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High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer.
Bertelsen B, Tuxen IV, Yde CW, Gabrielaite M, Torp MH, Kinalis S, Oestrup O, Rohrberg K, Spangaard I, Santoni-Rugiu E, Wadt K, Mau-Sorensen M, Lassen U, Nielsen FC. Bertelsen B, et al. Among authors: nielsen fc. NPJ Genom Med. 2019 Jun 21;4:13. doi: 10.1038/s41525-019-0087-6. eCollection 2019. NPJ Genom Med. 2019. PMID: 31263571 Free PMC article.
Personalized oncology: genomic screening in phase 1.
Tuxen IV, Jønson L, Santoni-Rugiu E, Hasselby JP, Nielsen FC, Lassen U. Tuxen IV, et al. Among authors: nielsen fc. APMIS. 2014 Aug;122(8):723-33. doi: 10.1111/apm.12293. APMIS. 2014. PMID: 25046202 Review.
[The genome and cancer treatment].
Nielsen FC, Lassen U. Nielsen FC, et al. Ugeskr Laeger. 2014 Nov 10;176(46):V07140419. Ugeskr Laeger. 2014. PMID: 25394934 Free article. Review. Danish.
A new NFIA:RAF1 fusion activating the MAPK pathway in pilocytic astrocytoma.
Yde CW, Sehested A, Mateu-Regué À, Østrup O, Scheie D, Nysom K, Nielsen FC, Rossing M. Yde CW, et al. Among authors: nielsen fc. Cancer Genet. 2016 Oct;209(10):440-444. doi: 10.1016/j.cancergen.2016.09.002. Epub 2016 Sep 16. Cancer Genet. 2016. PMID: 27810072 Free article.
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
Leinøe E, Zetterberg E, Kinalis S, Østrup O, Kampmann P, Norström E, Andersson N, Klintman J, Qvortrup K, Nielsen FC, Rossing M. Leinøe E, et al. Among authors: nielsen fc. Br J Haematol. 2017 Oct;179(2):308-322. doi: 10.1111/bjh.14863. Epub 2017 Jul 27. Br J Haematol. 2017. PMID: 28748566 Free PMC article. Clinical Trial.
329 results