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), 1 Dec 2022, In: Hereditary cancer in clinical practice. 20, 1, 36.

Research output: Contribution to journal › Article › Academic › peer-review

Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients (Breast Cancer Research, (2022), 24, 1, (69), 10.1186/s13058-022-01567-3)

Giardiello, D., Hooning, M. J., Hauptmann, M., Keeman, R., Heemskerk-Gerritsen, B. A. M., Becher, H., Blomqvist, C., Bojesen, S. E., Bolla, M. K., Camp, N. J., Czene, K., Devilee, P., Eccles, D. M., Fasching, P. A., Figueroa, J. D., Flyger, H., García-Closas, M., Haiman, C. A., Hamann, U., Hopper, J. L., & 19 othersJakubowska, A., Leeuwen, F. E., Lindblom, A., Lubiński, J., Margolin, S., Martinez, M. E., Nevanlinna, H., Nevelsteen, I., Pelders, S., Pharoah, P. D. P., Siesling, S., Southey, M. C., van der Hout, A. H., van Hest, L. P., Chang-Claude, J., Hall, P., Easton, D. F., Steyerberg, E. W. & Schmidt, M. K., 1 Dec 2022, In: Breast cancer research. 24, 1, 82.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

First estimates of diffuse gastric cancer risks for carriers of CTNNA1 germline pathogenic variants

Coudert, M., Drouet, Y., Delhomelle, H. L., Svrcek, M., Benusiglio, P. R., Coulet, F., Clark, D. F., Katona, B. W., van Hest, L. P., van der Kolk, L. E., Cats, A., van Dieren, J. M., Nehoray, B., Slavin, T., Spier, I., Hüneburg, R., Lobo, S., Oliveira, C., Boussemart, L., Masson, L., & 9 othersChiesa, J., Schwartz, M., Buecher, B., Golmard, L., Bouvier, A-M., Bonadona, V., Stoppa-Lyonnet, D., Lasset, C. & Colas, C., 29 Aug 2022, In: Journal of Medical Genetics. 59, 12, p. 1189-1195 7 p., 108740.

Research output: Contribution to journal › Article › Academic › peer-review

Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort

PTEN Study Group, 1 Dec 2022, In: European Journal of Medical Genetics. 65, 12, 104632.

Research output: Contribution to journal › Article › Academic › peer-review

PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients

Giardiello, D., Hooning, M. J., Hauptmann, M., Keeman, R., Heemskerk-Gerritsen, B. A. M., Becher, H., Blomqvist, C., Bojesen, S. E., Bolla, M. K., Camp, N. J., Czene, K., Devilee, P., Eccles, D. M., Fasching, P. A., Figueroa, J. D., Flyger, H., García-Closas, M., Haiman, C. A., Hamann, U., Hopper, J. L., & 19 othersJakubowska, A., Leeuwen, F. E., Lindblom, A., Lubiński, J., Margolin, S., Martinez, M. E., Nevanlinna, H., Nevelsteen, I., Pelders, S., Pharoah, P. D. P., Siesling, S., Southey, M. C., van der Hout, A. H., van Hest, L. P., Chang-Claude, J., Hall, P., Easton, D. F., Steyerberg, E. W. & Schmidt, M. K., 1 Dec 2022, In: Breast cancer research. 24, 1, 69.

Research output: Contribution to journal › Article › Academic › peer-review