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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2017 1
2018 1
2020 2
2022 3
2023 7

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13 results

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Page 1
RosettaDDGPrediction for high-throughput mutational scans: From stability to binding.
Sora V, Laspiur AO, Degn K, Arnaudi M, Utichi M, Beltrame L, De Menezes D, Orlandi M, Stoltze UK, Rigina O, Sackett PW, Wadt K, Schmiegelow K, Tiberti M, Papaleo E. Sora V, et al. Among authors: stoltze uk. Protein Sci. 2023 Jan;32(1):e4527. doi: 10.1002/pro.4527. Protein Sci. 2023. PMID: 36461907 Free PMC article.
Redefining germline predisposition in children with molecularly characterized ependymoma: a population-based 20-year cohort.
Foss-Skiftesvik J, Stoltze UK, van Overeem Hansen T, Ahlborn LB, Sørensen E, Ostrowski SR, Kullegaard SMA, Laspiur AO, Melchior LC, Scheie D, Kristensen BW, Skjøth-Rasmussen J, Schmiegelow K, Wadt K, Mathiasen R. Foss-Skiftesvik J, et al. Among authors: stoltze uk. Acta Neuropathol Commun. 2022 Aug 25;10(1):123. doi: 10.1186/s40478-022-01429-1. Acta Neuropathol Commun. 2022. PMID: 36008825 Free PMC article.
Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants.
Stoltze UK, Hagen CM, van Overeem Hansen T, Byrjalsen A, Gerdes AM, Yakimov V, Rasmussen S, Bækvad-Hansen M, Hougaard DM, Schmiegelow K, Hjalgrim H, Wadt K, Bybjerg-Grauholm J. Stoltze UK, et al. Genome Med. 2023 Mar 14;15(1):17. doi: 10.1186/s13073-023-01167-6. Genome Med. 2023. PMID: 36918911 Free PMC article.
Multi-ancestry genome-wide association study of 4069 children with glioma identifies 9p21.3 risk locus.
Foss-Skiftesvik J, Li S, Rosenbaum A, Hagen CM, Stoltze UK, Ljungqvist S, Hjalmars U, Schmiegelow K, Morimoto L, de Smith AJ, Mathiasen R, Metayer C, Hougaard D, Melin B, Walsh KM, Bybjerg-Grauholm J, Dahlin AM, Wiemels JL. Foss-Skiftesvik J, et al. Among authors: stoltze uk. Neuro Oncol. 2023 Sep 5;25(9):1709-1720. doi: 10.1093/neuonc/noad042. Neuro Oncol. 2023. PMID: 36810956 Free PMC article.
13 results