-
1
-
-
84871771432
-
Evaluation of BRCA1 mutations in an unselected patient population with triple-negative breast cancer
-
Rummel S, Varner E, Shriver CD, Ellsworth RE (2013) Evaluation of BRCA1 mutations in an unselected patient population with triple-negative breast cancer. Breast Cancer Res Treat 137(1):119-125
-
(2013)
Breast Cancer Res Treat
, vol.137
, Issue.1
, pp. 119-125
-
-
Rummel, S.1
Varner, E.2
Shriver, C.D.3
Ellsworth, R.E.4
-
2
-
-
57749092800
-
Triple-negative/basal-like breast cancer: Review
-
Rakha EA, Ellis IO (2009) Triple-negative/basal-like breast cancer: review. Pathology 41(1):40-47
-
(2009)
Pathology
, vol.41
, Issue.1
, pp. 40-47
-
-
Rakha, E.A.1
Ellis, I.O.2
-
3
-
-
84896722620
-
Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC)
-
Andres R, Pajares I, Balmana J, Llort G, Ramon YCT, Chirivella I, Aguirre E, Robles L, Lastra E, Perez-Segura P et al (2014) Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC). Clin Transl Oncol 16(3):280-284
-
(2014)
Clin Transl Oncol
, vol.16
, Issue.3
, pp. 280-284
-
-
Andres, R.1
Pajares, I.2
Balmana, J.3
Llort, G.4
Ramon, Y.C.T.5
Chirivella, I.6
Aguirre, E.7
Robles, L.8
Lastra, E.9
Perez-Segura, P.10
-
4
-
-
84890247728
-
Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: A meta-analysis
-
Tun NM, Villani G, Ong K, Yoe L, Bo ZM (2014) Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis. Clin Genet 85(1):43-48
-
(2014)
Clin Genet
, vol.85
, Issue.1
, pp. 43-48
-
-
Tun, N.M.1
Villani, G.2
Ong, K.3
Yoe, L.4
Bo, Z.M.5
-
5
-
-
33645084562
-
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 et al (2006) Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer. JAMA 295(12):1379-1388
-
(2006)
JAMA
, vol.295
, Issue.12
, pp. 1379-1388
-
-
Walsh, T.1
Casadei, S.2
Coats, K.H.3
Swisher, E.4
Stray, S.M.5
Higgins, J.6
Roach, K.C.7
Mandell, J.8
Lee, M.K.9
Ciernikova, S.10
-
6
-
-
18744401644
-
Genomic rearrangements in the BRCA1 and BRCA2 genes
-
Mazoyer S (2005) Genomic rearrangements in the BRCA1 and BRCA2 genes. Hum Mutat 25(5):415-422
-
(2005)
Hum Mutat
, vol.25
, Issue.5
, pp. 415-422
-
-
Mazoyer, S.1
-
7
-
-
70449529411
-
Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population
-
Seong MW, Cho SI, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS (2009) Low contribution of BRCA1/2 genomic rearrangement to high-risk breast cancer in the Korean population. Fam Cancer 8(4):505-508
-
(2009)
Fam Cancer
, vol.8
, Issue.4
, pp. 505-508
-
-
Seong, M.W.1
Cho, S.I.2
Noh, D.Y.3
Han, W.4
Kim, S.W.5
Park, C.M.6
Park, H.W.7
Kim, S.Y.8
Kim, J.Y.9
Park, S.S.10
-
8
-
-
84868200812
-
Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer
-
Kim H, Cho DY, Choi DH, Choi SY, Shin I, Park W, Huh SJ, Han SH, Lee MH, Ahn SH et al (2012) Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. Breast Cancer Res Treat 134(3):1315-1326
-
(2012)
Breast Cancer Res Treat
, vol.134
, Issue.3
, pp. 1315-1326
-
-
Kim, H.1
Cho, D.Y.2
Choi, D.H.3
Choi, S.Y.4
Shin, I.5
Park, W.6
Huh, S.J.7
Han, S.H.8
Lee, M.H.9
Ahn, S.H.10
-
9
-
-
70349985067
-
Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients and evidence of a founder mutation
-
Seong MW, Cho SI, Noh DY, Han WS, Kim SW, Park CM, Park HY, Kim SY, Kim JY, Park SS (2009) Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients and evidence of a founder mutation. Clin Genet 76(2):152-160
-
(2009)
Clin Genet
, vol.76
, Issue.2
, pp. 152-160
-
-
Seong, M.W.1
Cho, S.I.2
Noh, D.Y.3
Han, W.S.4
Kim, S.W.5
Park, C.M.6
Park, H.Y.7
Kim, S.Y.8
Kim, J.Y.9
Park, S.S.10
-
10
-
-
42149139456
-
ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007
-
DOI 10.1097/GIM.0b013e31816b5cae, PII 0012581720080400000009
-
Richards CS, Bale S, Bellissimo DB, Das S, Grody WW, Hegde MR, Lyon E, Ward BE (2008) Molecular Subcommittee of the ALQAC: aCMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007. Genet Med 10(4):294-300 (Pubitemid 351544132)
-
(2008)
Genetics in Medicine
, vol.10
, Issue.4
, pp. 294-300
-
-
Richards, C.S.1
Bale, S.2
Bellissimo, D.B.3
Das, S.4
Grody, W.W.5
Hegde, M.R.6
Lyon, E.7
Ward, B.E.8
-
11
-
-
33847147313
-
American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer
-
DOI 10.1200/JCO.2006.09.2775
-
Wolff AC, Hammond ME, Schwartz JN, Hagerty KL, Allred DC, Cote RJ, Dowsett M, Fitzgibbons PL, Hanna WM, Langer A et al (2007) American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer. J Clin Oncol 25(1):118-145 (Pubitemid 350003059)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.1
, pp. 118-145
-
-
Wolff, A.C.1
Hammond, M.E.H.2
Schwartz, J.N.3
Hagerty, K.L.4
Allred, D.C.5
Cote, R.J.6
Dowsett, M.7
Fitzgibbons, P.L.8
Hanna, W.M.9
Langer, A.10
McShane, L.M.11
Paik, S.12
Pegram, M.D.13
Perez, E.A.14
Press, M.F.15
Rhodes, A.16
Sturgeon, C.17
Taube, S.E.18
Tubbs, R.19
Vance, G.H.20
Van De, V.M.21
Wheeler, T.M.22
Hayes, D.F.23
more..
-
12
-
-
80755171231
-
BRCA1/2 mutations and triple negative breast cancers
-
Peshkin BN, Alabek ML, Isaacs C (2010) BRCA1/2 mutations and triple negative breast cancers. Breast Dis 32(1-2):25-33
-
(2010)
Breast Dis
, vol.32
, Issue.1-2
, pp. 25-33
-
-
Peshkin, B.N.1
Alabek, M.L.2
Isaacs, C.3
-
13
-
-
79958704558
-
Family history of breast cancer in first-degree relatives and triple-negative breast cancer risk
-
Phipps AI, Buist DS, Malone KE, Barlow WE, Porter PL, Kerlikowske K, Li CI (2011) Family history of breast cancer in first-degree relatives and triple-negative breast cancer risk. Breast Cancer Res Treat 126(3):671-678
-
(2011)
Breast Cancer Res Treat
, vol.126
, Issue.3
, pp. 671-678
-
-
Phipps, A.I.1
Buist, D.S.2
Malone, K.E.3
Barlow, W.E.4
Porter, P.L.5
Kerlikowske, K.6
Li, C.I.7
-
14
-
-
78649663247
-
Triple-negative breast cancer: Disease entity or title of convenience?
-
Carey L, Winer E, Viale G, Cameron D, Gianni L (2010) Triple-negative breast cancer: disease entity or title of convenience? Nat Rev Clin Oncol 7(12):683-692
-
(2010)
Nat Rev Clin Oncol
, vol.7
, Issue.12
, pp. 683-692
-
-
Carey, L.1
Winer, E.2
Viale, G.3
Cameron, D.4
Gianni, L.5
-
15
-
-
78449311361
-
Triple-negative breast cancer: Epidemiology and management options
-
Dawood S (2010) Triple-negative breast cancer: epidemiology and management options. Drugs 70(17):2247-2258
-
(2010)
Drugs
, vol.70
, Issue.17
, pp. 2247-2258
-
-
Dawood, S.1
-
16
-
-
84863984125
-
Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: Implications for genetic screening selection criteria: A hellenic cooperative oncology group study
-
Fostira F, Tsitlaidou M, Papadimitriou C, Pertesi M, Timotheadou E, Stavropoulou AV, Glentis S, Bournakis E, Bobos M, Pectasides D et al (2012) Prevalence of BRCA1 mutations among 403 women with triple-negative breast cancer: implications for genetic screening selection criteria: a hellenic cooperative oncology group study. Breast Cancer Res Treat 134(1):353-362
-
(2012)
Breast Cancer Res Treat
, vol.134
, Issue.1
, pp. 353-362
-
-
Fostira, F.1
Tsitlaidou, M.2
Papadimitriou, C.3
Pertesi, M.4
Timotheadou, E.5
Stavropoulou, A.V.6
Glentis, S.7
Bournakis, E.8
Bobos, M.9
Pectasides, D.10
-
17
-
-
79952253747
-
Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer
-
Gonzalez-Angulo AM, Timms KM, Liu S, Chen H, Litton JK, Potter J, Lanchbury JS, Stemke-Hale K, Hennessy BT, Arun BK et al (2011) Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer. Clin Cancer Res 17(5):1082-1089
-
(2011)
Clin Cancer Res
, vol.17
, Issue.5
, pp. 1082-1089
-
-
Gonzalez-Angulo, A.M.1
Timms, K.M.2
Liu, S.3
Chen, H.4
Litton, J.K.5
Potter, J.6
Lanchbury, J.S.7
Stemke-Hale, K.8
Hennessy, B.T.9
Arun, B.K.10
-
18
-
-
84858295021
-
BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years
-
Robertson L, Hanson H, Seal S, Warren-Perry M, Hughes D, Howell I, Turnbull C, Houlston R, Shanley S, Butler S et al (2012) BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years. Br J Cancer 106(6):1234-1238
-
(2012)
Br J Cancer
, vol.106
, Issue.6
, pp. 1234-1238
-
-
Robertson, L.1
Hanson, H.2
Seal, S.3
Warren-Perry, M.4
Hughes, D.5
Howell, I.6
Turnbull, C.7
Houlston, R.8
Shanley, S.9
Butler, S.10
-
19
-
-
84868217990
-
Triple-negative breast cancer and PTEN (phosphatase and tensin homologue)loss are predictors of BRCA1 germline mutations in women with early-onset and familial breast cancer, but not in women with isolated late-onset breast cancer
-
Phuah SY, Looi LM, Hassan N, Rhodes A, Dean S, Taib NA, Yip CH, Teo SH (2012) Triple-negative breast cancer and PTEN (phosphatase and tensin homologue)loss are predictors of BRCA1 germline mutations in women with early-onset and familial breast cancer, but not in women with isolated late-onset breast cancer. Breast Cancer Res 14(6):R142
-
(2012)
Breast Cancer Res
, vol.14
, Issue.6
-
-
Phuah, S.Y.1
Looi, L.M.2
Hassan, N.3
Rhodes, A.4
Dean, S.5
Taib, N.A.6
Yip, C.H.7
Teo, S.H.8
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