-
1
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
COI: 1:CAS:528:DC%2BC3cXjvFKqu78%3D, PID: 20354512
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov AS, Sunyaev SR (2010) A method and server for predicting damaging missense mutations. Nat Methods 7:248–249
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
2
-
-
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
-
COI: 1:CAS:528:DC%2BD3sXjslagtbg%3D, PID: 12677558
-
Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, Loman N, Olsson H, Johannsson O, Borg A, Pasini B, Radice P, Manoukian S, Eccles DM, Tang N, Olah E, Anton-Culver H, Warner E, Lubinski J, Gronwald J, Gorski B, Tulinius H, Thorlacius S, Eerola H, Nevanlinna H, Syrjakoski K, Kallioniemi OP, Thompson D, Evans C, Peto J, Lalloo F, Evans DG, Easton DF (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.D.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
Hopper, J.L.6
Loman, N.7
Olsson, H.8
Johannsson, O.9
Borg, A.10
Pasini, B.11
Radice, P.12
Manoukian, S.13
Eccles, D.M.14
Tang, N.15
Olah, E.16
Anton-Culver, H.17
Warner, E.18
Lubinski, J.19
Gronwald, J.20
Gorski, B.21
Tulinius, H.22
Thorlacius, S.23
Eerola, H.24
Nevanlinna, H.25
Syrjakoski, K.26
Kallioniemi, O.P.27
Thompson, D.28
Evans, C.29
Peto, J.30
Lalloo, F.31
Evans, D.G.32
Easton, D.F.33
more..
-
3
-
-
52049086689
-
Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer
-
PID: 18779615
-
Atchley DP, Albarracin CT, Lopez A, Valero V, Amos CI, Gonzalez-Angulo AM, Hortobagyi GN, Arun BK (2008) Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer. J Clin Oncol 26:4282–4288
-
(2008)
J Clin Oncol
, vol.26
, pp. 4282-4288
-
-
Atchley, D.P.1
Albarracin, C.T.2
Lopez, A.3
Valero, V.4
Amos, C.I.5
Gonzalez-Angulo, A.M.6
Hortobagyi, G.N.7
Arun, B.K.8
-
4
-
-
80052695765
-
BRCA in breast cancer: ESMO clinical practice guidelines
-
PID: 21908500
-
Balmana J, Diez O, Rubio IT, Cardoso F (2011) BRCA in breast cancer: ESMO clinical practice guidelines. Ann Oncol 22(Suppl 6):vi31–vi34
-
(2011)
Ann Oncol
, vol.22
, pp. vi31-vi34
-
-
Balmana, J.1
Diez, O.2
Rubio, I.T.3
Cardoso, F.4
-
5
-
-
79960834725
-
Relative contributions of BRCA1 and BRCA2 mutations to “triple-negative” breast cancer in Ashkenazi Women
-
COI: 1:CAS:528:DC%2BC3MXptVOitro%3D, PID: 21394499
-
Comen E, Davids M, Kirchhoff T, Hudis C, Offit K, Robson M (2011) Relative contributions of BRCA1 and BRCA2 mutations to “triple-negative” breast cancer in Ashkenazi Women. Breast Cancer Res Treat 129:185–190
-
(2011)
Breast Cancer Res Treat
, vol.129
, pp. 185-190
-
-
Comen, E.1
Davids, M.2
Kirchhoff, T.3
Hudis, C.4
Offit, K.5
Robson, M.6
-
6
-
-
84921898753
-
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
-
PID: 25452441
-
Couch FJ, Hart SN, Sharma P, Toland AE, Wang X, Miron P, Olson JE, Godwin AK, Pankratz VS, Olswold C, Slettedahl S, Hallberg E, Guidugli L, Davila JI, Beckmann MW, Janni W, Rack B, Ekici AB, Slamon DJ, Konstantopoulou I, Fostira F, Vratimos A, Fountzilas G, Pelttari LM, Tapper WJ, Durcan L, Cross SS, Pilarski R, Shapiro CL, Klemp J, Yao S, Garber J, Cox A, Brauch H, Ambrosone C, Nevanlinna H, Yannoukakos D, Slager SL, Vachon CM, Eccles DM, Fasching PA (2014) Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. J Clin Oncol 33:304–311
-
(2014)
J Clin Oncol
, vol.33
, pp. 304-311
-
-
Couch, F.J.1
Hart, S.N.2
Sharma, P.3
Toland, A.E.4
Wang, X.5
Miron, P.6
Olson, J.E.7
Godwin, A.K.8
Pankratz, V.S.9
Olswold, C.10
Slettedahl, S.11
Hallberg, E.12
Guidugli, L.13
Davila, J.I.14
Beckmann, M.W.15
Janni, W.16
Rack, B.17
Ekici, A.B.18
Slamon, D.J.19
Konstantopoulou, I.20
Fostira, F.21
Vratimos, A.22
Fountzilas, G.23
Pelttari, L.M.24
Tapper, W.J.25
Durcan, L.26
Cross, S.S.27
Pilarski, R.28
Shapiro, C.L.29
Klemp, J.30
Yao, S.31
Garber, J.32
Cox, A.33
Brauch, H.34
Ambrosone, C.35
Nevanlinna, H.36
Yannoukakos, D.37
Slager, S.L.38
Vachon, C.M.39
Eccles, D.M.40
Fasching, P.A.41
more..
-
7
-
-
84907298200
-
Genetic/familial high-risk assessment: breast and ovarian, version 1. 2014
-
COI: 1:CAS:528:DC%2BC2cXhvFGmtL%2FF
-
Daly MB, Pilarski R, Axilbund JE, Buys SS, Crawford B, Friedman S, Garber JE, Horton C, Kaklamani V, Klein C, Kohlmann W, Kurian A, Litton J, Madlensky L, Marcom PK, Merajver SD, Offit K, Pal T, Pasche B, Reiser G, Shannon KM, Swisher E, Voian NC, Weitzel JN, Whelan A, Wiesner GL, Dwyer MA, Kumar R (2014) Genetic/familial high-risk assessment: breast and ovarian, version 1. 2014. J Natl Compr Cancer Netw 12:1326–1338
-
(2014)
J Natl Compr Cancer Netw
, vol.12
, pp. 1326-1338
-
-
Daly, M.B.1
Pilarski, R.2
Axilbund, J.E.3
Buys, S.S.4
Crawford, B.5
Friedman, S.6
Garber, J.E.7
Horton, C.8
Kaklamani, V.9
Klein, C.10
Kohlmann, W.11
Kurian, A.12
Litton, J.13
Madlensky, L.14
Marcom, P.K.15
Merajver, S.D.16
Offit, K.17
Pal, T.18
Pasche, B.19
Reiser, G.20
Shannon, K.M.21
Swisher, E.22
Voian, N.C.23
Weitzel, J.N.24
Whelan, A.25
Wiesner, G.L.26
Dwyer, M.A.27
Kumar, R.28
more..
-
8
-
-
66249120367
-
Human splicing finder: an online bioinformatics tool to predict splicing signals
-
PID: 19339519
-
Desmet FO, Hamroun D, Lalande M, Collod-Beroud G, Claustres M, Beroud C (2009) Human splicing finder: an online bioinformatics tool to predict splicing signals. Nucleic Acids Res 37:e67
-
(2009)
Nucleic Acids Res
, vol.37
, pp. e67
-
-
Desmet, F.O.1
Hamroun, D.2
Lalande, M.3
Collod-Beroud, G.4
Claustres, M.5
Beroud, C.6
-
10
-
-
67650471685
-
Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers
-
COI: 1:CAS:528:DC%2BD1MXosVKrtrw%3D, PID: 19553641
-
Fong PC, Boss DS, Yap TA, Tutt A, Wu P, Mergui-Roelvink M, Mortimer P, Swaisland H, Lau A, O’Connor MJ, Ashworth A, Carmichael J, Kaye SB, Schellens JH, de Bono JS (2009) Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers. N Engl J Med 361:123–134
-
(2009)
N Engl J Med
, vol.361
, pp. 123-134
-
-
Fong, P.C.1
Boss, D.S.2
Yap, T.A.3
Tutt, A.4
Wu, P.5
Mergui-Roelvink, M.6
Mortimer, P.7
Swaisland, H.8
Lau, A.9
O’Connor, M.J.10
Ashworth, A.11
Carmichael, J.12
Kaye, S.B.13
Schellens, J.H.14
de Bono, J.S.15
-
11
-
-
0028330276
-
Risks of cancer in BRCA1-mutation carriers. Breast cancer linkage consortium
-
COI: 1:STN:280:DyaK2c7otVKitQ%3D%3D, PID: 7907678
-
Ford D, Easton DF, Bishop DT, Narod SA, Goldgar DE (1994) Risks of cancer in BRCA1-mutation carriers. Breast cancer linkage consortium. Lancet 343:692–695
-
(1994)
Lancet
, vol.343
, pp. 692-695
-
-
Ford, D.1
Easton, D.F.2
Bishop, D.T.3
Narod, S.A.4
Goldgar, D.E.5
-
12
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The breast cancer linkage consortium
-
COI: 1:CAS:528:DyaK1MXlvFeh, PID: 9497246
-
Ford D, Easton DF, Stratton M, Narod S, Goldgar D, Devilee P, Bishop DT, Weber B, Lenoir G, Chang-Claude J, Sobol H, Teare MD, Struewing J, Arason A, Scherneck S, Peto J, Rebbeck TR, Tonin P, Neuhausen S, Barkardottir R, Eyfjord J, Lynch H, Ponder BA, Gayther SA, Zelada-Hedman M (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.F.2
Stratton, M.3
Narod, S.4
Goldgar, D.5
Devilee, P.6
Bishop, D.T.7
Weber, B.8
Lenoir, G.9
Chang-Claude, J.10
Sobol, H.11
Teare, M.D.12
Struewing, J.13
Arason, A.14
Scherneck, S.15
Peto, J.16
Rebbeck, T.R.17
Tonin, P.18
Neuhausen, S.19
Barkardottir, R.20
Eyfjord, J.21
Lynch, H.22
Ponder, B.A.23
Gayther, S.A.24
Zelada-Hedman, M.25
more..
-
13
-
-
84880115555
-
In brief: BRCA1 and BRCA2
-
COI: 1:CAS:528:DC%2BC3sXhtFSit7vE, PID: 23620175
-
Foulkes WD, Shuen AY (2013) In brief: BRCA1 and BRCA2. J Pathol 230:347–349
-
(2013)
J Pathol
, vol.230
, pp. 347-349
-
-
Foulkes, W.D.1
Shuen, A.Y.2
-
14
-
-
78149483057
-
Triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BC3cXhsVCltr7P, PID: 21067385
-
Foulkes WD, Smith IE, Reis-Filho JS (2010) Triple-negative breast cancer. N Engl J Med 363:1938–1948
-
(2010)
N Engl J Med
, vol.363
, pp. 1938-1948
-
-
Foulkes, W.D.1
Smith, I.E.2
Reis-Filho, J.S.3
-
15
-
-
79961128939
-
Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany
-
PID: 22109790
-
Gadzicki D, Evans DG, Harris H, Julian-Reynier C, Nippert I, Schmidtke J, Tibben A, van Asperen CJ, Schlegelberger B (2011) Genetic testing for familial/hereditary breast cancer—comparison of guidelines and recommendations from the UK, France, the Netherlands and Germany. J Community Genet 2:53–69
-
(2011)
J Community Genet
, vol.2
, pp. 53-69
-
-
Gadzicki, D.1
Evans, D.G.2
Harris, H.3
Julian-Reynier, C.4
Nippert, I.5
Schmidtke, J.6
Tibben, A.7
van Asperen, C.J.8
Schlegelberger, B.9
-
16
-
-
79952253747
-
Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer
-
COI: 1:CAS:528:DC%2BC3MXis1eisbc%3D, PID: 21233401
-
Gonzalez-Angulo AM, Timms KM, Liu S, Chen H, Litton JK, Potter J, Lanchbury JS, Stemke-Hale K, Hennessy BT, Arun BK, Hortobagyi GN, Do KA, Mills GB, Meric-Bernstam F (2011) Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer. Clin Cancer Res 17:1082–1089
-
(2011)
Clin Cancer Res
, vol.17
, 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
Hortobagyi, G.N.11
Do, K.A.12
Mills, G.B.13
Meric-Bernstam, F.14
-
17
-
-
77954526150
-
American Society of Clinical Oncology/College of American Pathologists guideline recommendations for immunohistochemical testing of estrogen and progesterone receptors in breast cancer
-
PID: 20404251
-
Hammond ME, Hayes DF, Dowsett M, Allred DC, Hagerty KL, Badve S, Fitzgibbons PL, Francis G, Goldstein NS, Hayes M, Hicks DG, Lester S, Love R, Mangu PB, McShane L, Miller K, Osborne CK, Paik S, Perlmutter J, Rhodes A, Sasano H, Schwartz JN, Sweep FC, Taube S, Torlakovic EE, Valenstein P, Viale G, Visscher D, Wheeler T, Williams RB, Wittliff JL, Wolff AC (2010) American Society of Clinical Oncology/College of American Pathologists guideline recommendations for immunohistochemical testing of estrogen and progesterone receptors in breast cancer. J Clin Oncol 28:2784–2795
-
(2010)
J Clin Oncol
, vol.28
, pp. 2784-2795
-
-
Hammond, M.E.1
Hayes, D.F.2
Dowsett, M.3
Allred, D.C.4
Hagerty, K.L.5
Badve, S.6
Fitzgibbons, P.L.7
Francis, G.8
Goldstein, N.S.9
Hayes, M.10
Hicks, D.G.11
Lester, S.12
Love, R.13
Mangu, P.B.14
McShane, L.15
Miller, K.16
Osborne, C.K.17
Paik, S.18
Perlmutter, J.19
Rhodes, A.20
Sasano, H.21
Schwartz, J.N.22
Sweep, F.C.23
Taube, S.24
Torlakovic, E.E.25
Valenstein, P.26
Viale, G.27
Visscher, D.28
Wheeler, T.29
Williams, R.B.30
Wittliff, J.L.31
Wolff, A.C.32
more..
-
18
-
-
84861323251
-
Prevalence of BRCA mutations in an unselected population of triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BC38Xnt1Kgtbs%3D, PID: 22614657
-
Hartman AR, Kaldate RR, Sailer LM, Painter L, Grier CE, Endsley RR, Griffin M, Hamilton SA, Frye CA, Silberman MA, Wenstrup RJ, Sandbach JF (2012) Prevalence of BRCA mutations in an unselected population of triple-negative breast cancer. Cancer 118:2787–2795
-
(2012)
Cancer
, vol.118
, pp. 2787-2795
-
-
Hartman, A.R.1
Kaldate, R.R.2
Sailer, L.M.3
Painter, L.4
Grier, C.E.5
Endsley, R.R.6
Griffin, M.7
Hamilton, S.A.8
Frye, C.A.9
Silberman, M.A.10
Wenstrup, R.J.11
Sandbach, J.F.12
-
19
-
-
56949103031
-
What is triple-negative breast cancer?
-
COI: 1:CAS:528:DC%2BD1cXhsVKltr%2FE, PID: 19008097
-
Irvin WJ Jr, Carey LA (2008) What is triple-negative breast cancer? Eur J Cancer 44:2799–2805
-
(2008)
Eur J Cancer
, vol.44
, pp. 2799-2805
-
-
Irvin, W.J.1
Carey, L.A.2
-
20
-
-
49649087897
-
Classifying variants of undetermined significance in BRCA2 with protein likelihood ratios
-
PID: 19043619
-
Karchin R, Agarwal M, Sali A, Couch F, Beattie MS (2008) Classifying variants of undetermined significance in BRCA2 with protein likelihood ratios. Cancer Inform 6:203–216
-
(2008)
Cancer Inform
, vol.6
, pp. 203-216
-
-
Karchin, R.1
Agarwal, M.2
Sali, A.3
Couch, F.4
Beattie, M.S.5
-
21
-
-
0142178215
-
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
COI: 1:CAS:528:DC%2BD3sXotlWqt7Y%3D, PID: 14576434
-
King MC, Marks JH, Mandell JB (2003) Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 302:643–646
-
(2003)
Science
, vol.302
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
22
-
-
84871455595
-
Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges
-
COI: 1:CAS:528:DC%2BC3sXlsVKlsQ%3D%3D, PID: 23285130
-
Knies K, Schuster B, Ameziane N, Rooimans M, Bettecken T, de Winter J, Schindler D (2012) Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges. PLoS One 7:e52648
-
(2012)
PLoS One
, vol.7
, pp. e52648
-
-
Knies, K.1
Schuster, B.2
Ameziane, N.3
Rooimans, M.4
Bettecken, T.5
de Winter, J.6
Schindler, D.7
-
23
-
-
68149165614
-
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
-
COI: 1:CAS:528:DC%2BD1MXovVyns78%3D, PID: 19561590
-
Kumar P, Henikoff S, Ng PC (2009) Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm. Nat Protoc 4:1073–1081
-
(2009)
Nat Protoc
, vol.4
, pp. 1073-1081
-
-
Kumar, P.1
Henikoff, S.2
Ng, P.C.3
-
24
-
-
84896721529
-
New strategies for triple-negative breast cancer–deciphering the heterogeneity
-
COI: 1:CAS:528:DC%2BC2cXivVejsb0%3D, PID: 24536073
-
Mayer IA, Abramson VG, Lehmann BD, Pietenpol JA (2014) New strategies for triple-negative breast cancer–deciphering the heterogeneity. Clin Cancer Res 20:782–790
-
(2014)
Clin Cancer Res
, vol.20
, pp. 782-790
-
-
Mayer, I.A.1
Abramson, V.G.2
Lehmann, B.D.3
Pietenpol, J.A.4
-
25
-
-
0036466858
-
Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population
-
COI: 1:CAS:528:DC%2BD38XkvFegtg%3D%3D, PID: 11802209
-
Meindl A (2002) Comprehensive analysis of 989 patients with breast or ovarian cancer provides BRCA1 and BRCA2 mutation profiles and frequencies for the German population. Int J Cancer 97:472–480
-
(2002)
Int J Cancer
, vol.97
, pp. 472-480
-
-
Meindl, A.1
-
26
-
-
84920830655
-
Cancers associated with BRCA1 and BRCA2 mutations other than breast and ovarian
-
COI: 1:CAS:528:DC%2BC2MXivFWmsg%3D%3D, PID: 25224030
-
Mersch J, Jackson MA, Park M, Nebgen D, Peterson SK, Singletary C, Arun BK, Litton JK (2015) Cancers associated with BRCA1 and BRCA2 mutations other than breast and ovarian. Cancer 121:269–275
-
(2015)
Cancer
, vol.121
, pp. 269-275
-
-
Mersch, J.1
Jackson, M.A.2
Park, M.3
Nebgen, D.4
Peterson, S.K.5
Singletary, C.6
Arun, B.K.7
Litton, J.K.8
-
27
-
-
84861603883
-
BRCA2 mutations and triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BC38XosVensbc%3D, PID: 22666503
-
Meyer P, Landgraf K, Hogel B, Eiermann W, Ataseven B (2012) BRCA2 mutations and triple-negative breast cancer. PLoS One 7:e38361
-
(2012)
PLoS One
, vol.7
, pp. e38361
-
-
Meyer, P.1
Landgraf, K.2
Hogel, B.3
Eiermann, W.4
Ataseven, B.5
-
28
-
-
79151476662
-
Triple negative breast cancer: unmet medical needs
-
COI: 1:CAS:528:DC%2BC3MXhtVelsbw%3D, PID: 21161370
-
Pal SK, Childs BH, Pegram M (2011) Triple negative breast cancer: unmet medical needs. Breast Cancer Res Treat 125:627–636
-
(2011)
Breast Cancer Res Treat
, vol.125
, pp. 627-636
-
-
Pal, S.K.1
Childs, B.H.2
Pegram, M.3
-
29
-
-
84868136807
-
Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BC38Xhs1KisL3M, PID: 23110154
-
Pern F, Bogdanova N, Schurmann P, Lin M, Ay A, Langer F, Hillemanns P, Christiansen H, Park-Simon TW, Dork T (2012) Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer. PLoS One 7:e47993
-
(2012)
PLoS One
, vol.7
, pp. e47993
-
-
Pern, F.1
Bogdanova, N.2
Schurmann, P.3
Lin, M.4
Ay, A.5
Langer, F.6
Hillemanns, P.7
Christiansen, H.8
Park-Simon, T.W.9
Dork, T.10
-
30
-
-
0030787520
-
Improved splice site detection in Genie
-
COI: 1:CAS:528:DyaK2sXls1Whtbc%3D, PID: 9278062
-
Reese MG, Eeckman FH, Kulp D, Haussler D (1997) Improved splice site detection in Genie. J Comput Biol 4:311–323
-
(1997)
J Comput Biol
, vol.4
, pp. 311-323
-
-
Reese, M.G.1
Eeckman, F.H.2
Kulp, D.3
Haussler, D.4
-
31
-
-
84871771432
-
Evaluation of BRCA1 mutations in an unselected patient population with triple-negative breast cancer
-
PID: 23192404
-
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 137:119–125
-
(2013)
Breast Cancer Res Treat
, vol.137
, pp. 119-125
-
-
Rummel, S.1
Varner, E.2
Shriver, C.D.3
Ellsworth, R.E.4
-
32
-
-
84863727561
-
Guideline for the prevention and early detection of breast and ovarian cancer in high risk patients, particularly in women from HBOC (hereditary breast and ovarian cancer) families
-
PID: 22644217
-
Singer CF, Tea MK, Pristauz G, Hubalek M, Rappaport C, Riedl C, Helbich T (2012) Guideline for the prevention and early detection of breast and ovarian cancer in high risk patients, particularly in women from HBOC (hereditary breast and ovarian cancer) families. Wien Klin Wochenschr 124:334–339
-
(2012)
Wien Klin Wochenschr
, vol.124
, pp. 334-339
-
-
Singer, C.F.1
Tea, M.K.2
Pristauz, G.3
Hubalek, M.4
Rappaport, C.5
Riedl, C.6
Helbich, T.7
-
33
-
-
78651370824
-
The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population
-
COI: 1:CAS:528:DC%2BC3MXht1Kltbk%3D, PID: 21232165
-
Stegel V, Krajc M, Zgajnar J, Teugels E, De Greve J, Hocevar M, Novakovic S (2011) The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population. BMC Med Genet 12:9
-
(2011)
BMC Med Genet
, vol.12
, pp. 9
-
-
Stegel, V.1
Krajc, M.2
Zgajnar, J.3
Teugels, E.4
De Greve, J.5
Hocevar, M.6
Novakovic, S.7
-
34
-
-
84964698044
-
Optimizing chemotherapy in triple-negative breast cancer: the role of platinum
-
Telli M (2014) Optimizing chemotherapy in triple-negative breast cancer: the role of platinum. Am Soc Clin Oncol Educ Book. e37–e42
-
(2014)
Am Soc Clin Oncol Educ Book
, pp. e37-e42
-
-
Telli, M.1
-
35
-
-
84890247728
-
Risk of having BRCA1 mutation in high-risk women with triple-negative breast cancer: a meta-analysis
-
COI: 1:CAS:528:DC%2BC3sXhvFequ7jJ, PID: 24000781
-
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 85:43–48
-
(2014)
Clin Genet
, vol.85
, pp. 43-48
-
-
Tun, N.M.1
Villani, G.2
Ong, K.3
Yoe, L.4
Bo, Z.M.5
-
36
-
-
33847147313
-
American Society of Clinical Oncology/College of American Pathologists guideline recommendations for human epidermal growth factor receptor 2 testing in breast cancer
-
COI: 1:CAS:528:DC%2BD2sXht1ejs7Y%3D, PID: 17159189
-
Wolff AC, Hammond ME, Schwartz JN, Hagerty KL, Allred DC, Cote RJ, Dowsett M, Fitzgibbons PL, Hanna WM, Langer A, McShane LM, Paik S, Pegram MD, Perez EA, Press MF, Rhodes A, Sturgeon C, Taube SE, Tubbs R, Vance GH, van de Vijver M, Wheeler TM, Hayes DF (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 25:118–145
-
(2007)
J Clin Oncol
, vol.25
, pp. 118-145
-
-
Wolff, A.C.1
Hammond, M.E.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 Vijver, M.21
Wheeler, T.M.22
Hayes, D.F.23
more..
-
37
-
-
84925486358
-
Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BC2MXjtFeisbs%3D, PID: 25682074
-
Wong-Brown MW, Meldrum CJ, Carpenter JE, Clarke CL, Narod SA, Jakubowska A, Rudnicka H, Lubinski J, Scott RJ (2015) Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer. Breast Cancer Res Treat 150:71–80
-
(2015)
Breast Cancer Res Treat
, vol.150
, pp. 71-80
-
-
Wong-Brown, M.W.1
Meldrum, C.J.2
Carpenter, J.E.3
Clarke, C.L.4
Narod, S.A.5
Jakubowska, A.6
Rudnicka, H.7
Lubinski, J.8
Scott, R.J.9
|