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Colaris Clinical References

Aarnio M, Sankila R, Pukkala E, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer. 1999;81:214-218.
Aarnio M, Mecklin JP, Aaltonen LA, et al. Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome. Int J Cancer. 1995;64:430-3.

Burke W, Petersen G, Lynch P, et al. Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium. JAMA. 1997;277:915-9.

Caduff RF, Johnston CM, Svoboda-Newman SM, Poy EL, et al. Clinical and pathological significance of microsatellite instability in sporadic endometrial carcinoma. Am J Pathol. 1996:148:1671-1678.

Jarvinen HJ, Aarnio M, Mustonen H, et al. Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer. Gastroenterology. 2000;118:829-34.

Kowalski LD, Mutch DG, Herzog TJ, et al. Mutational analysis of MLH1 and MSH2 in 25 prospectively acquired RER+ endometrial cancers. Genes Chromosomes Cancer. 1997;18:219-227.

Kraus C, Kastl S, Gunther K, et al. A proven de novo germline mutation in HNPCC. J Med Genet. 1999;36:919-921.

Liu B, Parsons R, Papadopolous N, et al. Analysis of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients. Nat Med. 1996;2:169-174.

Liu B, Parsons RE, Hamilton SR, et al. hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds. Cancer Res. 1994;54:4590-4594.

Lynch H, Smyrk T. Hereditary nonpolyposis colorectal cancer (Lynch Syndrome): an updated review. Cancer. 1996;78:1149-1167.

Lynch HT, Fusaro RM, Lynch JF. Cancer genetics in the new era of molecular biology. Ann N Y Acad Sci. 1997;833:1-28.

Mecklin J-P, Sipponen P, Jarvinen HJ. Histopathology of colorectal carcinomas and adenomas in cancer family syndrome. Dis Colon Rectum. 1986;29:849.

Miyaki M, Konishi M, Tanaka K, et al. Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat Genet. 1997;17:271-272.

Nagy R, Sweet K, Eng C. Highly penetrant hereditary cancer syndromes. Oncogene. 2004;23:6445-70.

Nicolaides NC, Papadophoulos N, Liu B, et al. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature. 1994;371:75-80.

Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines. J Natl Cancer Inst. 1997;89:1758-1762.

Papadopoulos N, Nicolaides NC, Wei YF, et al. Mutation of a mutL homolog in hereditary colon cancer. Science. 1994;263:1625-1629.

Park JG, Vasen HFA, Park KJ, et al. Suspected hereditary nonpolyposis colorectal cancer — International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC) criteria and results of genetic diagnosis. Dis Colon Rectum. 1999;42:710-715.

Risinger JI, Berchuch A, Kohler MF, et al. Genetic instability of microsatellites in endometrial carcinoma. Cancer Res. 1993;53:5100-5103.

Salovaara R, Loukola A, Kristo P, et al. Population-based molecular detection of hereditary nonpolyposis colorectal cancer. J Clin Oncol. 2000;11:2193-200.

Sutter C, Gebert J, Bischoff P, et al. Molecular screening of potential HNPCC patients using a multiplex microsatellite PCR system. Mol Cell Probes. 1999;13:157-165.

Vasen HFA, Mecklin J-P, Meera Khan P, Lych HT. The International Collaborative Group on Hereditary Non-polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum. 1991;34:424-425.

Vasen HFA, Vignen J, Menko FH, et al. Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis. Gastroenterology 1996;110:1020-1027.

Vasen HFA, Watson P, Mecklin J-P, Lynch HT, and the ICG-HNPCC. New clinical criteria for hereditary non-polyposis colorectal cancer (HNPCC, Lynch Syndrome) proposed by the International Collaborative Group on HNPCC. Gastroenterology. 1999;116:1453-1456.

Wijnen JT, Vasen HFA, Meera Khan P, et al. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. N Eng J Med. 1998;339:511-518.

Wu Y, Nystrom-Lahti M, Osinga J, et al. MSH2 and MLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimentional DNA electrophoresis. Genes Chromosomes Cancer. 1997;18:269-278.

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