| Non-infectious chemotherapy-associated acute toxicities during childhood acute lymphoblastic leukemia therapy K Schmiegelow, K Müller, SS Mogensen, PR Mogensen, BO Wolthers, ... F1000Research 6, 2017 | 90 | 2017 |
| Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes A Byrjalsen, TVO Hansen, UK Stoltze, MM Mehrjouy, NM Barnkob, ... PLoS genetics 16 (12), e1009231, 2020 | 84 | 2020 |
| Pediatric cancer families’ participation in whole‐genome sequencing research in Denmark: Parent perspectives A Byrjalsen, U Stoltze, K Wadt, LL Hjalgrim, AM Gerdes, K Schmiegelow, ... European Journal of Cancer Care 27 (6), e12877, 2018 | 20 | 2018 |
| Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility NP Archer, V Perez-Andreu, U Stoltze, ME Scheurer, AV Wilkinson, ... PLoS One 12 (8), e0180488, 2017 | 20 | 2017 |
| Genetic predisposition and evolutionary traces of pediatric cancer risk: a prospective 5-year population-based genome sequencing study of children with CNS tumors UK Stoltze, J Foss-Skiftesvik, T van Overeem Hansen, A Byrjalsen, ... Neuro-Oncology 25 (4), 761-773, 2023 | 16 | 2023 |
| RosettaDDGPrediction for high‐throughput mutational scans: From stability to binding V Sora, AO Laspiur, K Degn, M Arnaudi, M Utichi, L Beltrame, ... Protein Science 32 (1), e4527, 2023 | 15 | 2023 |
| Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort J Foss-Skiftesvik, UK Stoltze, T van Overeem Hansen, LB Ahlborn, ... Acta neuropathologica communications 10 (1), 123, 2022 | 10 | 2022 |
| Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel A Byrjalsen, IJ Diets, J Bakhuizen, TO Hansen, K Schmiegelow, ... Familial Cancer 20 (4), 279-287, 2021 | 9 | 2021 |
| Epidemiology and Etiology of Childhood ALL M Tulstrup, UK Stoltze, K Schmiegelow, JJ Yang Childhood Acute Lymphoblastic Leukemia, 1-27, 2017 | 8 | 2017 |
| Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark U Stoltze, AB Skytte, H Roed, H Hasle, B Ejlertsen, T Overeem Hansen, ... Plos one 13 (1), e0190050, 2018 | 7 | 2018 |
| 9p21. 3 Microdeletion involving CDKN2A/2B in a young patient with multiple primary cancers and review of the literature MR Jensen, U Stoltze, TVO Hansen, M Bak, A Sehested, C Rechnitzer, ... Molecular Case Studies 8 (4), a006164, 2022 | 5 | 2022 |
| Germline whole genome sequencing in pediatric oncology in Denmark—Practitioner perspectives A Byrjalsen, UK Stoltze, A Castor, A Wahlberg Molecular genetics & genomic medicine 8 (8), e1276, 2020 | 5 | 2020 |
| Germline (epi) genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort UK Stoltze, M Hildonen, TVO Hansen, J Foss-Skiftesvik, A Byrjalsen, ... Journal of Medical Genetics 60 (9), 842-849, 2023 | 3 | 2023 |
| Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21. 3 risk locus J Foss-Skiftesvik, S Li, A Rosenbaum, CM Hagen, UK Stoltze, ... Neuro-oncology 25 (9), 1709-1720, 2023 | 3 | 2023 |
| Background sensitivity to chemotherapy-induced nausea and vomiting and response to antiemetics in paediatric patients: a genetic association study A Eliasen, J Kornholt, R Mathiasen, K Wadt, U Stoltze, J Brok, ... Pharmacogenetics and Genomics 32 (2), 72-78, 2022 | 3 | 2022 |
| Maternal versus paternal inheritance of a 132 bp 11p15. 5 microdeletion affecting KCNQ1OT1 and associated phenotypes UK Stoltze, TVO Hansen, JS Brok, K Grønskov, Z Tumer, LB Ahlborn, ... Journal of Medical Genetics 60 (2), 128-130, 2023 | 2 | 2023 |
| Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants UK Stoltze, CM Hagen, T van Overeem Hansen, A Byrjalsen, AM Gerdes, ... Genome Medicine 15 (1), 17, 2023 | 1 | 2023 |
| Double Batched DNA Sequencing is a reliable, cost-effective and scalable approach to genomic population screening U Stoltze, C Hagen, T Hansen, A Byrjalsen, AM Gerdes, V Yakimov, ... | 1 | 2022 |
| Germ line mutations causing paediatric cancer predisposition syndromes are common in children and adolescents with cancer UK Stoltze, A Byrjalsen, LL Hjalgrim, A Wahlberg, R Gupta, AM Gerdes, ... Ugeskrift for Laeger 180 (17), V07170566-V07170566, 2018 | 1 | 2018 |
| Actionability and familial uptake following opportunistic genomic screening in a pediatric cancer cohort S Hammer-Hansen, U Stoltze, E Bartels, TO Hansen, A Byrjalsen, ... European Journal of Human Genetics, 1-12, 2024 | | 2024 |
Karin WadtDepartment of Clinical Genetics在 regionh.dk 的电子邮件经过验证
