Syngal S - Search Results

1

Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families.

Wahlberg SS, Schmeits J, Thomas G, Loda M, Garber J, Syngal S, Kolodner RD, Fox E. Wahlberg SS, et al. Among authors: syngal s. Cancer Res. 2002 Jun 15;62(12):3485-92. Cancer Res. 2002. PMID: 12067992

2

Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.

Marsh DJ, Roth S, Lunetta KL, Hemminki A, Dahia PL, Sistonen P, Zheng Z, Caron S, van Orsouw NJ, Bodmer WF, Cottrell SE, Dunlop MG, Eccles D, Hodgson SV, Järvinen H, Kellokumpu I, Markie D, Neale K, Phillips R, Rozen P, Syngal S, Vijg J, Tomlinson IP, Aaltonen LA, Eng C. Marsh DJ, et al. Among authors: syngal s. Cancer Res. 1997 Nov 15;57(22):5017-21. Cancer Res. 1997. PMID: 9371495

3

Benefits of colonoscopic surveillance and prophylactic colectomy in patients with hereditary nonpolyposis colorectal cancer mutations.

Syngal S, Weeks JC, Schrag D, Garber JE, Kuntz KM. Syngal S, et al. Ann Intern Med. 1998 Nov 15;129(10):787-96. doi: 10.7326/0003-4819-129-10-199811150-00007. Ann Intern Med. 1998. PMID: 9841584

4

Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing.

Syngal S, Fox EA, Li C, Dovidio M, Eng C, Kolodner RD, Garber JE. Syngal S, et al. JAMA. 1999 Jul 21;282(3):247-53. doi: 10.1001/jama.282.3.247. JAMA. 1999. PMID: 10422993

5

Germ-line msh6 mutations in colorectal cancer families.

Kolodner RD, Tytell JD, Schmeits JL, Kane MF, Gupta RD, Weger J, Wahlberg S, Fox EA, Peel D, Ziogas A, Garber JE, Syngal S, Anton-Culver H, Li FP. Kolodner RD, et al. Among authors: syngal s. Cancer Res. 1999 Oct 15;59(20):5068-74. Cancer Res. 1999. PMID: 10537275

6

Phenotypic characteristics associated with the APC gene I1307K mutation in Ashkenazi Jewish patients with colorectal polyps.

Syngal S, Schrag D, Falchuk M, Tung N, Farraye FA, Chung D, Wright M, Whetsell A, Miller G, Garber JE. Syngal S, et al. JAMA. 2000 Aug 16;284(7):857-60. doi: 10.1001/jama.284.7.857. JAMA. 2000. PMID: 10938175

7

Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1.

Syngal S, Fox EA, Eng C, Kolodner RD, Garber JE. Syngal S, et al. J Med Genet. 2000 Sep;37(9):641-5. doi: 10.1136/jmg.37.9.641. J Med Genet. 2000. PMID: 10978352 Free PMC article.

8

A hereditary nonpolyposis colorectal carcinoma case associated with hypermethylation of the MLH1 gene in normal tissue and loss of heterozygosity of the unmethylated allele in the resulting microsatellite instability-high tumor.

Gazzoli I, Loda M, Garber J, Syngal S, Kolodner RD. Gazzoli I, et al. Among authors: syngal s. Cancer Res. 2002 Jul 15;62(14):3925-8. Cancer Res. 2002. PMID: 12124320

9

Cancer surveillance is often inadequate in people at high risk for colorectal cancer.

Stoffel EM, Garber JE, Grover S, Russo L, Johnson J, Syngal S. Stoffel EM, et al. Among authors: syngal s. J Med Genet. 2003 May;40(5):e54. doi: 10.1136/jmg.40.5.e54. J Med Genet. 2003. PMID: 12746408 Free PMC article. No abstract available.

10

One less thing to worry about: the shrinking spectrum of tumors in BRCA founder mutation carriers.

Garber JE, Syngal S. Garber JE, et al. Among authors: syngal s. J Natl Cancer Inst. 2004 Jan 7;96(1):2-3. doi: 10.1093/jnci/djh021. J Natl Cancer Inst. 2004. PMID: 14709725 No abstract available.

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