项目详细信息
Description of project aims
This project examines the heritability of melanoma predisposition within families. The aim is to identify genetic variants inherited within families with a high melanoma burden and/or related cancers that increase susceptibility to tumour development.
| 状态 | 活跃的 |
|---|---|
| 有效的开始/结束日期 | 1/08/17 → … |
协作伙伴
- University of the Highlands and Islands （主要的）
- Oncogenomics Group, QIMR Berghofer Medical Research Institute, Brisbane, Australia. (Project partner)
- National Cancer Institute (NCI), National Institute of Health (NIH), Bethesda, Maryland (Project partner)
- Experimental Cancer Genetics, Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK. (Project partner)
联合国可持续发展目标
2015 年，联合国成员国同意 17 项全球可持续发展目标 (SDG)，以消除贫困、保护地球并确保全人类的繁荣。此项目有助于实现下列可持续发展目标：
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Good health and well being
指纹
搜索该项目所涉及的研究主题。这些标签是基于奖励/奖项生成的。它们共同形成唯一的指纹。
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Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
GenoMEL Study Group, 1 8月 2019, 在: Journal of the American Academy of Dermatology. 81, 2, 页码 386-394 9 页码科研成果: Article › 同行评审
开放访问文档21 引用 （Scopus）83 下载量 (Pure) -
Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma
Johansson, P. A., Nathan, V., Bourke, L. M., Palmer, J. M., Zhang, T., Symmons, J., Howlie, M., Patch, A. M., Read, J., Holland, E. A., Schmid, H., Warrier, S., Glasson, W., Höiom, V., Wadt, K., Jönsson, G., Olsson, H., Ingvar, C., Mann, G. & Brown, K. M. 以及 2其他, , 1 10月 2019, 在: Melanoma Research. 29, 5, 页码 483-490 8 页码科研成果: Article › 同行评审
开放访问文档22 引用 （Scopus）112 下载量 (Pure) -
Germline variants in oculocutaneous albinism genes and predisposition to familial cutaneous melanoma
Nathan, V., Johansson, P. A., Palmer, J. M., Howlie, M., Hamilton, H. R., Wadt, K., Jönsson, G., Brooks, K. M., Pritchard, A. L. & Hayward, N. K., 24 6月 2019, 在: Pigment Cell and Melanoma Research. 32, 6, 页码 854-863 10 页码科研成果: Article › 同行评审
18 引用 （Scopus）