-
1
-
-
0038744296
-
Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies
-
Antoniou A, Pharoah P, Narod S, Risch H, Eyfjord J, et al. (2003) Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies. Am J Hum Genet 72: 1117-1130.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.2
Narod, S.3
Risch, H.4
Eyfjord, J.5
-
2
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium
-
Ford D, Easton D, Stratton M, Narod S, Goldgar D, et al. (1998) Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. Am J Hum Genet 62: 676-689.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.2
Stratton, M.3
Narod, S.4
Goldgar, D.5
-
3
-
-
0033769823
-
Patients with double primary tumors in the breast and ovary-clinical characteristics and BRCA1-2 mutations status
-
Fishman A, Dekel E, Chetrit A, Lerner-Geva L, Bar-Am A, et al. (2000) Patients with double primary tumors in the breast and ovary-clinical characteristics and BRCA1-2 mutations status. Gynecol Oncol 79: 74-78.
-
(2000)
Gynecol Oncol
, vol.79
, pp. 74-78
-
-
Fishman, A.1
Dekel, E.2
Chetrit, A.3
Lerner-Geva, L.4
Bar-Am, A.5
-
4
-
-
77956097177
-
BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasta and/or ovaries
-
Evans D, Ahmed M, Bayliss S, Howard E, Lalloo F, et al. (2010) BRCA1, BRCA2 and CHEK2 c.1100 delC mutations in patients with double primaries of the breasta and/or ovaries. J Med Genet 47: 561-566.
-
(2010)
J Med Genet
, vol.47
, pp. 561-566
-
-
Evans, D.1
Ahmed, M.2
Bayliss, S.3
Howard, E.4
Lalloo, F.5
-
5
-
-
79961113537
-
BRCA1/2 status and clinicopathologic characteristics of patients with double primary breast and ovarian cancer
-
Cvelbar M, Hocevar M, Vidmar G, Teugels E, (2011) BRCA1/2 status and clinicopathologic characteristics of patients with double primary breast and ovarian cancer. Neoplasma 58: 198-204.
-
(2011)
Neoplasma
, vol.58
, pp. 198-204
-
-
Cvelbar, M.1
Hocevar, M.2
Vidmar, G.3
Teugels, E.4
-
6
-
-
0033748806
-
Factors associated with decisions about clinical BRCA1/2 testing
-
Armstrong K, Calzone K, Stopfer J, Fitzgerald G, Coyne J, et al. (2000) Factors associated with decisions about clinical BRCA1/2 testing. Cancer Epidemiol Biomarkers Prev 9: 1251-1254.
-
(2000)
Cancer Epidemiol Biomarkers Prev
, vol.9
, pp. 1251-1254
-
-
Armstrong, K.1
Calzone, K.2
Stopfer, J.3
Fitzgerald, G.4
Coyne, J.5
-
7
-
-
74949116222
-
Weighing options for cancer risk reduction in carriers of BRCA1 and BRCA2 mutations
-
Stadler Z, Kauff N, (2010) Weighing options for cancer risk reduction in carriers of BRCA1 and BRCA2 mutations. J Clin Oncol 28: 189-191.
-
(2010)
J Clin Oncol
, vol.28
, pp. 189-191
-
-
Stadler, Z.1
Kauff, N.2
-
8
-
-
58749091606
-
Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation
-
Metcalfe K, Finch A, Poll A, Horsman D, Kim-Sing C, et al. (2009) Breast cancer risks in women with a family history of breast or ovarian cancer who have tested negative for a BRCA1 or BRCA2 mutation. Br J Cancer 100: 421-425.
-
(2009)
Br J Cancer
, vol.100
, pp. 421-425
-
-
Metcalfe, K.1
Finch, A.2
Poll, A.3
Horsman, D.4
Kim-Sing, C.5
-
9
-
-
77955749949
-
A KRAS-variant in Ovarian Cancer Acts as a Genetic Marker of Cancer Risk
-
Ratner E, Lu L, Boeke M, Barnett R, Nallur S, et al. (2010) A KRAS-variant in Ovarian Cancer Acts as a Genetic Marker of Cancer Risk. Cancer Research 15: 6509-6515.
-
(2010)
Cancer Research
, vol.15
, pp. 6509-6515
-
-
Ratner, E.1
Lu, L.2
Boeke, M.3
Barnett, R.4
Nallur, S.5
-
10
-
-
79953165309
-
A 3'-untranslated region KRAS variant and triple-negative breast cancer: a case-control and genetic analysis
-
Paranjape T, Heneghan H, Lindner R, Keane F, Hoffman A, et al. (2011) A 3'-untranslated region KRAS variant and triple-negative breast cancer: a case-control and genetic analysis. Lancet Oncology.
-
(2011)
Lancet Oncology
-
-
Paranjape, T.1
Heneghan, H.2
Lindner, R.3
Keane, F.4
Hoffman, A.5
-
11
-
-
54249117763
-
A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk
-
Chin L, Ratner E, Leng S, Zhai R, Nullur S, et al. (2008) A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer risk. Cancer Res 68: 8535-8540.
-
(2008)
Cancer Res
, vol.68
, pp. 8535-8540
-
-
Chin, L.1
Ratner, E.2
Leng, S.3
Zhai, R.4
Nullur, S.5
-
12
-
-
66749164641
-
A let-7 microRNA binding site polymorphism in the KRAS 3'UTR is associatied with reduced survival in oral cancers
-
Christensen B, Moyer B, Avissar M, Ouellet L, Plaza S, et al. (2009) A let-7 microRNA binding site polymorphism in the KRAS 3'UTR is associatied with reduced survival in oral cancers. Carcinogenesis 30: 1003-1007.
-
(2009)
Carcinogenesis
, vol.30
, pp. 1003-1007
-
-
Christensen, B.1
Moyer, B.2
Avissar, M.3
Ouellet, L.4
Plaza, S.5
-
13
-
-
79957925584
-
The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing
-
Pharoah P, Palmieri R, Ramus S, Gayther S, Andrulis I, et al. (2011) The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing. Clin Cancer Res online March 8th.
-
(2011)
Clin Cancer Res Online March
, vol.8
-
-
Pharoah, P.1
Palmieri, R.2
Ramus, S.3
Gayther, S.4
Andrulis, I.5
-
14
-
-
84867875190
-
A KRAS-variant is a Biomarker of Poor Outcome, Platinum Chemotherapy Resistance and a Potential Target for Therapy in Ovarian Cancer
-
Ratner E, Keane F, Lindner R, Tassi R, Paranjape T, et al. (2011) A KRAS-variant is a Biomarker of Poor Outcome, Platinum Chemotherapy Resistance and a Potential Target for Therapy in Ovarian Cancer. Oncogene Dec 5.
-
(2011)
Oncogene Dec
, vol.5
-
-
Ratner, E.1
Keane, F.2
Lindner, R.3
Tassi, R.4
Paranjape, T.5
-
15
-
-
79957896962
-
MicroRNA signatures differentiate melanoma subtypes
-
Chan E, Patel R, Nallur S, Bacchiocchi A, Hoyt K, et al. (2011) MicroRNA signatures differentiate melanoma subtypes. Cell Cycle 10 epub ahead of print.
-
(2011)
Cell Cycle 10, epub ahead of print
-
-
Chan, E.1
Patel, R.2
Nallur, S.3
Bacchiocchi, A.4
Hoyt, K.5
-
16
-
-
33645084562
-
Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer
-
Walsh T, Casadei S, Coats K, Swisher E, Stray S, et al. (2006) Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. JAMA 295: 1379-1388.
-
(2006)
JAMA
, vol.295
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.3
Swisher, E.4
Stray, S.5
-
17
-
-
52049088505
-
The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families
-
Palma M, Domchek S, Stopfer J, Erlichman J, Siegfried J, et al. (2008) The relative contribution of point mutations and genomic rearrangements in BRCA1 and BRCA2 in high-risk breast cancer families. Cancer Res 68: 7006-7014.
-
(2008)
Cancer Res
, vol.68
, pp. 7006-7014
-
-
Palma, M.1
Domchek, S.2
Stopfer, J.3
Erlichman, J.4
Siegfried, J.5
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