-
1
-
-
0028882346
-
The etiology of breast cancer - From epidemiology to prevention
-
Kuller LH. The etiology of breast cancer - from epidemiology to prevention. Public Health Reviews 1995; 23: 157-213.
-
(1995)
Public Health Reviews
, vol.23
, pp. 157-213
-
-
Kuller, L.H.1
-
2
-
-
0029558093
-
The genetic epidemiology of cancer
-
Claus EB. The genetic epidemiology of cancer. Cancer Surveys 1995; 25: 13-26.
-
(1995)
Cancer Surveys
, vol.25
, pp. 13-26
-
-
Claus, E.B.1
-
3
-
-
0030914999
-
Family history and the risk of breast cancer: A systematic review and meta-analysis
-
Pharoah PD, Day NE, Duffy S et al. Family history and the risk of breast cancer: A systematic review and meta-analysis. International Journal of Cancer 1997; 71: 800-9.
-
(1997)
International Journal of Cancer
, vol.71
, pp. 800-809
-
-
Pharoah, P.D.1
Day, N.E.2
Duffy, S.3
-
4
-
-
0343103400
-
Recent progress in breast cancer genetic epidemiology
-
Howell A, ed. Springer-Verlag
-
Bishop DT, Eby N, Chang-Claude J. Recent Progress in Breast Cancer Genetic Epidemiology. In: Howell A, ed. Endocrine Therapy of Breast Cancer VI. Vol. VI: Springer-Verlag 1994: 3-15.
-
(1994)
Endocrine Therapy of Breast Cancer VI
, vol.6
, pp. 3-15
-
-
Bishop, D.T.1
Eby, N.2
Chang-Claude, J.3
-
7
-
-
0025633582
-
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
-
Malkin D, Li FP, Strong LC et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 1990; 250: 1233-8.
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Strong, L.C.3
-
8
-
-
0022649866
-
The Cowden syndrome: A clinical and genetic study in 21 patients
-
Starink TM, van der Veen JP, Arwert F et al. The Cowden syndrome: a clinical and genetic study in 21 patients. Clinical Genetics 1986; 29: 222-33.
-
(1986)
Clinical Genetics
, vol.29
, pp. 222-233
-
-
Starink, T.M.1
Van Der Veen, J.P.2
Arwert, F.3
-
9
-
-
6844252284
-
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation
-
Marsh DJ, Coulon V, Lunetta KL et al. Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation. Human Molecular Genetics 1998; 7: 507-15.
-
(1998)
Human Molecular Genetics
, vol.7
, pp. 507-515
-
-
Marsh, D.J.1
Coulon, V.2
Lunetta, K.L.3
-
10
-
-
0031004088
-
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
-
Liaw D, Marsh DJ, Li J et al. Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome. Nature Genetics 1997; 16: 64-7.
-
(1997)
Nature Genetics
, vol.16
, pp. 64-67
-
-
Liaw, D.1
Marsh, D.J.2
Li, J.3
-
11
-
-
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: 1684-9.
-
(1990)
Science
, vol.250
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
-
12
-
-
42449107062
-
Familial breast-ovarian cancer locus on chromosome 17q12-q23
-
Narod SA, Feuteun J, Lynch HT et al. Familial breast-ovarian cancer locus on chromosome 17q12-q23. Lancet 1991; 338: 82-3.
-
(1991)
Lancet
, vol.338
, pp. 82-83
-
-
Narod, S.A.1
Feuteun, J.2
Lynch, H.T.3
-
13
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. The breast cancer linkage consortium
-
Easton DF, Bishop DT, Ford D et al. Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium. American Journal of Human Genetics 1993; 52: 678-701.
-
(1993)
American Journal of Human Genetics
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
-
14
-
-
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.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
-
15
-
-
0028834145
-
A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene: Implications for presymptomatic testing and screening
-
Shattuck-Eidens D, McClure M, Simard J et al. A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene: Implications for presymptomatic testing and screening. JAMA 1995; 273: 535-41.
-
(1995)
JAMA
, vol.273
, pp. 535-541
-
-
Shattuck-Eidens, D.1
McClure, M.2
Simard, J.3
-
16
-
-
0028141722
-
Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q
-
Stratton MR, Ford D, Neuhasen S et al. Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q. Nature Genetics 1994; 7: 103-7.
-
(1994)
Nature Genetics
, vol.7
, pp. 103-107
-
-
Stratton, M.R.1
Ford, D.2
Neuhasen, S.3
-
17
-
-
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: 2088-90.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
-
18
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J et al. Identification of the breast cancer susceptibility gene BRCA2. Nature 1995; 378 (Dec 21/28): 789-92.
-
(1995)
Nature
, vol.378
, Issue.DEC 21-28
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
-
19
-
-
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: 676-89.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
-
20
-
-
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. Nature Genetics 1995; 11: 428-33.
-
(1995)
Nature Genetics
, vol.11
, pp. 428-433
-
-
Gayther, S.A.1
Warren, W.2
Mazoyer, S.3
-
21
-
-
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: 102-10.
-
(1997)
Genes, Chromosomes & Cancer
, vol.18
, pp. 102-110
-
-
Xu, C.F.1
Chambers, J.A.2
Nicolai, H.3
-
22
-
-
19144367118
-
Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis
-
Gayther SA, Harrington P, Russell P et al. Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. Am J Hum Genet 1996; 58: 451-6.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 451-456
-
-
Gayther, S.A.1
Harrington, P.2
Russell, P.3
-
23
-
-
16944364123
-
BRCA sequence variations in 160 individuals referred to a breast/ovary family cancer clinic
-
Stoppa Lyonnet D. BRCA sequence variations in 160 individuals referred to a breast/ovary family cancer clinic. Am J of Hum Genet 1997; 60: 1021-30.
-
(1997)
Am J of Hum Genet
, vol.60
, pp. 1021-1030
-
-
Stoppa Lyonnet, D.1
-
24
-
-
0029812426
-
A common BRCA1 mutation in Norwegian breast and ovarian cancer families?
-
Andersen TI, Børresen A-L, Møller P. A common BRCA1 mutation in Norwegian breast and ovarian cancer families? Am J Hum Genet 1996; 59: 486-7.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 486-487
-
-
Andersen, T.I.1
Børresen, A.-L.2
Møller, P.3
-
25
-
-
19144364122
-
Founding BRCA1 mutations in hereditary breast and ovarian cancer in Southern Sweden
-
Johannsson O, Ostermeyer EA, Håkansson S et al. Founding BRCA1 mutations in hereditary breast and ovarian cancer in Southern Sweden. Am J Hum Genet 1996; 58: 441-50.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 441-450
-
-
Johannsson, O.1
Ostermeyer, E.A.2
Håkansson, S.3
-
26
-
-
16944367027
-
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
-
Hakansson S, Johannsson O, Johansson U et al. Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer. Am J Hum Genet 1997; 60: 1068-78.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1068-1078
-
-
Hakansson, S.1
Johannsson, O.2
Johansson, U.3
-
27
-
-
0032565070
-
Frequency of breast cancer attributable to BRCA1 in a population-based series of American women
-
Newman B. Frequency of breast cancer attributable to BRCA1 in a population-based series of American women. JAMA 1998; 279: 915-21.
-
(1998)
JAMA
, vol.279
, pp. 915-921
-
-
Newman, B.1
-
28
-
-
0032565074
-
BRCA1 mutations and breast cancer in the general population
-
Malone K. BRCA1 mutations and breast cancer in the general population. JAMA 1998; 279: 922-9.
-
(1998)
JAMA
, vol.279
, pp. 922-929
-
-
Malone, K.1
-
29
-
-
0028885339
-
An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families
-
Narod S, Ford D, Devilee P et al. An evaluation of genetic heterogeneity in 145 breast-ovarian cancer families. Am J Hum Genet 1995; 56: 254-64.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 254-264
-
-
Narod, S.1
Ford, D.2
Devilee, P.3
-
30
-
-
16944365740
-
Cancer risks in two large breast cancer families linked to BRCA2 on chromosome 13q12-13
-
Easton DF, 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 1997; 61: 120-8.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 120-128
-
-
Easton, D.F.1
Steele, L.2
Fields, P.3
-
31
-
-
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 Eng J Med 1997; 336: 1401-8.
-
(1997)
N Eng J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hartge, P.2
Wacholder, S.3
-
32
-
-
18344410703
-
Population-based study of breast cancer in carriers of BRCA2 mutation
-
Thorlacius S, Struewing JP, Hartge P et al. Population-based study of breast cancer in carriers of BRCA2 mutation. Lancet. 1998; 352: 1337-9.
-
(1998)
Lancet
, vol.352
, pp. 1337-1339
-
-
Thorlacius, S.1
Struewing, J.P.2
Hartge, P.3
-
33
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
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: 103-5.
-
(1997)
Nat Genet
, vol.15
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russell, P.3
-
34
-
-
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. Lancet 1997; 349: 1505-10.
-
(1997)
Lancet
, vol.349
, pp. 1505-1510
-
-
|