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Contact Details

Email
danielle.jenkins@otago.ac.nz
Position
Teaching Fellow
Department
Department of Anatomy
Qualifications
BSc PGDipSci MSc PhD
Teaching
  • Hubs 191 and 192 Human Body Systems
  • ANAT 101 Anatomy for Sport and Exercise
  • ANAT 243 Reproductive and Developmental Biology
  • ANAT 331 Functional Anatomy
  • Med Endocrinology

Research

Danielle is a Teaching Fellow / Kaiwhakaako in Te Tari KikoKiko / Department of Anatomy and teaches a range of topics from 100 - 300 level papers.

Danielle has a research background in molecular biology, and completed her PhD at the University of Otago (Department of Anatomy / Centre for Neuroendocrinology).

Publications

Mulligan, M. R., Jenkins, D. E., Damsteegt, E., Beck, C., & Bicknell, L. S. (2021). The developmental effects of disrupting DONSON: A gene involved in genetic microcephaly. New Zealand Medical Journal, 134(1537), (pp. 115). Retrieved from https://www.nzma.org.nz/journal Conference Contribution - Published proceedings: Abstract

Nair, B. B., Khant Aung, Z., Porteous, R., Prescott, M., Glendining, K. A., Jenkins, D. E., Augustine, R. A., Silva, M. S. B., Yip, S. H., Bouwer, G. T., Brown, C. H., Jasoni, C. L., Campbell, R. E., Bunn, S. J., Anderson, G. M., Grattan, D. R., Herbison, A. E., & Iremonger, K. J. (2021). Impact of chronic variable stress on neuroendocrine hypothalamus and pituitary in male and female C57BL/6J mice. Journal of Neuroendocrinology, 33, e12972. doi: 10.1111/jne.12972 Journal - Research Article

Knapp, K. M., Jenkins, D. E., Sullivan, R., Harms, F. L., von Elsner, L., Ockeloen, C. W., … Bicknell, L. S. (2021). MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency. European Journal of Human Genetics, 29, 1110-1120. doi: 10.1038/s41431-021-00839-4 Journal - Research Article

Knapp, K. M., Luu, R., Baerenfaenger, M., Zijlstra, F., Wessels, H. J. C. T., Jenkins, D., … Bicknell, L. S. (2020). Biallelic variants in SLC35C1 as a cause of isolated short stature with intellectual disability. Journal of Human Genetics, 65, 743-750. doi: 10.1038/s10038-020-0764-4 Journal - Research Article

Knapp, K. M., Poke, G., Jenkins, D., Truter, W., & Bicknell, L. S. (2019). Expanding the phenotypic spectrum associated with DPF2: A new case report. American Journal of Medical Genetics Part A, 179A, 1637-1641. doi: 10.1002/ajmg.a.61262 Journal - Research Other

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