-
1
-
-
0034686619
-
Genetic and hormonal risk factors in breast cancer
-
Martin AM, Weber BL: Genetic and hormonal risk factors in breast cancer. J Natl Cancer Inst 92:1126-1135, 2000
-
(2000)
J Natl Cancer Inst
, vol.92
, pp. 1126-1135
-
-
Martin, A.M.1
Weber, B.L.2
-
2
-
-
0037162110
-
Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations
-
Rebbeck TR, Lynch HT, Neuhausen SL, et al: Prophylactic oophorectomy in carriers of BRCA1 or BRCA2 mutations. N Engl J Med 346:1616-1622, 2002
-
(2002)
N Engl J Med
, vol.346
, pp. 1616-1622
-
-
Rebbeck, T.R.1
Lynch, H.T.2
Neuhausen, S.L.3
-
3
-
-
0037162115
-
Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation
-
Kauff ND, Satagopan JM, Robson ME, et al: Risk-reducing salpingo-oophorectomy in women with a BRCA1 or BRCA2 mutation. N Engl J Med 346:1609-1615, 2002
-
(2002)
N Engl J Med
, vol.346
, pp. 1609-1615
-
-
Kauff, N.D.1
Satagopan, J.M.2
Robson, M.E.3
-
4
-
-
0033199926
-
Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers
-
Rebbeck TR, Levin AM, Eisen A, et al: Breast cancer risk after bilateral prophylactic oophorectomy in BRCA1 mutation carriers. J Natl Cancer Inst 91:1475-1479, 1999
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1475-1479
-
-
Rebbeck, T.R.1
Levin, A.M.2
Eisen, A.3
-
5
-
-
0034597916
-
Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: A case-control study. Hereditary Breast Cancer Clinical Study Group
-
Narod SA, Brunet JS, Ghadirian P, et al: Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers: A case-control study. Hereditary Breast Cancer Clinical Study Group. Lancet 356:1876-1881, 2000
-
(2000)
Lancet
, vol.356
, pp. 1876-1881
-
-
Narod, S.A.1
Brunet, J.S.2
Ghadirian, P.3
-
6
-
-
0032514413
-
Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group
-
Narod SA, Risch H, Moslehi R, et al: Oral contraceptives and the risk of hereditary ovarian cancer. Hereditary Ovarian Cancer Clinical Study Group. N Engl J Med 339:424-428, 1998
-
(1998)
N Engl J Med
, vol.339
, pp. 424-428
-
-
Narod, S.A.1
Risch, H.2
Moslehi, R.3
-
7
-
-
0036157735
-
Family history of cancer, oral contraceptive use, and ovarian cancer risk
-
Walker GR, Schlesselman JJ, Ness RB: Family history of cancer, oral contraceptive use, and ovarian cancer risk. Am J Obstet Gynecol 186:8-14, 2002
-
(2002)
Am J Obstet Gynecol
, vol.186
, pp. 8-14
-
-
Walker, G.R.1
Schlesselman, J.J.2
Ness, R.B.3
-
8
-
-
0033552904
-
Efficacy of bilateral prophylactic mastectomy in women with a family history of breast cancer
-
Hartmann LC, Schaid DJ, Woods JE, et al: Efficacy of bilateral prophylactic mastectomy in women with a family history of breast cancer. N Engl J Med 340:77-84, 1999
-
(1999)
N Engl J Med
, vol.340
, pp. 77-84
-
-
Hartmann, L.C.1
Schaid, D.J.2
Woods, J.E.3
-
9
-
-
0035824069
-
Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers
-
Hartmann LC, Sellers TA, Schaid DJ, et al: Efficacy of bilateral prophylactic mastectomy in BRCA1 and BRCA2 gene mutation carriers. J Natl Cancer Inst 93:1633-1637, 2001
-
(2001)
J Natl Cancer Inst
, vol.93
, pp. 1633-1637
-
-
Hartmann, L.C.1
Sellers, T.A.2
Schaid, D.J.3
-
10
-
-
0035913275
-
Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation
-
Meijers-Heijboer H, van Geel B, van Putten WL, et al: Breast cancer after prophylactic bilateral mastectomy in women with a BRCA1 or BRCA2 mutation. N Engl J Med 345:159-164, 2001
-
(2001)
N Engl J Med
, vol.345
, pp. 159-164
-
-
Meijers-Heijboer, H.1
van Geel, B.2
van Putten, W.L.3
-
11
-
-
0036498727
-
Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers
-
Scheuer L, Kauff N, Robson M, et al: Outcome of preventive surgery and screening for breast and ovarian cancer in BRCA mutation carriers. J Clin Oncol 20:1260-1268, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 1260-1268
-
-
Scheuer, L.1
Kauff, N.2
Robson, M.3
-
12
-
-
0035865285
-
Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk
-
Brekelmans CT, Seynaeve C, Bartels CC, et al: Effectiveness of breast cancer surveillance in BRCA1/2 gene mutation carriers and women with high familial risk. J Clin Oncol 19:924-930, 2001
-
(2001)
J Clin Oncol
, vol.19
, pp. 924-930
-
-
Brekelmans, C.T.1
Seynaeve, C.2
Bartels, C.C.3
-
13
-
-
0036498780
-
Risk management in BRCA1 and BRCA2 mutation carriers: Lessons learned, challenges posed
-
DeMichele A, Weber BL: Risk management in BRCA1 and BRCA2 mutation carriers: Lessons learned, challenges posed. J Clin Oncol 20:1164-1166, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 1164-1166
-
-
DeMichele, A.1
Weber, B.L.2
-
14
-
-
0032537990
-
Tamoxifen for prevention of breast cancer: Report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study
-
Fisher B, Costantino JP, Wickerham DL, et al: Tamoxifen for prevention of breast cancer: Report of the National Surgical Adjuvant Breast and Bowel Project P-1 Study. J Natl Cancer Inst 90:1371-1388, 1998
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 1371-1388
-
-
Fisher, B.1
Costantino, J.P.2
Wickerham, D.L.3
-
15
-
-
0036157770
-
American Cancer Society guidelines for the early detection of cancer
-
Smith RA, Cokkinides V, von Eschenbach AC, et al: American Cancer Society guidelines for the early detection of cancer. CA Cancer J Clin 52:8-22, 2002
-
(2002)
CA Cancer J Clin
, vol.52
, pp. 8-22
-
-
Smith, R.A.1
Cokkinides, V.2
von Eschenbach, A.C.3
-
16
-
-
0027979310
-
Autosomal dominant inheritance of early-onset breast cancer: Implications for risk prediction
-
Claus EB, Risch N, Thompson WD: Autosomal dominant inheritance of early-onset breast cancer: Implications for risk prediction. Cancer 73:643-651, 1994
-
(1994)
Cancer
, vol.73
, pp. 643-651
-
-
Claus, E.B.1
Risch, N.2
Thompson, W.D.3
-
17
-
-
0024801278
-
Projecting individualized probabilities of developing breast cancer for white females who are being examined annually
-
Gail MH, Brinton LA, Byar DP, et al: Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. J Natl Cancer Inst 81:1879-1886, 1989
-
(1989)
J Natl Cancer Inst
, vol.81
, pp. 1879-1886
-
-
Gail, M.H.1
Brinton, L.A.2
Byar, D.P.3
-
18
-
-
0343918505
-
BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer
-
Couch FJ, DeShano ML, Blackwood MA, et al: BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. N Engl J Med 336:1409-1415, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1409-1415
-
-
Couch, F.J.1
DeShano, M.L.2
Blackwood, M.A.3
-
19
-
-
0030852505
-
BRCA1 sequence analysis in women at high risk for susceptibility mutations: Risk factor analysis and implications for genetic testing
-
Shattuck-Eidens D, Oliphant A, McClure M, et al: BRCA1 sequence analysis in women at high risk for susceptibility mutations: Risk factor analysis and implications for genetic testing. J Am Med Assoc 278:1242-1250, 1997
-
(1997)
J Am Med Assoc
, vol.278
, pp. 1242-1250
-
-
Shattuck-Eidens, D.1
Oliphant, A.2
McClure, M.3
-
20
-
-
0031832541
-
Sequence analysis of BRCA1 and BRCA2: Correlation of mutations with family history and ovarian cancer risk
-
Frank TS, Manley SA, Olopade OI, et al: Sequence analysis of BRCA1 and BRCA2: Correlation of mutations with family history and ovarian cancer risk. J Clin Oncol 16:2417-2425, 1998
-
(1998)
J Clin Oncol
, vol.16
, pp. 2417-2425
-
-
Frank, T.S.1
Manley, S.A.2
Olopade, O.I.3
-
21
-
-
0031917403
-
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2
-
Parmigiani G, Berry D, Aguilar O: Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2. Am J Hum Genet 62:145-158, 1998
-
(1998)
Am J Hum Genet
, vol.62
, pp. 145-158
-
-
Parmigiani, G.1
Berry, D.2
Aguilar, O.3
-
22
-
-
0031971484
-
Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes
-
Chang-Claude J, Dong J, Schmidt S, et al: Using gene carrier probability to select high risk families for identifying germline mutations in breast cancer susceptibility genes. J Med Genet 35:116-121, 1998
-
(1998)
J Med Genet
, vol.35
, pp. 116-121
-
-
Chang-Claude, J.1
Dong, J.2
Schmidt, S.3
-
23
-
-
0033237314
-
The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews
-
Hartge P, Struewing JP, Wacholder S, et al: The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews. Am J Hum Genet 64:963-970, 1999
-
(1999)
Am J Hum Genet
, vol.64
, pp. 963-970
-
-
Hartge, P.1
Struewing, J.P.2
Wacholder, S.3
-
24
-
-
0035793797
-
A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families
-
Vahteristo P, Eerola H, Tamminen A, et al: A probability model for predicting BRCA1 and BRCA2 mutations in breast and breast-ovarian cancer families. Br J Cancer 84:704-708, 2001
-
(2001)
Br J Cancer
, vol.84
, pp. 704-708
-
-
Vahteristo, P.1
Eerola, H.2
Tamminen, A.3
-
25
-
-
0033814256
-
A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center
-
Gilpin CA, Carson N, Hunter AG: A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center. Clin Genet 58:299-308, 2000
-
(2000)
Clin Genet
, vol.58
, pp. 299-308
-
-
Gilpin, C.A.1
Carson, N.2
Hunter, A.G.3
-
26
-
-
17544403741
-
Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer
-
Krainer M, Silva-Arrieta S, FitzGerald MG, et al: Differential contributions of BRCA1 and BRCA2 to early-onset breast cancer. N Engl J Med 336:1416-1421, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1416-1421
-
-
Krainer, M.1
Silva-Arrieta, S.2
FitzGerald, M.G.3
-
28
-
-
13344260688
-
Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer
-
FitzGerald MG, MacDonald DJ, Krainer M, et al: Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer. N Engl J Med 334:143-149, 1996
-
(1996)
N Engl J Med
, vol.334
, pp. 143-149
-
-
FitzGerald, M.G.1
MacDonald, D.J.2
Krainer, M.3
-
29
-
-
0034653903
-
Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases
-
Malone KE, Daling JR, Neal C, et al: Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases. Cancer 88:1393-1402, 2000
-
(2000)
Cancer
, vol.88
, pp. 1393-1402
-
-
Malone, K.E.1
Daling, J.R.2
Neal, C.3
-
30
-
-
14844331964
-
Predicted probability of breast cancer susceptibility gene mutations
-
Blackwood MA, Yang H, Margolin A, et al: Predicted probability of breast cancer susceptibility gene mutations. Breast Cancer Res Treat 69:223, 2001
-
(2001)
Breast Cancer Res Treat
, vol.69
, pp. 223
-
-
Blackwood, M.A.1
Yang, H.2
Margolin, A.3
-
31
-
-
0033516265
-
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
-
Peto J, Collins N, Barfoot R, et al: Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J Natl Cancer Inst 91:943-949, 1999
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 943-949
-
-
Peto, J.1
Collins, N.2
Barfoot, R.3
-
32
-
-
0037087536
-
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: Analysis of 10,000 individuals
-
Frank TS, Deffenbaugh AM, Reid JE, et al: Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: Analysis of 10,000 individuals. J Clin Oncol 20:1480-1490, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 1480-1490
-
-
Frank, T.S.1
Deffenbaugh, A.M.2
Reid, J.E.3
-
33
-
-
0031029633
-
Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history
-
Berry DA, Parmigiani G, Sanchez J, et al: Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history. J Natl Cancer Inst 89:227-238, 1997
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 227-238
-
-
Berry, D.A.1
Parmigiani, G.2
Sanchez, J.3
-
34
-
-
0028843102
-
Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium
-
Easton DF, Ford D, Bishop DT: Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium. Am J Hum Genet 56:265-271, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 265-271
-
-
Easton, D.F.1
Ford, D.2
Bishop, D.T.3
-
35
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium
-
Ford D, Easton DF, Stratton M, et al: 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
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
36
-
-
0032231617
-
Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patients
-
Fodor FH, Weston A, Bleiweiss IJ, et al: Frequency and carrier risk associated with common BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer patients. Am J Hum Genet 63:45-51, 1998
-
(1998)
Am J Hum Genet
, vol.63
, pp. 45-51
-
-
Fodor, F.H.1
Weston, A.2
Bleiweiss, I.J.3
-
37
-
-
0036605379
-
BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes
-
Berry DA, Iversen ES, Jr, Gudbjartsson DF, et al: BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. J Clin Oncol 20:2701-2712, 2002
-
(2002)
J Clin Oncol
, vol.20
, pp. 2701-2712
-
-
Berry, D.A.1
Iversen Jr, E.S.2
Gudbjartsson, D.F.3
-
38
-
-
0031035359
-
The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women
-
Abeliovich D, Kaduri L, Lerer I, et al: The founder mutations 185delAG and 5382insC in BRCA1 and 6174delT in BRCA2 appear in 60% of ovarian cancer and 30% of early-onset breast cancer patients among Ashkenazi women. Am J Hum Genet 60:505-514, 1997
-
(1997)
Am J Hum Genet
, vol.60
, pp. 505-514
-
-
Abeliovich, D.1
Kaduri, L.2
Lerer, I.3
-
39
-
-
16944363862
-
Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families
-
Levy-Lahad E, Catane R, Eisenberg S, et al: Founder BRCA1 and BRCA2 mutations in Ashkenazi Jews in Israel: Frequency and differential penetrance in ovarian cancer and in breast-ovarian cancer families. Am J Hum Genet 60:1059-1067, 1997
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1059-1067
-
-
Levy-Lahad, E.1
Catane, R.2
Eisenberg, S.3
-
40
-
-
0031281949
-
High frequency of BRCA1 and BRCA2 germline mutations in Ashkenazi Jewish ovarian cancer patients, regardless of family history
-
Beller U, Halle D, Catane R, et al: High frequency of BRCA1 and BRCA2 germline mutations in Ashkenazi Jewish ovarian cancer patients, regardless of family history. Gynecol Oncol 67:123-126, 1997
-
(1997)
Gynecol Oncol
, vol.67
, pp. 123-126
-
-
Beller, U.1
Halle, D.2
Catane, R.3
-
41
-
-
0032126139
-
Rates of Jewish ancestral mutations in BRCA1 and BRCA2 in borderline ovarian tumors
-
Gotlieb WH, Friedman E, Bar-Sade RB, et al: Rates of Jewish ancestral mutations in BRCA1 and BRCA2 in borderline ovarian tumors. J Natl Cancer Inst 90:995-1000, 1998
-
(1998)
J Natl Cancer Inst
, vol.90
, pp. 995-1000
-
-
Gotlieb, W.H.1
Friedman, E.2
Bar-Sade, R.B.3
-
42
-
-
0342940785
-
Pathology of familial breast cancer: Differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Breast Cancer Linkage Consortium
-
Pathology of familial breast cancer: differences between breast cancers in carriers of BRCA1 or BRCA2 mutations and sporadic cases. Breast Cancer Linkage Consortium. Lancet 349:1505-1510, 1997
-
(1997)
Lancet
, vol.349
, pp. 1505-1510
-
-
-
43
-
-
0018218939
-
Lobular carcinoma in situ of the breast: Detailed analysis of 99 patients with average follow-up of 24 years
-
Rosen PP, Kosloff C, Lieberman PH, et al: Lobular carcinoma in situ of the breast: Detailed analysis of 99 patients with average follow-up of 24 years. Am J Surg Pathol 2:225-251, 1978
-
(1978)
Am J Surg Pathol
, vol.2
, pp. 225-251
-
-
Rosen, P.P.1
Kosloff, C.2
Lieberman, P.H.3
-
44
-
-
0018098856
-
Lobular neoplasia (so-called lobular carcinoma in situ) of the breast
-
Haagensen CD, Lane N, Lattes R, et al: Lobular neoplasia (so-called lobular carcinoma in situ) of the breast. Cancer 42:737-769, 1978
-
(1978)
Cancer
, vol.42
, pp. 737-769
-
-
Haagensen, C.D.1
Lane, N.2
Lattes, R.3
-
45
-
-
0021931794
-
Risk factors for breast cancer in women with proliferate breast disease
-
Dupont WD, Page DL: Risk factors for breast cancer in women with proliferate breast disease. N Engl J Med 312:146-151, 1985
-
(1985)
N Engl J Med
, vol.312
, pp. 146-151
-
-
Dupont, W.D.1
Page, D.L.2
-
46
-
-
0026530997
-
A prospective study of benign breast disease and the risk of breast cancer
-
London SJ, Connolly JL, Schnitt SJ, et al: A prospective study of benign breast disease and the risk of breast cancer. JAMA 267:941-944, 1992
-
(1992)
JAMA
, vol.267
, pp. 941-944
-
-
London, S.J.1
Connolly, J.L.2
Schnitt, S.J.3
-
47
-
-
0037130889
-
Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program
-
Brose MS, Rebbeck TR, Calzone KA, et al: Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. J Natl Cancer Inst 94:1365-1372, 2002
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1365-1372
-
-
Brose, M.S.1
Rebbeck, T.R.2
Calzone, K.A.3
-
48
-
-
0037130887
-
Cancer incidence in BRCA1 mutation carriers
-
Thompson D, Easton DF: Cancer incidence in BRCA1 mutation carriers. J Natl Cancer Inst 94:1358-1365, 2002
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1358-1365
-
-
Thompson, D.1
Easton, D.F.2
-
49
-
-
0033731558
-
BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers
-
Shih HA, Nathanson KL, Seal S, et al: BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers. Clin Cancer Res 6:4259-4264, 2000
-
(2000)
Clin Cancer Res
, vol.6
, pp. 4259-4264
-
-
Shih, H.A.1
Nathanson, K.L.2
Seal, S.3
-
50
-
-
0033523268
-
Cancer risks in BRCA2 mutation carriers
-
The Breast Cancer Linkage Consortium
-
The Breast Cancer Linkage Consortium: Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst 91:1310-1316, 1999
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 1310-1316
-
-
-
51
-
-
0036644884
-
Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%
-
Murphy KM, Brune KA, Griffin C, et al: Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer: Deleterious BRCA2 mutations in 17%. Cancer Res 62:3789-3793, 2002
-
(2002)
Cancer Res
, vol.62
, pp. 3789-3793
-
-
Murphy, K.M.1
Brune, K.A.2
Griffin, C.3
-
52
-
-
0030139524
-
BRCA2 germline mutations in male breast cancer cases and breast cancer families
-
Couch FJ, Farid LM, DeShano ML, et al: BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nat Genet 13:123-125, 1996
-
(1996)
Nat Genet
, vol.13
, pp. 123-125
-
-
Couch, F.J.1
Farid, L.M.2
DeShano, M.L.3
-
53
-
-
0031018551
-
Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population
-
Friedman LS, Gayther SA, Kurosaki T, et al: Mutation analysis of BRCA1 and BRCA2 in a male breast cancer population. Am J Hum Genet 60:313-319, 1997
-
(1997)
Am J Hum Genet
, vol.60
, pp. 313-319
-
-
Friedman, L.S.1
Gayther, S.A.2
Kurosaki, T.3
-
54
-
-
84871473141
-
BRCA1 and BRCA2 germline mutations in male breast cancer cases
-
abstr 1650
-
Gerrero MR, Brose M, Couch FJ, et al: BRCA1 and BRCA2 germline mutations in male breast cancer cases. J Clin Oncol 20:413a, 2001 (abstr 1650)
-
(2001)
J Clin Oncol
, vol.20
-
-
Gerrero, M.R.1
Brose, M.2
Couch, F.J.3
-
55
-
-
0033583762
-
Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer
-
Tang NL, Pang CP, Yeo W, et al: Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer. J Natl Cancer Inst 91:882-885, 1999
-
(1999)
J Natl Cancer Inst
, vol.91
, pp. 882-885
-
-
Tang, N.L.1
Pang, C.P.2
Yeo, W.3
-
56
-
-
0034748511
-
Prevalence of breast cancer predisposition gene mutations in Chinese women and guidelines for genetic testing
-
Tang NL, Choy KW, Pang CP, et al: Prevalence of breast cancer predisposition gene mutations in Chinese women and guidelines for genetic testing. Clin Chim Acta 313:179-185, 2001
-
(2001)
Clin Chim Acta
, vol.313
, pp. 179-185
-
-
Tang, N.L.1
Choy, K.W.2
Pang, C.P.3
-
57
-
-
0033965408
-
The prevalence of BRCA1 mutations in Chinese patients with early onset breast cancer and affected relatives
-
Sng JH, Chang J, Feroze F, et al: The prevalence of BRCA1 mutations in Chinese patients with early onset breast cancer and affected relatives. Br J Cancer 82:538-542, 2000
-
(2000)
Br J Cancer
, vol.82
, pp. 538-542
-
-
Sng, J.H.1
Chang, J.2
Feroze, F.3
-
59
-
-
0033818032
-
Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer
-
Gao Q, Tomlinson G, Das S, et al: Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer. Hum Genet 107:186-191, 2000
-
(2000)
Hum Genet
, vol.107
, pp. 186-191
-
-
Gao, Q.1
Tomlinson, G.2
Das, S.3
-
60
-
-
0033818267
-
Protein truncating BRCA1 and BRCA2 mutations in African women with pre-menopausal breast cancer
-
Gao Q, Adebamowo CA, Fackenthal J, et al: Protein truncating BRCA1 and BRCA2 mutations in African women with pre-menopausal breast cancer. Hum Genet 107:192-194, 2000
-
(2000)
Hum Genet
, vol.107
, pp. 192-194
-
-
Gao, Q.1
Adebamowo, C.A.2
Fackenthal, J.3
-
61
-
-
16944363592
-
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
-
Petrij-Bosch A, Peelen T, van Vliet M, et al: BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nat Genet 17:341-345, 1997
-
(1997)
Nat Genet
, vol.17
, pp. 341-345
-
-
Petrij-Bosch, A.1
Peelen, T.2
van Vliet, M.3
-
62
-
-
0033909581
-
The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations
-
The BRCA1 Exon 13 Duplication Screening Group
-
The BRCA1 Exon 13 Duplication Screening Group: The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. Am J Hum Genet 67:207-212, 2000
-
(2000)
Am J Hum Genet
, vol.67
, pp. 207-212
-
-
-
63
-
-
0020573811
-
Practical guide for estimating risk for familial breast cancer
-
Ottman R, Pike MC, King MC, et al: Practical guide for estimating risk for familial breast cancer. Lancet 2:556-558, 1983
-
(1983)
Lancet
, vol.2
, pp. 556-558
-
-
Ottman, R.1
Pike, M.C.2
King, M.C.3
-
64
-
-
0021848579
-
Risk of familial breast cancer
-
Anderson DE, Badzioch MD: Risk of familial breast cancer. Cancer 56:383-387, 1985
-
(1985)
Cancer
, vol.56
, pp. 383-387
-
-
Anderson, D.E.1
Badzioch, M.D.2
-
66
-
-
84944368025
-
Family history and the risk of breast cancer
-
Sattin RW, Rubin GL, Webster LA, et al: Family history and the risk of breast cancer. JAMA 253:1908-1913, 1985
-
(1985)
JAMA
, vol.253
, pp. 1908-1913
-
-
Sattin, R.W.1
Rubin, G.L.2
Webster, L.A.3
-
67
-
-
0027956481
-
Quantitating familial cancer risk: A resource for clinical oncologists
-
Offit K, Brown K: Quantitating familial cancer risk: A resource for clinical oncologists. J Clin Oncol 12:1724-1736, 1994
-
(1994)
J Clin Oncol
, vol.12
, pp. 1724-1736
-
-
Offit, K.1
Brown, K.2
-
68
-
-
0026092912
-
Genetic analysis of breast cancer in the cancer and steroid hormone study
-
Claus EB, Risch N, Thompson WD: Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet 48:232-242, 1991
-
(1991)
Am J Hum Genet
, vol.48
, pp. 232-242
-
-
Claus, E.B.1
Risch, N.2
Thompson, W.D.3
-
69
-
-
0027731939
-
The calculation of breast cancer risk for women with a first degree family history of ovarian cancer
-
Claus EB, Risch N, Thompson WD: The calculation of breast cancer risk for women with a first degree family history of ovarian cancer. Breast Cancer Res Treat 28:115-120, 1993
-
(1993)
Breast Cancer Res Treat
, vol.28
, pp. 115-120
-
-
Claus, E.B.1
Risch, N.2
Thompson, W.D.3
-
70
-
-
0029771623
-
Agreement between breast cancer risk estimation methods
-
McGuigan KA, Ganz PA, Breant C: Agreement between breast cancer risk estimation methods. J Natl Cancer Inst 88:1315-1317, 1996
-
(1996)
J Natl Cancer Inst
, vol.88
, pp. 1315-1317
-
-
McGuigan, K.A.1
Ganz, P.A.2
Breant, C.3
-
71
-
-
0034894376
-
Comparisons of two breast cancer risk estimates in women with a family history of breast cancer
-
McTiernan A, Kuniyuki A, Yasui Y, et al: Comparisons of two breast cancer risk estimates in women with a family history of breast cancer. Cancer Epidemiol Biomarkers Prev 10:333-338, 2001
-
(2001)
Cancer Epidemiol Biomarkers Prev
, vol.10
, pp. 333-338
-
-
McTiernan, A.1
Kuniyuki, A.2
Yasui, Y.3
-
72
-
-
0028826709
-
Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence
-
Ford D, Easton DF, Peto J: Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence. Am J Hum Genet 57:1457-1462, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1457-1462
-
-
Ford, D.1
Easton, D.F.2
Peto, J.3
-
73
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing JP, Hartge P, Wacholder S, et al: The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews. N Engl J Med 336:1401-1408, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
-
74
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM, et al: The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 14:188-190, 1996
-
(1996)
Nat Genet
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
-
75
-
-
0029954317
-
BRCA1 mutations in young women with breast cancer
-
Struewing JP, Tarone RE, Brody LC, et al: BRCA1 mutations in young women with breast cancer. Lancet 347:1493, 1996
-
(1996)
Lancet
, vol.347
, pp. 1493
-
-
Struewing, J.P.1
Tarone, R.E.2
Brody, L.C.3
-
76
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
Roa BB, Boyd AA, Volcik K, et al: Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nat Genet 14:185-187, 1996
-
(1996)
Nat Genet
, vol.14
, pp. 185-187
-
-
Roa, B.B.1
Boyd, A.A.2
Volcik, K.3
-
77
-
-
0032565070
-
Frequency of breast cancer attributable to BRCA1 in a population-based series of American women
-
Newman B, Mu H, Butler LM, et al: Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. JAMA 279:915-921, 1998
-
(1998)
JAMA
, vol.279
, pp. 915-921
-
-
Newman, B.1
Mu, H.2
Butler, L.M.3
-
78
-
-
0031958466
-
BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: Relationship to family history and implications for genetic testing
-
Rubin SC, Blackwood MA, Bandera C, et al: BRCA1, BRCA2, and hereditary nonpolyposis colorectal cancer gene mutations in an unselected ovarian cancer population: Relationship to family history and implications for genetic testing. Am J Obstet Gynecol 178:670-677, 1998
-
(1998)
Am J Obstet Gynecol
, vol.178
, pp. 670-677
-
-
Rubin, S.C.1
Blackwood, M.A.2
Bandera, C.3
-
79
-
-
0031003498
-
Contribution of BRCA1 mutations to ovarian cancer
-
Stratton JF, Gayther SA, Russell P, et al: Contribution of BRCA1 mutations to ovarian cancer. N Engl J Med 336:1125-1130, 1997
-
(1997)
N Engl J Med
, vol.336
, pp. 1125-1130
-
-
Stratton, J.F.1
Gayther, S.A.2
Russell, P.3
-
80
-
-
0035819891
-
-
Rockhill B, Spiegelman D, Byrne C, et al: Validation of the Gail, et al model of breast cancer risk prediction and implications for chemoprevention. J Natl Cancer Inst 93:358-366, 2001
-
Rockhill B, Spiegelman D, Byrne C, et al: Validation of the Gail, et al model of breast cancer risk prediction and implications for chemoprevention. J Natl Cancer Inst 93:358-366, 2001
-
-
-
|