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Familial Cancer - 2023
27 articles | Last updated: 2025-12-03 14:12:56
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Inherited BRCA1 and RNF43 pathogenic variants in a familial colorectal cancer type X family
Cascade testing in Italian Hereditary Breast Ovarian Cancer families: a missed opportunity for cancer prevention?
Functional and phenotypic consequences of an unusual inversion in MSH2
Balancing the burden and benefits of colonoscopy in Lynch Syndrome
PREMM5 distinguishes sporadic from Lynch syndrome-associated MMR-deficient/MSI-high colorectal cancer
Combining clinical and molecular characterization of CDH1: a multidisciplinary approach to reclassification of a splicing variant
Prevalence and genetic spectrum associated with hereditary colorectal cancer syndromes, the need to improve cancer risk awareness, and family cascade testing in Vietnam
Germline whole genome sequencing in adults with multiple primary tumors
Willingness of individuals with Li-Fraumeni syndrome to participate in a cancer prevention trial: a survey study
Whole genome sequencing and disease pattern in patients with juvenile polyposis syndrome: a nationwide study
Mainstreamed genetic testing of breast cancer patients: experience from a single surgeon’s practice in a large US Academic Center
Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1
In deep bioinformatic characterization of a novel fumarate hydratase variant FH c.199T > G; (p.Tyr67Asp) in hereditary leiomyomatosis and renal cell carcinoma
A mosaic pathogenic variant in MSH6 causes MSH6-deficient colorectal and endometrial cancer in a patient classified as suspected Lynch syndrome: a case report
Ninth International Symposium on Hereditary Breast and Ovarian Cancer
Reclassification of two germline DICER1 splicing variants leads to DICER1 syndrome diagnosis
Colonoscopy surveillance in Lynch syndrome is burdensome and frequently delayed
Hematologic toxicities of chemotherapy in breast and ovarian cancer patients carrying BRCA1/BRCA2 germline pathogenic variants. A single center experience and review of the literature
Endoscopic and chemopreventive management of familial adenomatous polyposis syndrome
Perspectives on the implications of carrying putative pathogenic variants in the medulloblastoma predisposition genes ELP1 and GPR161
Hereditary acute myeloid leukemia associated with C-terminal CEBPA germline variants
Characteristics of familial pancreatic cancer families with additional colorectal carcinoma
Heritable methylation marks associated with prostate cancer risk
2022 CGA-IGC Annual Meeting: The collaborative group of the Americas on Inherited Gastrointestinal Cancer November 11–13, 2022
Evaluating the role of CHEK2 p.(Asp438Tyr) allele in inherited breast cancer predisposition
Pilot study of the prevalence of autoimmune disorders in Li-Fraumeni syndrome