Sally Dunwoodie
Sally Dunwoodie | |
|---|---|
| Personal details | |
| Born | Sally Lewers Dunwoodie |
| Nationality | Australian |
| Occupation | Embryologist, geneticist |
Sally Lewers Dunwoodie is an Australian scientist, specialising in genetic birth defects.[1]
Dunwoodie became an Officer of the Order of Australia in 2024 "For distinguished service to medical research as an embryologist and geneticist, particularly in the field of fetal and neonatal heart disease".[2]
Early life
[edit]Dunwoodie attended Queenwood School for Girls in Sydney, Australia, graduating in 1981.[3] She studied a Bachelor of Science with Honours at the University of Sydney.[4] She graduated with a PhD from the Children's Medical Research Institute.[4]
Scientific career
[edit]Dunwoodie completed postdoctoral training at the National Institute for Medical Research before starting work at the Victor Chang Cardiac Research Institute in 2000.[5] In 2022, Dunwoodie became the Deputy Director of the Victor Chang Cardiac Research Institute.[4]
Awards
[edit]- Fellow of the Australian Academy of Health and Medical Sciences, 2019-[6]
- Australian Museum Eureka Prize for Scientific Research (2018)[2]
- NSW Premier's Prize for Excellence in Medical Biological Sciences (2017)[2]
- Australian Financial Review Women of Influence (2015)[7][1]
Personal life
[edit]Dunwoodie has two children.[2]
Selected publications
[edit]- S. L. Dunwoodie (2009), "The role of hypoxia in development of the Mammalian embryo", Developmental cell, 17(6), pp. 755–773.[8]
- J. O. Szot, C. Campagnolo, Y. Cao, K. R. Iyer, H. Cuny, T. Drysdale, J. A. Flores-Daboub, W. Bi, L. Westerfield, P. Liu, T. Ngong Leung, K. W. Choy, G. Chapman, R. Xiao, V. M,. Siu, S. L. Dunwoodie (2020), "Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders", American Journal of Human Genetics, 106(1), pp. 129–136.[9]
- S. L. Dunwoodie, D. Henrique, S. M. Harrison, R. S. P. Beddington (1997), "Mouse Dll3: a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo", Development, 124(16), pp. 3065–3076.[10]
- G. Chapman, D. B. Sparrow, E. Kremmer, S. L. Dunwoodie (2011), "Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis", Human Molecular Genetics, 20(5), pp. 905–916.[11]
References
[edit]- ^ a b Stewart, Claire (16 July 2015). "Women of influence: How embryologist Sally Dunwoodie wins by 'striving to fail'". Australian Financial Review. Archived from the original on 1 July 2024. Retrieved 1 July 2024.
- ^ a b c d "Order of Australia awarded to Institute's Prof Sally Dunwoodie - Victor Chang Cardiac Research Institute". The Victor Chang Cardiac Research Institute. Archived from the original on 1 July 2024. Retrieved 1 July 2024.
- ^ "Queenwood - Professor Sally Dunwoodie". Queenwood School. Archived from the original on 1 July 2024. Retrieved 1 July 2024.
- ^ a b c "Professor Sally Dunwoodie - Victor Chang Cardiac Research Institute". The Victor Chang Cardiac Research Institute. Archived from the original on 18 March 2024. Retrieved 1 July 2024.
- ^ "External Speaker - Professor Sally Dunwoodie". Australian Regenerative Medicine Institute. Archived from the original on 1 July 2024. Retrieved 1 July 2024.
- ^ "Professor Sally Dunwoodie - AAHMS". Australian Academy of Health and Medical Sciences. 9 October 2019. Archived from the original on 1 July 2024. Retrieved 1 July 2024.
- ^ "Prof. Sally Dunwoodie - AFR Women of Influence". Retrieved 1 July 2024.
- ^ Dunwoodie, Sally L. (December 2009). "The Role of Hypoxia in Development of the Mammalian Embryo". Developmental Cell. 17 (6): 755–773. doi:10.1016/j.devcel.2009.11.008. ISSN 1534-5807. PMID 20059947.
- ^ Szot, Justin O.; Campagnolo, Carla; Cao, Ye; Iyer, Kavitha R.; Cuny, Hartmut; Drysdale, Thomas; Flores-Daboub, Josue A.; Bi, Weimin; Westerfield, Lauren; Liu, Pengfei; Leung, Tse Ngong; Choy, Kwong Wai; Chapman, Gavin; Xiao, Rui; Siu, Victoria M. (January 2020). "Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders". The American Journal of Human Genetics. 106 (1): 129–136. doi:10.1016/j.ajhg.2019.12.006. ISSN 0002-9297. PMC 7042491. PMID 31883644.
- ^ Dunwoodie, Sally L.; Henrique, Domingos; Harrison, Stephen M.; Beddington, Rosa S. P. (15 August 1997). "Mouse Dll3 : a novel divergent Delta gene which may complement the function of other Delta homologues during early pattern formation in the mouse embryo". Development. 124 (16): 3065–3076. doi:10.1242/dev.124.16.3065. ISSN 0950-1991. PMID 9272948.
- ^ Chapman, Gavin; Sparrow, Duncan B.; Kremmer, Elisabeth; Dunwoodie, Sally L. (7 December 2010). "Notch inhibition by the ligand Delta-Like 3 defines the mechanism of abnormal vertebral segmentation in spondylocostal dysostosis". Human Molecular Genetics. 20 (5): 905–916. doi:10.1093/hmg/ddq529. ISSN 1460-2083. PMID 21147753.
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