-
1
-
-
52949096470
-
Genetic predisposition to breast cancer: Past, present, and future
-
Turnbull C, Rahman N. Genetic predisposition to breast cancer: past, present, and future. Annu Rev Genomics Hum Genet. 2008; 9: 321-345
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 321-345
-
-
Turnbull, C.1
Rahman, N.2
-
2
-
-
69849107956
-
Polygenic susceptibility to breast cancer: Current state-of-the-art
-
Ghoussaini M, Pharoah PD. Polygenic susceptibility to breast cancer: current state-of-the-art. Future Oncol. 2009; 5(5): 689-701
-
(2009)
Future Oncol
, vol.5
, Issue.5
, pp. 689-701
-
-
Ghoussaini, M.1
Pharoah, P.D.2
-
3
-
-
77953615401
-
The inherited genetics of ovarian and endometrial cancer
-
Gayther SA, Pharoah PD. The inherited genetics of ovarian and endometrial cancer. Curr Opin Genet Dev. 2010; 20(3): 231-238
-
(2010)
Curr Opin Genet Dev
, vol.20
, Issue.3
, pp. 231-238
-
-
Gayther, S.A.1
Pharoah, P.D.2
-
4
-
-
0035098503
-
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
-
DOI 10.1086/318787
-
Risch HA, McLaughlin JR, Cole DE, et al. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. Am J Hum Genet. 2001; 68(3): 700- 710 (Pubitemid 32203724)
-
(2001)
American Journal of Human Genetics
, vol.68
, Issue.3
, pp. 700-710
-
-
Risch, H.A.1
McLaughlin, J.R.2
Cole, D.E.C.3
Rosen, B.4
Bradley, L.5
Kwan, E.6
Jack, E.7
Vesprini, D.J.8
Kuperstein, G.9
Abrahamson, J.L.A.10
Fan, I.11
Wong, B.12
Narod, S.A.13
-
5
-
-
0035125062
-
Variation in cancer risks, by mutation position, in BRCA2 mutation carriers
-
DOI 10.1086/318181
-
Thompson D, Easton D, Breast Cancer Linkage Consortium. Variation in cancer risks, by mutation position, in BRCA2 mutation carriers. Am J Hum Genet. 2001; 68(2): 410-419 (Pubitemid 32147810)
-
(2001)
American Journal of Human Genetics
, vol.68
, Issue.2
, pp. 410-419
-
-
Thompson, D.1
Easton, D.2
-
6
-
-
77956418209
-
High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from Belarus
-
Bogdanova NV, Antonenkova NN, Rogov YI, Karstens JH, Hillemanns P, Dörk T. High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from Belarus. Clin Genet. 2010; 78(4): 364-372
-
(2010)
Clin Genet.
, vol.78
, Issue.4
, pp. 364-372
-
-
Bogdanova, N.V.1
Antonenkova, N.N.2
Rogov, Y.I.3
Karstens, J.H.4
Hillemanns, P.5
Dörk, T.6
-
7
-
-
36749002743
-
RAD51 135GC modifies breast cancer risk among BRCA2 mutation carriers: Results from a combined analysis of 19 studies
-
DOI 10.1086/522611
-
Antoniou AC, Sinilnikova OM, Simard J, et al. RAD51 135G>C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies. Am J Hum Genet. 2007; 81(6): 1186-1200 (Pubitemid 350211449)
-
(2007)
American Journal of Human Genetics
, vol.81
, Issue.6
, pp. 1186-1200
-
-
Antoniou, A.C.1
Sinilnikova, O.M.2
Simard, J.3
Leone, M.4
Dumont, M.5
Neuhausen, S.L.6
Struewing, J.P.7
Stoppa-Lyonnet, D.8
Barjhoux, L.9
Hughes, D.J.10
Coupier, I.11
Belotti, M.12
Lasset, C.13
Bonadona, V.14
Bignon, Y.-J.15
Rebbeck, T.R.16
Wagner, T.17
Lynch, H.T.18
Domchek, S.M.19
Nathanson, K.L.20
Garber, J.E.21
Weitzel, J.22
Narod, S.A.23
Tomlinson, G.24
Olopade, O.I.25
Godwin, A.26
Isaacs, C.27
Jakubowska, A.28
Lubinski, J.29
Gronwald, J.30
Gorski, B.31
Byrski, T.32
Huzarski, T.33
Peock, S.34
Cook, M.35
Baynes, C.36
Murray, A.37
Rogers, M.38
Daly, P.A.39
Dorkins, H.40
Schmutzler, R.K.41
Versmold, B.42
Engel, C.43
Meindl, A.44
Arnold, N.45
Niederacher, D.46
Deissler, H.47
Spurdle, A.B.48
Chen, X.49
Waddell, N.50
Cloonan, N.51
Kirchhoff, T.52
Offit, K.53
Friedman, E.54
Kaufmann, B.55
Laitman, Y.56
Galore, G.57
Rennert, G.58
Lejbkowicz, F.59
Raskin, L.60
Andrulis, I.L.61
Ilyushik, E.62
Ozcelik, H.63
Devilee, P.64
Vreeswijk, M.P.G.65
Greene, M.H.66
Prindiville, S.A.67
Osorio, A.68
Benitez, J.69
Zikan, M.70
Szabo, C.I.71
Kilpivaara, O.72
Nevanlinna, H.73
Hamann, U.74
Durocher, F.75
Arason, A.76
Couch, F.J.77
Easton, D.F.78
Chenevix-Trench, G.79
Chompret, A.80
Bressac-de-Paillerets, B.81
Byrde, V.82
Capoulade, C.83
Lenoir, G.84
Uhrhammer, N.85
Gauthier-Villars, M.86
De Pauw, A.87
Sinilnikova, O.88
Giraud, S.89
Hardouin, A.90
Berthet, P.91
Sobol, H.92
Bourdon, V.93
Eisinger, F.94
Coulet, F.95
Colas, C.96
Soubrier, F.97
Peyrat, J.-P.98
Fournier, J.99
more..
-
8
-
-
79251507591
-
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
-
Ramus SJ, Kartsonaki C, Gayther SA, Pharoah PD, Sinilnikova OM, Beesley J. Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. J Natl Cancer Inst. 2011; 103(2): 105-116
-
(2011)
J Natl Cancer Inst
, vol.103
, Issue.2
, pp. 105-116
-
-
Ramus, S.J.1
Kartsonaki, C.2
Gayther, S.A.3
Pharoah, P.D.4
Sinilnikova, O.M.5
Beesley, J.6
-
9
-
-
33846625493
-
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
-
DOI 10.1038/ng1959, PII NG1959
-
Rahman N, Seal S, Thompson D, et al. PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet. 2007; 39(2): 165-167 (Pubitemid 46184346)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 165-167
-
-
Rahman, N.1
Seal, S.2
Thompson, D.3
Kelly, P.4
Renwick, A.5
Elliott, A.6
Reid, S.7
Spanova, K.8
Barfoot, R.9
Chagtai, T.10
Jayatilake, H.11
McGuffog, L.12
Hanks, S.13
Evans, D.G.14
Eccles, D.15
Easton, D.F.16
Stratton, M.R.17
-
10
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
DOI 10.1038/nature05609, PII NATURE05609
-
Erkko H, Xia B, Nikkilä J, et al. A recurrent mutation in PALB2 in Finnish cancer families. Nature. 2007; 446(7133): 316-319 (Pubitemid 46426155)
-
(2007)
Nature
, vol.446
, Issue.7133
, pp. 316-319
-
-
Erkko, H.1
Xia, B.2
Nikkila, J.3
Schleutker, J.4
Syrjakoski, K.5
Mannermaa, A.6
Kallioniemi, A.7
Pylkas, K.8
Karppinen, S.-M.9
Rapakko, K.10
Miron, A.11
Sheng, Q.12
Li, G.13
Mattila, H.14
Bell, D.W.15
Haber, D.A.16
Grip, M.17
Reiman, M.18
Jukkola-Vuorinen, A.19
Mustonen, A.20
Kere, J.21
Aaltonen, L.A.22
Kosma, V.-M.23
Kataja, V.24
Soini, Y.25
Drapkin, R.I.26
Livingston, D.M.27
Winqvist, R.28
more..
-
11
-
-
51649092869
-
Penetrance analysis of the PALB2 c.1592delT founder mutation
-
Erkko H, Dowty JG, Nikkilä J, et al. Penetrance analysis of the PALB2 c.1592delT founder mutation. Clin Cancer Res 2008;14(14):4667-4671
-
(2008)
Clin Cancer Res
, vol.14
, Issue.14
, pp. 4667-4671
-
-
Erkko, H.1
Dowty, J.G.2
Nikkilä, J.3
-
12
-
-
77649148280
-
A novel germline PALB2 deletion in Polish breast and ovarian cancer patients
-
Dansonka-Mieszkowska A, Kluska A, Moes J, et al. A novel germline PALB2 deletion in Polish breast and ovarian cancer patients. BMC Med Genet. 2010; 11: 20.
-
BMC Med Genet.
, vol.2010
, Issue.11
, pp. 20
-
-
Dansonka-Mieszkowska, A.1
Kluska, A.2
Moes, J.3
-
13
-
-
84862262488
-
Rare occurrence of PALB2 mutations in ovarian cancer patients from the Volga-Ural region
-
Prokofyeva D, Bogdanova N, Bermisheva M, et al. Rare occurrence of PALB2 mutations in ovarian cancer patients from the Volga-Ural region. Clin Genet. 2012; 82(1): 100-101
-
(2012)
Clin Genet
, vol.82
, Issue.1
, pp. 100-101
-
-
Prokofyeva, D.1
Bogdanova, N.2
Bermisheva, M.3
-
14
-
-
77951720395
-
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
-
Meindl A, Hellebrand H, Wiek C, et al. Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene. Nat Genet. 2010; 42(5): 410-414
-
(2010)
Nat Genet
, vol.42
, Issue.5
, pp. 410-414
-
-
Meindl, A.1
Hellebrand, H.2
Wiek, C.3
-
15
-
-
79960815893
-
RAD51C is a susceptibility gene for ovarian cancer
-
Pelttari LM, Heikkinen T, Thompson D, et al. RAD51C is a susceptibility gene for ovarian cancer. Hum Mol Genet. 2011; 20(16): 3278-3288
-
(2011)
Hum Mol Genet
, vol.20
, Issue.16
, pp. 3278-3288
-
-
Pelttari, L.M.1
Heikkinen, T.2
Thompson, D.3
-
16
-
-
80052264429
-
Germline mutations in RAD51D confer susceptibility to ovarian cancer
-
Loveday C, Turnbull C, Ramsay E, Hughes D, Ruark E, Frankum Jr. Germline mutations in RAD51D confer susceptibility to ovarian cancer. Nat Genet. 2011; 43(9): 879-882
-
(2011)
Nat Genet
, vol.43
, Issue.9
, pp. 879-882
-
-
Loveday, C.1
Turnbull, C.2
Ramsay, E.3
Hughes, D.4
Ruark, E.5
Frankum, J.R.6
-
17
-
-
33750465216
-
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
-
DOI 10.1038/ng1902, PII NG1902
-
Seal S, Thompson D, Renwick A, et al. Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles. Nat Genet. 2006; 38(11): 1239-1241 (Pubitemid 44646283)
-
(2006)
Nature Genetics
, vol.38
, Issue.11
, pp. 1239-1241
-
-
Seal, S.1
Thompson, D.2
Renwick, A.3
Elliott, A.4
Kelly, P.5
Barfoot, R.6
Chagtai, T.7
Jayatilake, H.8
Ahmed, M.9
Spanova, K.10
North, B.11
McGuffog, L.12
Evans, D.G.13
Eccles, D.14
Easton, D.F.15
Stratton, M.R.16
Rahman, N.17
-
18
-
-
36348986039
-
Germline E-cadherin mutations in familial lobular breast cancer
-
DOI 10.1136/jmg.2007.051268
-
Masciari S, Larsson N, Senz J, et al. Germline E-cadherin mutations in familial lobular breast cancer. J Med Genet. 2007; 44(11): 726-731 (Pubitemid 350155461)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.11
, pp. 726-731
-
-
Masciari, S.1
Larsson, N.2
Senz, J.3
Boyd, N.4
Kaurah, P.5
Kandel, M.J.6
Harris, L.N.7
Pinheiro, H.C.8
Troussard, A.9
Miron, P.10
Tung, N.11
Oliveira, C.12
Collins, L.13
Schnitt, S.14
Garber, J.E.15
Huntsman, D.16
-
19
-
-
79960010866
-
Germline mutations of the E-cadherin gene in families with inherited invasive lobular breast carcinoma but no diffuse gastric cancer
-
Xie ZM, Li LS, Laquet C, et al. Germline mutations of the E-cadherin gene in families with inherited invasive lobular breast carcinoma but no diffuse gastric cancer. Cancer. 2011; 117(14): 3112-3117
-
(2011)
Cancer
, vol.117
, Issue.14
, pp. 3112-3117
-
-
Xie, Z.M.1
Li, L.S.2
Laquet, C.3
-
20
-
-
0023244806
-
Breast and other cancers in families with ataxia-telangiectasia
-
Swift M, Reitnauer PJ, Morrell D, Chase CL. Breast and other cancers in families with ataxiatelangiectasia. N Engl J Med. 1987; 316(21): 1289- 1294 (Pubitemid 17084026)
-
(1987)
New England Journal of Medicine
, vol.316
, Issue.21
, pp. 1289-1294
-
-
Swift, M.1
Reitnauer, P.J.2
Morrell, D.3
Chase, C.L.4
-
21
-
-
0037365789
-
ATM and related protein kinases: Safeguarding genome integrity
-
DOI 10.1038/nrc1011
-
Shiloh Y. ATM and related protein kinases: safeguarding genome integrity. Nat Rev Cancer. 2003; 3(3): 155-168 (Pubitemid 37328868)
-
(2003)
Nature Reviews Cancer
, vol.3
, Issue.3
, pp. 155-168
-
-
Shiloh, Y.1
-
22
-
-
33746491583
-
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
-
DOI 10.1038/ng1837, PII NG1837
-
Renwick A, Thompson D, Seal S, et al. ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles. Nat Genet. 2006; 38(8): 873-875 (Pubitemid 44141653)
-
(2006)
Nature Genetics
, vol.38
, Issue.8
, pp. 873-875
-
-
Renwick, A.1
Thompson, D.2
Seal, S.3
Kelly, P.4
Chagtai, T.5
Ahmed, M.6
North, B.7
Jayatilake, H.8
Barfoot, R.9
Spanova, K.10
McGuffog, L.11
Evans, D.G.12
Eccles, D.13
Easton, D.F.14
Stratton, M.R.15
Rahman, N.16
-
23
-
-
34447096911
-
Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer
-
DOI 10.1093/carcin/bgl237
-
Pylkäs K, Tommiska J, Syrjäkoski K, et al. Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer. Carcinogenesis. 2007; 28(5): 1040-1045 (Pubitemid 47072188)
-
(2007)
Carcinogenesis
, vol.28
, Issue.5
, pp. 1040-1045
-
-
Pylkas, K.1
Tommiska, J.2
Syrjakoski, K.3
Kere, J.4
Gatei, M.5
Waddell, N.6
Allinen, M.7
Karppinen, S.-M.8
Rapakko, K.9
Kaariainen, H.10
Aittomaki, K.11
Blomqvist, C.12
Mustonen, A.13
Holli, K.14
Khanna, K.K.15
Kallioniemi, O.-P.16
Nevanlinna, H.17
Winqvist, R.18
-
24
-
-
70349912565
-
A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer
-
Bogdanova N, Cybulski C, Bermisheva M, et al. A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer. Breast Cancer Res Treat. 2009; 118(1): 207-211
-
(2009)
Breast Cancer Res Treat.
, vol.118
, Issue.1
, pp. 207-211
-
-
Bogdanova, N.1
Cybulski, C.2
Bermisheva, M.3
-
25
-
-
21044452905
-
Breast cancer predisposing alleles in Poland
-
DOI 10.1007/s10549-005-1409-1
-
Górski B, Cybulski C, Huzarski T, et al. Breast cancer predisposing alleles in Poland. Breast Cancer Res Treat. 2005; 92(1): 19-24 (Pubitemid 40875074)
-
(2005)
Breast Cancer Research and Treatment
, vol.92
, Issue.1
, pp. 19-24
-
-
Gorski, B.1
Cybulski, C.2
Huzarski, T.3
Byrski, T.4
Gronwald, J.5
Jakubowska, A.6
Stawicka, M.7
Gozdecka-Grodecka, S.8
Szwiec, M.9
Urbanski, K.10
Mitus, J.11
Marczyk, E.12
Dziuba, J.13
Wandzel, P.14
Surdyka, D.15
Haus, O.16
Janiszewska, H.17
Debniak, T.18
Toloczko-Grabarek, A.19
Medrek, K.20
Masojc, B.21
Mierzejewski, M.22
Kowalska, E.23
Narod, S.A.24
Lubinski, J.25
more..
-
26
-
-
33745225487
-
Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland
-
Steffen J, Nowakowska D, Niwinska A, et al. Germline mutations 657del5 of the NBS1 gene contribute significantly to the incidence of breast cancer in Central Poland. Int J Cancer. 2006; 119(2): 472-475
-
(2006)
Int J Cancer
, vol.119
, Issue.2
, pp. 472-475
-
-
Steffen, J.1
Nowakowska, D.2
Niwinska, A.3
-
27
-
-
38349052915
-
Nijmegen Breakage Syndrome mutations and risk of breast cancer
-
Bogdanova N, Feshchenko S, Schürmann P, et al. Nijmegen Breakage Syndrome mutations and risk of breast cancer. Int J Cancer. 2008; 122(4): 802-806
-
(2008)
Int J Cancer
, vol.122
, Issue.4
, pp. 802-806
-
-
Bogdanova, N.1
Feshchenko, S.2
Schürmann, P.3
-
28
-
-
33747884830
-
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
-
DOI 10.1093/carcin/bgi360, Special Issue on Chronic Pain
-
Heikkinen K, Rapakko K, Karppinen SM, et al. RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability. Carcinogenesis. 2006; 27(8): 1593-1599 (Pubitemid 44288048)
-
(2006)
Carcinogenesis
, vol.27
, Issue.8
, pp. 1593-1599
-
-
Heikkinen, K.1
Rapakko, K.2
Karppinen, S.-M.3
Erkko, H.4
Knuutila, S.5
Lundan, T.6
Mannermaa, A.7
Borresen-Dale, A.-L.8
Borg, A.9
Barkardottir, R.B.10
Petrini, J.11
Winqvist, R.12
-
29
-
-
56649086648
-
Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene
-
Bartkova J, Tommiska J, Oplustilova L, et al. Aberrations of the MRE11-RAD50-NBS1 DNA damage sensor complex in human breast cancer: MRE11 as a candidate familial cancer-predisposing gene. Mol Oncol. 2008; 2(4): 296-316
-
(2008)
Mol Oncol
, vol.2
, Issue.4
, pp. 296-316
-
-
Bartkova, J.1
Tommiska, J.2
Oplustilova, L.3
-
30
-
-
81055126264
-
Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
-
Walsh T, Casadei S, Lee MK, et al. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. Proc Natl Acad Sci USA. 2011; 108(44): 18032-18037
-
(2011)
Proc Natl Acad Sci USA
, vol.108
, Issue.44
, pp. 18032-18037
-
-
Walsh, T.1
Casadei, S.2
Lee, M.K.3
-
31
-
-
33749039966
-
The CHEK2 gene and inherited breast cancer susceptibility
-
DOI 10.1038/sj.onc.1209877, PII 1209877
-
Nevanlinna H, Bartek J. The CHEK2 gene and inherited breast cancer susceptibility. Oncogene. 2006; 25(43): 5912-5919 (Pubitemid 44453447)
-
(2006)
Oncogene
, vol.25
, Issue.43
, pp. 5912-5919
-
-
Nevanlinna, H.1
Bartek, J.2
-
32
-
-
18544389716
-
CHEK2-Breast Cancer Consortium. Lowpenetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations
-
Meijers-Heijboer H, van den Ouweland A, Klijn J, et al; CHEK2-Breast Cancer Consortium. Lowpenetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet. 2002; 31(1): 55-59
-
(2002)
Nat Genet
, vol.31
, Issue.1
, pp. 55-59
-
-
Meijers-Heijboer, H.1
Van Den Ouweland, A.2
Klijn, J.3
-
33
-
-
18444379055
-
A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer
-
DOI 10.1086/341943
-
Vahteristo P, Bartkova J, Eerola H, et al. A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer. Am J Hum Genet. 2002; 71(2): 432-438 (Pubitemid 34800260)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.2
, pp. 432-438
-
-
Vahteristo, P.1
Bartkova, J.2
Eerola, H.3
Syrjakoski, K.4
Ojala, S.5
Kilpivaara, O.6
Tamminen, A.7
Kononen, J.8
Aittomaki, K.9
Heikkila, P.10
Holli, K.11
Blomqvist, C.12
Bartek, J.13
Kallioniemi, O.-P.14
Nevanlinna, H.15
-
34
-
-
3042582651
-
CHEK21100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
-
CHEK2 Breast Cancer Case-Control Consortium
-
CHEK2 Breast Cancer Case-Control Consortium. CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet. 2004; 74(6): 1175-1182
-
(2004)
Am J Hum Genet.
, vol.74
, Issue.6
, pp. 1175-1182
-
-
-
35
-
-
84856014217
-
CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women
-
Adank MA, Jonker MA, Kluijt I, et al. CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. J Med Genet. 2011; 48(12): 860-863
-
(2011)
J Med Genet
, vol.48
, Issue.12
, pp. 860-863
-
-
Adank, M.A.1
Jonker, M.A.2
Kluijt, I.3
-
36
-
-
33847163983
-
A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland
-
DOI 10.1007/s10549-006-9320-y
-
Cybulski C, Wokołorczyk D, Huzarski T, et al. A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland. Breast Cancer Res Treat. 2007; 102(1): 119-122 (Pubitemid 46294966)
-
(2007)
Breast Cancer Research and Treatment
, vol.102
, Issue.1
, pp. 119-122
-
-
Cybulski, C.1
Wokolorczyk, D.2
Huzarski, T.3
Byrski, T.4
Gronwald, J.5
Gorski, B.6
Debniak, T.7
Masojc, B.8
Jakubowska, A.9
Van De Wetering, T.10
Narod, S.A.11
Lubinski, J.12
-
37
-
-
22044445244
-
Association of two mutations in the CHEK2 gene with breast cancer
-
DOI 10.1002/ijc.21022
-
Bogdanova N, Enssen-Dubrowinskaja N, Feshchenko S, et al. Association of two mutations in the CHEK2 gene with breast cancer. Int J Cancer. 2005; 116(2): 263-266 (Pubitemid 40967263)
-
(2005)
International Journal of Cancer
, vol.116
, Issue.2
, pp. 263-266
-
-
Bogdanova, N.1
Enssen-Dubrowinskaja, N.2
Feshchenko, S.3
Lazjuk, G.I.4
Rogov, Y.I.5
Dammann, O.6
Bremer, M.7
Karstens, J.H.8
Sohn, C.9
Dork, T.10
-
38
-
-
8844220451
-
CHEK2 is a multiorgan cancer susceptibility gene
-
DOI 10.1086/426403
-
Cybulski C, Górski B, Huzarski T, et al. CHEK2 is a multiorgan cancer susceptibility gene. Am J Hum Genet. 2004; 75(6): 1131-1135 (Pubitemid 39532081)
-
(2004)
American Journal of Human Genetics
, vol.75
, Issue.6
, pp. 1131-1135
-
-
Cybulski, C.1
Gorski, B.2
Huzarski, T.3
Masojc, B.4
Mierzejewski, M.5
Debniak, T.6
Teodorczyk, U.7
Byrski, T.8
Gronwald, J.9
Matyjasik, J.10
Zlowocka, E.11
Lenner, M.12
Grabowska, E.13
Nej, K.14
Castaneda, J.15
Medrek, K.16
Szymanska, A.17
Szymanska, J.18
Kurzawski, G.19
Suchy, J.20
Oszurek, O.21
Witek, A.22
Narod, S.A.23
Lubinski, J.24
more..
-
39
-
-
34250006413
-
Genome-wide association study identifies novel breast cancer susceptibility loci
-
DOI 10.1038/nature05887, PII NATURE05887
-
Easton DF, Pooley KA, Dunning AM, et al. Genomewide association study identifies novel breast cancer susceptibility loci. Nature. 2007; 447(7148): 1087-1093 (Pubitemid 47014426)
-
(2007)
Nature
, vol.447
, Issue.7148
, pp. 1087-1093
-
-
Easton, D.F.1
Pooley, K.A.2
Dunning, A.M.3
Pharoah, P.D.P.4
Thompson, D.5
Ballinger, D.G.6
Struewing, J.P.7
Morrison, J.8
Field, H.9
Luben, R.10
Wareham, N.11
Ahmed, S.12
Healey, C.S.13
Bowman, R.14
Meyer, K.B.15
Haiman, C.A.16
Kolonel, L.K.17
Henderson, B.E.18
Le Marchand, L.19
Brennan, P.20
Sangrajrang, S.21
Gaborieau, V.22
Odefrey, F.23
Shen, C.-Y.24
Wu, P.-E.25
Wang, H.-C.26
Eccles, D.27
Evans, D.G.28
Peto, J.29
Fletcher, O.30
Johnson, N.31
Seal, S.32
Stratton, M.R.33
Rahman, N.34
Chenevix-Trench, G.35
Bojesen, S.E.36
Nordestgaard, B.G.37
Axelsson, C.K.38
Garcia-Closas, M.39
Brinton, L.40
Chanock, S.41
Lissowska, J.42
Peplonska, B.43
Nevanlinna, H.44
Fagerholm, R.45
Eerola, H.46
Kang, D.47
Yoo, K.-Y.48
Noh, D.-Y.49
Ahn, S.-H.50
Hunter, D.J.51
Hankinson, S.E.52
Cox, D.G.53
Hall, P.54
Wedren, S.55
Liu, J.56
Low, Y.-L.57
Bogdanova, N.58
Schurmann, P.59
Dork, T.60
Tollenaar, R.A.E.M.61
Jacobi, C.E.62
Devilee, P.63
Klijn, J.G.M.64
Sigurdson, A.J.65
Doody, M.M.66
Alexander, B.H.67
Zhang, J.68
Cox, A.69
Brock, I.W.70
MacPherson, G.71
Reed, M.W.R.72
Couch, F.J.73
Goode, E.L.74
Olson, J.E.75
Meijers-Heijboer, H.76
Van Den Ouweland, A.77
Uitterlinden, A.78
Rivadeneira, F.79
Milne, R.L.80
Ribas, G.81
Gonzalez-Neira, A.82
Benitez, J.83
Hopper, J.L.84
McCredie, M.85
Southey, M.86
Giles, G.G.87
Schroen, C.88
Justenhoven, C.89
Brauch, H.90
Hamann, U.91
Ko, Y.-D.92
Spurdle, A.B.93
Beesley, J.94
Chen, X.95
Mannermaa, A.96
Kosma, V.-M.97
Kataja, V.98
Hartikainen, J.99
more..
-
40
-
-
67349237973
-
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
-
Ahmed S, Thomas G, Ghoussaini M, et al. Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Nat Genet. 2009; 41(5): 585-590.
-
(2009)
Nat Genet
, vol.41
, Issue.5
, pp. 585-590
-
-
Ahmed, S.1
Thomas, G.2
Ghoussaini, M.3
-
41
-
-
77957568513
-
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
-
Antoniou AC, Wang X, Fredericksen ZS, et al. A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. Nat Genet 2010;42(10):885-892
-
(2010)
Nat Genet
, vol.42
, Issue.10
, pp. 885-892
-
-
Antoniou, A.C.1
Wang, X.2
Fredericksen, Z.S.3
-
42
-
-
77952887426
-
Genomewide association study identifies five new breast cancer susceptibility loci
-
Turnbull C, Ahmed S, Morrison J, et al. Genomewide association study identifies five new breast cancer susceptibility loci. Nat Genet. 2010; 42(6): 504-507
-
(2010)
Nat Genet
, vol.42
, Issue.6
, pp. 504-507
-
-
Turnbull, C.1
Ahmed, S.2
Morrison, J.3
-
43
-
-
82255183150
-
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
-
Haiman CA, Chen GK, Vachon CM, et al. A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Nat Genet. 2011; 43(12): 1210-1214
-
(2011)
Nat Genet.
, vol.43
, Issue.12
, pp. 1210-1214
-
-
Haiman, C.A.1
Chen, G.K.2
Vachon, C.M.3
-
44
-
-
84859197861
-
Genome-wide association study in East Asians identifies novel susceptibility loci for breast cancer
-
Long J, Cai Q, Sung H, et al. Genome-wide association study in East Asians identifies novel susceptibility loci for breast cancer. PLoS Genet. 2012; 8(2): e1002532
-
(2012)
PLoS Genet
, vol.8
, Issue.2
-
-
Long, J.1
Cai, Q.2
Sung, H.3
-
45
-
-
84862776961
-
Genome-wide association analysis identifies threenew breast cancer susceptibility loci
-
Ghoussaini M, Fletcher O, Michailidou K, et al. Genome-wide association analysis identifies threenew breast cancer susceptibility loci. Nat Genet. 2012; 44(3): 312-318
-
(2012)
Nat Genet
, vol.44
, Issue.3
, pp. 312-318
-
-
Ghoussaini, M.1
Fletcher, O.2
Michailidou, K.3
-
46
-
-
69349102630
-
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
-
Song H, Ramus SJ, Tyrer J, et al. A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Nat Genet. 2009; 41(9): 996-1000
-
(2009)
Nat Genet.
, vol.41
, Issue.9
, pp. 996-1000
-
-
Song, H.1
Ramus, S.J.2
Tyrer, J.3
-
47
-
-
77957571905
-
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
-
Goode EL, Chenevix-Trench G, Song H, et al. A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Nat Genet. 2010; 42(10): 874-879
-
(2010)
Nat Genet.
, vol.42
, Issue.10
, pp. 874-879
-
-
Goode, E.L.1
Chenevix-Trench, G.2
Song, H.3
-
48
-
-
77957584092
-
Common variants at 19p13 are associated with susceptibility to ovarian cancer
-
Bolton KL, Tyrer J, Song H, et al. Common variants at 19p13 are associated with susceptibility to ovarian cancer. Nat Genet. 2010; 42(10): 880-884
-
(2010)
Nat Genet
, vol.42
, Issue.10
, pp. 880-884
-
-
Bolton, K.L.1
Tyrer, J.2
Song, H.3
-
49
-
-
46849098205
-
Multiple loci with different cancer specificities within the 8q24 gene desert
-
DOI 10.1093/jnci/djn190
-
Ghoussaini M, Song H, Koessler T, et al. Multiple loci with different cancer specificities within the 8q24 gene desert. J Natl Cancer Inst. 2008; 100(13): 962-966 (Pubitemid 351957516)
-
(2008)
Journal of the National Cancer Institute
, vol.100
, Issue.13
, pp. 962-966
-
-
Ghoussaini, M.1
Song, H.2
Koessler, T.3
Al Olama, A.A.4
Kote-Jarai, Z.5
Driver, K.E.6
Pooley, K.A.7
Ramus, S.J.8
Kjaer, S.K.9
Hogdall, E.10
DiCioccio, R.A.11
Whittemore, A.S.12
Gayther, S.A.13
Giles, G.G.14
Guy, M.15
Edwards, S.M.16
Morrison, J.17
Donovan, J.L.18
Hamdy, F.C.19
Dearnaley, D.P.20
Ardern-Jones, A.T.21
Hall, A.L.22
O'Brien, L.T.23
Gehr-Swain, B.N.24
Wilkinson, R.A.25
Brown, P.M.26
Hopper, J.L.27
Neal, D.E.28
Pharoah, P.D.P.29
Ponder, B.A.J.30
Eeles, R.A.31
Easton, D.F.32
Dunning, A.M.33
more..
-
50
-
-
77950405093
-
Genomewide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genomewide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls. Nature. 2010; 464(7289): 713-720
-
(2010)
Nature.
, vol.464
, Issue.7289
, pp. 713-720
-
-
-
51
-
-
45949085378
-
Polygenes, risk prediction, and targeted prevention of breast cancer
-
DOI 10.1056/NEJMsa0708739
-
Pharoah PD, Antoniou AC, Easton DF, Ponder BA. Polygenes, risk prediction, and targeted prevention of breast cancer. N Engl J Med. 2008; 358(26): 2796- 2803 (Pubitemid 351930854)
-
(2008)
New England Journal of Medicine
, vol.358
, Issue.26
, pp. 2796-2803
-
-
Pharoah, P.D.P.1
Antoniou, A.C.2
Easton, D.F.3
Ponder, B.A.J.4
-
52
-
-
79955793051
-
Polygenic susceptibility to prostate and breast cancer: Implications for personalised screening
-
Pashayan N, Duffy SW, Chowdhury S, et al. Polygenic susceptibility to prostate and breast cancer: implications for personalised screening. Br J Cancer. 2011; 104 (10): 1656-1663.
-
(2011)
Br J Cancer
, vol.104
, Issue.10
, pp. 1656-1663
-
-
Pashayan, N.1
Duffy, S.W.2
Chowdhury, S.3
-
53
-
-
84858295021
-
BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years
-
Robertson L, Hanson H, Seal S, et al. BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years. Br J Cancer. 2012; 106(6): 1234-1238
-
(2012)
Br J Cancer
, vol.106
, Issue.6
, pp. 1234-1238
-
-
Robertson, L.1
Hanson, H.2
Seal, S.3
-
54
-
-
80053366674
-
Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: Findings from the Breast Cancer Association Consortium
-
Broeks A, Schmidt MK, Sherman ME, et al. Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium. Hum Mol Genet. 2011; 20(16): 3289- 3303
-
(2011)
Hum Mol Genet
, vol.20
, Issue.16
, pp. 3289-3303
-
-
Broeks, A.1
Schmidt, M.K.2
Sherman, M.E.3
-
55
-
-
77954365472
-
Potential for targeting the fibroblast growth factor receptors in breast cancer
-
Hynes NE, Dey JH. Potential for targeting the fibroblast growth factor receptors in breast cancer. Cancer Res. 2010; 70(13): 5199-5202
-
(2010)
Cancer Res
, vol.70
, Issue.13
, pp. 5199-5202
-
-
Hynes, N.E.1
Dey, J.H.2
-
56
-
-
84856158117
-
Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer
-
Bolton KL, Chenevix-Trench G, Goh C, et al. Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer. JAMA. 2012; 307(4): 382-390
-
(2012)
JAMA
, vol.307
, Issue.4
, pp. 382-390
-
-
Bolton, K.L.1
Chenevix-Trench, G.2
Goh, C.3
-
57
-
-
79954560252
-
Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations
-
Dedes KJ, Wilkerson PM, Wetterskog D, Weigelt B, Ashworth A, Reis-Filho JS. Synthetic lethality of PARP inhibition in cancers lacking BRCA1 and BRCA2 mutations. Cell Cycle. 2011; 10(8): 1192- 1199
-
(2011)
Cell Cycle
, vol.10
, Issue.8
, pp. 1192-1199
-
-
Dedes, K.J.1
Wilkerson, P.M.2
Wetterskog, D.3
Weigelt, B.4
Ashworth, A.5
Reis-Filho, J.S.6
-
58
-
-
79959376888
-
Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR
-
Reaper PM, Griffiths MR, Long JM, et al. Selective killing of ATM- or p53-deficient cancer cells through inhibition of ATR. Nat Chem Biol. 2011; 7(7): 428- 430.
-
(2011)
Nat Chem Biol
, vol.7
, Issue.7
, pp. 428-430
-
-
Reaper, P.M.1
Griffiths, M.R.2
Long, J.M.3
|