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Familial Cancer - 2019

40 articles | Last updated: 2025-12-03 14:12:56
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T A T A T A T A
The (ir)relevance of the abandoned criterion II for the diagnosis of serrated polyposis syndrome: a retrospective cohort study
De novo pathogenic germline variant in PALB2 in a patient with pancreatic cancer
Clear cell chondrosarcoma in Von Hippel-Lindau disease
Renal cell carcinoma in young FH mutation carriers: case series and review of the literature ✓ ✓ Dutch
‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations
Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li–Fraumeni syndrome)
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case
Long-term positive psychological outcomes in an Australian pancreatic cancer screening program
A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature
Novel candidates in early-onset familial colorectal cancer
Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European ✓ ✓ as compared to European; individuals who identify as Hispanic, African or Asian and Pacific Islander
Health behaviours and beliefs in individuals with familial pancreatic cancer
Should unaffected female BRCA2 pathogenic variant carriers be told there is little or no advantage from risk reducing mastectomy?
Population frequencies of pathogenic alleles of BRCA1 and BRCA2: analysis of 173 Danish breast cancer pedigrees using the BOADICEA model
TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition?
Hereditary diffuse gastric cancer: cancer risk and the personal cost of preventive surgery
Energy balance related lifestyle factors and risk of endometrial and colorectal cancer among individuals with lynch syndrome: a systematic review
Multiple primary malignancies associated with a germline SMARCB1 pathogenic variant
Assessing a single SNP located at TERT/CLPTM1L multi-cancer risk region as a genetic modifier for risk of pancreatic cancer and melanoma in Dutch CDKN2A mutation carriers
Ability of known susceptibility SNPs to predict colorectal cancer risk for persons with and without a family history
Endoscopic full thickness resection for early colon cancer in Lynch syndrome
Targeted next generation sequencing screening of Lynch syndrome in Tunisian population
The incidence of consecutive manifestations in Von Hippel-Lindau disease
Genetic counseling referral for ovarian cancer patients: a call to action
Implication of DNA repair genes in Lynch-like syndrome
Hereditary gastric cancer: what’s new? Update 2013–2018
Pediatric craniopharyngioma in association with familial adenomatous polyposis
NTHL1-associate polyposis: first Australian case report
International society for gastrointestinal hereditary tumours—InSiGHT
Progress report: familial pancreatic cancer
Implementation of a Systematic Tumor Screening Program for Lynch Syndrome in an Integrated Health Care Setting
Moving into the mainstream: healthcare professionals’ views of implementing treatment focussed genetic testing in breast cancer care
Phenotypic confirmation of oligodontia, colorectal polyposis and cancer in a family carrying an exon 7 nonsense variant in the AXIN2 gene
Mutated SON putatively causes a cancer syndrome comprising high-risk medulloblastoma combined with café-au-lait spots
Exploring the preferences of involved health professionals regarding the implementation of an online decision aid to support couples during reproductive decision-making in hereditary cancer: a mixed m
Progress report on the major clinical advances in patient-oriented research into familial melanoma (2013–2018)
Recent advances in Lynch syndrome
Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis
TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort