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Vanessa Lattimore

Research Fellow

PhD(Otago)

Email vanessa.lau@otago.ac.nz
Tel +64 3 364 3628

Research interests

Dr Vanessa Lau is investigating familial breast cancer genetics by evaluating BRCA1 and BRCA2 sequence variants with modulate isoform expression.

Otago profile

Vanessa Lattimore thumbnail
PhD candidate Vanessa Lattimore has a strong history of breast cancer in her family. Three of five sisters in her family tree either suffered from or died of breast cancer.
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Publications

Stylianou, C. E., Wiggins, G. A. R., Lau, V. L., Dennis, J., Shelling, A. N., Wilson, M., Sykes, P., … Pearson, J., & Walker, L. C. (2024). Germline copy number variants and endometrial cancer risk. Human Genetics. Advance online publication. doi: 10.1007/s00439-024-02707-9 Journal - Research Article

Lau, A. W. K., Lau, V. L., & Sakowska, M. M. (2023). Evolution of sentinel lymph node biopsy for breast cancer patients in a rural setting: 10 years' experience. New Zealand Medical Journal/Te ara tika o te hauora hapori, 136(1575), 42-49. Retrieved from https://journal.nzma.org.nz/ Journal - Research Article

Lattimore, V., Parsons, M. T., Spurdle, A. B., Pearson, J., Lehnert, K., Sullivan, J., … Morrin, H., Robinson, B., & Walker, L. (2021). Under-ascertainment of breast cancer susceptibility gene carriers in a cohort of New Zealand female breast cancer patients. Breast Cancer Research & Treatment, 185, 583-590. doi: 10.1007/s10549-020-05986-8 Journal - Research Article

Lattimore, V., Parsons, M., Spurdle, A., Pearson, J., Northcott, H., Lehnert, K., … Morrin, H., Robinson, B., & Walker, L. (2020). Potential under-ascertainment of New Zealand women at high-risk of breast cancer in clinical care [Invited]. Proceedings of the Genetics Otago (GO) Zoom Symposium. Retrieved from https://blogs.otago.ac.nz/go/2020-3/ Conference Contribution - Published proceedings: Abstract

Walker, L. C., Lattimore, V. L., Kvist, A., Kleiblova, P., Zemankova, P., de Jong, L., Wiggins, G. A. R., Hakkaart, C., Cree, S. L., … Kennedy, M. A., … de la Hoya, M. (2019). Comprehensive assessment of BARD1 messenger ribonucleic acid splicing with implications for variant classification. Frontiers in Genetics, 10, 1139. doi: 10.3389/fgene.2019.01139 Journal - Research Article

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