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Human Molecular Genetics|July 31, 2018
Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanomaFangyi Gu, Ting-Huei Chen, Ruth M Pfeiffer, et al.
Journal of Medical Genetics|August 15, 2006
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continentsAlisa M Goldstein, May Chan, Mark Harland, et al.
Journal of the American Academy of Dermatology|February 8, 2019
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICTNicholas J Taylor, Nandita Mitra, Lu Qian, et al.
Cancer Research|October 19, 2006
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMELAlisa M Goldstein, May Chan, Mark Harland, et al.
The Journal of Investigative Dermatology|August 24, 2017
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma FamiliesNicholas J Taylor, Nandita Mitra, Alisa M Goldstein, et al.
Nature Genetics|April 2, 2014
Rare missense variants in POT1 predispose to familial cutaneous malignant melanomaJianxin Shi, Xiaohong R Yang, Bari Ballew, et al.
Research Square|May 25, 2026
A high-penetrance intergenic variant at 9p21 confers melanoma susceptibilityMaria Teresa Landi, Linh Bui-Raborn, Lorenza Pastorino, et al.
Nature Genetics|July 7, 2009
Genome-wide association study identifies three loci associated with melanoma riskD Timothy Bishop, Florence Demenais, Mark M Iles, et al.
Nature Genetics|October 11, 2011
Genome-wide association study identifies three new melanoma susceptibility lociJennifer H Barrett, Mark M Iles, Mark Harland, et al.
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