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Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
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Germline Genetic Features of Young Individuals With Colorectal Cancer.
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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
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Increasing disparities in the age-related incidences of colon and rectal cancers in the United States, 1975-2010.
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Association of Obesity With Risk of Early-Onset Colorectal Cancer Among Women.
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Germline mutations affecting the proofreading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas.
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Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
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Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
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Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
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Rare disruptive mutations and their contribution to the heritable risk of colorectal cancer.
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Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.
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Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
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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.