PubMed (cited) for id: 609310

Year	Number of Results
1991	1
1993	1
1994	5
1995	1
1997	1
1999	1
2000	1
2001	2
2002	1
2008	1
2009	3
2010	1
2013	1
2024	0

1

Cancer risks for MLH1 and MSH2 mutation carriers.

Dowty JG, Win AK, Buchanan DD, Lindor NM, Macrae FA, Clendenning M, Antill YC, Thibodeau SN, Casey G, Gallinger S, Marchand LL, Newcomb PA, Haile RW, Young GP, James PA, Giles GG, Gunawardena SR, Leggett BA, Gattas M, Boussioutas A, Ahnen DJ, Baron JA, Parry S, Goldblatt J, Young JP, Hopper JL, Jenkins MA. Dowty JG, et al. Hum Mutat. 2013 Mar;34(3):490-7. doi: 10.1002/humu.22262. Hum Mutat. 2013. PMID: 23255516 Free PMC article.

2

Risk of urothelial bladder cancer in Lynch syndrome is increased, in particular among MSH2 mutation carriers.

van der Post RS, Kiemeney LA, Ligtenberg MJ, Witjes JA, Hulsbergen-van de Kaa CA, Bodmer D, Schaap L, Kets CM, van Krieken JH, Hoogerbrugge N. van der Post RS, et al. J Med Genet. 2010 Jul;47(7):464-70. doi: 10.1136/jmg.2010.076992. J Med Genet. 2010. PMID: 20591884 Free PMC article.

3

Risk of pancreatic cancer in families with Lynch syndrome.

Kastrinos F, Mukherjee B, Tayob N, Wang F, Sparr J, Raymond VM, Bandipalliam P, Stoffel EM, Gruber SB, Syngal S. Kastrinos F, et al. JAMA. 2009 Oct 28;302(16):1790-5. doi: 10.1001/jama.2009.1529. JAMA. 2009. PMID: 19861671 Free PMC article.

4

Germ line MLH1 and MSH2 mutations in Taiwanese Lynch syndrome families: characterization of a founder genomic mutation in the MLH1 gene.

Tang R, Hsiung C, Wang JY, Lai CH, Chien HT, Chiu LL, Liu CT, Chen HH, Wang HM, Chen SX, Hsieh LL; TCOG HNPCC Consortium. Tang R, et al. Clin Genet. 2009 Apr;75(4):334-45. doi: 10.1111/j.1399-0004.2009.01162.x. Clin Genet. 2009. PMID: 19419416

5

The G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndrome.

Clyne M, Offman J, Shanley S, Virgo JD, Radulovic M, Wang Y, Ardern-Jones A, Eeles R, Hoffmann E, Yu VP. Clyne M, et al. Br J Cancer. 2009 Jan 27;100(2):376-80. doi: 10.1038/sj.bjc.6604860. Epub 2009 Jan 13. Br J Cancer. 2009. PMID: 19142183 Free PMC article.

6

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations.

Barrow E, Alduaij W, Robinson L, Shenton A, Clancy T, Lalloo F, Hill J, Evans DG. Barrow E, et al. Clin Genet. 2008 Sep;74(3):233-42. doi: 10.1111/j.1399-0004.2008.01035.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18554281

7

Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.

Cravo M, Afonso AJ, Lage P, Albuquerque C, Maia L, Lacerda C, Fidalgo P, Chaves P, Cruz C, Nobre-Leitão C. Cravo M, et al. Gut. 2002 Mar;50(3):405-12. doi: 10.1136/gut.50.3.405. Gut. 2002. PMID: 11839723 Free PMC article.

8

The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas.

Cunningham JM, Kim CY, Christensen ER, Tester DJ, Parc Y, Burgart LJ, Halling KC, McDonnell SK, Schaid DJ, Walsh Vockley C, Kubly V, Nelson H, Michels VV, Thibodeau SN. Cunningham JM, et al. Am J Hum Genet. 2001 Oct;69(4):780-90. doi: 10.1086/323658. Epub 2001 Aug 24. Am J Hum Genet. 2001. PMID: 11524701 Free PMC article.

9

Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds.

Scott RJ, McPhillips M, Meldrum CJ, Fitzgerald PE, Adams K, Spigelman AD, du Sart D, Tucker K, Kirk J. Scott RJ, et al. Am J Hum Genet. 2001 Jan;68(1):118-127. doi: 10.1086/316942. Epub 2000 Dec 7. Am J Hum Genet. 2001. PMID: 11112663 Free PMC article.

10

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer.

Bapat BV, Madlensky L, Temple LK, Hiruki T, Redston M, Baron DL, Xia L, Marcus VA, Soravia C, Mitri A, Shen W, Gryfe R, Berk T, Chodirker BN, Cohen Z, Gallinger S. Bapat BV, et al. Hum Genet. 1999 Feb;104(2):167-76. doi: 10.1007/s004390050931. Hum Genet. 1999. PMID: 10190329

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