Thomas van Overeem Hansen

Thomas van Overeem Hansen

Clinical Professor

Member of:

  • Clinical Genetics


  1. 2023
  2. Published

    Molecular reclassification reveals low prevalence of germline predisposition in children with ependymoma

    Foss-Skiftesvik, J., Mathiasen, René, Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin, Schmiegelow, Kjeld & Stoltze, U. K., 2023, In: Acta Neuropathologica Communications. 11, 1, 94.

    Research output: Contribution to journalComment/debateResearchpeer-review

  3. Published

    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 journalJournal articleResearchpeer-review

  4. Published

    Survival, surveillance, and genetics in patients with Peutz–Jeghers syndrome: A nationwide study

    Jelsig, A. M., Hansen, Thomas van Overeem, Gede, L. B., Qvist, N., Christensen, L. L., Lautrup, C. K., Frederiksen, J. H., Sunde, L., Ousager, L. B., Ljungmann, K., Bertelsen, B. & Karstensen, John Gásdal, 2023, In: Clinical Genetics. 104, 1, p. 81-89 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    The effect of a single SMARCA4 exon deletion on RNA splicing: Implications for variant classification

    Byrjalsen, A., Stoltze, U., Mehrjouy, M., Frederiksen, J. H., Bak, M., Birkedal, U., Hasle, H., Gerdes, Anne-Marie Axø, Schmiegelow, Kjeld, Wadt, Karin Anna Wallentin & Hansen, Thomas van Overeem, 2023, In: Molecular Genetics and Genomic Medicine. 11, 10, 7 p., e2232.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Update of penetrance estimates in Birt-Hogg-Dubé syndrome

    Bruinsma, F. J., Dowty, J. G., Win, A. K., Goddard, L. C., Agrawal, P., Attina', D., Bissada, N., De Luise, M., Eisen, D. B., Furuya, M., Gasparre, G., Genuardi, M., Gerdes, A. M., Hansen, T. V. O., Houweling, A. C., Johannesma, P. C., Lencastre, A., Lim, D., Lindor, N. M., Luzzi, V. & 20 others, Lynch, M., Maffé, A., Menko, F. H., Michels, G., Pulido, J. S., Ryu, J. H., Sattler, E. C., Steinlein, O. K., Tomassetti, S., Tucker, K., Turchetti, D., Van De Beek, I., Van Riel, L., Van Steensel, M., Zenone, T., Zompatori, M., Walsh, J., Bondavalli, D., Maher, E. R. & Winship, I. M., 2023, In: Journal of Medical Genetics. 60, 4, p. 317-326 10 p.

    Research output: Contribution to journalReviewResearchpeer-review

  7. Published

    Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study

    Jelsig, A. M., Hansen, Thomas van Overeem, Gede, L. B., Qvist, N., Christensen, L. L., Lautrup, C. K., Ljungmann, K., Christensen, L. T., Rønlund, K., Tørring, P. M., Bertelsen, B., Sunde, Lone & Karstensen, John Gásdal, 2023, In: Familial Cancer. 22, p. 429–436 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. 2022
  9. 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 journalJournal articleResearchpeer-review

  10. Published

    9p21.3 Microdeletion involving CDKN2A/2B in a young patient with multiple primary cancers and review of the literature

    Jensen, M. R., Stoltze, U., Hansen, Thomas van Overeem, Bak, M., Sehested, A., Rechnitzer, C., Mathiasen, René, Scheie, David, Larsen, K. B., Olsen, T. E., Muhic, A., Skjøth, Jane, Rossing, Caroline Maria, Schmiegelow, Kjeld & Wadt, Karin Anna Wallentin, 2022, In: Cold Spring Harbor molecular case studies. 8, 4, a006164.

    Research output: Contribution to journalReviewResearchpeer-review

  11. Published

    Clinical implications of genetic testing in familial intermediate and late-onset colorectal cancer

    Djursby, M., Hansen, Thomas van Overeem, Wadt, Karin Anna Wallentin, Madsen, M. B., Berchtold, L. A., Lautrup, C. K., Markholt, S., Jensen, U. B., Krogh, L. N., Lundsgaard, M., Gerdes, Anne-Marie Axø, Nilbert, M. & Therkildsen, C., 2022, In: Human Genetics. 141, p. 1925–1933

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points-based ACMG/AMP approach

    Thomassen, M., Mesman, R. L. S., Hansen, T. V. O., Menendez, M., Rossing, M., Esteban-Sánchez, A., Tudini, E., Törngren, T., Parsons, M. T., Pedersen, I. S., Teo, S. H., Kruse, T. A., Møller, P., Borg, Å., Jensen, U. B., Christensen, L. L., Singer, C. F., Muhr, D., Santamarina, M., Brandao, R. & 30 others, Andresen, B. S., Feng, B., Canson, D., Richardson, M. E., Karam, R., Pesaran, T., LaDuca, H., Conner, B. R., Abualkheir, N., Hoang, L., Calléja, F. M. G. R., Andrews, L., James, P. A., Bunyan, D., Hamblett, A., Radice, P., Goldgar, D. E., Walker, L. C., Engel, C., Claes, K. B. M., Macháčková, E., Baralle, D., Viel, A., Wappenschmidt, B., Lazaro, C., Vega, A., Vreeswijk, M. P. G., de la Hoya, M., Spurdle, A. B. & ENIGMA Consortium, E. C., 2022, In: Human Mutation. 43, 12, p. 1921-1944

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 33972371