Ulrik Kristoffer Stoltze
Rigshospitalet(DK)
Publications by Year
Research Areas
Genomics and Rare Diseases, Acute Lymphoblastic Leukemia research, Childhood Cancer Survivors' Quality of Life, BRCA gene mutations in cancer, Glioma Diagnosis and Treatment
Most-Cited Works
- → Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes(2020)109 cited
- → Non-infectious chemotherapy-associated acute toxicities during childhood acute lymphoblastic leukemia therapy(2017)95 cited
- → RosettaDDGPrediction for high‐throughput mutational scans: From stability to binding(2022)80 cited
- → Pediatric cancer families’ participation in whole-genome sequencing research in Denmark: Parent perspectives(2018)23 cited
- → Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors(2022)20 cited
- → Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel(2021)19 cited
- → Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility(2017)18 cited
- → Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort(2022)16 cited
- → Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus(2023)14 cited
- → The evolutionary impact of childhood cancer on the human gene pool(2024)13 cited