Suter-Giorgini, Nicola - University of Leicester

个人简介

As a teaching-based Lecturer, Dr Suter-Giorgini is involved in the development of teaching aids to help students learn about genetics in new and innovative ways, as well as to be a resource for the development of teaching ideas from lab research-based members of staff. Dr Suter-Giorgini also has general undergraduate teaching responsibilities, personal tutees and final year analytical project students. After gaining a PhD from the University of Leicester in 1998, Dr Suter-Giorgini was a bench scientist at the Fred Hutchinson Cancer Research Center (FHCRC) in Seattle, USA for several years carrying out population-based research into the genetics of breast cancer. Following a short stint as an industry liaison officer also at FHCRC, Dr Suter-Giorgini taught degree-level biological sciences in Seattle for two years, after which she returned to the University of Leicester and worked for the GENIE CETL (Centre for Excellence in Teaching and Learning) in the position she currently holds.

研究领域

Current research interests include: Investigation of the use of Concept Inventories to enhance student learning, team-based learning, undergraduate research projects

近期论文

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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.