-
1
-
-
0033516265
-
Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer
-
Peto J, Collins N, Barfoot R et al (1999) Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer. J Natl Cancer Inst 91(11):943-949
-
(1999)
J Natl Cancer Inst
, vol.91
, Issue.11
, pp. 943-949
-
-
Peto, J.1
Collins, N.2
Barfoot, R.3
-
2
-
-
18344410703
-
Population-based study of risk of breast cancer in carriers of BRCA2 mutation
-
Thorlacius S, Struewing JP, Hartge P et al (1998) Population-based study of risk of breast cancer in carriers of BRCA2 mutation. Lancet 352(9137):1337-13379
-
(1998)
Lancet
, vol.352
, Issue.9137
, pp. 1337-13379
-
-
Thorlacius, S.1
Struewing, J.P.2
Hartge, P.3
-
3
-
-
0033570046
-
Ethnic differences in cancer risk resulting from genetic variation
-
Neuhausen SL (1999) Ethnic differences in cancer risk resulting from genetic variation. Cancer 86(Suppl 11):2575-2582
-
(1999)
Cancer
, vol.86
, Issue.SUPPL. 11
, pp. 2575-2582
-
-
Neuhausen, S.L.1
-
4
-
-
0033838645
-
Founder BRCA 1 and 2 mutations among a consecutive series of Ashkenazi Jewish ovarian cancer patients
-
Tobias DH, Eng C, McCurdy LD et al (2000) Founder BRCA 1 and 2 mutations among a consecutive series of Ashkenazi Jewish ovarian cancer patients. Gynecol Oncol 78(2):148-151
-
(2000)
Gynecol Oncol
, vol.78
, Issue.2
, pp. 148-151
-
-
Tobias, D.H.1
Eng, C.2
McCurdy, L.D.3
-
5
-
-
0035880897
-
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
-
Loman N, Johannsson O, Kristoffersson U, Olsson H, Borg A (2001) Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. J Natl Cancer Inst 93(16):1215-1223
-
(2001)
J Natl Cancer Inst
, vol.93
, Issue.16
, pp. 1215-1223
-
-
Loman, N.1
Johannsson, O.2
Kristoffersson, U.3
Olsson, H.4
Borg, A.5
-
6
-
-
0037836054
-
Population attributes affecting the prevalence of BRCA mutation carriers in epithelial ovarian cancer cases in israel
-
Hirsh-Yechezkel G, Chetrit A, Lubin F et al (2003) Population attributes affecting the prevalence of BRCA mutation carriers in epithelial ovarian cancer cases in israel. Gynecol Oncol 89(3):494-498
-
(2003)
Gynecol Oncol
, vol.89
, Issue.3
, pp. 494-498
-
-
Hirsh-Yechezkel, G.1
Chetrit, A.2
Lubin, F.3
-
7
-
-
19144364122
-
Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden
-
Johannsson O, Ostermeyer EA, Hakansson S et al (1996) Founding BRCA1 mutations in hereditary breast and ovarian cancer in southern Sweden. Am J Hum Genet 58(3):441-450
-
(1996)
Am J Hum Genet
, vol.58
, Issue.3
, pp. 441-450
-
-
Johannsson, O.1
Ostermeyer, E.A.2
Hakansson, S.3
-
8
-
-
0034813329
-
A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer
-
Einbeigi Z, Bergman A, Kindblom LG et al (2001) A founder mutation of the BRCA1 gene in Western Sweden associated with a high incidence of breast and ovarian cancer. Eur J Cancer 37(15):1904-1909
-
(2001)
Eur J Cancer
, vol.37
, Issue.15
, pp. 1904-1909
-
-
Einbeigi, Z.1
Bergman, A.2
Kindblom, L.G.3
-
9
-
-
21244445093
-
A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques
-
Bergman A, Flodin A, Engwall Y et al (2005) A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques. Fam Cancer 4:89-96
-
(2005)
Fam Cancer
, vol.4
, pp. 89-96
-
-
Bergman, A.1
Flodin, A.2
Engwall, Y.3
-
10
-
-
0034748570
-
The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation
-
Bergman A, Einbeigi Z, Olofsson U et al (2001) The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation. Eur J Hum Genet 9(10):787-793
-
(2001)
Eur J Hum Genet
, vol.9
, Issue.10
, pp. 787-793
-
-
Bergman, A.1
Einbeigi, Z.2
Olofsson, U.3
-
11
-
-
0037152091
-
Risk of ovarian cancer in breast-cancer patients with a family history of breast or ovarian cancer: A population-based cohort study
-
Bergfeldt K, Rydh B, Granath F et al (2002) Risk of ovarian cancer in breast-cancer patients with a family history of breast or ovarian cancer: a population-based cohort study. Lancet 360(9337):891-894
-
(2002)
Lancet
, vol.360
, Issue.9337
, pp. 891-894
-
-
Bergfeldt, K.1
Rydh, B.2
Granath, F.3
-
12
-
-
0036262531
-
Clustering of individuals with both breast and ovarian cancer - a possible indicator of BRCA founder mutations
-
Einbeigi Z, Meis-Kindblom JM, Kindblom LG, Wallgren A, Karlsson P (2002) Clustering of individuals with both breast and ovarian cancer - a possible indicator of BRCA founder mutations. Acta Oncol 41(2):153-157
-
(2002)
Acta Oncol
, vol.41
, Issue.2
, pp. 153-157
-
-
Einbeigi, Z.1
Meis-Kindblom, J.M.2
Kindblom, L.G.3
Wallgren, A.4
Karlsson, P.5
-
13
-
-
33847165127
-
ICD-7. International classification of diseases, injuries and causes of death
-
World Health Organisation , Geneva
-
World Health Organisation (1957) ICD-7. International classification of diseases, injuries and causes of death. 1955 revision, Geneva
-
(1957)
1955 revision
-
-
-
14
-
-
0033987736
-
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
-
den Dunnen JT, Antonarakis SE (2000) Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat 15(1):7-12
-
(2000)
Hum Mutat
, vol.15
, Issue.1
, pp. 7-12
-
-
den Dunnen, J.T.1
Antonarakis, S.E.2
-
15
-
-
0036591552
-
Characterization of common BRCA1 and BRCA2 variants
-
Deffenbaugh AM, Frank TS, Hoffman M, Cannon-Albright L, Neuhausen SL (2002) Characterization of common BRCA1 and BRCA2 variants. Genet Test 6(2):119-121
-
(2002)
Genet Test
, vol.6
, Issue.2
, pp. 119-121
-
-
Deffenbaugh, A.M.1
Frank, T.S.2
Hoffman, M.3
Cannon-Albright, L.4
Neuhausen, S.L.5
-
16
-
-
0035057806
-
BRCA1 and BRCA2 and the genetics of breast and ovarian cancer
-
Welcsh PL, King MC (2001) BRCA1 and BRCA2 and the genetics of breast and ovarian cancer. Hum Mol Genet 10(7):705-713
-
(2001)
Hum Mol Genet
, vol.10
, Issue.7
, pp. 705-713
-
-
Welcsh, P.L.1
King, M.C.2
-
17
-
-
0032755991
-
A high frequency of sequence alterations is due to formali fixation of archival specimens
-
Williams C, Pontén F, Moberg C et al (1999) A high frequency of sequence alterations is due to formali fixation of archival specimens. Am J Pathology 155:1467-1471
-
(1999)
Am J Pathology
, vol.155
, pp. 1467-1471
-
-
Williams, C.1
Pontén, F.2
Moberg, C.3
-
18
-
-
0033982554
-
Overestimated risk of second primary malignancies in ovarian cancer patients
-
Bergfeldt K, Silfversward C, Einhorn S, Hall P (2000) Overestimated risk of second primary malignancies in ovarian cancer patients. Eur J Cancer 36(1):100-105
-
(2000)
Eur J Cancer
, vol.36
, Issue.1
, pp. 100-105
-
-
Bergfeldt, K.1
Silfversward, C.2
Einhorn, S.3
Hall, P.4
-
19
-
-
0031105976
-
Tumour biological features of BRCA1-induced breast and ovarian cancer
-
Johannsson OT, Idvall I, Anderson C et al (1997) Tumour biological features of BRCA1-induced breast and ovarian cancer. Eur J Cancer 33(3):362-371
-
(1997)
Eur J Cancer
, vol.33
, Issue.3
, pp. 362-371
-
-
Johannsson, O.T.1
Idvall, I.2
Anderson, C.3
-
20
-
-
1642554820
-
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: Results of a prospective study in Southern Sweden
-
Malander S, Ridderheim M, Masback A et al (2004) One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations: results of a prospective study in Southern Sweden. Eur J Cancer 40(3):422-428
-
(2004)
Eur J Cancer
, vol.40
, Issue.3
, pp. 422-428
-
-
Malander, S.1
Ridderheim, M.2
Masback, A.3
-
21
-
-
0035318296
-
BRCA1 and BRCA2 mutations among Finnish ovarian carcinoma families
-
Sarantaus L, Auranen A, Nevanlinna H (2001) BRCA1 and BRCA2 mutations among Finnish ovarian carcinoma families. Int J Oncol 18(4):831-835
-
(2001)
Int J Oncol
, vol.18
, Issue.4
, pp. 831-835
-
-
Sarantaus, L.1
Auranen, A.2
Nevanlinna, H.3
-
22
-
-
0142178215
-
Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2
-
King MC, Marks JH, Mandell JB (2003) Breast and ovarian cancer risks due to inherited mutations in BRCA1 and BRCA2. Science 302(5645):643-646
-
(2003)
Science
, vol.302
, Issue.5645
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
23
-
-
0034990616
-
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
-
Bergthorsson JT, Ejlertsen B, Olsen JH et al (2001) BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age. J Med Genet 38(6):361-368
-
(2001)
J Med Genet
, vol.38
, Issue.6
, pp. 361-368
-
-
Bergthorsson, J.T.1
Ejlertsen, B.2
Olsen, J.H.3
-
24
-
-
4143060219
-
BRCA1 mutations in a population-based study of breast cancer in Stockholm County
-
Margolin S, Werelius BF, Fornander T, Lindblom A (2004) BRCA1 mutations in a population-based study of breast cancer in Stockholm County. Genet Test 8:127-132
-
(2004)
Genet Test
, vol.8
, pp. 127-132
-
-
Margolin, S.1
Werelius, B.F.2
Fornander, T.3
Lindblom, A.4
-
25
-
-
0033031573
-
Three per cent of Norwegian ovarian cancers are caused by BRCA1 1675delA or 1135insA
-
Dørum A, Hovig E, Trope C, Inganas M, Moller P (1999) Three per cent of Norwegian ovarian cancers are caused by BRCA1 1675delA or 1135insA. Eur J Cancer 35(5):779-781
-
(1999)
Eur J Cancer
, vol.35
, Issue.5
, pp. 779-781
-
-
Dørum, A.1
Hovig, E.2
Trope, C.3
Inganas, M.4
Moller, P.5
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