These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
377 related articles for article (PubMed ID: 12094328)
1. A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Vahteristo P; Bartkova J; Eerola H; Syrjäkoski K; Ojala S; Kilpivaara O; Tamminen A; Kononen J; Aittomäki K; Heikkilä P; Holli K; Blomqvist C; Bartek J; Kallioniemi OP; Nevanlinna H Am J Hum Genet; 2002 Aug; 71(2):432-8. PubMed ID: 12094328 [TBL] [Abstract][Full Text] [Related]
2. Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Meijers-Heijboer H; van den Ouweland A; Klijn J; Wasielewski M; de Snoo A; Oldenburg R; Hollestelle A; Houben M; Crepin E; van Veghel-Plandsoen M; Elstrodt F; van Duijn C; Bartels C; Meijers C; Schutte M; McGuffog L; Thompson D; Easton D; Sodha N; Seal S; Barfoot R; Mangion J; Chang-Claude J; Eccles D; Eeles R; Evans DG; Houlston R; Murday V; Narod S; Peretz T; Peto J; Phelan C; Zhang HX; Szabo C; Devilee P; Goldgar D; Futreal PA; Nathanson KL; Weber B; Rahman N; Stratton MR; Nat Genet; 2002 May; 31(1):55-9. PubMed ID: 11967536 [TBL] [Abstract][Full Text] [Related]
3. The CHEK2*1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families. Oldenburg RA; Kroeze-Jansema K; Kraan J; Morreau H; Klijn JG; Hoogerbrugge N; Ligtenberg MJ; van Asperen CJ; Vasen HF; Meijers C; Meijers-Heijboer H; de Bock TH; Cornelisse CJ; Devilee P Cancer Res; 2003 Dec; 63(23):8153-7. PubMed ID: 14678969 [TBL] [Abstract][Full Text] [Related]
4. CHEK2 1100delC is not a risk factor for male breast cancer population. Syrjäkoski K; Kuukasjärvi T; Auvinen A; Kallioniemi OP Int J Cancer; 2004 Jan; 108(3):475-6. PubMed ID: 14648717 [TBL] [Abstract][Full Text] [Related]
5. Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women. Friedrichsen DM; Malone KE; Doody DR; Daling JR; Ostrander EA Breast Cancer Res; 2004; 6(6):R629-35. PubMed ID: 15535844 [TBL] [Abstract][Full Text] [Related]
6. Excess breast cancer risk in first degree relatives of CHEK2∗1100delC positive familial breast cancer cases. Adank MA; Verhoef S; Oldenburg RA; Schmidt MK; Hooning MJ; Martens JW; Broeks A; Rookus M; Waisfisz Q; Witte BI; Jonker MA; Meijers-Heijboer H Eur J Cancer; 2013 May; 49(8):1993-9. PubMed ID: 23415889 [TBL] [Abstract][Full Text] [Related]
7. Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility. Schutte M; Seal S; Barfoot R; Meijers-Heijboer H; Wasielewski M; Evans DG; Eccles D; Meijers C; Lohman F; Klijn J; van den Ouweland A; Futreal PA; Nathanson KL; Weber BL; Easton DF; Stratton MR; Rahman N; Am J Hum Genet; 2003 Apr; 72(4):1023-8. PubMed ID: 12610780 [TBL] [Abstract][Full Text] [Related]
8. Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. Walsh T; Casadei S; Coats KH; Swisher E; Stray SM; Higgins J; Roach KC; Mandell J; Lee MK; Ciernikova S; Foretova L; Soucek P; King MC JAMA; 2006 Mar; 295(12):1379-88. PubMed ID: 16551709 [TBL] [Abstract][Full Text] [Related]
9. Correlation of CHEK2 protein expression and c.1100delC mutation status with tumor characteristics among unselected breast cancer patients. Kilpivaara O; Bartkova J; Eerola H; Syrjäkoski K; Vahteristo P; Lukas J; Blomqvist C; Holli K; Heikkilä P; Sauter G; Kallioniemi OP; Bartek J; Nevanlinna H Int J Cancer; 2005 Feb; 113(4):575-80. PubMed ID: 15472904 [TBL] [Abstract][Full Text] [Related]
10. Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals. Jekimovs CR; Chen X; Arnold J; Gatei M; Richard DJ; Spurdle AB; Khanna KK; Chenevix-Trench G; Br J Cancer; 2005 Feb; 92(4):784-90. PubMed ID: 15700044 [TBL] [Abstract][Full Text] [Related]
11. The CHEK2 1100delC mutation is not present in Korean patients with breast cancer cases tested for BRCA1 and BRCA2 mutation. Choi DH; Cho DY; Lee MH; Park HS; Ahn SH; Son BH; Haffty BG Breast Cancer Res Treat; 2008 Dec; 112(3):569-73. PubMed ID: 18175216 [TBL] [Abstract][Full Text] [Related]
12. BRCA1, BRCA2 and CHEK2 (1100 del C) germline mutations in hereditary breast and ovarian cancer families in South India. Rajkumar T; Soumittra N; Nancy NK; Swaminathan R; Sridevi V; Shanta V Asian Pac J Cancer Prev; 2003; 4(3):203-8. PubMed ID: 14507240 [TBL] [Abstract][Full Text] [Related]
13. German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer. Rashid MU; Jakubowska A; Justenhoven C; Harth V; Pesch B; Baisch C; Pierl CB; Brüning T; Ko Y; Benner A; Wichmann HE; Brauch H; Hamann U; Eur J Cancer; 2005 Dec; 41(18):2896-903. PubMed ID: 16239104 [TBL] [Abstract][Full Text] [Related]
14. 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; 26(4):542-8. PubMed ID: 18172190 [TBL] [Abstract][Full Text] [Related]
15. Evaluation of the contribution of the three breast cancer susceptibility genes CHEK2, STK11, and PALB2 in non-BRCA1/2 French Canadian families with high risk of breast cancer. Guénard F; Pedneault CS; Ouellette G; Labrie Y; Simard J; ; Durocher F Genet Test Mol Biomarkers; 2010 Aug; 14(4):515-26. PubMed ID: 20722467 [TBL] [Abstract][Full Text] [Related]
16. Limited relevance of the CHEK2 gene in hereditary breast cancer. Dufault MR; Betz B; Wappenschmidt B; Hofmann W; Bandick K; Golla A; Pietschmann A; Nestle-Krämling C; Rhiem K; Hüttner C; von Lindern C; Dall P; Kiechle M; Untch M; Jonat W; Meindl A; Scherneck S; Niederacher D; Schmutzler RK; Arnold N Int J Cancer; 2004 Jun; 110(3):320-5. PubMed ID: 15095295 [TBL] [Abstract][Full Text] [Related]
17. Two new CHEK2 germ-line variants detected in breast cancer/sarcoma families negative for BRCA1, BRCA2, and TP53 gene mutations. Manoukian S; Peissel B; Frigerio S; Lecis D; Bartkova J; Roversi G; Radice P; Bartek J; Delia D Breast Cancer Res Treat; 2011 Nov; 130(1):207-15. PubMed ID: 21562711 [TBL] [Abstract][Full Text] [Related]
18. CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. CHEK2 Breast Cancer Case-Control Consortium Am J Hum Genet; 2004 Jun; 74(6):1175-82. PubMed ID: 15122511 [TBL] [Abstract][Full Text] [Related]
19. 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; 200(2):149-52. PubMed ID: 14568168 [TBL] [Abstract][Full Text] [Related]
20. 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; Brekelmans C; Jagmohan S; Franken P; Verkuijlen P; van den Ouweland A; Chapman P; Tops C; Möslein G; Burn J; Lynch H; Klijn J; Fodde R; Schutte M Am J Hum Genet; 2003 May; 72(5):1308-14. PubMed ID: 12690581 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]