Foss-Skiftesvik, Ulrik Kristoffer StoltzeChild'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 26, 2024
The role of pathogenic TCF12 variants in children with coronal craniosynostosis-a systematic review with addition of two novel casesJon Foss-Skiftesvik, Carl Christian Larsen, Ulrik Kristoffer Stoltze, et al.Ugeskrift for Laeger|May 3, 2018
[Germ line mutations causing paediatric cancer predisposition syndromes are common in children and adolescents with cancer]Ulrik Kristoffer Stoltze, Anna Byrjalsen, Lisa Lyngsie Hjalgrim, et al.F1000Research|April 18, 2017
Non-infectious chemotherapy-associated acute toxicities during childhood acute lymphoblastic leukemia therapyKjeld Schmiegelow, Klaus Müller, Signe Sloth Mogensen, et al.Nature Communications|February 29, 2024
The evolutionary impact of childhood cancer on the human gene poolUlrik Kristoffer Stoltze, Jon Foss-Skiftesvik, Thomas van Overeem Hansen, et al.Molecular Oncology|August 11, 2025
Data-driven discovery of gene expression markers distinguishing pediatric acute lymphoblastic leukemia subtypesMona Nourbakhsh, Nikola Tom, Anna Schrøder Lassen, et al.Cancer Genetics|May 9, 2026
Novel truncating WT1 germline variant in a case of familial Wilms tumorMira Marie Laustsen, Ulrik Kristoffer Stoltze, Karen Bonde Larsen, et al.Journal of Medical Genetics|April 5, 2023
Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohortUlrik Kristoffer Stoltze, Mathis Hildonen, Thomas Van Overeem Hansen, et al.NAR Genomics and Bioinformatics|February 18, 2026
DoBSeqWF: a framework for sensitive detection of individual genetic variation in pooled sequencing dataMads Cort Nielsen, Christian Munch Hagen, Ulrik Kristoffer Stoltze, et al.Protein Science : a Publication of the Protein Society|December 3, 2022
RosettaDDGPrediction for high-throughput mutational scans: From stability to bindingValentina Sora, Adrian Otamendi Laspiur, Kristine Degn, et al.Pageof 2