-
1
-
-
14944385553
-
Global cancer statistics, 2002
-
Parkin DM, Bray F, Ferlay J, et al. Global cancer statistics, 2002. CA Cancer J Clin 2005;55:74-108.
-
(2005)
CA Cancer J Clin
, vol.55
, pp. 74-108
-
-
Parkin, D.M.1
Bray, F.2
Ferlay, J.3
-
2
-
-
0036488497
-
Modifiers of risk of hereditary breast and ovarian cancer
-
Narod SA. Modifiers of risk of hereditary breast and ovarian cancer. Nat Rev Cancer 2002;2:113-123 (Pubitemid 37328798)
-
(2002)
Nature Reviews Cancer
, vol.2
, Issue.2
, pp. 113-123
-
-
Narod, S.A.1
-
3
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994;266:66-71. (Pubitemid 24345325)
-
(1994)
Science
, vol.266
, Issue.5182
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
4
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
DOI 10.1038/ng0396-333
-
Tavtigian SV, Simard J, Rommens J, et al. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat Genet 1996;12:333-337 (Pubitemid 26080098)
-
(1996)
Nature Genetics
, vol.12
, Issue.3
, pp. 333-337
-
-
Tavtigian, S.V.1
Simard, J.2
Rommens, J.3
Couch, F.4
Shattuck-Eidens, D.5
Neuhausen, S.6
Merajver, S.7
Thorlacius, S.8
Offit, K.9
Stoppa-Lyonnet, D.10
Belanger, C.11
Bell, R.12
Berry, S.13
Bogden, R.14
Chen, Q.15
Davis, T.16
Dumont, M.17
Frye, C.18
Hattier, T.19
Jammulapati, S.20
Janecki, T.21
Jiang, P.22
Kehrer, R.23
Leblanc, J.-F.24
Mitchell, J.T.25
McArthur-Morrison, J.26
Nguyen, K.27
Peng, Y.28
Samson, C.29
Schroeder, M.30
Snyder, S.C.31
Steele, L.32
Stringfellow, M.33
Stroup, C.34
Swedlund, B.35
Swensen, J.36
Teng, D.37
Thomas, A.38
Tran, T.39
Tran, T.40
Tranchant, M.41
Weaver-Feldhaus, J.42
Wong, A.K.C.43
Shizuya, H.44
Eyfjord, J.E.45
Cannon-Albright, L.46
Labrie, F.47
Skolnick, M.H.48
Weber, B.49
Kamb, A.50
Goldgar, D.E.51
more..
-
5
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994;265:2088-2090 (Pubitemid 24325690)
-
(1994)
Science
, vol.265
, Issue.5181
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
6
-
-
0028330276
-
Risks of cancer in BRC/4/-mutation carriers. Breast cancer linkage consortium
-
Ford D, Easton DF, Bishop DT, et al. Risks of cancer in BRC/4/-mutation carriers. Breast Cancer Linkage Consortium. Lancet 1994;343:692-695
-
(1994)
Lancet
, vol.343
, pp. 692-695
-
-
Ford, D.1
Easton, D.F.2
Bishop, D.T.3
-
7
-
-
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 1998;62:676-689
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
9
-
-
0028844202
-
Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation
-
Gayther Sa, Warren W, Mazoyer S, et al. Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation. Nat Genet 1995;11:428-433
-
(1995)
Nat Genet
, vol.11
, pp. 428-433
-
-
Gayther Sa1
Warren, W.2
Mazoyer, S.3
-
10
-
-
0343918505
-
BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer
-
DOI 10.1056/NEJM199705153362002
-
Couch FJ, DeShano ML, Blackwood MA, etal. BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. N Engl J Med 1997;336:1409-1415 (Pubitemid 27208599)
-
(1997)
New England Journal of Medicine
, vol.336
, Issue.20
, pp. 1409-1415
-
-
Couch, F.J.1
DeShano, M.L.2
Blackwood, M.A.3
Calzone, K.4
Stopfer, J.5
Campeau, L.6
Ganguly, A.7
Rebbeck, T.8
Weber, B.L.9
Jablon, L.10
Cobleigh, M.A.11
Hoskins, K.12
Garber, J.E.13
-
11
-
-
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 1998;16:2417-2425 (Pubitemid 28309036)
-
(1998)
Journal of Clinical Oncology
, vol.16
, Issue.7
, pp. 2417-2425
-
-
Frank, T.S.1
Manley, S.A.2
Olopade, O.I.3
Cummings, S.4
Garber, J.E.5
Bernhardt, B.6
Antman, K.7
Russo, D.8
Wood, M.E.9
Mullineau, L.10
Isaacs, C.11
Peshkin, B.12
Buys, S.13
Venne, V.14
Rowley, P.T.15
Loader, S.16
Offit, K.17
Robson, M.18
Hampel, H.19
Brener, D.20
Winer, E.P.21
Clark, S.22
Weber, B.23
Strong, L.C.24
Rieger, P.25
McClure, M.26
Ward, B.E.27
Shattuck-Eidens, D.28
Oliphant, A.29
Skolnick, M.H.30
Thomas, A.31
more..
-
12
-
-
0029655346
-
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families
-
Serova O, Montagna M, Torchard D, etal. A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families. Am J Hum Genet 1996;58:42-51.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 42-51
-
-
Serova, O.1
Montagna, M.2
Torchard, D.3
-
13
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
DOI 10.1038/ng0197-103
-
Gayther SA, Mangion J, Russell P, et al. Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. Nat Genet 1997;15:103-105 (Pubitemid 27014960)
-
(1997)
Nature Genetics
, vol.15
, Issue.1
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russell, P.3
Seal, S.4
Barfoot, R.5
Ponder, B.A.J.6
Stratton, M.R.7
Easton, D.8
-
14
-
-
17344372404
-
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study
-
Neuhausen SL, Godwin AK, Gershoni-Baruch R, et al. Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. Am J Hum Genet 1998;62:1381-1388
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1381-1388
-
-
Neuhausen, S.L.1
Godwin, A.K.2
Gershoni-Baruch, R.3
-
15
-
-
0035125062
-
Variation in cancer risks, by mutation position, in BRCA2 mutation carriers
-
DOI 10.1086/318181
-
Thompson D, Easton D. Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. Am J Hum Genet 2001;68:410-419 (Pubitemid 32147810)
-
(2001)
American Journal of Human Genetics
, vol.68
, Issue.2
, pp. 410-419
-
-
Thompson, D.1
Easton, D.2
-
16
-
-
65849088882
-
-
(accessed 15 December 2008)
-
Al-Mulla F. http://www.al-mulla.org/breastcancer.html (accessed 15 December 2008).
-
-
-
Al-Mulla, F.1
-
17
-
-
84892372742
-
The robust inference for the Cox proportional hazards model
-
Lin DY, Wei LJ. The robust inference for the Cox proportional hazards model. J Am Stat Assoc 1989;84:1074-1078
-
(1989)
J Am Stat Assoc
, vol.84
, pp. 1074-1078
-
-
Lin, D.Y.1
Wei, L.J.2
-
18
-
-
84871466818
-
-
National Human Genome Research Institute, (accessed 15 December 2008)
-
National Human Genome Research Institute. Breast Cancer Information Core database. http://research.nhgri.nih.gov/bic/ (accessed 15 December 2008).
-
Breast Cancer Information Core database
-
-
-
19
-
-
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 2003;72:1117-1130 (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..
-
20
-
-
0035102533
-
A marginal likelihood approach for estimating penetrance from kin-cohort designs
-
Chatterjee N, Wacholder S. A marginal likelihood approach for estimating penetrance from kin-cohort designs. Biometrics 2001;57:245-252 (Pubitemid 32200163)
-
(2001)
Biometrics
, vol.57
, Issue.1
, pp. 245-252
-
-
Chatterjee, N.1
Wacholder, S.2
-
21
-
-
0033912293
-
Bias and efficiency in family-based gene-characterization studies: Conditional, prospective, retrospective, and joint likelihoods
-
DOI 10.1086/302808
-
Kraft P, Thomas DC. Bias and efficiency in family-based gene-characterization studies: conditional, prospective, retrospective, and joint likelihoods. Am J Hum Genet 2000;66:1119-1131 (Pubitemid 30470509)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.3
, pp. 1119-1131
-
-
Kraft, P.1
Thomas, D.C.2
-
23
-
-
0031000719
-
Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia
-
Gayther SA, Harrington P, Russell P, et al. Frequently occurring germ-line mutations of the BRCA1 gene in ovarian cancer families from Russia. Am J Hum Genet 1997;60:1239-1242 (Pubitemid 27194110)
-
(1997)
American Journal of Human Genetics
, vol.60
, Issue.5
, pp. 1239-1242
-
-
Gayther, S.A.1
Harrington, P.2
Russell, P.3
Kharkevich, G.4
Garkavtseva, R.F.5
Ponder, B.A.J.6
-
24
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius S, Olafsdottir G, Tryggvadottir L, et al. A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat Genet 1996;13:117-119 (Pubitemid 126528241)
-
(1996)
Nature Genetics
, vol.13
, Issue.1
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Tryggvadottir, L.3
Neuhausen, S.4
Jonasson, J.G.5
Tavtigian, S.V.6
Tulinius, H.7
Ogmundsdottir, H.M.8
Eyfjord, J.E.9
-
25
-
-
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 2000;67:207-212
-
(2000)
Am J Hum Genet
, vol.67
, pp. 207-212
-
-
-
26
-
-
0031033343
-
Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families
-
Xu CF, Chambers JA, Nicolai H, et al. Mutations and alternative splicing of the BRCA1 gene in UK breast/ovarian cancer families. Genes Chromosomes Cancer 1997; 18:102-110
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 102-110
-
-
Xu, C.F.1
Chambers, J.A.2
Nicolai, H.3
-
27
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall JM, Lee MK, Newman B, et al. Linkage of early-onset familial breast cancer to chromosome 17q21. Science 1990;250:1684-1689 (Pubitemid 120031871)
-
(1990)
Science
, vol.250
, Issue.4988
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
Morrow, J.E.4
Anderson, L.A.5
Huey, B.6
King, M.-C.7
-
28
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families
-
Phelan CM, Lancaster JM, Tonin P, etal. Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. Nat Genet 1996;13:120-122 (Pubitemid 126528242)
-
(1996)
Nature Genetics
, vol.13
, Issue.1
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
Gumbs, C.4
Cochran, C.5
Carter, R.6
Ghadirian, P.7
Perret, C.8
Moslehi, R.9
Dion, F.10
Faucher, M.-C.11
Dole, K.12
Karimi, S.13
Foulkes, W.14
Lounis, H.15
Warner, E.16
Goss, P.17
Anderson, D.18
Larsson, C.19
Narod, S.A.20
Futreal, P.A.21
more..
-
30
-
-
0033799478
-
Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing
-
Unger MA, Nathanson KL, Calzone K, et al. Screening for genomic rearrangements in families with breast and ovarian cancer identifies BRCA1 mutations previously missed by conformation-sensitive gel electrophoresis or sequencing. Am J Hum Genet 2000;67:841-850
-
(2000)
Am J Hum Genet
, vol.67
, pp. 841-850
-
-
Unger, M.A.1
Nathanson, K.L.2
Calzone, K.3
-
31
-
-
33746907114
-
Detection of a novel alu-mediated BRCA1 exon 13 duplication in Chinese breast cancer patients and implications for genetic testing [5]
-
DOI 10.1111/j.1399-0004.2006.00637.x
-
Yap KP, Ang P, Lim IH, et al. Detection of a novel Alu-mediated BRCA1 exon 13 duplication in Chinese breast cancer patients and implications for genetic testing. Clin Genet 2006;70:80-82 (Pubitemid 44192742)
-
(2006)
Clinical Genetics
, vol.70
, Issue.1
, pp. 80-82
-
-
Yap, K.P.-L.1
Ang, P.2
Lim, I.H.-K.3
Ho, G.H.4
Lee, A.S.-G.5
-
32
-
-
0024847169
-
Cancer incidence in Jewish migrants to Israel, 1961-1981
-
Steinitz R, Parkin DM, Young JL, et al. Cancer incidence in Jewish migrants to Israel, 1961-1981. IARC Sci Publ 1989:1-311.
-
(1989)
IARC Sci Publ
, pp. 1-311
-
-
Steinitz, R.1
Parkin, D.M.2
Young, J.L.3
-
33
-
-
22244467729
-
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: A combined analysis of 22 population based studies
-
DOI 10.1136/jmg.2004.024133
-
Antoniou AC, Pharoah PD, Narod S, etal. Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies. J Med Genet 2005;42:602-603 (Pubitemid 40993838)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.7
, pp. 602-603
-
-
Antoniou, A.C.1
Pharoah, P.D.P.2
Narod, S.3
Risch, H.A.4
Eyfjord, J.E.5
Hopper, J.L.6
Olsson, H.7
Johannsson, O.8
Borg, A.9
Pasini, B.10
Radice, P.11
Manoukian, S.12
Eccles, D.M.13
Tang, N.14
Olah, E.15
Anton-Culver, H.16
Warner, E.17
Lubinski, J.18
Gronwald, J.19
Gorski, B.20
Tulinius, H.21
Thorlacius, S.22
Eerola, H.23
Nevanlinna, H.24
Syrjakoski, K.25
Kallioniemi, O.-P.26
Thompson, D.27
Evans, C.28
Peto, J.29
Lalloo, F.30
Evans, D.G.31
Easton, D.F.32
more..
-
34
-
-
0036848138
-
The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons
-
Perrin-Vidoz L, Sinilnikova OM, Stoppa-Lyonnet D, et al. The nonsense-mediated mRNA decay pathway triggers degradation of most BRCA1 mRNAs bearing premature termination codons. Hum Mol Genet 2002;11:2805-2814 (Pubitemid 35331813)
-
(2002)
Human Molecular Genetics
, vol.11
, Issue.23
, pp. 2805-2814
-
-
Perrin-Vidoz, L.1
Sinilnikova, O.M.2
Stoppa-Lyonnet, D.3
Lenoir, G.M.4
Mazoyer, S.5
-
35
-
-
33749034203
-
The 185delAG mutation (c.68-69delAG) in the BRCA1 gene triggers translation reinitiation at a downstream AUG codon
-
DOI 10.1002/humu.20384
-
Buisson M, Anczukow 0, Zetoune AB, et al. The 185delAG mutation (c.68-69delAG) in the BRCA1 gene triggers translation reinitiation at a downstream AUG codon. Hum Mutat 2006;27:1024-1029 (Pubitemid 44454055)
-
(2006)
Human Mutation
, vol.27
, Issue.10
, pp. 1024-1029
-
-
Buisson, M.1
Anczukow, O.2
Zetoune, A.B.3
Ware, M.D.4
Mazoyer, S.5
-
36
-
-
33751583981
-
Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients
-
Rashid MU, Zaidi A, Torres D, et al. Prevalence of BRCA1 and BRCA2 mutations in Pakistani breast and ovarian cancer patients. Int J Cancer 2006;119:2832-2839
-
(2006)
Int J Cancer
, vol.119
, pp. 2832-2839
-
-
Rashid, M.U.1
Zaidi, A.2
Torres, D.3
|