Finn Cilius Nielsen

Finn Cilius Nielsen

Clinical Professor

Member of:

  • Clinical Biochemistry


  1. 2018
  2. Published

    Incidence and prevalence of sporadic and hereditary MTC in Denmark 1960-2014: a nationwide study

    Mathiesen, J. S., Kroustrup, J. P., Vestergaard, P., Stochholm, K., Poulsen, P. L., Rasmussen, Å. K., Feldt-Rasmussen, U., Schytte, S., Londero, S. C., Pedersen, H. B., Hahn, C. H., Djurhuus, B. D., Bentzen, J., Möller, S., Gaustadnes, M., Rossing, M., Nielsen, F. C., Brixen, K., Frederiksen, A. L., Godballe, C. & 1 others, Danish Thyroid Cancer Group (DATHYRCA), D. T. C. G. (., 2018, In: Endocrine Connections. 7, 6, p. 829-839 11 p.

    Research output: Contribution to journalJournal articlepeer-review

  3. Published

    MicroRNA-based classifiers for diagnosis of oral cavity squamous cell carcinoma in tissue and plasma

    Pedersen, N. J., Jensen, D. H., Lelkaitis, G., Kiss, K., Charabi, Birgitte Wittenborg, Ullum, H., Specht, Lena, Schmidt, A. Y., Nielsen, Finn Cilius & von Buchwald, Christian, 2018, In: Oral Oncology. 83, p. 46-52

    Research output: Contribution to journalJournal articlepeer-review

  4. Published

    Molecular subtyping of breast cancer improves identification of both high and low risk patients

    Rossing, M., Østrup, O., Majewski, W. W., Kinalis, S., Jensen, M. B., Knoop, A., Kroman, Niels Thorndahl, Talman, M. L., Hansen, T. V. O., Ejlertsen, B. & Nielsen, Finn Cilius, 2018, In: Acta Oncologica. 57, 1, p. 58-66

    Research output: Contribution to journalJournal articlepeer-review

  5. Published

    Mutational landscape assessed in tumor tissue and cell-free DNA during neratinib treatment of patients with HER2 mutated solid tumors

    Spanggaard, I., Oestrup, O., Bertelsen, B., Rohrberg, K. S., de Schmidt, A. Y., Tuxen, I. V., Ahlborn, L. B., Hasselby, Jane Preuss, Santoni Rugiu, Eric, Marvig, R. L., Lassen, Ulrik Niels, Nielsen, Finn Cilius, Yde, C. W. & Mau-Sørensen, M., 2018, In: European Journal of Cancer. 103, Suppl. 1, p. E142-E143 2 p.

    Research output: Contribution to journalConference abstract in journal

  6. Published

    Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations

    EMBRACE, E., 2018, In: Human Mutation. 39, 5, p. 593-620 28 p.

    Research output: Contribution to journalJournal articlepeer-review

  7. Published

    Using microarray-based subtyping methods for breast cancer in the era of high-throughput RNA sequencing

    Pedersen, C. B., Nielsen, Finn Cilius, Rossing, M. & Olsen, L. R., 2018, In: Molecular Oncology. 12, 12, p. 2136-2146 11 p.

    Research output: Contribution to journalJournal articlepeer-review

  8. 2017
  9. Published

    Correlation between HPV status at T and N sites of oropharyngeal squamous cell carcinomas

    Josiassen, M. V., Charabi, Birgitte Wittenborg, Lajer, C. B., Garnaes, E., Hamilton Therkildsen, M., Norrild, B., Specht, Lena, Nielsen, Finn Cilius & von Buchwald, Christian, Dec 2017, In: Acta Oto-Laryngologica. 137, 12, p. 1260-1264 5 p.

    Research output: Contribution to journalJournal articlepeer-review

  10. Published

    Founder effect of the RETC611Y mutation in multiple endocrine neoplasia 2A in Denmark: a nationwide Study

    Sloth Mathiesen, J., Kroustrup, J. P., Vestergaard, P., Krag, K. S., Poulsen, P. L., Rasmussen, Å. K., Feldt-Rasmussen, Ulla, Gaustadnes, M., Ørntoft, T. F., Rossing, M., Nielsen, Finn Cilius, Albrechtsen, Anders, Brixen, K., Godballe, C. & Frederiksen, A. L., Dec 2017, In: Thyroid. 27, 12, p. 1505-1510 6 p.

    Research output: Contribution to journalJournal articlepeer-review

  11. Published

    Next-Generation Sequencing-Based Detection of Germline Copy Number Variations in BRCA1/BRCA2: Validation of a One-Step Diagnostic Workflow

    Schmidt, A. Y., Hansen, T. V. O., Ahlborn, L. B., Jønson, L., Yde, C. W. & Nielsen, Finn Cilius, Nov 2017, In: The Journal of molecular diagnostics : JMD. 19, 6, p. 809-816 8 p.

    Research output: Contribution to journalJournal articlepeer-review

  12. Published

    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, Klaus, Nielsen, Finn Cilius & Rossing, M., Oct 2017, In: British Journal of Haematology. 179, 2, p. 308-322 15 p.

    Research output: Contribution to journalJournal articlepeer-review

Previous 1...4 5 6 7 8 9 10 11 ...25 Next

ID: 6797