-
2
-
-
33746398408
-
Polygenic inherited predisposition to breast cancer
-
Ponder BA, Antoniou A, Dunning A, Easton DF, Pharoah PD. Polygenic inherited predisposition to breast cancer. Cold Spring Harb Symp Quant Biol. 2005; 70: 35-41.
-
(2005)
Cold Spring Harb Symp Quant Biol
, vol.70
, pp. 35-41
-
-
Ponder, B.A.1
Antoniou, A.2
Dunning, A.3
Easton, D.F.4
Pharoah, P.D.5
-
3
-
-
0037685164
-
Breast and ovarian cancer
-
Wooster R, Weber BL. Breast and ovarian cancer. N Engl J Med. 2003; 348: 2339-47.
-
(2003)
N Engl J Med
, vol.348
, pp. 2339-2347
-
-
Wooster, R.1
Weber, B.L.2
-
4
-
-
56249103144
-
Inherited susceptibility to common cancers
-
Foulkes WD. Inherited susceptibility to common cancers. N Engl J Med. 2008; 359: 2143-53.
-
(2008)
N Engl J Med
, vol.359
, pp. 2143-2153
-
-
Foulkes, W.D.1
-
5
-
-
18544389716
-
CHEK2-breast cancer consortium. 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, et al; CHEK2-Breast Cancer Consortium. Low-penetrance susceptibility to breast cancer due to CHEK2(∗)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002; 31: 55-9.
-
(2002)
Nat Genet
, vol.31
, pp. 55-59
-
-
Meijers-Heijboer, H.1
Van Den Ouweland, A.2
Klijn, J.3
-
6
-
-
3042582651
-
CHEK2 breast cancer case-control consortium. 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. CHEK2∗1100delC and susceptibility to breast cancer: a collaborative analysis involving 10, 860 breast cancer cases and 9, 065 controls from 10 studies. Am J Hum Genet. 2004; 74: 1175-82.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1175-1182
-
-
-
7
-
-
39149141409
-
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. 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; 26: 542-8.
-
(2008)
J Clin Oncol
, vol.26
, pp. 542-548
-
-
Weischer, M.1
Bojesen, S.E.2
Ellervik, C.3
Tybjaerg-Hansen, A.4
Nordestgaard, B.G.5
-
8
-
-
77954579781
-
Testing for CHEK2 in the cancer genetics clinic: Ready for prime time?
-
Narod SA. Testing for CHEK2 in the cancer genetics clinic: ready for prime time? Clin Genet. 2010; 78: 1-7.
-
(2010)
Clin Genet
, vol.78
, pp. 1-7
-
-
Narod, S.A.1
-
9
-
-
0345669750
-
Breast Cancer Linkage Consortium. Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility
-
Schutte M, Seal S, Barfoot R, et al; Breast Cancer Linkage Consortium. Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility. Am J Hum Genet. 2003; 72: 1023-8.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1023-1028
-
-
Schutte, M.1
Seal, S.2
Barfoot, R.3
-
10
-
-
58349121873
-
Family history, genetic testing, and clinical risk prediction: Pooled analysis of CHEK2 1100delC in 1, 828 bilateral breast cancers and 7, 030 controls
-
Fletcher O, Johnson N, Dos Santos Silva I, et al. Family history, genetic testing, and clinical risk prediction: pooled analysis of CHEK2 1100delC in 1, 828 bilateral breast cancers and 7, 030 controls. Cancer Epidemiol Biomarkers Prev. 2009; 18: 230-4.
-
(2009)
Cancer Epidemiol Biomarkers Prev
, vol.18
, pp. 230-234
-
-
Fletcher, O.1
Johnson, N.2
Dos Santos Silva, I.3
-
11
-
-
80053594059
-
Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer
-
Cybulski C, Wokołorczyk D, Jakubowska A, et al. Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer. J Clin Oncol. 2011; 29: 3747-52.
-
(2011)
J Clin Oncol
, vol.29
, pp. 3747-3752
-
-
Cybulski, C.1
Wokołorczyk, D.2
Jakubowska, A.3
-
12
-
-
27544515629
-
Interaction between CHEK2∗1100delC and other low-penetrance breast-cancer susceptibility genes: A familial study
-
Johnson N, Fletcher O, Naceur-Lombardelli C, dos Santos Silva I, Ashworth A, Peto J. Interaction between CHEK2∗1100delC and other low-penetrance breast-cancer susceptibility genes: a familial study. Lancet. 2005; 366: 1554-7.
-
(2005)
Lancet
, vol.366
, pp. 1554-1557
-
-
Johnson, N.1
Fletcher, O.2
Naceur-Lombardelli, C.3
Dos Santos Silva, I.4
Ashworth, A.5
Peto, J.6
-
13
-
-
84876683067
-
Excess breast cancer risk in first degree relatives of CHEK2 1100delC positive familial breast cancer cases
-
Adank MA, Verhoef S, Oldenburg RA, et al. Excess breast cancer risk in first degree relatives of CHEK2 1100delC positive familial breast cancer cases. Eur J Cancer. 2013; 49: 1993-9.
-
(2013)
Eur J Cancer
, vol.49
, pp. 1993-1999
-
-
Adank, M.A.1
Verhoef, S.2
Oldenburg, R.A.3
-
14
-
-
0347626108
-
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, et al. The CHEK2∗1100delC variant acts as a breast cancer risk modifier in non-BRCA1/BRCA2 multiple-case families. Cancer Res. 2003; 63: 8153-7.
-
(2003)
Cancer Res
, vol.63
, pp. 8153-8157
-
-
Oldenburg, R.A.1
Kroeze-Jansema, K.2
Kraan, J.3
-
15
-
-
42049120693
-
Frequency of the CHEK2 1100delC mutation among women with breast cancer: An international study
-
Zhang S, Phelan CM, Zhang P, et al. Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international study. Cancer Res. 2008; 68: 2154-7.
-
(2008)
Cancer Res
, vol.68
, pp. 2154-2157
-
-
Zhang, S.1
Phelan, C.M.2
Zhang, P.3
-
16
-
-
34250315627
-
Increased risk of breast cancer associated with CHEK2∗1100delC
-
Weischer M, Bojesen SE, Tybjaerg-Hansen A, Axelsson CK, Nordestgaard BG. Increased risk of breast cancer associated with CHEK2∗1100delC. J Clin Oncol. 2007; 25: 57-63. .
-
(2007)
J Clin Oncol
, vol.25
, pp. 57-63
-
-
Weischer, M.1
Bojesen, S.E.2
Tybjaerg-Hansen, A.3
Axelsson, C.K.4
Nordestgaard, B.G.5
-
17
-
-
6344261987
-
Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2∗1100delC variant
-
De Bock GH, Schutte M, Krol-Warmerdam EM, et al. Tumour characteristics and prognosis of breast cancer patients carrying the germline CHEK2∗1100delC variant. J Med Genet. 2004; 41: 731-5.
-
(2004)
J Med Genet
, vol.41
, pp. 731-735
-
-
De Bock, G.H.1
Schutte, M.2
Krol-Warmerdam, E.M.3
-
18
-
-
84906937926
-
Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: Impact of adjuvant chemotherapy
-
Kriege M, Hollestelle A, Jager A, et al. Survival and contralateral breast cancer in CHEK2 1100delC breast cancer patients: impact of adjuvant chemotherapy. Br J Cancer. 2014; 111: 1004-13.
-
(2014)
Br J Cancer
, vol.111
, pp. 1004-1013
-
-
Kriege, M.1
Hollestelle, A.2
Jager, A.3
-
19
-
-
0942279575
-
Excess risk for contralateral breast cancer in CHEK2∗1100delC germline mutation carriers
-
Broeks A, de Witte L, Nooijen A, et al. Excess risk for contralateral breast cancer in CHEK2∗1100delC germline mutation carriers. Breast Cancer Res Treat. 2004; 83: 91-3.
-
(2004)
Breast Cancer Res Treat
, vol.83
, pp. 91-93
-
-
Broeks, A.1
De Witte, L.2
Nooijen, A.3
-
20
-
-
39449090355
-
Risk for contralateral breast cancer among carriers of the CHEK2∗1100delC mutation in the WECARE Study
-
WECARE Study Collaborative Group
-
Mellemkjaer L, Dahl C, Olsen JH, et al; WECARE Study Collaborative Group. Risk for contralateral breast cancer among carriers of the CHEK2∗1100delC mutation in the WECARE Study. Br J Cancer. 2008; 98: 728-33.
-
(2008)
Br J Cancer
, vol.98
, pp. 728-733
-
-
Mellemkjaer, L.1
Dahl, C.2
Olsen, J.H.3
-
21
-
-
77956097177
-
BRCA1 BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries
-
Evans DG, Ahmed M, Bayliss S, Howard E, Lalloo F, Wallace A. BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasts and/or ovaries. J Med Genet. 2010; 47: 561-6.
-
(2010)
J Med Genet
, vol.47
, pp. 561-566
-
-
Evans, D.G.1
Ahmed, M.2
Bayliss, S.3
Howard, E.4
Lalloo, F.5
Wallace, A.6
-
22
-
-
84870526600
-
The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: A retrospective cohort study
-
Rhiem K, Engel C, Graeser M, et al. The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort study. Breast Cancer Res. 2012; 14: R156.
-
(2012)
Breast Cancer Res
, vol.14
, pp. R156
-
-
Rhiem, K.1
Engel, C.2
Graeser, M.3
-
23
-
-
84870744620
-
CHEK2∗1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer
-
Weischer M, Nordestgaard BG, Pharoah P, et al. CHEK2∗1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer. J Clin Oncol. 2012; 30: 4308-16.
-
(2012)
J Clin Oncol
, vol.30
, pp. 4308-4316
-
-
Weischer, M.1
Nordestgaard, B.G.2
Pharoah, P.3
-
24
-
-
34547735957
-
Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2∗1100delC germline mutation
-
Schmidt MK, Tollenaar RA, de Kemp SR, et al. Breast cancer survival and tumor characteristics in premenopausal women carrying the CHEK2∗1100delC germline mutation. J Clin Oncol. 2007; 25: 64-9.
-
(2007)
J Clin Oncol
, vol.25
, pp. 64-69
-
-
Schmidt, M.K.1
Tollenaar, R.A.2
De Kemp, S.R.3
-
25
-
-
84856014217
-
CHEK2∗1100delC homozygosity is associated with a high breast cancer risk in women
-
Adank MA, Jonker MA, Kluijt I, et al. CHEK2∗1100delC homozygosity is associated with a high breast cancer risk in women. J Med Genet. 2011; 48: 860-3.
-
(2011)
J Med Genet
, vol.48
, pp. 860-863
-
-
Adank, M.A.1
Jonker, M.A.2
Kluijt, I.3
-
26
-
-
84890789926
-
CHEK2∗1100delC homozygosity in the Netherlands - Prevalence and risk of breast and lung cancer
-
Huijts PEA, Hollestelle A, Balliu B, et al. CHEK2∗1100delC homozygosity in the Netherlands - prevalence and risk of breast and lung cancer. Eur J Hum Genet. 2014; 22: 46-51.
-
(2014)
Eur J Hum Genet
, vol.22
, pp. 46-51
-
-
Pea, H.1
Hollestelle, A.2
Balliu, B.3
|