Thomas van Overeem Hansen
Clinical Professor
- 2013
- Published
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
- Published
Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
Permuth-Wey, J., Lawrenson, K., Shen, H. C., Velkova, A., Tyrer, J. P., Chen, Z., Lin, H-Y., Chen, Y. A., Tsai, Y-Y., Qu, X., Ramus, S. J., Karevan, R., Lee, J., Lee, N., Larson, M. C., Aben, K. K., Anton-Culver, H., Antonenkova, N., Antoniou, A. C., Armasu, S. M. & 160 others, , 2013, In: Nature Communications. 4, p. 1-12 1627.Research output: Contribution to journal › Journal article › Research › peer-review
- 2012
- 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
- 2011
- Published
A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics
Moltke, Ida, Albrechtsen, Anders, Hansen, Thomas van Overeem, Nielsen, Finn Cilius & Nielsen, Rasmus, 2011, In: Genome Research. 21, 7, p. 1168-80 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Ramus, S. J., Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J., Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., Allavena, A. & 31 others, , 2011, In: National Cancer Institute. Journal (Print). 103, 2, p. 105-16 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2010
- 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, , 1 Oct 2010, In: Nature Genetics. 42, 10, p. 885-92 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
Gaudet, M. M., Kirchhoff, T., Green, T., Vijai, J., Korn, J. M., Guiducci, C., Segrè, A. V., McGee, K., McGuffog, L., Kartsonaki, C., Morrison, J., Healey, S., Sinilnikova, O. M., Stoppa-Lyonnet, D., Mazoyer, S., Gauthier-Villars, M., Sobol, H., Longy, M., Frenay, M., GEMO Study Collaborators & 31 others, , 1 Oct 2010, In: P L o S Genetics. 6, 10, p. e1001183Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations
Steffensen, A. Y., Jønson, L., Ejlertsen, B., Gerdes, Anne-Marie Axø, Nielsen, Finn Cilius & Hansen, Thomas van Overeem, 1 Sep 2010, In: Familial Cancer. 9, 3, p. 283-7 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Ancient human genome sequence of an extinct Palaeo-Eskimo
Rasmussen, M., Li, Y., Lindgreen, S., Pedersen, J. S., Albrechtsen, A., Moltke, I., Metspalu, M., Metspalu, E., Kivisild, T., Gupta, R., Bertalan, M., Nielsen, K., Gilbert, T., Wang, Y., Raghavan, M., Campos, P., Kamp, H. L. M., Wilson, A. S., Gledhill, A., Tridico, S. & 32 others, , 11 Feb 2010, In: Nature. 463, 7282, p. 757-762 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Identification of a novel BRCA1 nucleotide 4803delCC/c.4684delCC mutation and a nucleotide 249T>A/c.130T>A (p.Cys44Ser) mutation in two Greenlandic Inuit families: implications for genetic screening of Greenlandic Inuit families with high risk for breast and/or ovarian cancer
Hansen, Thomas van Overeem, Jønson, L., Albrechtsen, Anders, Steffensen, A. Y., Bergsten, E. B., Myrhøj, T., Ejlertsen, Bent Laursen & Nielsen, Finn Cilius, 2010, In: Breast Cancer Research and Treatment. 124, 1, p. 259-264 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 33972371
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IMP3 RNP safe houses prevent miRNA-directed HMGA2 mRNA decay in cancer and development
Research output: Contribution to journal › Journal article › Research › peer-review
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Ancient human genome sequence of an extinct Palaeo-Eskimo
Research output: Contribution to journal › Journal article › Research › peer-review
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30
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Combinatorial batching of DNA for ultralow-cost detection of pathogenic variants
Research output: Contribution to journal › Journal article › Research › peer-review
Published