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Identification of 22 susceptibility loci associated with testicular germ cell tumors
Vitamin D–VDR signaling inhibits Wnt/β-Catenin–mediated melanoma progression and promotes antitumor immunity
MX 2 is a novel regulator of cell cycle in melanoma cells
Transcriptomic analysis reveals prognostic molecular signatures of stage I melanoma
High-resolution copy number patterns from clinically relevant FFPE material
Genetic and environmental determinants of immune response to cutaneous melanoma
β-Catenin–mediated immune evasion pathway frequently operates in primary cutaneous melanomas
Large-scale sequencing of testicular germ cell tumour (TGCT) cases excludes major TGCT predisposition gene
Comparative genomics reveals that loss of lunatic fringe (LFNG) promotes melanoma metastasis
Design considerations for genetic linkage and association studies
Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor
Identification of four new susceptibility loci for testicular germ cell tumour
Independent replication of a melanoma subtype gene signature and evaluation of its prognostic value and biological correlates in a population cohort
Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14
Germline MRE11 variants predictive of radiotherapy outcomes in bladder cancer by next-generation sequencing
Design considerations for genetic linkage and association studies
Melanoma sentinel node biopsy and prediction models for relapse and overall survival
Patterns of expression of DNA repair genes and relapse from melanoma
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer
Gene expression profiling of paraffin-embedded primary melanoma using the DASL assay identifies increased osteopontin expression as predictive of reduced relapse-free survival
Replication of the recessive STBMS1 locus but with dominant inheritance
A genome-wide association study of testicular germ cell tumor
Enhanced linkage of a locus on chromosome 2 to premature coronary artery disease in the absence of hypercholesterolemia
Heterozygote excess is repeatedly observed in females at the BRCA2 locus N372H
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
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