-
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
-
DOI 10.1086/375033
-
Antoniou A, Pharoah PD, Narod S, et al: 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 (Pubitemid 36530000)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.5
, pp. 1117-1130
-
-
Antoniou, A.1
Pharoah, P.D.P.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..
-
2
-
-
34248170114
-
Meta-analysis of BRCA1 and BRCA2 penetrance
-
DOI 10.1200/JCO.2006.09.1066
-
Chen S, Parmigiani G: Meta-analysis of BRCA1 and BRCA2 penetrance. J Clin Oncol 25: 1329-1333, 2007 (Pubitemid 46706879)
-
(2007)
Journal of Clinical Oncology
, vol.25
, Issue.11
, pp. 1329-1333
-
-
Chen, S.1
Parmigiani, G.2
-
3
-
-
77952982796
-
Genetic/ familial high-risk assessment: Breast and ovarian
-
Daly MB, Axilbund JE, Buys S, et al: Genetic/ familial high-risk assessment: Breast and ovarian. J Natl Compr Canc Netw 8:562-594, 2010
-
(2010)
J Natl Compr Canc Netw
, vol.8
, pp. 562-594
-
-
Daly, M.B.1
Axilbund, J.E.2
Buys, S.3
-
4
-
-
33846425741
-
Phenocopies in BRCA1 and BRCA2 families: Evidence for modifier genes and implications for screening
-
DOI 10.1136/jmg.2006.043091
-
Smith A, Moran A, Boyd MC, et al: Phenocopies in BRCA1 and BRCA2 families: Evidence for modifier genes and implications for screening. J Med Genet 44:10-15, 2007 (Pubitemid 46142833)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.1
, pp. 10-15
-
-
Smith, A.1
Moran, A.2
Boyd, M.C.3
Bulman, M.4
Shenton, A.5
Smith, L.6
Iddenden, R.7
Woodward, E.R.8
Lalloo, F.9
Maher, E.R.10
Evans, D.G.R.11
-
5
-
-
34248345996
-
Phenocopies in breast cancer 1 (BRCA1) families: Implications for genetic counselling
-
Gronwald J, Cybulski C, Lubinski J, et al: Phenocopies in breast cancer 1 (BRCA1) families: Implications for genetic counselling. J Med Genet 44:e76, 2007
-
(2007)
J Med Genet
, vol.44
-
-
Gronwald, J.1
Cybulski, C.2
Lubinski, J.3
-
6
-
-
34548579074
-
A prospective study of breast cancer risk in relatives of BRCA1/ BRCA2 mutation carriers
-
Rowan E, Poll A, Narod SA: A prospective study of breast cancer risk in relatives of BRCA1/ BRCA2 mutation carriers. J Med Genet 44:e89, 2007
-
(2007)
J Med Genet
, vol.44
-
-
Rowan, E.1
Poll, A.2
Narod, S.A.3
-
7
-
-
74849110212
-
Breast cancer risks in individuals testing negative for a known family mutation in BRCA1 or BRCA2
-
Domchek SM, Gaudet MM, Stopfer JE, et al: Breast cancer risks in individuals testing negative for a known family mutation in BRCA1 or BRCA2. Breast Cancer Res Treat 119:409-414, 2010
-
(2010)
Breast Cancer Res Treat
, vol.119
, pp. 409-414
-
-
Domchek, S.M.1
Gaudet, M.M.2
Stopfer, J.E.3
-
8
-
-
78651092651
-
No evidence of excess breast cancer risk among mutation-negative women from BRCA mutation-positive families
-
Korde LA, Mueller CM, Loud JT, et al: No evidence of excess breast cancer risk among mutation-negative women from BRCA mutation-positive families. Breast Cancer Res Treat 125:169- 173, 2011
-
(2011)
Breast Cancer Res Treat
, vol.125
, pp. 169-173
-
-
Korde, L.A.1
Mueller, C.M.2
Loud, J.T.3
-
9
-
-
34548589165
-
Phenocopies: Actual risk or self-fulfilling prophecy?
-
Eisinger F: Phenocopies: Actual risk or self-fulfilling prophecy? J Med Genet 44:e87, 2007
-
(2007)
J Med Genet
, vol.44
-
-
Eisinger, F.1
-
10
-
-
7044272596
-
The Breast Cancer Family Registry: An infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer
-
John EM, Hopper JL, Beck JC, et al: The Breast Cancer Family Registry: An infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer. Breast Cancer Res 6:R375-R389, 2004
-
(2004)
Breast Cancer Res
, vol.6
-
-
John, E.M.1
Hopper, J.L.2
Beck, J.C.3
-
11
-
-
67649214899
-
BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: An open resource for collaborative research
-
Neuhausen SL, Ozcelik H, Southey MC, et al: BRCA1 and BRCA2 mutation carriers in the Breast Cancer Family Registry: An open resource for collaborative research. Breast Cancer Res Treat 116: 379-386, 2009
-
(2009)
Breast Cancer Res Treat
, vol.116
, pp. 379-386
-
-
Neuhausen, S.L.1
Ozcelik, H.2
Southey, M.C.3
-
12
-
-
0031032930
-
Multi-stage sampling in genetic epidemiology
-
Whittemore AS, Halpern J: Multi-stage sampling in genetic epidemiology. Stat Med 16:153-167, 1997 (Pubitemid 27029294)
-
(1997)
Statistics in Medicine
, vol.16
, Issue.1-3
, pp. 153-167
-
-
Whittemore, A.S.1
Halpern, J.2
-
13
-
-
0027433113
-
Conformation-sensitive gel electrophoresis for rapid detection of single- base differences in double-stranded PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes
-
DOI 10.1073/pnas.90.21.10325
-
Ganguly A, Rock MJ, Prockop DJ: Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: Evidence for solvent-induced bends in DNA heteroduplexes. Proc Natl Acad Sci U S A 90: 10325-10329, 1993 (Pubitemid 23328305)
-
(1993)
Proceedings of the National Academy of Sciences of the United States of America
, vol.90
, Issue.21
, pp. 10325-10329
-
-
Ganguly, A.1
Rock, M.J.2
Prockop, D.J.3
-
14
-
-
0032539612
-
Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: Comparison with denaturing gradient gel electrophoresis and nucleotide sequencing
-
DOI 10.1073/pnas.95.4.1681
-
Körkkö J, Annunen S, Pihlajamaa T, et al: Conformation sensitive gel electrophoresis for simple and accurate detection of mutations: Comparison with denaturing gradient gel electrophoresis and nucleotide sequencing. Proc Natl Acad Sci U S A 95:1681-1685, 1998 (Pubitemid 28103453)
-
(1998)
Proceedings of the National Academy of Sciences of the United States of America
, vol.95
, Issue.4
, pp. 1681-1685
-
-
Korkko, J.1
Annunen, S.2
Pihlajamaa, T.3
Prockop, D.J.4
Ala-Kokko, L.5
-
15
-
-
32244437594
-
High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison
-
DOI 10.1016/j.ygeno.2005.11.008, PII S0888754305003277
-
Davies H, Dicks E, Stephens P, et al: High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison. Genomics 87:427-432, 2006 (Pubitemid 43214515)
-
(2006)
Genomics
, vol.87
, Issue.3
, pp. 427-432
-
-
Davies, H.1
Dicks, E.2
Stephens, P.3
Cox, C.4
Teague, J.5
Greenman, C.6
Bignell, G.7
O'Meara, S.8
Edkins, S.9
Parker, A.10
Stevens, C.11
Menzies, A.12
Blow, M.13
Bottomley, B.14
Dronsfield, M.15
Futreal, P.A.16
Stratton, M.R.17
Wooster, R.18
-
16
-
-
34250782433
-
Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes
-
DOI 10.1038/nprot.2006.482, PII NPROT.2006.482
-
Velasco E, Infante M, Durán M, et al: Heteroduplex analysis by capillary array electrophoresis for rapid mutation detection in large multiexon genes. Nat Protoc 2:237-246, 2007 (Pubitemid 47040089)
-
(2007)
Nature Protocols
, vol.2
, Issue.1
, pp. 237-246
-
-
Velasco, E.1
Infante, M.2
Duran, M.3
Perez-Cabornero, L.4
Sanz, D.J.5
Esteban-Cardenosa, E.6
Miner, C.7
-
17
-
-
37549036689
-
Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups
-
John EM, Miron A, Gong G, et al: Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups. JAMA 298:2869-2876, 2007
-
(2007)
JAMA
, vol.298
, pp. 2869-2876
-
-
John, E.M.1
Miron, A.2
Gong, G.3
-
18
-
-
18444394315
-
Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations
-
DOI 10.1002/humu.10097
-
Andrulis IL, Anton-Culver H, Beck J, et al: Comparison of DNA- and RNA-based methods for detection of truncating BRCA1 mutations. Hum Mutat 20:65-73, 2002 (Pubitemid 34747718)
-
(2002)
Human Mutation
, vol.20
, Issue.1
, pp. 65-73
-
-
Andrulis, I.L.1
Anton-Culver, H.2
Beck, J.3
Bove, B.4
Boyd, J.5
Buys, S.6
Godwin, A.K.7
Hopper, J.L.8
Li, F.9
Neuhausen, S.L.10
Ozcelik, H.11
Peel, D.12
Santella, R.M.13
Southey, M.C.14
Van Orsouw, N.J.15
Venter, D.J.16
Vijg, J.17
Whittemore, A.S.18
-
19
-
-
77957242033
-
Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations
-
Dite GS, Whittemore AS, Knight JA, et al: Increased cancer risks for relatives of very early-onset breast cancer cases with and without BRCA1 and BRCA2 mutations. Br J Cancer 103:1103-1108, 2010
-
(2010)
Br J Cancer
, vol.103
, pp. 1103-1108
-
-
Dite, G.S.1
Whittemore, A.S.2
Knight, J.A.3
-
20
-
-
84876083286
-
-
National Human Genome Research Institute: Breast Cancer Information Core. http://research.nhgri .nih.gov/bic/
-
Breast Cancer Information Core
-
-
-
21
-
-
0142063079
-
Polygenic Inheritance of Breast Cancer: Implications for Design of Association Studies
-
DOI 10.1002/gepi.10261
-
Antoniou AC, Easton DF: Polygenic inheritance of breast cancer: Implications for design of association studies. Genet Epidemiol 25:190-202, 2003 (Pubitemid 37296594)
-
(2003)
Genetic Epidemiology
, vol.25
, Issue.3
, pp. 190-202
-
-
Antoniou, A.C.1
Easton, D.F.2
-
23
-
-
1842680082
-
A breast cancer prediction model incorporating familial and personal risk factors
-
DOI 10.1002/sim.1668
-
Tyrer J, Duffy SW, Cuzick J: A breast cancer prediction model incorporating familial and personal risk factors. Stat Med 23:1111-1130, 2004 (Pubitemid 38477070)
-
(2004)
Statistics in Medicine
, vol.23
, Issue.7
, pp. 1111-1130
-
-
Tyrer, J.1
Duffy, S.W.2
Cuzick, J.3
-
24
-
-
0023838218
-
Likelihood analysis of multi-state models for disease incidence and mortality
-
Kalbfleisch JD, Lawless JF: Likelihood analysis of multi-state models for disease incidence and mortality. Stat Med 7:149-160, 1988 (Pubitemid 18045527)
-
(1988)
Statistics in Medicine
, vol.7
, Issue.1-2
, pp. 149-160
-
-
Kalbfleisch, J.D.1
Lawless, J.F.2
-
25
-
-
0034671638
-
Familial breast and ovarian cancer: A swedish population-based register study
-
DOI 10.1093/aje/152.12.1154
-
Anderson H, Bladstrom A, Olsson H, et al: Familial breast and ovarian cancer: A Swedish population-based register study. Am J Epidemiol 152:1154-1163, 2000 (Pubitemid 32005753)
-
(2000)
American Journal of Epidemiology
, vol.152
, Issue.12
, pp. 1154-1163
-
-
Anderson, H.1
Bladstrom, A.2
Olsson, H.3
Moller, T.R.4
-
26
-
-
0036578764
-
Polygenic susceptibility to breast cancer and implications for prevention
-
Pharoah PD, Antoniou A, Bobrow M, et al: Polygenic susceptibility to breast cancer and implications for prevention. Nat Genet 31:33-36, 2002
-
(2002)
Nat Genet
, vol.31
, pp. 33-36
-
-
Pharoah, P.D.1
Antoniou, A.2
Bobrow, M.3
-
28
-
-
0037151382
-
On the use of familial aggregation in population-based case probands for calculating penetrance
-
Begg CB: On the use of familial aggregation in population-based case probands for calculating penetrance. J Natl Cancer Inst 94:1221-1226, 2002
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 1221-1226
-
-
Begg, C.B.1
-
29
-
-
77952917993
-
Assessing women at high risk of breast cancer: A review of risk assessment models
-
Amir E, Freedman OC, Seruga B, et al: Assessing women at high risk of breast cancer: A review of risk assessment models. J Natl Cancer Inst 102:680-691, 2010
-
(2010)
J Natl Cancer Inst
, vol.102
, pp. 680-691
-
-
Amir, E.1
Freedman, O.C.2
Seruga, B.3
|