Contribution of Inherited Variants to Hereditary Cancer Syndrome Predisposition
Author:
Affiliation:
1. Department of Medical Genetics, Ankara Yıldırım Beyazıt University
2. Department of Medical Genetics, Ankara City Hospital
Publisher
Tohoku University Medical Press
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
https://www.jstage.jst.go.jp/article/tjem/258/4/258_2022.J087/_pdf
Reference21 articles.
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2. Anderson, C.L., Munawar, S., Reilly, L., Kamp, T.J., January, C.T., Delisle, B.P. & Eckhardt, L.L. (2022) How functional genomics can keep pace with VUS identification. Front. Cardiovasc. Med., 9, 900431.
3. Colas, C., Golmard, L., de Pauw, A., Caputo, S.M. & Stoppa-Lyonnet, D. (2019) “Decoding hereditary breast cancer” benefits and questions from multigene panel testing. Breast, 45, 29-35.
4. de Oliveira, J.M., Zurro, N.B., Coelho, A.V.C., Caraciolo, M.P., de Alexandre, R.B., Cervato, M.C., Minillo, R.M., de Vasconcelos Carvalho Neto, G., Grivicich, I. & Oliveira, J.B. (2022) The genetics of hereditary cancer risk syndromes in Brazil: a comprehensive analysis of 1682 patients. Eur. J. Hum. Genet., 30, 818-823.
5. de Voer, R.M., Hahn, M.M., Mensenkamp, A.R., Hoischen, A., Gilissen, C., Henkes, A., Spruijt, L., van Zelst-Stams, W.A., Kets, C.M., Verwiel, E.T., Nagtegaal, I.D., Schackert, H.K., van Kessel, A.G., Hoogerbrugge, N., Ligtenberg, M.J., et al. (2015) Deleterious germline BLM mutations and the risk for early-onset colorectal cancer. Sci. Rep., 5, 14060.
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