Thomas van Overeem Hansen

Thomas van Overeem Hansen

Clinical Professor

Member of:

  • Clinical Genetics


Publication year:
All
1 - 10 out of 57Page size: 10
Sort by: 1st author
  1. Published

    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

  2. Published

    MicroRNA dysregulation in adenoid cystic carcinoma of the salivary gland in relation to prognosis and gene fusion status: a cohort study

    Andreasen, S., Tan, Q., Agander, T. K., Hansen, Thomas van Overeem, Steiner, P., Bjørndal, K., Høgdall, Estrid Vilma Solyom, Larsen, S. R., Erentaite, D., Olsen, C. H., Ulhøi, B. P., Heegaard, Steffen, Wessel, Irene & Homøe, Preben, Sep 2018, In: Virchows Archiv. 473, 3, p. 329-340

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

    Antoniou, A. C., Wang, X., Fredericksen, Z. S., McGuffog, L., Tarrell, R., Sinilnikova, O. M., Healey, S., Morrison, J., Kartsonaki, C., Lesnick, T., Ghoussaini, M., Barrowdale, D., Peock, S., Cook, M., Oliver, C., Frost, D., Eccles, D., Evans, D. G., Eeles, R., Izatt, L. & 31 others, Chu, C., Douglas, F., Paterson, J., Stoppa-Lyonnet, D., Houdayer, C., Mazoyer, S., Giraud, S., Lasset, C., Remenieras, A., Caron, O., Hardouin, A., Berthet, P., Hogervorst, F. B. L., Rookus, M. A., Jager, A., van den Ouweland, A., Hoogerbrugge, N., van der Luijt, R. B., Meijers-Heijboer, H., Gómez García, E. B., Devilee, P., Vreeswijk, M. P. G., Lubinski, J., Jakubowska, A., Gronwald, J., Huzarski, T., Byrski, T., Gerdes, Anne-Marie Axø, Hansen, Thomas van Overeem, Nielsen, Finn Cilius & EMBRACE, E., 1 Oct 2010, In: Nature Genetics. 42, 10, p. 885-92 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. Published

    Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy

    Barington, M., Dunø, M., Birkedal, U., Vissing, John, Born, A. P., Krag, T., Hansen, Thomas van Overeem & Østergaard, Elsebet, 2023, In: Neuromuscular Disorders. 33, 7, p. 539-545 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. Accepted/In press

    Novel Alu insertion in the ZEB2 gene causing Mowat-Wilson syndrome

    Barington, M., Bak, M., Kjartansdóttir, K. R., Hansen, Thomas van Overeem, Birkedal, U., Østergaard, Elsebet & Hove, H. B., 2024, (Accepted/In press) In: American Journal of Medical Genetics, Part A.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. Published

    Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

    GEMO Study Collaborators, G. S. C., EMBRACE Collaborators, E. C., kConFab Investigators, K. I., HEBON Investigators, H. I., BRCA1, B. & BRCA2, B., Jan 2022, In: National Cancer Institute. Journal (Online). 114, 1, p. 109-122 14 p., 147.

    Research output: Contribution to journal › Journal article › Research › peer-review

  7. Published

    Genomforskningsprojekt påviser TP53-mutation hos en pige med rabdomyosarkom

    Behrendt-Møller, I., Stoltze, U., Hjalgrim, L. L., Hansen, Thomas van Overeem, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 9 Aug 2021, In: Ugeskrift for Laeger. 183, 32, 4 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. Published

    Von Hippel-Lindau disease (vHL)

    Binderup, M. L. M., Bisgaard, S. M. L., Harbud, V., Møller, H. U., Gimsing, S., Friis-Hansen, Lennart Jan, Hansen, Thomas van Overeem, Bagi, P., Knigge, Ulrich, Kosteljanetz, M., Bøgeskov, L., Thomsen, C., Gerdes, Anne-Marie Axø, Ousager, L. B. & Sunde, L., Dec 2013, In: Danish Medical Journal. 60, 12, p. B4763

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. Published

    Male with an apparently normal phenotype carrying a BRCA1 exon 20 duplication in trans to a BRCA1 frameshift variant

    Block, I., Mateu-Regué, À., Do, T. T. N., Miceikaite, I., Sdogati, D., Larsen, M. J., Hao, Q., Nielsen, H. R., Boonen, S. E., Skytte, A. B., Jensen, U. B., Høffding, L. K., De Nicolo, A., Viel, A., Tudini, E., Parsons, M. T., Hansen, T. V. O., Rossing, M., Kruse, T. A., Spurdle, A. B. & 1 others, Thomassen, M., 2024, In: Breast Cancer Research. 26, 1, 14 p., 6.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. Published

    Aortic dissection in a young male with persistent ductus arteriosus and a novel variant in MYLK

    Boelman, M. B., Hansen, Thomas van Overeem, Smith, M. N., Hammer-Hansen, S., Christensen, Alex Hørby & Diness, Birgitte Rode, 2024, In: American Journal of Medical Genetics, Part A. 194, 3, 6 p., e63458.

    Research output: Contribution to journal › Journal article › Research › peer-review

Previous 1 2 3 4 5 6 Next

ID: 33972371