-
1
-
-
33644755351
-
The CHEK2*1100delC allelic variant and risk of breast cancer: Screening results from the Breast Cancer Family Registry
-
Bernstein JL, Teraoka SN, John EM, et al: The CHEK2*1100delC allelic variant and risk of breast cancer: Screening results from the Breast Cancer Family Registry. Cancer Epidemiol Biomarkers Prev 15:348-352, 2006
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 348-352
-
-
Bernstein, J.L.1
Teraoka, S.N.2
John, E.M.3
-
2
-
-
34249857115
-
Analysis of PALB2/FANCN-associated breast cancer families
-
Tischkowitz M, Xia B, Sabbaghian N, et al: Analysis of PALB2/FANCN-associated breast cancer families. Proc Natl Acad Sci USA 104:6788-6793, 2007
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 6788-6793
-
-
Tischkowitz, M.1
Xia, B.2
Sabbaghian, N.3
-
3
-
-
33749023605
-
ATM and breast cancer susceptibility
-
Ahmed M, Rahman N: ATM and breast cancer susceptibility. Oncogene 25:5906-5911, 2006
-
(2006)
Oncogene
, vol.25
, pp. 5906-5911
-
-
Ahmed, M.1
Rahman, N.2
-
4
-
-
33749039966
-
The CHEK2 gene and inherited breast cancer susceptibility
-
Nevanlinna H, Bartek J: The CHEK2 gene and inherited breast cancer susceptibility. Oncogene 25:5912-5919, 2006
-
(2006)
Oncogene
, vol.25
, pp. 5912-5919
-
-
Nevanlinna, H.1
Bartek, J.2
-
5
-
-
36248979794
-
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts
-
Bell DW, Kim SH, Godwin AK, et al: Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts. Int J Cancer 121:2661-2667, 2007
-
(2007)
Int J Cancer
, vol.121
, pp. 2661-2667
-
-
Bell, D.W.1
Kim, S.H.2
Godwin, A.K.3
-
6
-
-
39149141409
-
CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: Meta-analysis of 26,000 patient cases and 27,000 controls
-
Weischer M, Bojesen SE, Ellervik C, et al: CHEK2*1100delC genotyping for clinical assessment of breast cancer risk: Meta-analysis of 26,000 patient cases and 27,000 controls. J Clin Oncol 26:542-548, 2008
-
(2008)
J Clin Oncol
, vol.26
, pp. 542-548
-
-
Weischer, M.1
Bojesen, S.E.2
Ellervik, C.3
-
7
-
-
0033601346
-
Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome
-
Bell DW, Varley JM, Szydlo TE, et al: Heterozygous germ line hCHK2 mutations in Li-Fraumeni syndrome. Science 286:2528-2531, 1999
-
(1999)
Science
, vol.286
, pp. 2528-2531
-
-
Bell, D.W.1
Varley, J.M.2
Szydlo, T.E.3
-
8
-
-
33846012859
-
A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers
-
Thompson D, Seal S, Schutte M, et al: A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers. Cancer Epidemiol Biomarkers Prev 15:2542-2545, 2006
-
(2006)
Cancer Epidemiol Biomarkers Prev
, vol.15
, pp. 2542-2545
-
-
Thompson, D.1
Seal, S.2
Schutte, M.3
-
9
-
-
34248170114
-
Meta-analysis of BRCA1 and BRCA2 penetrance
-
Chen S, Parmigiani G: Meta-analysis of BRCA1 and BRCA2 penetrance. J Clin Oncol 25:1329-1333, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 1329-1333
-
-
Chen, S.1
Parmigiani, G.2
-
10
-
-
0037011665
-
CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours
-
Sodha N, Bullock S, Taylor R, et al: CHEK2 variants in susceptibility to breast cancer and evidence of retention of the wild type allele in tumours. Br J Cancer 87:1445-1448, 2002
-
(2002)
Br J Cancer
, vol.87
, pp. 1445-1448
-
-
Sodha, N.1
Bullock, S.2
Taylor, R.3
-
11
-
-
18444379055
-
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
-
Vahteristo P, Bartkova J, Eerola H, et al: A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet 71:432-438, 2002
-
(2002)
Am J Hum Genet
, vol.71
, pp. 432-438
-
-
Vahteristo, P.1
Bartkova, J.2
Eerola, H.3
-
12
-
-
28244457585
-
German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer
-
Rashid MU, Jakubowksa A, Justenhoven C, et al: German populations with infrequent CHEK2*1100delC and minor associations with early-onset and familial breast cancer. Eur J Cancer 41:2896-2903, 2005
-
(2005)
Eur J Cancer
, vol.41
, pp. 2896-2903
-
-
Rashid, M.U.1
Jakubowksa, A.2
Justenhoven, C.3
-
13
-
-
0037151382
-
On the use of familial aggregation in population-based case probands for calculating penetrance
-
Begg CB: On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst 94:1221-1226, 2002
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1221-1226
-
-
Begg, C.B.1
-
14
-
-
33845659623
-
BRCA mutation frequency and penetrance: New data, old debate
-
Offit K: BRCA mutation frequency and penetrance: New data, old debate. J Natl Cancer Inst 98:1675-1677, 2006
-
(2006)
J Natl Cancer Inst
, vol.98
, pp. 1675-1677
-
-
Offit, K.1
-
15
-
-
34250315627
-
Increased risk of breast cancer associated with CHEK2*1100delC
-
Weischer M, Bojesen SE, Tybjaerg-Hansen A, et al: Increased risk of breast cancer associated with CHEK2*1100delC. J Clin Oncol 25:57-63, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 57-63
-
-
Weischer, M.1
Bojesen, S.E.2
Tybjaerg-Hansen, A.3
-
16
-
-
3042582651
-
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 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 74:1175-1182, 2004
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1175-1182
-
-
-
17
-
-
2542449310
-
Frequency of CHEK2* 1100delC in New York breast cancer cases and controls
-
Offit K, Pierce H, Kirchhoff T, et al: Frequency of CHEK2* 1100delC in New York breast cancer cases and controls. BMC Med Genet 15:4:1, 2003
-
(2003)
BMC Med Genet
, vol.15
, Issue.4
, pp. 1
-
-
Offit, K.1
Pierce, H.2
Kirchhoff, T.3
-
18
-
-
21644484444
-
Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women
-
Friedrichsen DM, Malone KE, Doody DR, et al: Frequency of CHEK2 mutations in a population based, case-control study of breast cancer in young women. Breast Cancer Res 6:R629-R635, 2004
-
(2004)
Breast Cancer Res
, vol.6
-
-
Friedrichsen, D.M.1
Malone, K.E.2
Doody, D.R.3
-
19
-
-
0344825130
-
The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population
-
Osorio A, Rodriguez-Lopez R, Diez O, et al: The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population. Int J Cancer 108:54-56, 2004
-
(2004)
Int J Cancer
, vol.108
, pp. 54-56
-
-
Osorio, A.1
Rodriguez-Lopez, R.2
Diez, O.3
-
20
-
-
0642340839
-
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, et al: BRCA1, BRCA2 and CHEK2 (1100 del C) germline mutations in hereditary breast and ovarian cancer families in South India. Asian Pac J Cancer Prev 4:203-208, 2003
-
(2003)
Asian Pac J Cancer Prev
, vol.4
, pp. 203-208
-
-
Rajkumar, T.1
Soumittra, N.2
Nancy, N.K.3
-
21
-
-
14044272193
-
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population
-
Shaag A, Walsh T, Renbaum P, et al: Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population. Hum Mol Genet 14:555-563, 2005
-
(2005)
Hum Mol Genet
, vol.14
, pp. 555-563
-
-
Shaag, A.1
Walsh, T.2
Renbaum, P.3
-
22
-
-
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 25:64-69, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 64-69
-
-
Schmidt, M.K.1
Tollenaar, R.A.2
de Kemp, S.R.3
-
23
-
-
34547738991
-
CHEK2 mutation and hereditary breast cancer
-
Narod SA, Lynch HT: CHEK2 mutation and hereditary breast cancer. J Clin Oncol 25:6-7, 2007
-
(2007)
J Clin Oncol
, vol.25
, pp. 6-7
-
-
Narod, S.A.1
Lynch, H.T.2
-
24
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
Easton DF, Pooley KA, Dunning AM, et al: Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447:1087-1093, 2007
-
(2007)
Nature
, vol.447
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
|