Craft, E.V., Billington, C., O’Sullivan, R., Watson, W., Suter-Giorgini, N., Singletary, J., King, E., Perfirgines, M., Cashmore, A. and Barwell, J., 2015. Supporting families with Cancer: A patient centred survivorship model of care. Familial cancer, 14(4), pp.637-640.

Singletary, J.H., Bartle, C.L., Svirydzenka, N., Suter-Giorgini, N.M., Cashmore, A.M. and Dogra, N., 2015. Young people’s perceptions of mental and physical health in the context of general wellbeing. Health Education Journal, 74(3), pp.257-269.

Kramer, C., Suter-Giorgini, N., Moss, K. and Trent, N., 2013. The Mutation Game– A Versatile Educational Tool. New Traditional Games for Learning: A Case Book, p.20.

Kramer, C., Barber, R., Cashmore, A., Dalgleish, R., Suter-Giorgini, N., Willmott, C. and CETL, G., 2007. Linking DNA structure and sequencing using model based learning. In Proceedings of the Science Learning and Teaching Conference (2007) (pp. 107-109).

Malone, K.E., Daling, J.R., Doody, D.R., Hsu, L., Bernstein, L., Coates, R.J., Marchbanks, P.A., Simon, M.S., McDonald, J.A., Norman, S.A. and Strom, B.L., 2006. Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. Cancer research, 66(16), pp.8297-8308.

Suter, N.M., Malone, K.E., Daling, J.R., Doody, D.R. and Ostrander, E.A., 2003. Androgen receptor (CAG) n and (GGC) n polymorphisms and breast cancer risk in a population-based case-control study of young women. Cancer Epidemiology Biomarkers & Prevention, 12(2), pp.127-135.

Zhi, X., Szabo, C., Chopin, S., Suter, N., Wang, Q.S., Ostrander, E.A., Sinilnikova, O.M., Lenoir, G.M., Goldgar, D. and Shi, Y.R., 2002. BRCA1 and BRCA2 sequence variants in Chinese breast cancer families. Human mutation, 20(6), pp.474-474.

Breen, M., Jouquand, S., Renier, C., Mellersh, C.S., Hitte, C., Holmes, N.G., Chéron, A., Suter, N., Vignaux, F., Bristow, A.E. and Priat, C., 2001. Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes. Genome Research, 11(10), pp.1784-1795.

Teraoka, S.N., Malone, K.E., Doody, D.R., Suter, N.M., Ostrander, E.A., Daling, J.R. and Concannon, P., 2001. Increased frequency of ATM mutations in breast carcinoma patients with early onset disease and positive family history. Cancer, 92(3), pp.479-487.

Malone, K.E., Daling, J.R., Neal, C., Suter, N.M., O'Brien, C., Cushing‐Haugen, K., Jonasdottir, T.J., Thompson, J.D. and Ostrander, E.A., 2000. Frequency of BRCA1/BRCA2 mutations in a population‐based sample of young breast carcinoma cases. Cancer, 88(6), pp.1393-1402.



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Department of Genetics
University of Leicester

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Professor Jacqui Shaw

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