Hereditary Cancer in Clinical Practice

Papers
(The H4-Index of Hereditary Cancer in Clinical Practice is 12. 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 2022-06-01 to 2026-06-01.)
ArticleCitations
Association analysis of germline mutations in CHEK2, PALB2, NBN and RECQL with the risk of ductal carcinoma in situ in Polish women53
Two novel multiple endocrine neoplasia type 1 variants caused thymic neuroendocrine tumor: a case report37
A second hereditary cancer predisposition syndrome in a patient with lynch syndrome and three primary cancers22
Skin cancer risk in hereditary mixed cancer syndromes18
A genome-wide association study in Swedish colorectal cancer patients with gastric- and prostate cancer in relatives17
Primary fallopian tube cancer followed by primary breast cancer in RAD51C mutation carrier treated with niraparib as first line maintenance therapy: a case report15
Size matters in telomere biology disorders ‒ expanding phenotypic spectrum in patients with long or short telomeres14
Prostate Cancer: genetics in practice now and in the future13
Impact of germline MMR gene variants on immune checkpoint inhibitors response in patients with MSI-H/dMMR digestive cancers: a retrospective cohort analysis13
Genotype–phenotype correlation of BMPR1a disease causing variants in juvenile polyposis syndrome13
Progression of duodenal neoplasia to advanced adenoma in patients with familial adenomatous polyposis13
Preoperative multimodal ultrasonic imaging in a case of Peutz-Jeghers syndrome complicated by atypical lobular endocervical glandular hyperplasia: a case report and literature review12
Genetic testing for hereditary breast cancer in Poland: 1998–202212
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