Associated Papers
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Supplement: 12887_2024_4553_MOESM1_ESM.xlsx › trio.hg38.filter
Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.
Karageorgos I et al.
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Supplement: 40246_2015_34_MOESM1_ESM.xlsx › FamilyA
Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives.
Webb EL et al.
Human Molecular Genetics, 2006
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