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Times Cited
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A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
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POT1 loss-of-function variants predispose to familial melanoma.
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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
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Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma.
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Germline mutations in shelterin complex genes are associated with familial glioma.
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A mutation in the POT1 gene is responsible for cardiac angiosarcoma in TP53-negative Li-Fraumeni-like families.
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Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.
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Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair.
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Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer.
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Genetic Variants That Predispose to DNA Double-Strand Breaks in Lymphocytes From a Subset of Patients With Familial Colorectal Carcinomas.
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11
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.