Polygenic score distribution differences across European ancestry populations: implications for breast cancer risk prediction

NBCS Collaborators, ABCTB Investigators & kConFab Investigators, 2024, In: Breast Cancer Research. 26, 1, 14 p., 189.

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

Rare Germline Variants in DNA Repair Genes Detected in BRCA-Negative Finnish Patients with Early-Onset Breast Cancer

Kurkilahti, V., Rathinakannan, V. S., Nynäs, E., Goel, N., Aittomäki, K., Nevanlinna, H., Fey, V., Kankuri-Tammilehto, M. & Schleutker, J., Sept 2024, In: Cancers. 16, 17, 2955.

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

Understanding the genetic complexity of puberty timing across the allele frequency spectrum

ABCTB Investigators , The Lifelines Cohort Study, The Danish Blood Donor Study, The Biobank Japan Project, the China Kadoorie Biobank Collaborative Group, Kentistou, K. A., Kaisinger, L. R., Stankovic, S., Järvelin, M. R., Eriksson, J. G., Nevanlinna, H., Palotie, A., Tikkanen, E. & Widen, E., Jul 2024, In: Nature Genetics. 56, 7, p. 1397-1411 15 p.

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

Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry

NBCS Collaborators, CTS Consortium, Mueller, S. H., Lai, A. G., Valkovskaya, M., Blomqvist, C., Nevanlinna, H., Zheng, W. & Dunning, A. M., 26 Jan 2023, In: Genome medicine. 15, 1, 18 p., 7.

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

A likelihood ratio approach for utilizing case-control data in the clinical classification of rare sequence variants: Application to BRCA1 and BRCA2

Zanti, M., O'Mahony, D. G., Parsons, M. T., Li, H., Dennis, J., Aittomäki, K., Andrulis, I. L., Anton-Culver, H., Aronson, K. J., Augustinsson, A., Becher, H., Bojesen, S. E., Bolla, M. K., Brenner, H., Brown, M. A., Buys, S. S., Canzian, F., Caputo, S. M., Castelao, J. E. & Chang-Claude, J. & 104 others, Czene, K., Daly, M. B., De Nicolo, A., Devilee, P., Dörk, T., Dunning, A. M., Dwek, M., Eccles, D. M., Engel, C., Gareth Evans, D., Fasching, P. A., Gago-Dominguez, M., García-Closas, M., García-Sáenz, J. A., Gentry-Maharaj, A., Geurts-Giele, W. R. R., Giles, G. G., Glendon, G., Goldberg, M. S., Gómez Garcia, E. B., Göendert, M., Guénel, P., Hahnen, E., Haiman, C. A., Hall, P., Hamann, U., Harkness, E. F., Hogervorst, F. B. L., Hollestelle, A., Hoppe, R., Hopper, J. L., Houdayer, C., Houlston, R. S., Howell, A., Jakimovska, M., Jakubowska, A., Jernström, H., John, E. M., Kaaks, R., Kitahara, C. M., Koutros, S., Kraft, P., Kristensen, V. N., Lacey, J. V., Lambrechts, D., Léoné, M., Lindblom, A., Lubiski, J., Lush, M., Mannermaa, A., Manoochehri, M., Manoukian, S., Margolin, S., Martinez, M. E., Menon, U., Milne, R. L., Monteiro, A. N., Murphy, R. A., Neuhausen, S. L., Nevanlinna, H., Newman, W. G., Offit, K., Park, S. K., James, P., Peterlongo, P., Peto, J., Plaseska-Karanfilska, D., Punie, K., Radice, P., Rashid, M. U., Rennert, G., Romero, A., Rosenberg, E. H., Saloustros, E., Sandler, D. P., Schmidt, M. K., Schmutzler, R. K., Shu, X. O., Simard, J., Southey, M. C., Stone, J., Stoppa-Lyonnet, D., Tamimi, R. M., Tapper, W. J., Taylor, J. A., Teo, S. H., Teras, L. R., Terry, M. B., Thomassen, M., Troester, M. A., Vachon, C. M., Vega, A., Vreeswijk, M. P. G., Wang, Q., Wappenschmidt, B., Weinberg, C. R., Wolk, A., Zheng, W., Feng, B., Couch, F. J., Spurdle, A. B., Easton, D. F., Goldgar, D. E. & Michailidou, K., Sept 2023, In: Human mutation. 2023, 17 p., 9961341.

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