每年的项目
个人学者
Academic Qualifications
B.Med.Sc (1st class honours; specialisation in cellular and molecular biology)
Ph.D (Psychiatry; Genetics of Alzheimer's Disease)
Research Expertise
Dr Pritchard's research group investigates three main areas, centred around the study of melanoma. These include:
a) The genetics of melanoma susceptibility: what makes someone more likely to develop melanoma? What increases the risk of melanoma development in certain families?
b) The genomics of melanoma: what changes to the genome of melanoma drive the initiation, development and progression of melanomas?
c) The immunological control of melanoma: how does the immune system recognise melanoma cells? How do melanoma cells escape the immune system control?
Dr Pritchard's research group is interested in all types of melanoma, including skin, acral (sole of feet/palm of hands and fingernail beds), uveal (eye) and mucosal (e.g. oral, nasal, rectal) melanomas.
Research links
Google Scholar: Antonia Pritchard
Web of Science ResearcherID: F-4288-2010
ORCID: 0000-0001-5336-0454
Twitter: @antoniagage
外部职位
Visiting Scientist, Oncogenomics Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
7月 2017 → …
与联合国可持续发展目标相关的专业知识
2015 年,联合国成员国同意 17 项可持续发展目标 (SDG),以消除贫困、保护地球并确保全人类的繁荣。此人的工作有助于实现下列可持续发展目标:
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Good health and well being
学术指纹
- 1 相似学者
合作关系和合作领域
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Identification of genetic predisposition to familial melanoma and related cancers
Pritchard, A. (PI), Mustard, C. (CoI) & Hutchison, S. (PI)
1/08/17 → …
项目: Research
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The T-cell immune response to melanoma
Pritchard, A. (PI), Hutchison, S. (PI) & Mustard, C. (CoI)
Ride to Conquer Cancer, Australian Skin and Skin Cancer (ASSC) Centre
1/08/17 → …
项目: Research
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Use of lung ascites to diagnose mesothelioma by detecting genetic changes to BAP1
Pritchard, A. (PI)
1/01/22 → 31/12/22
项目: Research
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Whole genome landscapes of uveal melanoma show an ultraviolet radiation signature in iris tumours
Johansson, P. A., Brooks, K., Newell, F., Palmer, J. M., Wilmott, J. S., Pritchard, A. L., Broit, N., Wood, S., Carlino, M. S., Leonard, C., Koufariotis, L. T., Nathan, V., Beasley, A. B., Howlie, M., Dawson, R., Rizos, H., Schmidt, C. W., Long, G. V., Hamilton, H. & Kiilgaard, J. F. 以及 15其他, , 15 5月 2020, 在: Nature Communications. 11, 页码 1-8 8 页码, 2408 (2020).科研成果: Article › 同行评审
开放访问文档138 引用 (Scopus)210 下载量 (Pure) -
Whole-genome landscapes of major melanoma subtypes
Hayward, N. K., Wilmott, J. S., Waddell, N., Johansson, P. A., Field, M. A., Nones, K., Patch, A.-M., Kakavand, H., Alexandrov, L. B., Burke, H., Jakrot, V., Kazakoff, S., Holmes, O., Leonard, C., Sabarinathan, R., Mularoni, L., Wood, S., Xu, Q., Waddell, N. & Tembe, V. 以及 29其他, , 11 5月 2017, 在: Nature. 545, 7653, 页码 175-180 6 页码科研成果: Article › 同行评审
1262 引用 (Scopus) -
Exploration of peptides bound to MHC class I molecules in melanoma
Pritchard, A. L., Hastie, M. L., Neller, M., Gorman, J. J., Schmidt, C. W. & Hayward, N. K., 5月 2015, 在: Pigment Cell and Melanoma Research. 28, 3, 页码 281-294 14 页码科研成果: Article › 同行评审
20 引用 (Scopus) -
Exome Sequencing to Predict Neoantigens in Melanoma
Pritchard, A. L., Burel, J. G., Neller, M. A., Hayward, N. K., Lopez, J. A., Fatho, M., Lennerz, V., Woelfel, T. & Schmidt, C. W., 9月 2015, 在: Cancer Immunology Research. 3, 9, 页码 992-998 7 页码科研成果: Article › 同行评审
54 引用 (Scopus) -
Nonsense Mutations in the Shelterin Complex Genes ACD and TERF2IP in Familial Melanoma
Aoude, L. G., Pritchard, A. L., Robles-Espinoza, C. D., Wadt, K., Harland, M., Choi, J., Gartside, M., Quesada, V., Johansson, P. A., Palmer, J. M., Ramsay, A. J., Zhang, X., Jones, K., Symmons, J., Holland, E. A., Schmid, H., Bonazzi, V., Woods, S., Dutton-Regester, K. & Stark, M. S. 以及 19其他, , 1 2月 2015, 在: JNCI: Journal of the National Cancer Institute. 107, 2, 7 页码科研成果: Article › 同行评审
164 引用 (Scopus) -
POT1 loss-of-function variants predispose to familial melanoma
Robles-Espinoza, C. D., Harland, M., Ramsay, A. J., Aoude, L. G., Quesada, V., Ding, Z., Pooley, K. A., Pritchard, A. L., Tiffen, J. C., Petljak, M., Palmer, J. M., Symmons, J., Johansson, P. A., Stark, M. S., Gartside, M. G., Snowden, H., Montgomery, G. W., Martin, N. G., Lite, J. Z. & Choi, J. 以及 10其他, , 5月 2014, 在: Nature Genetics. 46, 5, 页码 478-481 4 页码科研成果: Article › 同行评审
354 引用 (Scopus) -
Genetic architecture of multiple primary cutaneous melanoma in the absence of high-penetrance susceptibility genes
Johansson, P. A., Palmer, J. M., Brooks, K. M., Herbert Chan, H., Pritchard, A. L., Wilson, D., Martin, L. K., Guitera, P. & Hayward, N. K., 26 2月 2026, 在: Journal of Investigative Dermatology.科研成果: Article › 同行评审
1 引用 (Scopus)
活动
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Upstream deletion: is it associated with familial melanoma?
Pritchard, A. (Speaker)
19 3月 2018 → 23 3月 2018活动: Invited talk
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RSE@Inverness
Pritchard, A. (Member)
30 9月 2017活动: Types of Public engagement and outreach - Festival/Exhibition
新闻 / 媒体
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Study to Measure Cell-Free DNA Capture Potential of BioCaptis Device
Megson, I. & Pritchard, A.
15/12/23
1 项目 媒体报道
新闻 / 媒体: Research
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Biocaptiva to conduct ex-vivo study to evaluate potential of BioCaptis device to capture cell free DNA to improve pleural disease diagnosis
Megson, I. & Pritchard, A.
16/10/23
1 项目 媒体报道
新闻 / 媒体: Research
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Biocaptiva to conduct ex-vivo study to evaluate potential of BioCaptis device to capture cell free DNA to improve pleural disease diagnosis
Megson, I. & Pritchard, A.
16/10/23
1 项目 媒体报道
新闻 / 媒体: Research