Similar articles for PMID: 12624141

Year	Number of Results
1994	1
1995	1
1996	1
1997	4
1998	8
1999	4
2000	6
2001	9
2002	13
2003	13
2004	10
2005	14
2006	1
2011	1
2013	1
2024	0

1

Cancer risk in 348 French MSH2 or MLH1 gene carriers.

Parc Y, Boisson C, Thomas G, Olschwang S. Parc Y, et al. J Med Genet. 2003 Mar;40(3):208-13. doi: 10.1136/jmg.40.3.208. J Med Genet. 2003. PMID: 12624141 Free PMC article. No abstract available.

2

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

Vasen HF, Stormorken A, Menko FH, Nagengast FM, Kleibeuker JH, Griffioen G, Taal BG, Moller P, Wijnen JT. Vasen HF, et al. J Clin Oncol. 2001 Oct 15;19(20):4074-80. doi: 10.1200/JCO.2001.19.20.4074. J Clin Oncol. 2001. PMID: 11600610

3

Colorectal and extracolonic cancer variations in MLH1/MSH2 hereditary nonpolyposis colorectal cancer kindreds and the general population.

Lin KM, Shashidharan M, Ternent CA, Thorson AG, Blatchford GJ, Christensen MA, Lanspa SJ, Lemon SJ, Watson P, Lynch HT. Lin KM, et al. Dis Colon Rectum. 1998 Apr;41(4):428-33. doi: 10.1007/BF02235755. Dis Colon Rectum. 1998. PMID: 9559626

4

Genetic testing in hereditary non-polyposis colorectal cancer families with a MSH2, MLH1, or MSH6 mutation.

Wagner A, Tops C, Wijnen JT, Zwinderman K, van der Meer C, Kets M, Niermeijer MF, Klijn JG, Tibben A, Vasen HF, Meijers-Heijboer H. Wagner A, et al. J Med Genet. 2002 Nov;39(11):833-7. doi: 10.1136/jmg.39.11.833. J Med Genet. 2002. PMID: 12414824 Free PMC article. No abstract available.

5

Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer.

Lin KM, Shashidharan M, Thorson AG, Ternent CA, Blatchford GJ, Christensen MA, Watson P, Lemon SJ, Franklin B, Karr B, Lynch J, Lynch HT. Lin KM, et al. J Gastrointest Surg. 1998 Jan-Feb;2(1):67-71. doi: 10.1016/s1091-255x(98)80105-4. J Gastrointest Surg. 1998. PMID: 9841970

6

Clinical findings with implications for genetic testing in families with clustering of colorectal cancer.

Wijnen JT, Vasen HF, Khan PM, Zwinderman AH, van der Klift H, Mulder A, Tops C, Møller P, Fodde R. Wijnen JT, et al. N Engl J Med. 1998 Aug 20;339(8):511-8. doi: 10.1056/NEJM199808203390804. N Engl J Med. 1998. PMID: 9709044 Free article.

7

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.

Plaschke J, Engel C, Krüger S, Holinski-Feder E, Pagenstecher C, Mangold E, Moeslein G, Schulmann K, Gebert J, von Knebel Doeberitz M, Rüschoff J, Loeffler M, Schackert HK. Plaschke J, et al. J Clin Oncol. 2004 Nov 15;22(22):4486-94. doi: 10.1200/JCO.2004.02.033. Epub 2004 Oct 13. J Clin Oncol. 2004. PMID: 15483016

8

Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer.

Piñol V, Castells A, Andreu M, Castellví-Bel S, Alenda C, Llor X, Xicola RM, Rodríguez-Moranta F, Payá A, Jover R, Bessa X; Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Piñol V, et al. JAMA. 2005 Apr 27;293(16):1986-94. doi: 10.1001/jama.293.16.1986. JAMA. 2005. PMID: 15855432

9

Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer.

Caldés T, Godino J, Sanchez A, Corbacho C, De la Hoya M, Lopez Asenjo J, Saez C, Sanz J, Benito M, Ramon Y Cajal S, Diaz-Rubio E. Caldés T, et al. Oncol Rep. 2004 Sep;12(3):621-9. Oncol Rep. 2004. PMID: 15289847

10

Identifying hereditary nonpolyposis colorectal cancer.

Lynch HT, Smyrk TC. Lynch HT, et al. N Engl J Med. 1998 May 21;338(21):1537-8. doi: 10.1056/NEJM199805213382109. N Engl J Med. 1998. PMID: 9593794 No abstract available.

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