 | Up a level |
2022
Heitz, F., Weber-Lassalle, K., Ernst, C., Moellenhoff, K., De Gregorio, N., Hauke, J., Dietrich, D., Borde, J., Jackisch, C., Park-Simon, T-W, Hanker, L. C., Pohl-Rescigno, E., Prieske, K., Kommoss, S., Marme, F., Stingl, J. C., Rita, S., Harter, P. and Hahnen, E. (2022). Chemotherapy-induced mutations in genes of clonal hematopoiesis increase the risk of myeloid neoplasms. Geburtshilfe Frauenheilkd., 82 (10). S. E88 - 1. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1438-8804
2018
Pohl, E., Borde, J., Hauke, J., Schmidt, S., Weber-Lassalle, K., Ernst, C., Niederacher, D., Arnold, N., Hellebrand, H., Meindl, A., Gehrig, A., Schmidt, G., Dutrannoy, V., Kast, K., Hahnen, E. and Schmutzler, R. (2018). Beyond CHEK2 in breast cancer: Search for additional moderately penetrant risk gene variants by analyzing the oligogenic disease course in CHEK2 mutation carriers. Eur. J. Hum. Genet., 26. S. 535 - 537. LONDON: NATURE PUBLISHING GROUP. ISSN 1476-5438
Weber-Lassalle, K., Weber-Lassalle, K., Borde, J., Weber-Lassalle, N., Klaschik, K., Neidhardt, G., Richters, L., Hauke, J., Hahnen, E. and Schmutzler, R. K. (2018). Germline loss-of-function variants in BARD1 are associated with familial breast cancer. Oncol. Res. Treat., 41. S. 3 - 4. BASEL: KARGER. ISSN 2296-5262