Victoria Stokes

Lecturer in Clinical Medicine

Oxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM)

Publications

Hannan, Fadil & Stevenson, Mark & Bayliss, Asha & Stokes, Victoria & Stewart, Michelle & Kooblall, Kreepa & Gorvin, Caroline & Codner, Gemma & Teboul, Lydia & Wells, Sara & Thakker, Rajesh. (2021). Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2. Human molecular genetics. 30. 10.1093/hmg/ddab076.

Hannan, Fadil & Stevenson, Mark & Bayliss, Asha & Stokes, Victoria & Stewart, Michelle & Kooblall, Kreepa & Gorvin, Caroline & Codner, Gemma & Teboul, Lydia & Wells, Sara & Thakker, Rajesh. (2020). Ap2s1 mutation in mice causes familial hypocalciuric hypercalcemia type 3. 10.1101/2020.08.10.244244.

Onopiuk, Marta & Eby, Bonnie & Nesin, Vasyl & Ngo, Peter & Lerner, Megan & Gorvin, Caroline & Stokes, Victoria & Thakker, Rajesh & Brandi, Maria & Chang, Wenhan & Humphrey, Mary & Tsiokas, Leonidas & Lau, Kai. (2020). Control of PTH secretion by the TRPC1 ion channel. JCI Insight. 5. 10.1172/jci.insight.132496.

Gorvin, Caroline & Stokes, Victoria & Boon, Hannah & Cranston, Treena & Gluck, Anna & Bahl, Shailina & Homfray, Tessa & Aung, Theingi & Shine, Brian & Lines, Kate & Hannan, Fadil & Thakker, Rajesh. (2019). Activating Mutations of the G-protein Subunit α 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2. Journal of Clinical Endocrinology & Metabolism. 105. 10.1210/clinem/dgz251.

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