-
1
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families
-
Ford D., Easton D.F., Stratton M.et al. Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. Am. J. Hum. Genet. 62:1998;676-689.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
2
-
-
0028330276
-
Consortium BCL. Risks of cancer in BRCA1-mutation carriers
-
Ford D., Easton D.F., Bishop D.T., Narod S.A., Goldgar D.E. Consortium BCL. Risks of cancer in BRCA1-mutation carriers. Lancet. 343:1994;692-695.
-
(1994)
Lancet
, vol.343
, pp. 692-695
-
-
Ford, D.1
Easton, D.F.2
Bishop, D.T.3
Narod, S.A.4
Goldgar, D.E.5
-
3
-
-
0027494344
-
Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Iclandic families, and possible relationship to prostatic cancer
-
Arason A., Barkadóttir R.B., Egilsson V. Linkage analysis of chromosome 17q markers and breast-ovarian cancer in Iclandic families, and possible relationship to prostatic cancer. Am. J. Hum. Genet. 52:1993;711-717.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 711-717
-
-
Arason, A.1
Barkadóttir, R.B.2
Egilsson, V.3
-
4
-
-
8044220285
-
Recommendations for follow-up care of individuals with an inherited predisposition to cancer
-
Burke W., Petersen G., Lynch P.et al. Recommendations for follow-up care of individuals with an inherited predisposition to cancer. JAMA. 227:1997;915-919.
-
(1997)
JAMA
, vol.227
, pp. 915-919
-
-
Burke, W.1
Petersen, G.2
Lynch, P.3
-
6
-
-
0028819984
-
Different tumor types from BRCA2 carriers show wild-type chromosome deletion on 13q12-q13
-
Gudmundsson J., Johannesdottir G., Bergthorsson J.T.et al. Different tumor types from BRCA2 carriers show wild-type chromosome deletion on 13q12-q13. Cancer Res. 55:1995;4830-4832.
-
(1995)
Cancer Res.
, vol.55
, pp. 4830-4832
-
-
Gudmundsson, J.1
Johannesdottir, G.2
Bergthorsson, J.T.3
-
7
-
-
0028784972
-
A large multisitic cancer family linked to BRCA2
-
Tonin P., Ghadirian P., Phelan C.et al. A large multisitic cancer family linked to BRCA2. J. Med. Genet. 32:1995;982-984.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 982-984
-
-
Tonin, P.1
Ghadirian, P.2
Phelan, C.3
-
8
-
-
0029792883
-
Mutations in the BRCA2 gene in hepatocellular carcinomas
-
Katagiri T., Nakamura Y., Miki Y. Mutations in the BRCA2 gene in hepatocellular carcinomas. Cancer Res. 56:1996;4475-4557.
-
(1996)
Cancer Res.
, vol.56
, pp. 4475-4557
-
-
Katagiri, T.1
Nakamura, Y.2
Miki, Y.3
-
9
-
-
12644253827
-
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas
-
Goggins M., Schutte M., Lu J.et al. Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. Cancer Res. 56:1996;5360-5364.
-
(1996)
Cancer Res.
, vol.56
, pp. 5360-5364
-
-
Goggins, M.1
Schutte, M.2
Lu, J.3
-
10
-
-
16044366171
-
Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families
-
Tonin P., Weber B., Offit K.et al. Frequency of recurrent BRCA1 and BRCA2 mutations in Ashkenazi Jewish breast cancer families. Nature Med. 2:1996;1179-1183.
-
(1996)
Nature Med.
, vol.2
, pp. 1179-1183
-
-
Tonin, P.1
Weber, B.2
Offit, K.3
-
11
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius S., Olafsdottir G., Jonasson L.et al. A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat. Genet. 13:1996;117-119.
-
(1996)
Nat. Genet.
, vol.13
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Jonasson, L.3
-
12
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 sitespecific breast cancer families
-
Phelan C.M., Lancaster J.M., Tonin P.et al. Mutation analysis of the BRCA2 gene in 49 sitespecific breast cancer families. Nat. Genet. 13:1996;120-122.
-
(1996)
Nat. Genet.
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
-
13
-
-
16944365740
-
Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13
-
Easton D.F., Steele L., Fields P.et al. Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13. Am. J. Hum. Genet. 61:1997;120-128.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 120-128
-
-
Easton, D.F.1
Steele, L.2
Fields, P.3
-
15
-
-
0027433563
-
Consortium BCL. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The Breast Cancer Linkage Consortium
-
Easton D.F., Bishop D.T., Ford D., Crockford G.P. Consortium BCL. Genetic linkage analysis in familial breast and ovarian cancer. results from 214 families. The Breast Cancer Linkage Consortium Am. J. Hum. Genet. 52:1993;678-701.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
Crockford, G.P.4
-
16
-
-
0028843102
-
Consortium BCL. Breast and ovarian cancer incidence in BRCA1-mutation carriers
-
Easton D.F., Ford D., Bishop D.T. Consortium BCL. Breast and ovarian cancer incidence in BRCA1-mutation carriers. Am. J. Hum. Genet. 56:1995;265-271.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 265-271
-
-
Easton, D.F.1
Ford, D.2
Bishop, D.T.3
-
17
-
-
0030910022
-
The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews
-
Struewing J.P., 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. 336:1997;1401-1408.
-
(1997)
N. Engl. J. Med.
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
-
18
-
-
0028863564
-
Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185del AG in Ashkenazi Jewish families
-
Friedman L.S., Szabo C.I., Ostermeyer E.A.et al. Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185del AG in Ashkenazi Jewish families. Am. J. Hum. Genet. 57:1995;1284-1297.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 1284-1297
-
-
Friedman, L.S.1
Szabo, C.I.2
Ostermeyer, E.A.3
-
20
-
-
0031984310
-
Is hereditary site-specific ovarian cancer a distinct genetic condition?
-
Liede A., Tonin P.N., Sun C.C.et al. Is hereditary site-specific ovarian cancer a distinct genetic condition? Am. J. Med. Genet. 75:1998;55-58.
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 55-58
-
-
Liede, A.1
Tonin, P.N.2
Sun, C.C.3
-
21
-
-
0032053728
-
BRCA2 germline mutations are frequent in male breast cancer patients without a family history of the disease
-
Haraldsson K., Loman N., Johannsson O., Olsson H., Borg Å BRCA2 germline mutations are frequent in male breast cancer patients without a family history of the disease. Cancer Res. 58:1998;1367-1371.
-
(1998)
Cancer Res.
, vol.58
, pp. 1367-1371
-
-
Haraldsson, K.1
Loman, N.2
Johannsson, O.3
Olsson, H.4
Borg, Å.5
-
22
-
-
0031105976
-
Tumour biological features of BRCA1-induced breast and ovarian cancer
-
Johannsson O.T., Idvall I., Anderson C., Borg Å., Egilsson V., Olsson H. Tumour biological features of BRCA1-induced breast and ovarian cancer. Eur. J. Cancer. 33:1997;362-371.
-
(1997)
Eur. J. Cancer
, vol.33
, pp. 362-371
-
-
Johannsson, O.T.1
Idvall, I.2
Anderson, C.3
Borg, Å.4
Egilsson, V.5
Olsson, H.6
-
23
-
-
16944367027
-
Moderate frequency of BRCA1 and BRCA2 germ-line mutation in Scandinavian familial breast cancer
-
Håkansson S., Johannsson O., Johansson U.et al. Moderate frequency of BRCA1 and BRCA2 germ-line mutation in Scandinavian familial breast cancer. Am. J. Hum. Genet. 60:1997;1068-1078.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1068-1078
-
-
Håkansson, S.1
Johannsson, O.2
Johansson, U.3
|