-
1
-
-
34247569300
-
Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from the California cancer Registry
-
PID: 17387718
-
Bauer KR, Brown M, Cress RD (2007) Descriptive analysis of estrogen receptor (ER)-negative, progesterone receptor (PR)-negative, and HER2-negative invasive breast cancer, the so-called triple-negative phenotype: a population-based study from the California cancer Registry. Cancer 109(9):1721–1728
-
(2007)
Cancer
, vol.109
, Issue.9
, pp. 1721-1728
-
-
Bauer, K.R.1
Brown, M.2
Cress, R.D.3
-
2
-
-
70849089229
-
Epidemiology of breast cancer subtypes in two prospective cohort studies of breast cancer survivors
-
PID: 19463150
-
Kwan ML, Kushi LH, Weltzien E et al (2009) Epidemiology of breast cancer subtypes in two prospective cohort studies of breast cancer survivors. Breast Cancer Res 11(3):R31. doi:10.1186/bcr2261
-
(2009)
Breast Cancer Res
, vol.11
, Issue.3
, pp. R31
-
-
Kwan, M.L.1
Kushi, L.H.2
Weltzien, E.3
-
3
-
-
80755171231
-
BRCA1/2 mutations and triple negative breast cancers
-
PID: 21778580
-
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
-
4
-
-
64749086562
-
The prevalence of BRCA1 mutations among young women with triple-negative breast cancer
-
COI: 1:CAS:528:DC%2BD1MXjvVSitLg%3D, PID: 19298662
-
Young SR, Pilarski RT, Donenberg T et al (2009) The prevalence of BRCA1 mutations among young women with triple-negative breast cancer. BMC Cancer 9:86. doi:10.1186/1471-2407-9-86
-
(2009)
BMC Cancer
, vol.9
, pp. 86
-
-
Young, S.R.1
Pilarski, R.T.2
Donenberg, T.3
-
5
-
-
52049086689
-
Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer
-
PID: 18779615
-
Atchley DP, Albarracin CT, Lopez A et al (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
-
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
-
COI: 1:CAS:528:DC%2BC2MXjs1Glsr8%3D, PID: 25452441
-
Couch FJ, Hart SN, Sharma P et al (2015) 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
-
(2015)
J Clin Oncol
, vol.33
, pp. 304-311
-
-
Couch, F.J.1
Hart, S.N.2
Sharma, P.3
-
7
-
-
0038298773
-
Breast cancers among very young premenopausal women (United States)
-
PID: 12749720
-
Althuis MD, Brogan DD, Coates RJ (2003) Breast cancers among very young premenopausal women (United States). Cancer Causes Control 14(2):151–160
-
(2003)
Cancer Causes Control
, vol.14
, Issue.2
, pp. 151-160
-
-
Althuis, M.D.1
Brogan, D.D.2
Coates, R.J.3
-
8
-
-
84874718584
-
Early onset Breast Cancer in a Registry-based sample of African-American women: BRCA mutation prevalence, and other personal and system-level clinical characteristics
-
COI: 1:CAS:528:DC%2BC3sXjs1entbY%3D, PID: 23320992
-
Pal T, Bonner D, Kim J et al (2013) Early onset Breast Cancer in a Registry-based sample of African-American women: BRCA mutation prevalence, and other personal and system-level clinical characteristics. Breast J 19(2):189–192
-
(2013)
Breast J
, vol.19
, Issue.2
, pp. 189-192
-
-
Pal, T.1
Bonner, D.2
Kim, J.3
-
9
-
-
37549036689
-
Prevalence of pathogenic BRCA1 mutation carriers in 5 U.S. racial/ethnic groups
-
COI: 1:CAS:528:DC%2BD1cXmvFOr, PID: 18159056
-
John EM, Miron A, Gong G et al (2007) Prevalence of pathogenic BRCA1 mutation carriers in 5 U.S. racial/ethnic groups. JAMA 298(24):2869–2876
-
(2007)
JAMA
, vol.298
, Issue.24
, pp. 2869-2876
-
-
John, E.M.1
Miron, A.2
Gong, G.3
-
10
-
-
33748092354
-
Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years
-
COI: 1:CAS:528:DC%2BD28XotFWqu74%3D, PID: 16912212
-
Malone KE, Daling JR, Doody DR et al (2006) Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. Cancer Res 66(16):8297–8308
-
(2006)
Cancer Res
, vol.66
, Issue.16
, pp. 8297-8308
-
-
Malone, K.E.1
Daling, J.R.2
Doody, D.R.3
-
11
-
-
32944456493
-
Racial differences in the incidence of BRCA1 and BRCA2 mutations in a cohort of early onset breast cancer patients: African American compared to white women
-
COI: 1:CAS:528:DC%2BD28XitF2hu78%3D, PID: 15983021
-
Haffty BG, Silber A, Matloff E et al (2006) Racial differences in the incidence of BRCA1 and BRCA2 mutations in a cohort of early onset breast cancer patients: African American compared to white women. J Med Genet 43:133–137
-
(2006)
J Med Genet
, vol.43
, pp. 133-137
-
-
Haffty, B.G.1
Silber, A.2
Matloff, E.3
-
12
-
-
26844544418
-
Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry
-
COI: 1:CAS:528:DC%2BD2MXhtFCitLnJ, PID: 16234499
-
Nanda R, Schumm LP, Cummings S et al (2005) Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry. JAMA 294(15):1925–1933
-
(2005)
JAMA
, vol.294
, Issue.15
, pp. 1925-1933
-
-
Nanda, R.1
Schumm, L.P.2
Cummings, S.3
-
13
-
-
65649112508
-
BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer
-
COI: 1:CAS:528:DC%2BD1MXlvFOhsrw%3D, PID: 19241424
-
Hall MJ, Reid JE, Burbidge LA et al (2009) BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer. Cancer 115(10):2222–2233
-
(2009)
Cancer
, vol.115
, Issue.10
, pp. 2222-2233
-
-
Hall, M.J.1
Reid, J.E.2
Burbidge, L.A.3
-
14
-
-
84867884099
-
Clinical significance of large rearrangements in BRCA1 and BRCA2
-
COI: 1:CAS:528:DC%2BC38XhsFCjsL3K, PID: 22544547
-
Judkins T, Rosenthal E, Arnell C et al (2012) Clinical significance of large rearrangements in BRCA1 and BRCA2. Cancer 118(21):5210–5216
-
(2012)
Cancer
, vol.118
, Issue.21
, pp. 5210-5216
-
-
Judkins, T.1
Rosenthal, E.2
Arnell, C.3
-
15
-
-
84883813542
-
Prevalence of BRCA mutations among women with triple-negative breast cancer (TNBC) in a genetic counseling cohort
-
PID: 23975317
-
Greenup R, Buchanan A, Lorizio W et al (2013) Prevalence of BRCA mutations among women with triple-negative breast cancer (TNBC) in a genetic counseling cohort. Ann Surg Oncol 20(10):3254–3258
-
(2013)
Ann Surg Oncol
, vol.20
, Issue.10
, pp. 3254-3258
-
-
Greenup, R.1
Buchanan, A.2
Lorizio, W.3
-
16
-
-
37549072095
-
®). Genetic/Familial High-Risk Assessment: Breast and Ovarian
-
®). Genetic/Familial High-Risk Assessment: Breast and Ovarian. Version 2.2015. www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf, Accessed 8 July 2015
-
(2015)
Version
, pp. 2
-
-
-
17
-
-
84928550017
-
Adherence patterns to National Comprehensive Cancer Network Guidelines for referral of women with breast cancer to genetics professionals
-
Stuckey A, Febbraro T, Laprise J, et al (2014) Adherence patterns to National Comprehensive Cancer Network Guidelines for referral of women with breast cancer to genetics professionals. Am J Clin Oncol 2014 [Epub ahead of print]
-
(2014)
Am J Clin Oncol
, vol.2014
, Issue.[Epub ahead of print]
-
-
Stuckey, A.1
Febbraro, T.2
Laprise, J.3
-
18
-
-
84899102829
-
BRCA sequencing and large rearrangement testing in young Black women with breast cancer
-
Pal T, Bonner D, Cragun D et al (2014) BRCA sequencing and large rearrangement testing in young Black women with breast cancer. J Commun Genet 5(2):157–165
-
(2014)
J Commun Genet
, vol.5
, Issue.2
, pp. 157-165
-
-
Pal, T.1
Bonner, D.2
Cragun, D.3
-
19
-
-
16944364123
-
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group
-
COI: 1:CAS:528:DyaK2sXjtlOru7c%3D, PID: 9150149
-
Stoppa-Lyonnet D, Laurent-Puig P, Essioux L et al (1997) BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Institut Curie Breast Cancer Group. Am J Hum Genet 60(5):1021–1030
-
(1997)
Am J Hum Genet
, vol.60
, Issue.5
, pp. 1021-1030
-
-
Stoppa-Lyonnet, D.1
Laurent-Puig, P.2
Essioux, L.3
-
20
-
-
84973336984
-
Unique genetic characteristics of BRCA mutation carriers in a cohort of Arab American women
-
Shatavi SV, Dohany, L, Chisti MM, et al. (2013) Unique genetic characteristics of BRCA mutation carriers in a cohort of Arab American women. J Clin Oncol 31, (suppl;aabstr 1541)
-
(2013)
J Clin Oncol
, vol.31
-
-
Shatavi, S.V.1
Dohany, L.2
Chisti, M.M.3
-
21
-
-
84939290542
-
Current variant of uncertain significance rates in BRCA1/2 and Lynch syndrome testing (MLH1, MSH2, MSH6
-
EPCAM) American College of Medical Genetics and Genomics annual meeting, Charlotte
-
Eggington JM, Burbidge LA, Roa B, et al (2012) Current variant of uncertain significance rates in BRCA1/2 and Lynch syndrome testing (MLH1, MSH2, MSH6, PMS2, EPCAM) American College of Medical Genetics and Genomics annual meeting, Charlotte
-
(2012)
PMS2
-
-
Eggington, J.M.1
Burbidge, L.A.2
Roa, B.3
-
22
-
-
84973356066
-
Mutation and uncertain variant findings in ethnic minority patients undergoing multi-gene panel testing for cancer risk assessment at a safety-net public hospital (Abstract 3428S). Presented at the 64th Annual Meeting of the American Society of Human Genetics
-
Ricker CN, Sturgeon JD, Gruber SB (2014) Mutation and uncertain variant findings in ethnic minority patients undergoing multi-gene panel testing for cancer risk assessment at a safety-net public hospital (Abstract 3428S). Presented at the 64th Annual Meeting of the American Society of Human Genetics, on October 2014 in San Diego
-
(2014)
on October 2014 in San Diego
-
-
Ricker, C.N.1
Sturgeon, J.D.2
Gruber, S.B.3
-
23
-
-
84908881428
-
Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients
-
LaDuca H, Stuenkel AJ, Dolinsky JS et al (2014) Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Gene Med 16(11):830–837
-
(2014)
Gene Med
, vol.16
, Issue.11
, pp. 830-837
-
-
LaDuca, H.1
Stuenkel, A.J.2
Dolinsky, J.S.3
-
24
-
-
84918798338
-
Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel
-
COI: 1:CAS:528:DC%2BC2cXitFWlsrbN, PID: 25186627
-
Tung N, Battelli C, Allen B et al (2015) Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel. Cancer 121(1):25–33
-
(2015)
Cancer
, vol.121
, Issue.1
, pp. 25-33
-
-
Tung, N.1
Battelli, C.2
Allen, B.3
-
25
-
-
83755180749
-
Long-term outcome of BRCA1/BRCA2 testing: risk reduction and surveillance
-
PID: 21717445
-
Schwartz MD, Isaacs C, Graves KD et al (2012) Long-term outcome of BRCA1/BRCA2 testing: risk reduction and surveillance. Cancer 118(2):510–517
-
(2012)
Cancer
, vol.118
, Issue.2
, pp. 510-517
-
-
Schwartz, M.D.1
Isaacs, C.2
Graves, K.D.3
-
26
-
-
40949154795
-
Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers
-
PID: 18344704
-
Bradbury AR, Comfort NI, Dignam JJ et al (2008) Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers. Genet Med 10:161–166
-
(2008)
Genet Med
, vol.10
, pp. 161-166
-
-
Bradbury, A.R.1
Comfort, N.I.2
Dignam, J.J.3
-
27
-
-
33747445937
-
Risk reduction behaviors and provider communication following genetic counseling and BRCA1 mutation testing in an African American kindred
-
PID: 16865561
-
Kinney AY, Simonsen SE, Baty BJ (2006) Risk reduction behaviors and provider communication following genetic counseling and BRCA1 mutation testing in an African American kindred. J Genet Couns 15:293–305
-
(2006)
J Genet Couns
, vol.15
, pp. 293-305
-
-
Kinney, A.Y.1
Simonsen, S.E.2
Baty, B.J.3
-
28
-
-
33745667036
-
”Why take it if you don’t have anything?” breast cancer risk perceptions and prevention choices at a public hospital
-
PID: 16808782
-
Salant T, Ganschow PS, Olopade OI (2006) ”Why take it if you don’t have anything?” breast cancer risk perceptions and prevention choices at a public hospital. J Gen Intern Med 21:779–785
-
(2006)
J Gen Intern Med
, vol.21
, pp. 779-785
-
-
Salant, T.1
Ganschow, P.S.2
Olopade, O.I.3
-
29
-
-
84868010151
-
Receipt of genetic counseling recommendations among black women at high risk for BRCA mutations
-
COI: 1:CAS:528:DC%2BC38XhsFOqtLfL
-
Thompson HS, Sussner K, Schwartz MD et al (2012) Receipt of genetic counseling recommendations among black women at high risk for BRCA mutations. Genet Test Molec Biomark 16(11):1257–1262
-
(2012)
Genet Test Molec Biomark
, vol.16
, Issue.11
, pp. 1257-1262
-
-
Thompson, H.S.1
Sussner, K.2
Schwartz, M.D.3
-
30
-
-
32944474116
-
Recruiting African American women to participate in hereditary breast cancer research
-
PID: 16258097
-
Halbert CH, Brewster K, Collier A et al (2005) Recruiting African American women to participate in hereditary breast cancer research. J Clin Oncol 23(31):7967–7973
-
(2005)
J Clin Oncol
, vol.23
, Issue.31
, pp. 7967-7973
-
-
Halbert, C.H.1
Brewster, K.2
Collier, A.3
-
31
-
-
84866888895
-
Barriers to genetic testing for breast cancer risk among ethnic minority women: an exploratory study
-
PID: 22870568
-
Glenn BA, Chawla N, Bastani R (2012) Barriers to genetic testing for breast cancer risk among ethnic minority women: an exploratory study. Ethn Dis 22(3):267–273
-
(2012)
Ethn Dis
, vol.22
, Issue.3
, pp. 267-273
-
-
Glenn, B.A.1
Chawla, N.2
Bastani, R.3
-
32
-
-
37849013468
-
Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer
-
PID: 18165638
-
Susswein LR, Skrzynia C, Lange LA et al (2008) Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer. J Clin Oncol 26:32–36
-
(2008)
J Clin Oncol
, vol.26
, pp. 32-36
-
-
Susswein, L.R.1
Skrzynia, C.2
Lange, L.A.3
-
33
-
-
80053386277
-
Ethnic, racial and cultural identity and perceived benefits and barriers related to genetic testing for breast cancer among at-risk women of African descent in New York City
-
COI: 1:STN:280:DC%2BC3MflvFykuw%3D%3D, PID: 21540561
-
Sussner KM, Edwards TA, Thompson HS et al (2011) Ethnic, racial and cultural identity and perceived benefits and barriers related to genetic testing for breast cancer among at-risk women of African descent in New York City. Public Health Genomics 14(6):356–370
-
(2011)
Public Health Genomics
, vol.14
, Issue.6
, pp. 356-370
-
-
Sussner, K.M.1
Edwards, T.A.2
Thompson, H.S.3
-
34
-
-
84861589732
-
The influence of health care policies and health care system disrupt on willingness to undergo genetic testing
-
PID: 22473221
-
Armstrong K, Putt M, Halbert CH et al (2012) The influence of health care policies and health care system disrupt on willingness to undergo genetic testing. Med Care 50(5):381–387
-
(2012)
Med Care
, vol.50
, Issue.5
, pp. 381-387
-
-
Armstrong, K.1
Putt, M.2
Halbert, C.H.3
-
35
-
-
84939290544
-
-
Affordable Care Act Implementation FAQs–Set 12. Accessed on April 15 2015
-
Affordable Care Act Implementation FAQs–Set 12. http://www.cms.gov/CCIIO/Resources/Fact-Sheets-and-FAQs/aca_implementation_faqs12.html. Accessed on April 15 2015
-
-
-
-
36
-
-
84922104283
-
Inherited predispostion to breast cancer among African American women
-
COI: 1:CAS:528:DC%2BC2cXitVWkur%2FO, PID: 25428789
-
Churpek JE, Walsh T, Zheng Y et al (2015) Inherited predispostion to breast cancer among African American women. Breast Cancer Res Treat 149(1):31–39
-
(2015)
Breast Cancer Res Treat
, vol.149
, Issue.1
, pp. 31-39
-
-
Churpek, J.E.1
Walsh, T.2
Zheng, Y.3
-
37
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
COI: 1:CAS:528:DC%2BD1MXltFOrurk%3D, PID: 19383810
-
Heikkinen T, Kärkkäinen H, Aaltonen K et al (2009) The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res 15(9):3214–3222
-
(2009)
Clin Cancer Res
, vol.15
, Issue.9
, pp. 3214-3222
-
-
Heikkinen, T.1
Kärkkäinen, H.2
Aaltonen, K.3
-
38
-
-
84905842087
-
Breast-cancer risk in families with mutations in PALB2
-
PID: 25099575
-
Antoniou AC, Casadei S, Heikkinen T et al (2014) Breast-cancer risk in families with mutations in PALB2. N Engl J Med 371(6):497–506
-
(2014)
N Engl J Med
, vol.371
, Issue.6
, pp. 497-506
-
-
Antoniou, A.C.1
Casadei, S.2
Heikkinen, T.3
|