-
1
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
a
-
(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
Rehbeck, 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..
-
3
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
a
-
(1997)
N. Engl. J. Med.
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
Baker, S.M.4
Berlin, M.5
McAdams, M.6
Timmerman, M.M.7
Brody, L.C.8
Tucker, M.A.9
-
4
-
-
18344410703
-
Population-based study of risk of breast cancer in carriers of BRCA2 mutation
-
a
-
(1998)
Lancet
, vol.352
, pp. 1337-1339
-
-
Thorlacius, S.1
Struewing, J.P.2
Hartge, P.3
Olafsdottir, G.H.4
Sigvaldason, H.5
Tryggvadottir, L.6
Wacholder, S.7
Tulinius, H.8
Eyfjord, J.E.P.9
-
5
-
-
0032826284
-
Population-based estimate of the average age-specific cumulative risk of breast cancer for a defined set of protein- truncating mutations in BRCA1 and BRCA2
-
a
-
(1999)
Cancer Epidemiol. Biomark. Prev.
, vol.8
, pp. 741-747
-
-
Hopper, J.L.1
Southey, M.C.2
Dite, G.S.3
Jolley, D.J.4
Giles, G.G.5
McCredie, M.R.E.6
Easton, D.F.7
Venter, D.J.8
-
6
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
-
a
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 254-264
-
-
Narod, S.A.1
Ford, D.2
Devilee, P.3
Barkardottir, R.B.4
Lynch, H.T.5
Smith, S.A.6
Ponder, B.A.7
Weber, B.L.8
Garber, J.E.9
Birch, J.M.10
Cornelis, R.S.11
Kelsell, D.P.12
Spurr, N.K.13
Smyth, E.14
Haites, N.15
Sobol, H.16
Bignon, Y.J.17
Chang-Claude, J.18
Hamann, U.19
Lindblom, A.20
Borg, A.21
Piver, M.S.22
Gallion, H.H.23
Struewing, J.P.24
Whittemore, A.S.25
Tonin, P.26
Goldgar, D.E.27
Easton, D.F.28
more..
-
7
-
-
13344268996
-
Ovarian cancer risk in BRCA1 carriers is modified by the HRASI variable number of tandem repeat (VNTR) locus
-
a
-
(1996)
Nat. Genet.
, vol.12
, pp. 309-311
-
-
Phelan, C.M.1
Rebbeck, T.R.2
Weber, B.L.3
Devilee, P.4
Ruttledge, M.H.5
Lynch, H.T.6
Lenoir, G.M.7
Stratton, M.R.8
Easton, D.F.9
Ponder, B.A.10
Cannon, A.L.11
Larsson, C.12
Goldgar, D.E.13
Narod, S.A.14
-
8
-
-
0001516492
-
Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat
-
a
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1371-1377
-
-
Rebbeck, T.R.1
Kantoff, P.N.2
Krithivas, K.3
Neuhausen, S.4
Blackwood, M.A.5
Godwin, A.K.6
Daly, M.B.7
Narod, S.A.8
Garber, J.E.9
Lynch, H.T.10
Weber, B.L.11
Brown, M.12
-
13
-
-
0028981764
-
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer
-
a
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1-7
-
-
Struewing, J.P.1
Brody, L.C.2
Erdos, M.R.3
Kase, R.G.4
Giambarresi, T.R.5
Smith, S.A.6
Collins, F.S.7
Tucker, M.A.8
-
15
-
-
0033287525
-
Design and analysis issues in a population-based, case-control-family study of the genetic epidemiology of breast cancer and the Co-operative Family Registry for Breast Cancer Studies (CFRBCS)
-
a
-
(1999)
J. Natl. Cancer Inst. Monogr.
, vol.26
, pp. 95-100
-
-
Hopper, J.L.1
Chenevix-Trench, G.2
Jolley, D.J.3
Dite, G.S.4
Jenkins, M.A.5
Venter, D.J.6
McCredie, M.R.7
Giles, G.G.8
-
17
-
-
0035954651
-
Parity, oral contraceptives, and the risk of ovarian cancer among carriers and noncarriers of a BRCA1 or BRCA2 mutation
-
a
-
(2001)
N. Engl. J. Med.
, vol.345
, pp. 235-240
-
-
Modan, B.1
Hartge, P.2
Hirsch-Yechezkel, G.3
Chetrit, A.4
Lubin, F.5
Beller, U.6
Ben-Baruch, G.7
Fishman, A.8
Menczer, J.9
Ebbers, S.M.10
Tucker, M.A.11
Wacholder, S.12
Struewing, J.P.13
Friedman, E.14
Piura, B.15
-
18
-
-
0033769823
-
Patients with double primary tumors in the breast and ovary-clinical characteristics and BRCA1-2 mutations status
-
a
-
(2000)
Gynecol. Oncol.
, vol.79
, pp. 74-78
-
-
Fishman, A.1
Dekel, E.2
Chetrit, A.3
Lerner-Geva, L.4
Bar-Am, A.5
Beck, D.6
Beller, U.7
Ben-Baruch, G.8
Piura, B.9
Friedman, E.10
Struewing, J.P.11
Modan, B.12
-
21
-
-
0033566756
-
Common nonsense mutations in RAD52
-
a
-
(1999)
Cancer Res.
, vol.59
, pp. 3883-3888
-
-
Bell, D.W.1
Wahrer, D.C.R.2
Kang, D.H.3
MacMahon, M.S.4
FitzGerald, M.G.5
Ishioka, C.6
Isselbacher, K.J.7
Krainer, M.8
Haber, D.A.9
-
22
-
-
17144455028
-
Identification of Rad5l alteration in patients with bilateral breast cancer
-
a
-
(2000)
J. Hum. Genet.
, vol.45
, pp. 133-137
-
-
Kato, M.1
Yano, K.2
Matsuo, F.3
Saito, H.4
Katagiri, T.5
Kurumizaka, H.6
Yoshimoto, M.7
Kasumi, F.8
Akiyama, F.9
Sakamoto, G.10
Nagawa, H.11
Nakamura, Y.12
Miki, Y.13
-
24
-
-
0035853077
-
A single nucleotide polymorphism in the RAD51 gene modifies cancer risk in BRCA2 but not BRCA1 carriers
-
a
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 3232-3236
-
-
Levy-Lahad, E.1
Lahad, A.2
Eisenberg, S.3
Dagan, E.4
Paperna, T.5
Kasinetz, L.6
Catane, R.7
Kaufman, B.8
Beller, U.9
Renbaum, P.10
Gershoni-Baruch, R.11
-
26
-
-
0032253553
-
Translational control by repressor proteins binding to the 5′UTR of mRNAs
-
a
-
(1998)
Methods Mol. Biol.
, vol.77
, pp. 379-397
-
-
Gray, N.K.1
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