Items where authors include "Mann, GJ"
Article
Steinberg, J, Iles, MM orcid.org/0000-0002-2603-6509, Lee, JY et al. (11 more authors) (2022) Independent evaluation of melanoma polygenic risk scores in UK and Australian prospective cohorts. British Journal of Dermatology, 186 (5). pp. 823-834. ISSN 0007-0963
Mangantig, E, MacGregor, S, Iles, MM orcid.org/0000-0002-2603-6509 et al. (17 more authors) (2020) Germline variants are associated with increased primary melanoma tumor thickness at diagnosis. Human Molecular Genetics, 29 (21). pp. 3578-3587. ISSN 0964-6906
Law, MH, Aoude, LG, Duffy, DL et al. (19 more authors) (2020) Multiplex melanoma families are enriched for polygenic risk. Human Molecular Genetics. ISSN 0964-6906
Vuong, K, Armstrong, BK, Drummond, M et al. (12 more authors) (2020) Development and external validation study of a melanoma risk prediction model incorporating clinically assessed naevi and solar lentigines. The British Journal of Dermatology, 182 (5). pp. 1262-1268. ISSN 0007-0963
Landi, MT, Bishop, DT orcid.org/0000-0002-8752-8785, MacGregor, S et al. (158 more authors) (2020) Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nature Genetics, 52 (5). pp. 494-504. ISSN 1061-4036
Cust, AE, Drummond, M, Bishop, DT orcid.org/0000-0002-8752-8785 et al. (15 more authors) (2019) Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure. Journal of the European Academy of Dermatology and Venereology, 33 (10). pp. 1874-1885. ISSN 0926-9959
Cust, AE, Drummond, M, Kanetsky, PA et al. (18 more authors) (2018) Assessing the incremental contribution of common genomic variants to melanoma risk prediction in two population-based studies. Journal of Investigative Dermatology, 138 (12). pp. 2617-2624. ISSN 0022-202X
Liyanage, UE, Law, MH, Ong, JS et al. (7 more authors) (2018) Polyunsaturated fatty acids and risk of melanoma: A Mendelian randomisation analysis. International Journal of Cancer, 143 (3). pp. 508-514. ISSN 0020-7136
Artomov, M, Stratigos, AJ, Kim, I et al. (21 more authors) (2017) Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing. JNCI: Journal of the National Cancer Institute, 109 (12). djx083. ISSN 0027-8874
Taylor, NJ, Mitra, N, Goldstein, AM et al. (41 more authors) (2017) Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families. Journal of Investigative Dermatology, 137 (12). pp. 2606-2612. ISSN 0022-202X
Jouenne, F, Chauvot de Beauchene, I, Bollaert, E et al. (33 more authors) (2017) Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma. Journal of Medical Genetics, 54 (9). pp. 607-612. ISSN 0022-2593
Vuong, K, Armstrong, BK, Weiderpass, E et al. (12 more authors) (2016) Development and External Validation of a Melanoma Risk Prediction Model Based on Self-assessed Risk Factors. JAMA Dermatology, 152 (8). p. 889. ISSN 2168-6068
Law, M, Bishop, DT orcid.org/0000-0002-8752-8785, Lee, JE et al. (78 more authors) (2015) Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Nature Genetics, 47 (9). pp. 987-995. ISSN 1061-4036