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 2022-01-01 to 2026-01-01.)
ArticleCitations
A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives45
Association analysis of germline mutations in CHEK2, PALB2, NBN and RECQL with the risk of ductal carcinoma in situ in Polish women25
Skin cancer risk in hereditary mixed cancer syndromes23
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers19
Primary fallopian tube cancer followed by primary breast cancer in RAD51C mutation carrier treated with niraparib as first line maintenance therapy: a case report18
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres16
Prostate Cancer: genetics in practice now and in the future13
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
Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system12
Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland12
Delineating the role of osteoprotegerin as a marker of breast cancer risk among women with a BRCA1 mutation11
Genetic testing for hereditary breast cancer in Poland: 1998–202211
Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review11
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