CHEK2 1100delC and colorectal cancer. [J Med Genet. 2003] - PubMed

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The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype. [Am J Hum Genet. 2003]
The CHEK2 1100delC mutation identifies families with a hereditary breast and colorectal cancer phenotype.
Meijers-Heijboer H, Wijnen J, Vasen H, Wasielewski M, Wagner A, Hollestelle A, Elstrodt F, van den Bos R, de Snoo A, Fat GT, et al. Am J Hum Genet. 2003 May; 72(5):1308-14. Epub 2003 Apr 10.
Contribution of the CHEK2 1100delC variant to risk of multiple colorectal adenoma and carcinoma. [Cancer Lett. 2003]
Contribution of the CHEK2 1100delC variant to risk of multiple colorectal adenoma and carcinoma.
Lipton L, Fleischmann C, Sieber OM, Thomas HJ, Hodgson SV, Tomlinson IP, Houlston RS. Cancer Lett. 2003 Oct 28; 200(2):149-52.
Homozygosity for a CHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype. [J Pathol. 2005]
Homozygosity for a CHEK2*1100delC mutation identified in familial colorectal cancer does not lead to a severe clinical phenotype.
van Puijenbroek M, van Asperen CJ, van Mil A, Devilee P, van Wezel T, Morreau H. J Pathol. 2005 Jun; 206(2):198-204.
Review CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls. [J Clin Oncol. 2008]
Review CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: meta-analyses of 26,000 patient cases and 27,000 controls.
Weischer M, Bojesen SE, Ellervik C, Tybjaerg-Hansen A, Nordestgaard BG. J Clin Oncol. 2008 Feb 1; 26(4):542-8. Epub 2008 Jan 2.
Review Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene? [Fam Cancer. 2001]
Review Apparent Mendelian inheritance of breast and colorectal cancer: chance, genetic heterogeneity or a new gene?
Lipton L, Thomas HJ, Eeles RA, Houlston RS, Longmuir M, Davison R, Hodgson SV, Murday VA, Norbury CG, Taylor C, et al. Fam Cancer. 2001; 1(3-4):189-95.

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Cited by 5 PubMed Central articles

Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals. [Breast Cancer Res. 2011]
Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals.
Kuusisto KM, Bebel A, Vihinen M, Schleutker J, Sallinen SL. Breast Cancer Res. 2011 Feb 28; 13(1):R20. Epub 2011 Feb 28.
The checkpointkinase 2 (CHK2) 1100delC germ line mutation is not associated with the development of squamous cell carcinoma of the head and neck (SCCHN). [J Negat Results Biomed. 2010]
The checkpointkinase 2 (CHK2) 1100delC germ line mutation is not associated with the development of squamous cell carcinoma of the head and neck (SCCHN).
Scheckenbach K, Papadopoulou G, Hoffmann TK, Chaker A, Bier H, Schipper J, Balz V, Wagenmann M. J Negat Results Biomed. 2010 Dec 25; 9:10. Epub 2010 Dec 25.
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers. [Cancer Epidemiol Biomarkers Pr...]
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers.
Thompson D, Seal S, Schutte M, McGuffog L, Barfoot R, Renwick A, Eeles R, Sodha N, Houlston R, Shanley S, et al. Cancer Epidemiol Biomarkers Prev. 2006 Dec; 15(12):2542-5.

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