Watson P - Search Results

1

Prediction of germline mutations and cancer risk in the Lynch syndrome.

Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K, Watson P, Gruber SB, Euhus D, Kinzler KW, Jass J, Gallinger S, Lindor NM, Casey G, Ellis N, Giardiello FM, Offit K, Parmigiani G; Colon Cancer Family Registry. Chen S, et al. Among authors: watson p. JAMA. 2006 Sep 27;296(12):1479-87. doi: 10.1001/jama.296.12.1479. JAMA. 2006. PMID: 17003396 Free PMC article.

2

Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard.

Chen S, Watson P, Parmigiani G. Chen S, et al. Among authors: watson p. Biostatistics. 2005 Jul;6(3):450-64. doi: 10.1093/biostatistics/kxi021. Epub 2005 Apr 14. Biostatistics. 2005. PMID: 15831578 Free PMC article.

3

History and molecular genetics of Lynch syndrome in family G: a century later.

Douglas JA, Gruber SB, Meister KA, Bonner J, Watson P, Krush AJ, Lynch HT. Douglas JA, et al. Among authors: watson p. JAMA. 2005 Nov 2;294(17):2195-202. doi: 10.1001/jama.294.17.2195. JAMA. 2005. PMID: 16264161

4

Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.

Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, Jass JR, Dunlop M, Wyllie A, Peltomäki P, de la Chapelle A, Hamilton SR, Vogelstein B, Kinzler KW. Liu B, et al. Among authors: watson p. Nat Med. 1996 Feb;2(2):169-74. doi: 10.1038/nm0296-169. Nat Med. 1996. PMID: 8574961

5

Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR).

Chao EC, Velasquez JL, Witherspoon MS, Rozek LS, Peel D, Ng P, Gruber SB, Watson P, Rennert G, Anton-Culver H, Lynch H, Lipkin SM. Chao EC, et al. Among authors: watson p. Hum Mutat. 2008 Jun;29(6):852-60. doi: 10.1002/humu.20735. Hum Mutat. 2008. PMID: 18383312 Free article.

6

Tobacco use and increased colorectal cancer risk in patients with hereditary nonpolyposis colorectal cancer (Lynch syndrome).

Watson P, Ashwathnarayan R, Lynch HT, Roy HK. Watson P, et al. Arch Intern Med. 2004 Dec 13-27;164(22):2429-31. doi: 10.1001/archinte.164.22.2429. Arch Intern Med. 2004. PMID: 15596632

7

The epidemiology of endometrial cancer in hereditary nonpolyposis colorectal cancer.

Vasen HF, Watson P, Mecklin JP, Jass JR, Green JS, Nomizu T, Müller H, Lynch HT. Vasen HF, et al. Among authors: watson p. Anticancer Res. 1994 Jul-Aug;14(4B):1675-8. Anticancer Res. 1994. PMID: 7979205

8

TGFBR1*6A may contribute to hereditary colorectal cancer.

Bian Y, Caldes T, Wijnen J, Franken P, Vasen H, Kaklamani V, Nafa K, Peterlongo P, Ellis N, Baron JA, Burn J, Moeslein G, Morrison PJ, Chen Y, Ahsan H, Watson P, Lynch HT, de la Chapelle A, Fodde R, Pasche B. Bian Y, et al. Among authors: watson p. J Clin Oncol. 2005 May 1;23(13):3074-8. doi: 10.1200/JCO.2005.00.281. J Clin Oncol. 2005. PMID: 15860866

9

The tumor spectrum in the Lynch syndrome.

Watson P, Riley B. Watson P, et al. Fam Cancer. 2005;4(3):245-8. doi: 10.1007/s10689-004-7994-z. Fam Cancer. 2005. PMID: 16136385 Review.

10

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.

Liu B, Parsons RE, Hamilton SR, Petersen GM, Lynch HT, Watson P, Markowitz S, Willson JK, Green J, de la Chapelle A, et al. Liu B, et al. Among authors: watson p. Cancer Res. 1994 Sep 1;54(17):4590-4. Cancer Res. 1994. PMID: 8062247

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