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Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants.
Haque B, Cheerie D, Pan A, Curtis M, Nalpathamkalam T, Nguyen J, Salhab C, Thiruvahindrapuram B, Zhang J, Couse M, Hartley T, Morrow MM, Price EM, Walker S, Malkin D, Roth FP, Costain G. Haque B, et al. Among authors: pan a. PLoS Genet. 2025 Jan 6;21(1):e1011540. doi: 10.1371/journal.pgen.1011540. Online ahead of print. PLoS Genet. 2025. PMID: 39761285 Free article.
1,913 results