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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
- 2018
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Mark
Phenocopies in melanoma-prone families with germ-line CDKN2A mutations
(
- Contribution to journal › Article
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Mark
Cell-type-specific eQTL of primary melanocytes facilitates identification of melanoma susceptibility genes
(
- 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
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutations
(
- Contribution to journal › Article
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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
- 2015
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Mark
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.
(
- Contribution to journal › Article
- 2014
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Mark
The Effect on Melanoma Risk of Genes Previously Associated With Telomere Length
(
- Contribution to journal › Article