| Initial clinical validation of Health Heritage, a patient-facing tool for personal and family history collection and cancer risk assessment |
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| Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defect |
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| Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer |
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| Risk of thyroid cancer among Caribbean Hispanic patients with familial adenomatous polyposis |
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| Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients |
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| Determining the familial risk distribution of colorectal cancer: a data mining approach |
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| Mismatch repair deficiency concordance between primary colorectal cancer and corresponding metastasis |
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| Associations between allergic conditions and pediatric brain tumors in Neurofibromatosis type 1 |
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| Screening of the BRCA1 gene in Brazilian patients with breast and/or ovarian cancer via high-resolution melting reaction analysis |
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| Non-genetic health professionals’ attitude towards, knowledge of and skills in discussing and ordering genetic testing for hereditary cancer |
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| Erratum to: Methylation of the miR-126 gene associated with glioma progression |
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| Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis? |
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| Development of a novel PTT assay for mutation detection in PALB2 large exons and PALB2 screening in medullary breast cancer |
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| Correlation between the germline methylation status in ERβ promoter and the risk in prostate cancer: a prospective study |
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| CYP1A1 and GSTP1 gene variations in breast cancer: a systematic review and case–control study |
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| Diagnostic values of osteopontin combined with CA125 for ovarian cancer: a meta-analysis |
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| Methylation of the miR-126 gene associated with glioma progression |
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| Surveillance using capsule endoscopy is safe in post-colectomy patients with familial adenomatous polyposis: a prospective Japanese study |
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| Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary |
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| Genetic testing for Lynch syndrome: family communication and motivation |
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| Germline TERT promoter mutations are rare in familial melanoma |
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| Association between the FTOrs8050136 polymorphism and cancer risk: a meta-analysis |
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| Aortopulmonary window parathyroid gland causing primary hyperparathyroidism in men type 1 syndrome |
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| First report of somatic mosaicism for mutations in STK11 in four patients with Peutz–Jeghers syndrome |
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| Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer? |
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| Screening of HELQ in breast and ovarian cancer families |
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| Birt–Hogg–Dubé syndrome: novel FLCN frameshift deletion in daughter and father with renal cell carcinomas |
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| Rhabdoid tumor predisposition syndrome caused by SMARCB1 constitutional deletion: prenatal detection of new case of recurrence in siblings due to gonadal mosaicism |
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| The knowledge value-chain of genetic counseling for breast cancer: an empirical assessment of prediction and communication processes |
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| Association of APC I1307K and E1317Q polymorphisms with colorectal cancer among Egyptian subjects |
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| The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer |
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| Ovarian tumors related to intronic mutations in DICER1: a report from the international ovarian and testicular stromal tumor registry |
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| Incidental diagnosis of HLRCC following investigation for Asperger Syndrome: actionable and actioned |
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| Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patient |
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| Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives |
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✓ |
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Chinese |
| POLE mutations in families predisposed to cutaneous melanoma |
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| The effect of personal medical history and family history of cancer on the uptake of risk-reducing salpingo-oophorectomy |
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| Risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: a 30-year semi-prospective analysis |
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| Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene |
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| Risk reducing salpingectomy and delayed oophorectomy in high risk women: views of cancer geneticists, genetic counsellors and gynaecological oncologists in the UK |
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| Massive gastric polyposis associated with a germline SMAD4 gene mutation |
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| Metastatic sympathetic paraganglioma in a patient with loss of the SDHC gene |
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| Challenges to clinical utilization of hereditary cancer gene panel testing: perspectives from the front lines |
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| High accuracy of family history of melanoma in Danish melanoma cases |
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| BRCA1 gene variant p.P142H associated with male breast cancer: a two-generation genealogic study and literature review |
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| Supporting families with Cancer: A patient centred survivorship model of care |
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| Coexistence of paraganglioma/pheochromocytoma and papillary thyroid carcinoma: a four-case series analysis |
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| Follicular variant of papillary thyroid cancer in Alström syndrome |
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| BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study |
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| A functional HOTAIR rs920778 polymorphism does not contributes to gastric cancer in a Turkish population: a case–control study |
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✓ |
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Turkish population |
| International society for gastrointestinal hereditary tumours—InSiGHT |
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| Psychological distress related to BRCA testing in ovarian cancer patients |
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| Prevalence and detection of psychosocial problems in cancer genetic counseling |
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| Survival in familial colorectal cancer: a Danish cohort study |
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| Childhood cancers in families with and without Lynch syndrome |
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| Genotype–phenotype analysis of von Hippel–Lindau syndrome in fifteen Indian families |
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| Birt–Hogg–Dubé syndrome and intracranial vascular pathologies |
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| 3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity |
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| Zebrafish xenotransplantation as a tool for in vivo cancer study |
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| A novel POLE mutation associated with cancers of colon, pancreas, ovaries and small intestine |
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| Specific Alu elements involved in a significant percentage of copy number variations of the STK11 gene in patients with Peutz–Jeghers syndrome |
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| Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study |
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| Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews |
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✓ |
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North-African Jews |
| Erratum to: Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers |
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| Implementing a telephone based peer support intervention for women with a BRCA1/2 mutation |
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| Germline mutations predisposing to non-small cell lung cancer |
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| Validation of an online questionnaire for identifying people at risk of familial and hereditary colorectal cancer |
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| Clinical characterization and mutation spectrum in Caribbean Hispanic families with Lynch syndrome |
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| Pitfalls in the diagnosis of biallelic PMS2 mutations |
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| Genetic screening in patients with Retinoblastoma in Israel |
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| The analysis of a large Danish family supports the presence of a susceptibility locus for adenoma and colorectal cancer on chromosome 11q24 |
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| Mutations of HNRNPA0 and WIF1 predispose members of a large family to multiple cancers |
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| The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an |
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| Heterozygous germline mutations in NBS1 among Korean patients with high-risk breast cancer negative for BRCA1/2 mutation |
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| Timing of risk reducing mastectomy in breast cancer patients carrying a BRCA1/2 mutation: retrospective data from the Dutch HEBON study |
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| Large genomic rearrangements in the familial breast and ovarian cancer gene BRCA1 are associated with an increased frequency of high risk features |
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| Polymorphisms of the XRCC1 gene and breast cancer risk in the Mexican population |
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| Analysis of PALB2 in a cohort of Italian breast cancer patients: identification of a novel PALB2 truncating mutation |
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| Defective DNA mismatch repair activity is common in sebaceous neoplasms, and may be an ineffective approach to screen for Lynch syndrome |
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| The effect of oral 3,3′-diindolylmethane supplementation on the 2:16α-OHE ratio in BRCA1 mutation carriers |
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| High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations |
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| Germline RAD51B truncating mutation in a family with cutaneous melanoma |
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| Exome sequencing reveals three novel candidate predisposition genes for diffuse gastric cancer |
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| The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers |
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| A risk of digestive tract neoplasms susceptibility in miR-146a and miR-196a2 |
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