Research output per year
Research output per year
Personal profile
Research
Hereditary cancer risk – lifelong risk and lifelong follow-up.
5-10% of cancer patients have an inherited gene variant that influences cancer development. Screening for hereditary cancer risk is crucial for tailoring treatment and preventing future cancers in patients and their families.
In both my clinical work and research, I am dedicated to developing diagnostic methods, risk communication, and follow-up for patients with hereditary cancer risk.
Areas of expertise
- Clinical Genetics
- Oncogenetics
- Hereditary cancer predisposition
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Collaborations and top research areas from the last five years
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
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The c.1744G > C, p.(Glu582Gln) missense variant in coding exon 14 of APC increases skipping of a natural occurring isoform and causes Familial Adenomatous Polyposis
Jelsig, A. M., Boelman, M. B., Birkedal, U., Hübertz, J., Al-Zehawi, L., Lautrup, C., Karstensen, J. G. & van Overeem Hansen, T., Jan 2026, In: Journal of Cancer Research and Clinical Oncology. 152, 1, 3.Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Letter › peer-review
Open Access -
Childhood Cancer Predisposition and Evolutionary Constraints: Novel Lessons from Germline Genomes from 1,127 Children with Cancer
Stoltze, U. K., Hansen, T. V. O., Foss-Skiftesvik, J., Byrjalsen, A., Henriksen, K. A., Otamendi Laspiur, A., Gerdes, A. M., Ostrowski, S. R., Sørensen, E., Bak, M., Lautrup, C. K., Grønskov, K., Papaleo, E., Hasle, H., Mikkelsen, T. S., Wehner, P., Saksager, A. B., Andersen, M. K., Kjærsgaard, M. & Hjortshøj, T. D. & 15 others, , 3 Nov 2025, In: Clinical Cancer Research. 31, 21, p. 4495-4509 15 p.Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review
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A registry-based study on universal screening for defective mismatch repair in colorectal cancer in Denmark highlights disparities in screening uptake and counselling referrals
Durhuus, J. A., Galanakis, M., Maltesen, T., Therkildsen, C., Rosthøj, S., Klarskov, L. L., Lautrup, C. K., Andersen, O. & Nilbert, M. C., Aug 2024, In: Translational Oncology. 46, 102013.Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review
Open Access3 Citations (Scopus) -
Automated variant re-evaluation is labor-balanced and gives clinically relevant results: Hereditary cardiac disease as a use case
Grosen, A., Lautrup, C. K., Bahsen, E., Jensen, H. K. & Lildballe, D. L., Dec 2024, In: European Journal of Medical Genetics. 72, 104981.Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Journal article › Research › peer-review
Open Access -
Expanding the understanding of telomere biology disorder with reports from two families harboring variants in ZCCHC8 and TERC
Nitschke, N. J., Jelsig, A. M., Lautrup, C., Lundsgaard, M., Severinsen, M. T., Cowland, J. B., Maroun, L. L., Andersen, M. K. & Grønbæk, K., Aug 2024, In: Clinical Genetics. 106, 2, p. 187-192 6 p.Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaper › Letter › peer-review
Open Access2 Citations (Scopus)