Hereditary Cancer in Clinical Practice

Papers
(The H4-Index of Hereditary Cancer in Clinical Practice is 11. 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 2021-07-01 to 2025-07-01.)
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 guideline19
Primary fallopian tube cancer followed by primary breast cancer in RAD51C mutation carrier treated with niraparib as first line maintenance therapy: a case report18
“Left in limbo”: Exploring how patients with colorectal cancer interpret and respond to a suspected Lynch syndrome diagnosis16
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres15
Genotype–phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome14
Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland13
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposis12
Prostate Cancer: genetics in practice now and in the future12
Genetic testing for hereditary breast cancer in Poland: 1998–202211
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system11
Correction to: Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis11
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