Finn Cilius Nielsen
Clinical Professor
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Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes
Fachal, L., Aschard, H., Beesley, J., Barnes, D. R., Allen, J., Kar, S., Pooley, K. A., Dennis, J., Michailidou, K., Turman, C., Soucy, P., Lemaçon, A., Lush, M., Tyrer, J. P., Ghoussaini, M., Marjaneh, M. M., Jiang, X., Agata, S., Aittomäki, K., Alonso, M. R. & 35 others, , 2020, In: Nature Genetics. 52, 1, p. 56-73 18 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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 journal › Journal article › Research › peer-review
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Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods
Milman, N., Koefoed, P., Pedersen, P., Nielsen, Finn Cilius & Eiberg, Hans Rudolf Lytchoff, 2003, In: European Journal of Haematology. 71, 6, p. 403-7 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Frequency of the hemochromatosis HFE mutations C282Y, H63D, and S65C in blood donors in the Faroe Islands
Milman, N., á Steig, T., Koefoed, P., Pedersen, P., Fenger, K. & Nielsen, Finn Cilius, 2004, In: Annals of Hematology. 84, 3, p. 146-9 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Functional analysis of HNPCC-related missense mutations in MSH2
Lützen, A., de Wind, N., Georgijevic, D., Nielsen, Finn Cilius & Rasmussen, Lene Juel, 14 Oct 2008, In: Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 645, 1-2, p. 44-55 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Functional characterization of BRCA1 gene variants by mini-gene splicing assay
Steffensen, A. Y., Dandanell, M., Jønson, L., Ejlertsen, B., Gerdes, Anne-Marie Axø, Nielsen, Finn Cilius & Hansen, T. V., Dec 2014, In: European Journal of Human Genetics. 22, 12, p. 1362-1368 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Functional characterization of MLH1 missense variants identified in Lynch Syndrome patients
Andersen, S. D., Liberti, S. E., Lützen, A., Drost, M., Bernstein, I., Nilbert, Mef Christina, Dominguez, M., Nyström, M., Hansen, Thomas van Overeem, Christoffersen, J. W., Jäger, A. C., de Wind, N., Nielsen, Finn Cilius, Tørring, P. M. & Rasmussen, Lene Juel, Dec 2012, In: Human Mutation. 33, 12, p. 1647-1655 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients
Petersen, S. M., Dandanell, M., Rasmussen, Lene Juel, Gerdes, Anne-Marie Axø, Krogh, L. N., Bernstein, I., Okkels, H., Wikman, F., Nielsen, Finn Cilius & Hansen, Thomas van Overeem, 2013, In: BMC Medical Genetics. 14, p. 103Research output: Contribution to journal › Journal article › Research › peer-review
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Gene Expression in the Human Endolymphatic Sac: The Solute Carrier Molecules in Endolymphatic Fluid Homeostasis
Møller, M. N., Kirkeby, Svend, Vikeså, J., Nielsen, Finn Cilius & Cayé-Thomasen, Per, Jun 2015, In: Otology & Neurotology. 36, 5, p. 915-22 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Gene expression demonstrates an immunological capacity of the human endolymphatic sac
Møller, M. N., Kirkeby, Svend, Vikeså, J., Nielsen, Finn Cilius & Cayé-Thomasen, Per, Aug 2015, In: The Laryngoscope. 125, 8, p. E269-75 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 6797
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IMP3 RNP safe houses prevent miRNA-directed HMGA2 mRNA decay in cancer and development
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RNA assemblages orchestrate complex cellular processes
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Cancers of unknown primary origin (CUP) are characterized by chromosomal instability (CIN) compared to metastasis of know origin
Research output: Contribution to journal › Journal article › Research › peer-review
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