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
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
Prostate Cancer: genetics in practice now and in the future13
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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