Associated Papers
Scalable approaches for generating, validating and incorporating data from high-throughput functional assays to improve clinical variant classification.
Padigepati SR et al.
Human Genetics, 2024
39085601 (PubMed )
Supplement: 439_2024_2691_MOESM2_ESM.xlsx › MSH2
Clinical Impact of Detecting Low-Frequency Variants in Cell-Free DNA on Treatment of Castration-Resistant Prostate Cancer.
Mizuno K et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2021
34526361 (PubMed )
Supplement: 10780432ccr212328-sup-268178_2_supp_7341418_qy5jxd.pdf
Diagnostic yield of a custom-designed multi-gene cancer panel in Irish patients with breast cancer.
McVeigh ÚM et al.
Irish Journal of Medical Science, 2020
Interactions between meat intake and genetic variation in relation to colorectal cancer.
Andersen V et al.
Genes & Nutrition, 2015
25491747 (PubMed )
Supplement: 12263_2014_448_MOESM1_ESM.docx
Beta2-microglobulin mutations in microsatellite unstable colorectal tumors.
Kloor M et al.
International Journal of Cancer, 2007
Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient in the MSH2 mismatch repair protein.
Phung QH et al.
The Journal of Experimental Medicine, 1998
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