-
2
-
-
29144509766
-
BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases
-
doi:10.1002/cncr.21536
-
PAL T, permuth-wey J, BETTS JA, KRISCHER JP, FIORICA J et al. BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer 2005; 104: 2807-2816. doi:10.1002/cncr.21536
-
(2005)
Cancer
, vol.104
, pp. 2807-2816
-
-
Pal, T.1
Permuth-Wey, J.2
Betts, J.A.3
Krischer, J.P.4
Fiorica, J.5
-
3
-
-
0031029633
-
Probability of carrying a mutation of breast- ovarian cancer gene BRCA1 based on family history
-
doi:10.1093/jnci/89.3.227
-
BERRY DA, PARMIGIANI G, SANCHEZ J, SCHILDKRAUT J, WINER E. Probability of carrying a mutation of breast- ovarian cancer gene BRCA1 based on family history. Journal of National Cancer Institute 1997; 89: 227-238. doi:10.1093/jnci/89.3.227
-
(1997)
Journal of National Cancer Institute
, vol.89
, pp. 227-238
-
-
Berry, D.A.1
Parmigiani, G.2
Sanchez, J.3
Schildkraut, J.4
Winer, E.5
-
4
-
-
0034754914
-
Germline BRCA1-2 Mutations in Non-Ashkenazi Families with Double Primary Breast and Ovarian Cancer
-
doi:10.1006/gyno.2001.6431
-
SCHORGE JO, MAHONEY NM, MILLER DS, COLEMAN RL, MULLER CY et al. Germline BRCA1-2 Mutations in Non-Ashkenazi Families with Double Primary Breast and Ovarian Cancer. Gynecologic Oncology 2001; 83: 383-387. doi:10.1006/gyno.2001.6431
-
(2001)
Gynecologic Oncology
, vol.83
, pp. 383-387
-
-
Schorge, J.O.1
Mahoney, N.M.2
Miller, D.S.3
Coleman, R.L.4
Muller, C.Y.5
-
5
-
-
0033731558
-
BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers
-
SHIH HA, NATHANSON KL, SEAL S, COLLINS N, STRETTON MR et al. BRCA1 and BRCA2 mutations in breast cancer families with multiple primary cancers. Clinical Cancer Re- searh 2000; 6: 4259-4264.
-
(2000)
Clinical Cancer Re- Searh
, vol.6
, pp. 4259-4264
-
-
Shih, H.A.1
Nathanson, K.L.2
Seal, S.3
Collins, N.4
Stretton, M.R.5
-
6
-
-
14644438527
-
Risk factors and prognostic factors in patients with double primary cancer: Epithelial ovarian cancer and breast cancer
-
CVELBAR M, Ursič-Vrščaj M, RAKAR S. Risk factors and prognostic factors in patients with double primary cancer: Epithelial ovarian cancer and breast cancer. European Journal of Gynaecological Oncology 2005; 26: 59-63.
-
(2005)
European Journal of Gynaecological Oncology
, vol.26
, pp. 59-63
-
-
Cvelbar, M.1
Ursič-Vrščaj, M.2
Rakar, S.3
-
8
-
-
0031953979
-
A second primary malignancy in a cohort of patients with epithelial ovarian cancer - characteristics of diagnosis
-
FISHMAN A, AVIRAM R, BEYTH Y, BERNHEIM J, ALTARAS M. A second primary malignancy in a cohort of patients with epithelial ovarian cancer - characteristics of diagnosis. European Journal of Gynaecologic Oncology 1998; 19: 280-283.
-
(1998)
European Journal of Gynaecologic Oncology
, vol.19
, pp. 280-283
-
-
Fishman, A.1
Aviram, R.2
Beyth, Y.3
Bernheim, J.4
Altaras, M.5
-
9
-
-
0033769823
-
Patients with double primary tumors in the breast and ovary - clinical characteristics and BRCA1-2 mutations status
-
doi:10.1006/gyno.2000.5895
-
Fishman A, Dekel E, Chetrit A, Lerner-Geva L, Baram A et al. Patients with double primary tumors in the breast and ovary - clinical characteristics and BRCA1-2 mutations status. Gynecologic Oncology 2000; 79: 74-78. doi:10.1006/gyno.2000.5895
-
(2000)
Gynecologic Oncology
, vol.79
, pp. 74-78
-
-
Fishman, A.1
Dekel, E.2
Chetrit, A.3
Lerner-Geva, L.4
Baram, A.5
-
10
-
-
0029034155
-
Rapid detection of BRCA1 mutations by the protein truncation test
-
doi:10.1038/ng0695-208
-
HOGERVORST FB, CORNELIS RS, BOUT M, VAN VLIET M, OOSTERWIJK JC et al. Rapid detection of BRCA1 mutations by the protein truncation test. Nat Genet 1995 Jun; 10: 208-12. doi:10.1038/ng0695-208
-
(1995)
Nat Genet
, vol.10
, pp. 208-212
-
-
Hogervorst, F.B.1
Cornelis, R.S.2
Bout, M.3
Vliet, M.4
Oosterwijk, J.C.5
-
11
-
-
33745728357
-
A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: Application in a Duch cancer clinic setting
-
doi:10.1002/humu.20340
-
van der Hout AH, van den Ouweland AM, van der Luijt RB, Gille HJ, BODMER D et al. A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Duch cancer clinic setting. Hum Mutat 2006 Jul; 27: 654-66. doi:10.1002/humu.20340
-
(2006)
Hum Mutat
, vol.27
, pp. 654-666
-
-
van der Hout, A.H.1
van den Ouweland, A.M.2
van der Luijt, R.B.3
Gille, H.J.4
Bodmer, D.5
-
12
-
-
0036927010
-
BRCA2 founder mutation in Slovenian breast cancer families
-
doi:10.1038/sj.ejhg.5200886
-
KRAJC M, DE GRÈVE J, GOELEN G, TEUGELS E. BRCA2 founder mutation in Slovenian breast cancer families. European Journal of Human Genetics 2002; 10: 879-882. doi:10.1038/sj.ejhg.5200886
-
(2002)
European Journal of Human Genetics
, vol.10
, pp. 879-882
-
-
Krajc, M.1
Grève, J.2
Goelen, G.3
Teugels, E.4
-
14
-
-
85067779673
-
Genetic counselling and testing in slovenian breast and ovarian cancer families
-
In: Žgajnar J e tal, eds, onkološki vikend; 2006 May 26-27; Laško, Slovenija. Ljubljana: Kancerološko združenje Slovenskega zdravniškega društva, Onkološki inštitut Ljubljana in Zveza slovenskih društev za boj proti raku
-
Krajc M, Žgajnar J, Bešić N, Hočevar M, Bilban Jakopin C et al. Genetic counselling and testing in slovenian breast and ovarian cancer families. In: Žgajnar J e tal, eds. Geni in rak-19. onkološki vikend; 2006 May 26-27; Laško, Slovenija. Ljubljana: Kancerološko združenje Slovenskega zdravniškega društva, Onkološki inštitut Ljubljana in Zveza slovenskih društev za boj proti raku; 2006: 48-58.
-
(2006)
Geni In Rak-19
, pp. 48-58
-
-
Krajc, M.1
Žgajnar, J.2
Bešić, N.3
Hočevar, M.4
Bilban, J.C.5
-
15
-
-
46949098149
-
Hereditary breast cancer: New genetic developments, new therapeutic evenues
-
doi:10.1007/s00439-008-0529-1
-
CAMPEAU PM, FOULKES WD, TISCHKOWITZ MD. Hereditary breast cancer: new genetic developments, new therapeutic evenues. Human Genetics 2008; 124: 31-42. doi:10.1007/s00439-008-0529-1
-
(2008)
Human Genetics
, vol.124
, pp. 31-42
-
-
Campeau, P.M.1
Foulkes, W.D.2
Tischkowitz, M.D.3
-
16
-
-
33846317838
-
Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patients
-
doi:10.1016/j.ejca.2006.09.021
-
RAZIS E, BOUKOVINAS I, XENIDIS N, RAZIS E, Bou-Kovinas I et al. Novel genomic rearrangements in the BRCA1 gene detected in Greek breast/ovarian cancer patients. European Journal of Cancer 2007; 43: 443-453. doi:10.1016/j.ejca.2006.09.021
-
(2007)
European Journal of Cancer
, vol.43
, pp. 443-453
-
-
Razis, E.1
Boukovinas, I.2
Xenidis, N.3
Razis, E.4
Bou-Kovinas, I.5
-
18
-
-
10744229650
-
Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2
-
MENKISZAK J, GRONWALD J, GÓRSKI B, BYRSKI T, HUZARSKI T et al. Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2. European Journal of Gynaecologic Oncology 2004, 25: 99-100.
-
(2004)
European Journal of Gynaecologic Oncology
, vol.25
, pp. 99-100
-
-
Menkiszak, J.1
Gronwald, J.2
Górski, B.3
Byrski, T.4
Huzarski, T.5
-
19
-
-
23944476784
-
Hereditary ovarian cancer
-
doi:10.1016/j.humpath.2005.06.006
-
PRAT J, RIBÉ A, GALLARDO A. Hereditary ovarian cancer. Human Pathology 2005; 36: 861-870. doi:10.1016/j.humpath.2005.06.006
-
(2005)
Human Pathology
, vol.36
, pp. 861-870
-
-
Prat, J.1
Ribé, A.2
Gallardo, A.3
-
20
-
-
0034600109
-
Clinicopathologic Features of BRCA-Linked and Sporadic Ovarian Cancer
-
BOYD J, SONODA Y, FEDERICI M, BOGOMOLNIY F, RHEI E et al. Clinicopathologic Features of BRCA-Linked and Sporadic Ovarian Cancer. JAMA 2000; 283: 2260-2265.
-
(2000)
JAMA
, vol.283
, pp. 2260-2265
-
-
Boyd, J.1
Sonoda, Y.2
Federici, M.3
Bogomolniy, F.4
Rhei, E.5
-
22
-
-
20444387248
-
A comparison of bilateral breast cancers in BRCA carriers. Cancer Epidemiology
-
doi:10.1158/1055-9965. EPI-05-0070
-
WEITZEL JN, ROBSON M, PASINI B, MANOUKIAN S, STOPPA-LYONNET D et al. A comparison of bilateral breast cancers in BRCA carriers. Cancer Epidemiology, Biomarkers & Prevention 2005; 14:1534-1538. doi:10.1158/1055-9965. EPI-05-0070
-
(2005)
Biomarkers & Prevention
, vol.14
, pp. 1534-1538
-
-
Weitzel, J.N.1
Robson, M.2
Pasini, B.3
Manoukian, S.4
Stoppa-Lyonnet, D.5
-
23
-
-
33644841624
-
High risk of contralateral breast carcinoma in women with hereditaty7familial non-BRCA1/BRCA2 breast carcinoma
-
doi:10.1002/cncr.21753
-
SHAHEDI K, EMANUELSSON M, WIKLUND F, Gron-Berg H. High risk of contralateral breast carcinoma in women with hereditaty7familial non-BRCA1/BRCA2 breast carcinoma. Cancer 2006; 106: 1237-1242. doi:10.1002/cncr.21753
-
(2006)
Cancer
, vol.106
, pp. 1237-1242
-
-
Shahedi, K.1
Emanuelsson, M.2
Wiklund, F.3
Gron-Berg, H.4
-
24
-
-
2942739225
-
Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers
-
doi:10.1200/JCO.2004.04.033
-
METCALFE K, LYNCH HT, GHADIRIAN P, TUNG N, OLLIVOTTO I et al. Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers. Journal of Clinical Oncology 2004; 22: 2328-2335. doi:10.1200/JCO.2004.04.033
-
(2004)
Journal of Clinical Oncology
, vol.22
, pp. 2328-2335
-
-
Metcalfe, K.1
Lynch, H.T.2
Ghadirian, P.3
Tung, N.4
Ollivotto, I.5
-
25
-
-
26844519521
-
Familial breast cancer: Characteristics and outcome of BRCA 1-2 positive and negative cases
-
VERONESI A, DE GIACOMI C, MAGRI MD, LOMBARDI D, ZANETTI M et al. Familial breast cancer: characteristics and outcome of BRCA 1-2 positive and negative cases. BMC Cancer 2005, 5: 70. http://www.biomedcentral.com/1471-2407/5/70
-
(2005)
BMC Cancer
, vol.5
, pp. 70
-
-
Veronesi, A.1
Giacomi, C.2
Magri, M.D.3
Lombardi, D.4
Zanetti, M.5
|