[Hereditary diffuse gastric cancer (HDGC): presentation of a family with a new mutation of the CDH1 gene]. |
17955726 |
Acta Gastroenterol Latinoam |
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States. |
14871915 |
JAMA |
Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR). |
18383312 |
Hum Mutat |
Advances in counselling and surveillance of patients at risk for pancreatic cancer. |
17872573 |
Gut |
Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers. |
17245541 |
Breast Cancer Res Treat |
American founder mutation for Lynch syndrome. Prevalence estimates and implications. |
16353207 |
Cancer |
BRCA1 and pancreatic cancer: pedigree findings and their causal relationships. |
15796958 |
Cancer Genet Cytogenet |
Cancer in Jews: introduction and overview. |
15516840 |
Fam Cancer |
Cancer risk in mismatch repair gene mutation carriers. |
14574017 |
Fam Cancer |
Carrier risk status changes resulting from mutation testing in hereditary non-polyposis colorectal cancer and hereditary breast-ovarian cancer. |
12920070 |
J Med Genet |
Challenging colonic polyposis pedigrees: differential diagnosis, surveillance, and management concerns. |
14734220 |
Cancer Genet Cytogenet |
Challenging pancreatic cancer-prone pedigrees: a nosologic dilemma. |
12492191 |
Am J Gastroenterol |
Colon cancer screening practices following genetic testing for hereditary nonpolyposis colon cancer (HNPCC) mutations. |
15451763 |
Arch Intern Med |
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers. |
18355772 |
Am J Hum Genet |
Downregulation of death-associated protein kinase 1 (DAPK1) in chronic lymphocytic leukemia. |
17540169 |
Cell |
Familial adenomatous polyposis and extracolonic cancer. |
11713930 |
Dig Dis Sci |
Familial adenomatous polyposis in children younger than age ten years: a multidisciplinary clinic experience. |
18157572 |
Dis Colon Rectum |
Familial multiple myeloma: a family study and review of the literature. |
11584064 |
J Natl Cancer Inst |
Familial pancreatic carcinoma in Jews. |
15516847 |
Fam Cancer |
Familial sarcoma: challenging pedigrees. |
14584079 |
Cancer |
Family with acute myelocytic leukemia, breast, ovarian, and gastrointestinal cancer. |
12377407 |
Cancer Genet Cytogenet |
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. |
17545690 |
JAMA |
Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international study. |
18381420 |
Cancer Res |
Gastric cancer: new genetic developments. |
15895459 |
J Surg Oncol |
Germline RAP80 mutations and susceptibility to breast cancer. |
18306035 |
Breast Cancer Res Treat |
Hereditary breast cancer: part I. Diagnosing hereditary breast cancer syndromes. |
18086272 |
Breast J |
Hereditary breast cancer: part II. Management of hereditary breast cancer: implications of molecular genetics and pathology. |
18086271 |
Breast J |
Hereditary breast-ovarian cancer at the bedside: role of the medical oncologist. |
12586815 |
J Clin Oncol |
Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. |
17381417 |
Future Oncol |
Hereditary cancer: family history, diagnosis, molecular genetics, ecogenetics, and management strategies. |
11900873 |
Biochimie |
Hereditary chronic lymphocytic leukemia: an extended family study and literature review. |
12407690 |
Am J Med Genet |
Hereditary colorectal cancer. |
12621137 |
N Engl J Med |
Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy. |
18442100 |
Cancer |
Hereditary nonpolyposis colorectal cancer (Lynch Syndrome) in Argentina: report from a referral hospital register. |
17846840 |
Dis Colon Rectum |
Hereditary nonpolyposis colorectal carcinoma (HNPCC) and HNPCC-like families: Problems in diagnosis, surveillance, and management. |
14692024 |
Cancer |
History and molecular genetics of Lynch syndrome in family G: a century later. |
16264161 |
JAMA |
Immunology and the Lynch syndrome. |
18395102 |
Gastroenterology |
Inflammatory bowel disease in Ashkenazi Jews: implications for familial colorectal cancer. |
15516846 |
Fam Cancer |
Inherited predisposition to cancer: a historical overview. |
15264268 |
Am J Med Genet C Semin Med Genet |
International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriers. |
18196574 |
Int J Cancer |
Intra-abdominal carcinomatosis after prophylactic oophorectomy in women of hereditary breast ovarian cancer syndrome kindreds associated with BRCA1 and BRCA2 mutations. |
15863145 |
Gynecol Oncol |
Loss of surface and cyst epithelial basement membranes and preneoplastic morphologic changes in prophylactic oophorectomies. |
14669280 |
Cancer |
Lynch syndrome and the role of the registered nurse: commentary on "hereditary nonpolyposis colorectal cancer (Lynch syndrome): molecular pathogenesis and clinical approaches ti diagnosis and management for nurses". |
18077772 |
Biol Res Nurs |
Lynch syndrome: genetics, natural history, genetic counseling, and prevention. |
11060321 |
J Clin Oncol |
Lynch syndrome: history and current status. |
15528784 |
Dis Markers |
Multiple primary cancer, including transitional cell carcinoma of the upper uroepithelial tract in a multigeneration HNPCC family: molecular genetic, diagnostic, and management implications. |
12650804 |
Am J Gastroenterol |
Mutational load distribution analysis yields metrics reflecting genetic instability during pancreatic carcinogenesis. |
18337498 |
Proc Natl Acad Sci U S A |
Origins and prevalence of the American Founder Mutation of MSH2. |
18381419 |
Cancer Res |
Patient responses to the disclosure of BRCA mutation tests in hereditary breast-ovarian cancer families. |
16527602 |
Cancer Genet Cytogenet |
Phenotypic and genotypic heterogeneity in the Lynch syndrome: diagnostic, surveillance and management implications. |
16479259 |
Eur J Hum Genet |
Phenotypic heterogeneity in multiple myeloma families. |
15681516 |
J Clin Oncol |
Phenotypic variation in eight extended CDKN2A germline mutation familial atypical multiple mole melanoma-pancreatic carcinoma-prone families: the familial atypical mole melanoma-pancreatic carcinoma syndrome. |
11815963 |
Cancer |
Predictors of contralateral prophylactic mastectomy in women with a BRCA1 or BRCA2 mutation: the Hereditary Breast Cancer Clinical Study Group. |
18195327 |
J Clin Oncol |
RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. |
17999359 |
Am J Hum Genet |
Risk-reducing salpingo-oophorectomy for the prevention of BRCA1- and BRCA2-associated breast and gynecologic cancer: a multicenter, prospective study. |
18268356 |
J Clin Oncol |
Screening adherence in BRCA1/2 families is associated with primary physicians' behavior. |
14755459 |
Am J Med Genet A |
The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome. |
18398828 |
Int J Cancer |
Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay. |
12660027 |
Cancer Genet Cytogenet |
Toward a consensus in molecular diagnosis of hereditary nonpolyposis colorectal cancer (Lynch syndrome). |
17312298 |
J Natl Cancer Inst |
Tumor-infiltrating lymphocytes are a marker for microsatellite instability in colorectal carcinoma. |
11413533 |
Cancer |
Understanding the development of human bladder cancer by using a whole-organ genomic mapping strategy. |
18458673 |
Lab Invest |
Who should be sent for genetic testing in hereditary colorectal cancer syndromes? |
17687158 |
J Clin Oncol |