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- 2020
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Mark
Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility
(
- Contribution to journal › Article
- 2019
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Mark
Estimating CDKN2A mutation carrier probability among global familial melanoma cases using GenoMELPREDICT
(
- Contribution to journal › Article
- 2017
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Mark
Germline Variation at CDKN2A and Associations with Nevus Phenotypes among Members of Melanoma Families
(
- Contribution to journal › Article
- 2016
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Mark
Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families.
(
- Contribution to journal › Article
- 2013
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Mark
A variant in FTO shows association with melanoma risk not due to BMI
(
- Contribution to journal › Article
- 2011
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Mark
Genome-wide association study identifies three new melanoma susceptibility loci
(
- Contribution to journal › Article
- 2009
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Mark
Genome-wide association study identifies three loci associated with melanoma risk
(
- Contribution to journal › Article
- 2007
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Mark
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents
(
- Contribution to journal › Article
- 2006
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Mark
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
(
- Contribution to journal › Article