Thomas van Overeem Hansen
Clinical Professor
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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
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Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC), T. E. H. T. G. (. A. T. I. M. R. C. (., 2022, In: Hereditary Cancer in Clinical Practice. 20, 36.Research output: Contribution to journal › Journal article › Research › peer-review
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Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2
AOCS Group, A. G., CZECANCA Consortium, C. C., The Consortium of Investigators of Modifiers of BRCA1/2, T. C. O. I. O. M. O. B., Evidence-based Network for the Interpretation of Germline Mutant Alleles Consortium, E. N. F. T. I. O. G. M. A. C., HEBON Investigators, H. I. & GEMO Study Collaborators, G. S. C., 2023, In: British Journal of Cancer. 128, 12, p. 2283-2294 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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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A distal Sp 1-element is necessary for maximal activity of the human gastrin gene promoter
R. Bundgaard, J., Hansen, Thomas van Overeem, Friis-Hansen, Lennart Jan, Rourke, I. J., van Solinge, W. W., Nielsen, Finn Cilius & Rehfeld, Jens Frederik, 7 Aug 1995, In: FEBS Letters. 369, 2-3, p. 225-228 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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The genetic prehistory of the New World Arctic
Raghavan, M., DeGiorgio, M., Albrechtsen, A., Moltke, I., Skoglund, P., Korneliussen, T. S., Grønnow, B., Appelt, M., Gulløv, H. C., Friesen, T. M., Fitzhugh, W., Malmström, H. S., Rasmussen, S., Olsen, J., Melchior, L. C., Fuller, B. T., Fahrni, S. M., Stafford jr., T., Grimes, V., Renouf, M. A. P. & 36 others, , 2014, In: Science. 345, 6200, 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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
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Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel
InSiGHT-ClinGen Hereditary Colon Cancer/Polyposis Variant Curation Expert Panel, I. H. C. C. V. C. E. P., 2024, In: Genetics in Medicine. 26, 2, 21 p., 100992.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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32
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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