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Works
8
High frequency of BRAF mutations in nevi
Identification of combination gene sets for glioma classification.
Genome-wide scanning for linkage in Finnish breast cancer families
Germline alterations of the RNASEL gene, a candidate HPC1 gene at 1q25, in patients and families with prostate cancer
Evidence for a prostate cancer susceptibility locus on the X chromosome
Molecular classification of familial non-BRCA1/BRCA2 breast cancer
Notch and NOXA-related pathways in melanoma cells.
Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing