Hereditary Cancer in Clinical Practice

Papers
(The H4-Index of Hereditary Cancer in Clinical Practice is 10. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-06-01 to 2025-06-01.)
ArticleCitations
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers36
A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives25
Risk reduction strategies for BRCA1/2 hereditary ovarian cancer syndromes: a clinical practice guideline17
Primary fallopian tube cancer followed by primary breast cancer in RAD51C mutation carrier treated with niraparib as first line maintenance therapy: a case report16
“Left in limbo”: Exploring how patients with colorectal cancer interpret and respond to a suspected Lynch syndrome diagnosis15
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres15
Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland13
Genotype–phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome13
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposis12
Prostate Cancer: genetics in practice now and in the future11
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system10
A novel germline mutation in hMLH1 in three Korean women with endometrial cancer in a family of Lynch syndrome: case report and literature review10
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