Watson P - Search Results

1

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.

2

Cancer risk in mismatch repair gene mutation carriers.

Watson P, Lynch HT. Watson P, et al. Fam Cancer. 2001;1(1):57-60. doi: 10.1023/a:1011590617833. Fam Cancer. 2001. PMID: 14574017 Review.

3

Multiple HNPCC tumours: ask the family!

Lynch HT, Watson P. Lynch HT, et al. Among authors: watson p. Gut. 1998 Nov;43(5):596-7. doi: 10.1136/gut.43.5.596. Gut. 1998. PMID: 9824333 Free PMC article. No abstract available.

4

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

5

Extracolonic cancer in hereditary nonpolyposis colorectal cancer.

Watson P, Lynch HT. Watson P, et al. Cancer. 1993 Feb 1;71(3):677-85. doi: 10.1002/1097-0142(19930201)71:3<677::aid-cncr2820710305>3.0.co;2-#. Cancer. 1993. PMID: 8431847

6

A nonsense mutation in MLH1 causes exon skipping in three unrelated HNPCC families.

Stella A, Wagner A, Shito K, Lipkin SM, Watson P, Guanti G, Lynch HT, Fodde R, Liu B. Stella A, et al. Among authors: watson p. Cancer Res. 2001 Oct 1;61(19):7020-4. Cancer Res. 2001. PMID: 11585727

7

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

8

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

Wagner A, Barrows A, Wijnen JT, van der Klift H, Franken PF, Verkuijlen P, Nakagawa H, Geugien M, Jaghmohan-Changur S, Breukel C, Meijers-Heijboer H, Morreau H, van Puijenbroek M, Burn J, Coronel S, Kinarski Y, Okimoto R, Watson P, Lynch JF, de la Chapelle A, Lynch HT, Fodde R. Wagner A, et al. Among authors: watson p. Am J Hum Genet. 2003 May;72(5):1088-100. doi: 10.1086/373963. Epub 2003 Mar 25. Am J Hum Genet. 2003. PMID: 12658575 Free PMC article.

9

The tumor spectrum in HNPCC.

Watson P, Lynch HT. Watson P, et al. Anticancer Res. 1994 Jul-Aug;14(4B):1635-9. Anticancer Res. 1994. PMID: 7979199 Review.

10

AFAP: variety is the spice of life.

Lynch HT, Watson P. Lynch HT, et al. Among authors: watson p. Gut. 1998 Oct;43(4):451-2. doi: 10.1136/gut.43.4.451a. Gut. 1998. PMID: 9824565 Free PMC article. No abstract available.

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