| Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma |
|
|
|
|
|
|
|
|
|
| Case report: renal cell carcinoma segregating with a t(2;3)(q37.3;q13.2) chromosomal translocation in an Ashkenazi Jewish family |
|
|
|
|
|
|
✓ |
|
Ashkenazi Jewish family |
| Familial gastric cancer: update for practice management |
|
|
|
|
|
|
|
|
|
| A new frameshift MEN1 gene mutation associated with familial malignant insulinomas |
|
|
|
|
|
|
|
|
|
| Linkage to chromosome 2q32.2-q33.3 in familial serrated neoplasia (Jass syndrome) |
|
|
|
|
|
|
|
|
|
| Mutation analysis of the PALB2 cancer predisposition gene in familial melanoma |
|
|
|
|
|
|
|
|
|
| Deranged Wnt signaling is frequent in hereditary nonpolyposis colorectal cancer |
|
|
|
|
|
|
|
|
|
| The impact of cancer pathology confirmation on clinical management of a family history of cancer |
|
|
|
|
|
|
|
|
|
| Non-truncating hMLH1 variants identified in Slovenian gastric cancer patients are not associated with Lynch Syndrome: a functional analysis report |
|
|
|
|
|
|
|
|
|
| IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer |
|
|
|
|
|
|
|
|
|
| Mutation analysis of the APC gene in unrelated Korean patients with FAP: four novel mutations with unusual phenotype |
|
|
|
|
|
|
|
|
|
| The impact of positive cancer family history on the clinical features and outcome of patients with non-small cell lung cancer |
|
|
|
|
|
|
|
|
|
| Recent advances in the genetics of SDH-related paraganglioma and pheochromocytoma |
|
|
|
|
|
|
|
|
|
| Lack of GNAQ germline mutations in uveal melanoma patients with high risk for hereditary cancer predisposition |
|
|
|
|
|
|
|
|
|
| Two BRCA1/2 founder mutations in Jews of Sephardic origin |
|
|
|
|
|
|
✓ |
|
Jews of Sephardic origin |
| Care for patients with multiple endocrine neoplasia type 1: the current evidence base |
|
|
|
|
|
|
|
|
|
| Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis |
|
|
|
|
|
|
|
|
|
| Strictly defined familial male breast cancer |
|
|
|
|
|
|
|
|
|
| Gene expression in response to ionizing radiation and family history of gastric cancer |
|
|
|
|
|
|
|
|
|
| An analysis of the efficacy of serial screening for familial nasopharyngeal carcinoma based on Markov chain models |
|
|
|
|
|
|
|
|
|
| Colorectal cancer: no longer the issue in familial adenomatous polyposis? |
|
|
|
|
|
|
|
|
|
| Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis |
|
|
|
|
|
|
|
|
|
| Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumor |
|
|
|
|
|
|
|
|
|
| Genetic epidemiological analysis reveals a multi-gene additive model for gastric cancer |
|
|
|
|
|
|
|
|
|
| Cancer survivors: familial risk perception and management advice given to their relatives |
|
|
|
|
|
|
|
|
|
| A new mutation of BRCA2 gene in an Italian healthy woman with familial breast cancer history |
|
|
|
|
|
|
|
|
|
| An exploration of the communication preferences regarding genetic testing in individuals from families with identified breast/ovarian cancer mutations |
|
|
|
|
|
|
|
|
|
| Hereditary prostate cancer as a feature of Lynch Syndrome |
|
|
|
|
|
|
|
|
|
| BRCA1 mutations and colorectal cancer in Poland |
|
|
|
|
|
|
|
|
|
| Shortened time interval between colorectal cancer diagnosis and risk testing for hereditary colorectal cancer is not related to higher psychological distress |
|
|
|
|
|
|
|
|
|
| Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome |
|
|
|
|
|
|
|
|
|
| Communicating genetic risk information within families: a review |
|
|
|
|
|
|
|
|
|
| What I wish I’d known before surgery: BRCA carriers’ perspectives after bilateral salipingo-oophorectomy |
|
|
|
|
|
|
|
|
|
| A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives |
|
|
|
|
|
|
|
|
|
| PALB2: a novel inactivating mutation in a Italian breast cancer family |
|
|
|
|
|
|
|
|
|
| CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland |
|
|
|
|
|
|
|
|
|
| Contribution of CDKN2A/P16 INK4A, P14 ARF, CDK4 and BRCA1/2 germline mutations in individuals with suspected genetic predisposition to uveal melanoma |
|
|
|
|
|
|
|
|
|
| BRCA1 and BRCA2 families and the risk of skin cancer |
|
|
|
|
|
|
|
|
|
| Real world experience with cancer genetic counseling via telephone |
|
|
|
|
|
|
|
|
|
| Hereditary predisposition rather than environmental factor are likely to explain the familial link between uveal melanoma and other cancers |
|
|
|
|
|
|
|
|
|
| Thymoma associated with malignancies may herald a hereditary cancer syndrome |
|
|
|
|
|
|
|
|
|
| An intronic mutation in MLH1 associated with familial colon and breast cancer |
|
|
|
|
|
|
|
|
|
| Similarities in solar ultraviolet irradiance and other environmental factors may explain much of the family link between uveal melanoma and other cancers |
|
|
|
|
|
|
|
|
|
| Frequency of extracolonic tumors in Brazilian families with Lynch syndrome: analysis of a hereditary colorectal cancer institutional registry |
|
|
|
|
|
|
|
|
|
| Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer |
|
|
|
|
|
|
✓ |
|
French Canadian |
| A functional varient in microRNA-146a is associated with risk of esophageal squamous cell carcinoma in Chinese Han |
|
|
|
|
|
|
|
|
|
| Regular surveillance for Li-fraumeni syndrome: advice, adherence and perceived benefits |
|
|
|
|
|
|
|
|
|
| MYH biallelic mutation can inactivate the two genetic pathways of colorectal cancer by APC or MLH1 transversions |
|
|
|
|
|
|
|
|
|
| Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters |
|
|
|
|
|
|
|
|
|
| Pancreatic cancer risk counselling and screening: impact on perceived risk and psychological functioning |
|
|
|
|
|
|
|
|
|
| Papillary thyroid cancer in a patient with MUTYH-associated polyposis (MAP) |
|
|
|
|
|
|
|
|
|
| The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers |
|
|
|
|
|
|
|
|
|
| Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives |
|
|
|
|
|
|
|
|
|
| Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations |
|
|
|
|
|
|
|
|
|
| Selective COX-2 inhibition affects fatty acids, but not COX mRNA expression in patients with FAP |
|
|
|
|
|
|
|
|
|
| Peutz-Jeghers syndrome: a study of long-term surgical morbidity and causes of mortality |
|
|
|
|
|
|
|
|
|
| A novel mutation of the Succinate Dehydrogenase B Gene in a Korean Family with Pheochromocytoma |
|
|
|
|
|
|
|
|
|
| Complete BRCA mutation screening in breast and ovarian cancer predisposition families from a North-Eastern Romanian population |
|
|
|
|
|
|
|
|
|
| Screening for large genomic rearrangements of the BRIP1 and CHK1 genes in Finnish breast cancer families |
|
|
|
|
|
|
|
|
|
| Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation |
|
|
|
|
|
|
|
|
|
| Abstracts 3rd Biennial Meeting of InSiGHT (International Society for Gastrointestinal Hereditary Tumours) |
|
|
|
|
|
|
|
|
|
| Can a phenotype for recessive inheritance in breast cancer be defined? |
|
|
|
|
|
|
|
|
|
| Report of the Combined Meeting of the International Society for Gastrointestinal Hereditary Tumours, the Human Variome Project and the National Cancer Institute Colon Cancer Family Registry, Duesseldo |
|
|
|
|
|
|
|
|
|
| FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review |
|
|
|
|
|
|
|
|
|
| Erratum to: Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation |
|
|
|
|
|
|
|
|
|
| Breast cancer susceptibility variants alter risk in familial ovarian cancer |
|
|
|
|
|
|
|
|
|
| Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of PENN II model to previous study |
|
|
|
|
|
|
|
|
|
| Magnetic resonance colonography for colorectal cancer screening in patients with Lynch syndrome gene mutation |
|
|
|
|
|
|
|
|
|
| Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations |
|
|
|
|
|
|
|
|
|
| Survey of familial glioma and role of germline p16 INK4A /p14 ARF and p53 mutation |
|
|
|
|
|
|
|
|
|
| Successful oxytocin-assisted nipple aspiration in women at increased risk for breast cancer |
|
|
|
|
|
|
|
|
|
| Surgical prophylaxis in familial adenomatous polyposis: do pre-existing desmoids outside the abdominal cavity matter? |
|
|
|
|
|
|
|
|
|
| Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes |
|
|
|
|
|
|
|
|
|
| Familial adenomatous polyposis (FAP) and gender. Does gender influence the genetic transmission of FAP? |
|
|
|
|
|
|
|
|
|
| Screening for germline DND1 mutations in testicular cancer patients |
|
|
|
|
|
|
|
|
|
| Differences in clinical and pathological characteristics of colorectal cancer in Arab as compared to Jewish patients in Northern Israel |
|
|
|
|
|
|
|
|
|
| Atypical identification of Lynch syndrome by immunohistochemistry and microsatellite instability analysis on jejunal adenocarcinoma |
|
|
|
|
|
|
|
|
|
| Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland |
|
|
|
|
|
|
|
|
|
| RASSF1A polymorphism in familial breast cancer |
|
|
|
|
|
|
|
|
|
| Analysis of mismatch repair gene mutations in Turkish HNPCC patients |
|
|
|
|
|
|
|
|
|
| Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers |
|
|
|
|
|
|
|
|
|
| The Second Birt Hogg Dubé Symposium |
|
|
|
|
|
|
|
|
|
| Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis |
|
|
|
|
|
|
|
|
|
| Location in the large bowel influences the APC mutations observed in FAP adenomas |
|
|
|
|
|
|
|
|
|
| Prevalence of BRCA2 and CDKN2a mutations in German familial pancreatic cancer families |
|
|
|
|
|
|
|
|
|
| Relationship of BRCA1 and BRCA2 mutations with cancer burden in the family and tumor incidence |
|
|
|
|
|
|
|
|
|
| Cancer family history characterization in an unselected cohort of 121 patients with uveal melanoma |
|
|
|
|
|
|
|
|
|
| Can self-esteem, mastery and perceived stigma predict long-term adjustment in women carrying a BRCA1/2-mutation? Evidence from a multi-center study |
|
|
|
|
|
|
|
|
|
| Assessment of clinical practices among cancer genetic counselors |
|
|
|
|
|
|
|
|
|
| Carney triad versus Carney Stratakis syndrome: two cases which illustrate the difficulty in distinguishing between these conditions in individual patients |
|
|
|
|
|
|
|
|
|
| “I have always believed I was at high risk…” The role of expectation in emotional responses to the receipt of an average, moderate or high cancer genetic risk assessment result: a thematic analysis of |
|
|
|
|
|
|
|
|
|
| Introduction |
|
|
|
|
|
|
|
|
|
| High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome |
|
|
|
|
|
|
|
|
|
| Update multiple endocrine neoplasia type 2 |
|
|
|
|
|
|
|
|
|
| Pregnancy after prophylactic total gastrectomy |
|
|
|
|
|
|
|
|
|
| Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome |
|
|
|
|
|
|
|
|
|
| LOH analysis should not be used as a tool to assess whether UVs of BRCA1/2 are pathogenic or not |
|
|
|
|
|
|
|
|
|
| A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma |
|
|
|
|
|
|
|
|
|