-
1
-
-
52949096470
-
Genetic predisposition to breast cancer: Past, present, and future
-
Turnbull C, Rahman N (2008) Genetic predisposition to breast cancer: past, present, and future. Annu Rev Genomics Hum Genet 9:321-345
-
(2008)
Annu Rev Genomics Hum Genet
, vol.9
, pp. 321-345
-
-
Turnbull, C.1
Rahman, N.2
-
2
-
-
46949098149
-
Hereditary breast cancer: New genetic developments, new therapeutic avenues
-
Campeau PM, Foulkes WD, Tischkowitz MD (2008) Hereditary breast cancer: new genetic developments, new therapeutic avenues. Hum Genet 124:31-42
-
(2008)
Hum Genet
, vol.124
, pp. 31-42
-
-
Campeau, P.M.1
Foulkes, W.D.2
Tischkowitz, M.D.3
-
3
-
-
77952600845
-
Susceptibility pathways in Fanconi's anemia and breast cancer
-
D'Andrea AD (2010) Susceptibility pathways in Fanconi's anemia and breast cancer. New Engl J Med 362:1909-1919
-
(2010)
New Engl J Med
, vol.362
, pp. 1909-1919
-
-
D'Andrea, A.D.1
-
4
-
-
84880922362
-
The complex genetic landscape of familial breast cancer
-
in press. Advanced online 2013 Apr 5
-
Melchor L, Benítez J (2013) The complex genetic landscape of familial breast cancer. Hum Genet, in press. Advanced online 2013 Apr 5
-
(2013)
Hum Genet
-
-
Melchor, L.1
Benítez, J.2
-
5
-
-
33745200945
-
Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2
-
Xia B, Sheng Q, Nakanishi K, Ohashi A, Wu J, Christ N, Liu X, Jasin M, Couch FJ, Livingston DM (2006) Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. Mol Cell 22:719-729
-
(2006)
Mol Cell
, vol.22
, pp. 719-729
-
-
Xia, B.1
Sheng, Q.2
Nakanishi, K.3
Ohashi, A.4
Wu, J.5
Christ, N.6
Liu, X.7
Jasin, M.8
Couch, F.J.9
Livingston, D.M.10
-
6
-
-
66349096607
-
PALB2 is an integral component of the BRCA complex required for homologous recombination repair
-
Sy SM, Huen MS, Chen J (2009) PALB2 is an integral component of the BRCA complex required for homologous recombination repair. Proc Natl Acad Sci USA 106:7155-7160
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 7155-7160
-
-
Sy, S.M.1
Huen, M.S.2
Chen, J.3
-
7
-
-
77957329128
-
PALB2/FANCN: Recombining cancer and Fanconi anemia
-
Tischkowitz M, Xia B (2010) PALB2/FANCN: recombining cancer and Fanconi anemia. Cancer Res 70:7353-7359
-
(2010)
Cancer Res
, vol.70
, pp. 7353-7359
-
-
Tischkowitz, M.1
Xia, B.2
-
8
-
-
33846601829
-
Fanconi anemia is associated with a defect in the BRCA2 partner PALB2
-
DOI 10.1038/ng1942, PII NG1942
-
Xia B, Dorsman JC, Ameziane N, de Vries Y, Rooimans MA, Sheng Q, Pals G, Errami A, Gluckman E, Llera J, Wang W, Livingston DM, Joenje H, de Winter JP (2007) Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. Nat Genet 39:159-161 (Pubitemid 46184344)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 159-161
-
-
Xia, B.1
Dorsman, J.C.2
Ameziane, N.3
De Vries, Y.4
Rooimans, M.A.5
Sheng, Q.6
Pals, G.7
Errami, A.8
Gluckman, E.9
Llera, J.10
Wang, W.11
Livingston, D.M.12
Joenje, H.13
De Winter, J.P.14
-
9
-
-
33846569450
-
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
-
DOI 10.1038/ng1947, PII NG1947
-
Reid S, Schindler D, Hanenberg H, Barker K, Hanks S, Kalb R, Neveling K, Kelly P, Seal S, Freund M, Wurm M, Batish SD, Lach FP, Yetgin S, Neitzel H, Ariffin H, Tischkowitz M, Mathew CG, Auerbach AD, Rahman N (2007) Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. Nat Genet 39:162-164 (Pubitemid 46184345)
-
(2007)
Nature Genetics
, vol.39
, Issue.2
, pp. 162-164
-
-
Reid, S.1
Schindler, D.2
Hanenberg, H.3
Barker, K.4
Hanks, S.5
Kalb, R.6
Neveling, K.7
Kelly, P.8
Seal, S.9
Freund, M.10
Wurm, M.11
Batish, S.D.12
Lach, F.P.13
Yetgin, S.14
Neitzel, H.15
Ariffin, H.16
Tischkowitz, M.17
Mathew, C.G.18
Auerbach, A.D.19
Rahman, N.20
more..
-
10
-
-
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, Kelly P, Renwick A, Elliott A, Reid S, Spanova K, Barfoot R, Chagtai T, Jayatilake H, McGuffog L, Hanks S, Evans DG, Eccles D, Breast Cancer Susceptibility Collaboration (UK), Easton DF, Stratton MR (2007) PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. Nat Genet 39:165-167 (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
-
11
-
-
33847227378
-
A recurrent mutation in PALB2 in Finnish cancer families
-
DOI 10.1038/nature05609, PII NATURE05609
-
Erkko H, Xia B, Nikkilä J, Schleutker J, Syrjäkoski K, Mannermaa A, Kallioniemi A, Pylkäs K, Karppinen SM, Rapakko K, Miron A, Sheng Q, Li G, Mattila H, Bell DW, Haber DA, Grip M, Reiman M, Jukkola-Vuorinen A, Mustonen A, Kere J, Aaltonen LA, Kosma VM, Kataja V, Soini Y, Drapkin RI, Livingston DM, Winqvist R (2007) A recurrent mutation in PALB2 in Finnish cancer families. Nature 446:316-319 (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..
-
12
-
-
64849092309
-
Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene
-
Jones S, Hruban RH, Kamiyama M, Borges M, Zhang X, Parsons DW, Lin JC, Palmisano E, Brune K, Jaffee EM, Iacobuzio-Donahue CA, Maitra A, Parmigiani G, Kern SE, Velculescu VE, Kinzler KW, Vogelstein B, Eshleman JR, Goggins M, Klein AP (2009) Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. Science 324:217
-
(2009)
Science
, vol.324
, pp. 217
-
-
Jones, S.1
Hruban, R.H.2
Kamiyama, M.3
Borges, M.4
Zhang, X.5
Parsons, D.W.6
Lin, J.C.7
Palmisano, E.8
Brune, K.9
Jaffee, E.M.10
Iacobuzio-Donahue, C.A.11
Maitra, A.12
Parmigiani, G.13
Kern, S.E.14
Velculescu, V.E.15
Kinzler, K.W.16
Vogelstein, B.17
Eshleman, J.R.18
Goggins, M.19
Klein, A.P.20
more..
-
13
-
-
79952741549
-
Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer
-
Casadei S, Norquist BM, Walsh T, Stray S, Mandell JB, Lee MK, Stamatoyannopoulos JA, King MC (2011) Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer. Cancer Res 71:2222-2229
-
(2011)
Cancer Res
, vol.71
, pp. 2222-2229
-
-
Casadei, S.1
Norquist, B.M.2
Walsh, T.3
Stray, S.4
Mandell, J.B.5
Lee, M.K.6
Stamatoyannopoulos, J.A.7
King, M.C.8
-
14
-
-
51649092869
-
Penetrance analysis of the PALB2 c.1592delT founder mutation
-
Erkko H, Dowty JG, Nikkilä J, Syrjäkoski K, Mannermaa A, Pylkäs K, Southey MC, Holli K, Kallioniemi A, Jukkola-Vuorinen A, Kataja V, Kosma VM, Xia B, Livingston DM, Winqvist R, Hopper JL (2008) Penetrance analysis of the PALB2 c.1592delT founder mutation. Clin Cancer Res 14:4667-4671
-
(2008)
Clin Cancer Res
, vol.14
, pp. 4667-4671
-
-
Erkko, H.1
Dowty, J.G.2
Nikkilä, J.3
Syrjäkoski, K.4
Mannermaa, A.5
Pylkäs, K.6
Southey, M.C.7
Holli, K.8
Kallioniemi, A.9
Jukkola-Vuorinen, A.10
Kataja, V.11
Kosma, V.M.12
Xia, B.13
Livingston, D.M.14
Winqvist, R.15
Hopper, J.L.16
-
15
-
-
84888197794
-
The incidence of PALB2 c.3113G > A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia
-
in press. Advanced online 2013 Mar 8
-
Teo ZL, Sawyer SD, James PA, Mitchell G, Trainer AH, Lindeman GJ, Shackleton K, Cicciarelli L, Southey MC (2013) The incidence of PALB2 c.3113G > A in women with a strong family history of breast and ovarian cancer attending familial cancer centres in Australia. Fam Cancer, in press. Advanced online 2013 Mar 8
-
(2013)
Fam Cancer
-
-
Teo, Z.L.1
Sawyer, S.D.2
James, P.A.3
Mitchell, G.4
Trainer, A.H.5
Lindeman, G.J.6
Shackleton, K.7
Cicciarelli, L.8
Southey, M.C.9
-
16
-
-
84874368165
-
Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families
-
Teo ZL, Park DJ, Provenzano E, Chatfield CA, Odefrey FA, Nguyen-Dumont T, Confab K, Dowty JG, Hopper JL, Winship I, Goldgar DE, Southey MC (2013) Prevalence of PALB2 mutations in Australasian multiple-case breast cancer families. Breast Cancer Res 15(1):R17
-
(2013)
Breast Cancer Res
, vol.15
, Issue.1
-
-
Teo, Z.L.1
Park, D.J.2
Provenzano, E.3
Chatfield, C.A.4
Odefrey, F.A.5
Nguyen-Dumont, T.6
Confab, K.7
Dowty, J.G.8
Hopper, J.L.9
Winship, I.10
Goldgar, D.E.11
Southey, M.C.12
-
17
-
-
84872023611
-
Contribution of the PALB2 c.2323C > T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent
-
Tischkowitz M, Sabbaghian N, Hamel N, Pouchet C, Foulkes WD, Mes-Masson AM, Provencher DM, Tonin PN (2013) Contribution of the PALB2 c.2323C > T [p.Q775X] founder mutation in well-defined breast and/or ovarian cancer families and unselected ovarian cancer cases of French Canadian descent. BMC Med Genet 14:5
-
(2013)
BMC Med Genet
, vol.14
, pp. 5
-
-
Tischkowitz, M.1
Sabbaghian, N.2
Hamel, N.3
Pouchet, C.4
Foulkes, W.D.5
Mes-Masson, A.M.6
Provencher, D.M.7
Tonin, P.N.8
-
18
-
-
77649148280
-
A novel germline PALB2 deletion in polish breast and ovarian cancer patients
-
Dansonka-Mieszkowska A, Kluska A, Moes J, Dabrowska M, Nowakowska D, Niwinska A, Derlatka P, Cendrowski K, Kupryjanczyk J (2010) A novel germline PALB2 deletion in polish breast and ovarian cancer patients. BMC Med Genet 11:20
-
(2010)
BMC Med Genet
, vol.11
, pp. 20
-
-
Dansonka-Mieszkowska, A.1
Kluska, A.2
Moes, J.3
Dabrowska, M.4
Nowakowska, D.5
Niwinska, A.6
Derlatka, P.7
Cendrowski, K.8
Kupryjanczyk, J.9
-
19
-
-
79958732548
-
PALB2 mutations in German and Russian patients with bilateral breast cancer
-
Bogdanova N, Sokolenko AP, Iyevleva AG, Abysheva SN, Blaut M, Bremer M, Christiansen H, Rave-Fränk M, Dörk T, Imyanitov EN (2011) PALB2 mutations in German and Russian patients with bilateral breast cancer. Breast Cancer Res Treat 126:545-550
-
(2011)
Breast Cancer Res Treat
, vol.126
, pp. 545-550
-
-
Bogdanova, N.1
Sokolenko, A.P.2
Iyevleva, A.G.3
Abysheva, S.N.4
Blaut, M.5
Bremer, M.6
Christiansen, H.7
Rave-Fränk, M.8
Dörk, T.9
Imyanitov, E.N.10
-
20
-
-
22044445244
-
Association of two mutations in the CHEK2 gene with breast cancer
-
DOI 10.1002/ijc.21022
-
Bogdanova N, Enssen-Dubrowinskaja N, Feshchenko S, Lazjuk GI, Rogov YI, Dammann O, Bremer M, Karstens JH, Sohn C, Dörk T (2005) Association of two mutations in the CHEK2 gene with breast cancer. Int J Cancer 116:263-266 (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
-
22
-
-
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 (2007) Genome-wide association study identifies novel breast cancer susceptibility loci. Nature 447:1087-1093 (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, M.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, O.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..
-
23
-
-
38349052915
-
Nijmegen breakage syndrome mutations and risk of breast cancer
-
Bogdanova N, Feshchenko S, Schürmann P, Waltes R, Wieland B, Hillemanns P, Rogov YI, Dammann O, Bremer M, Karstens JH, Sohn C, Varon R, Dörk T (2008) Nijmegen breakage syndrome mutations and risk of breast cancer. Int J Cancer 122:802-806
-
(2008)
Int J Cancer
, vol.122
, pp. 802-806
-
-
Bogdanova, N.1
Feshchenko, S.2
Schürmann, P.3
Waltes, R.4
Wieland, B.5
Hillemanns, P.6
Rogov, Y.I.7
Dammann, O.8
Bremer, M.9
Karstens, J.H.10
Sohn, C.11
Varon, R.12
Dörk, T.13
-
24
-
-
70349912565
-
A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer
-
Bogdanova N, Cybulski C, Bermisheva M, Datsyuk I, Yamini P, Hillemanns P, Antonenkova NN, Khusnutdinova E, Lubinski J, Dörk T (2009) A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer. Breast Cancer Res Treat 118:207-211
-
(2009)
Breast Cancer Res Treat
, vol.118
, pp. 207-211
-
-
Bogdanova, N.1
Cybulski, C.2
Bermisheva, M.3
Datsyuk, I.4
Yamini, P.5
Hillemanns, P.6
Antonenkova, N.N.7
Khusnutdinova, E.8
Lubinski, J.9
Dörk, T.10
-
25
-
-
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 (2010) High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from Belarus. Clin Genet 78:364-372
-
(2010)
Clin Genet
, vol.78
, 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
-
26
-
-
84880630260
-
Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations
-
Prokofyeva D, Bogdanova N, Dubrowinskaja N, Bermisheva M, Takhirova Z, Antonenkova N, Turmanov N, Datsyuk I, Gantsev S, Christiansen H, Park-Simon TW, Hillemanns P, Khusnutdinova E, Dörk T (2013) Nonsense mutation p.Q548X in BLM, the gene mutated in Bloom's syndrome, is associated with breast cancer in Slavic populations. Breast Cancer Res Treat 137:533-539
-
(2013)
Breast Cancer Res Treat
, vol.137
, pp. 533-539
-
-
Prokofyeva, D.1
Bogdanova, N.2
Dubrowinskaja, N.3
Bermisheva, M.4
Takhirova, Z.5
Antonenkova, N.6
Turmanov, N.7
Datsyuk, I.8
Gantsev, S.9
Christiansen, H.10
Park-Simon, T.W.11
Hillemanns, P.12
Khusnutdinova, E.13
Dörk, T.14
-
27
-
-
84875703379
-
Large-scale genotyping identifies 41 new loci associated with breast cancer risk
-
Michailidou K, Hall P, Gonzalez-Neira A et al (2013) Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Nat Genet 45:353-361
-
(2013)
Nat Genet
, vol.45
, pp. 353-361
-
-
Michailidou, K.1
Hall, P.2
Gonzalez-Neira, A.3
-
28
-
-
84868136807
-
Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer
-
Pern F, Bogdanova N, Schürmann P, Lin M, Ay A, Länger F, Hillemanns P, Christiansen H, Park-Simon TW, Dörk T (2012) Mutation analysis of BRCA1, BRCA2, PALB2 and BRD7 in a hospital-based series of German patients with triple-negative breast cancer. PLoS ONE 7(10):e47993
-
(2012)
PLoS ONE
, vol.7
, Issue.10
-
-
Pern, F.1
Bogdanova, N.2
Schürmann, P.3
Lin, M.4
Ay, A.5
Länger, F.6
Hillemanns, P.7
Christiansen, H.8
Park-Simon, T.W.9
Dörk, T.10
-
29
-
-
34249857115
-
Analysis of PALB2/FANCN-associated breast cancer families
-
DOI 10.1073/pnas.0701724104
-
Tischkowitz M Xia B, Sabbaghian N, Reis-Filho JS, Hamel N, Li G, van Beers EH, Li L, Khalil T, Quenneville LA, Omeroglu A, Poll A, Lepage P, Wong N, Nederlof PM, Ashworth A, Tonin PN, Narod SA, Livingston DM, Foulkes WD (2007) Analysis of PALB2/FANCN-associated breast cancer families. Proc Natl Acad Sci USA 104:6788-6793 (Pubitemid 47175579)
-
(2007)
Proceedings of the National Academy of Sciences of the United States of America
, vol.104
, Issue.16
, pp. 6788-6793
-
-
Tischkowitz, M.1
Xia, B.2
Sabbaghian, N.3
Reis-Filho, J.S.4
Hamel, N.5
Li, G.6
Van Beers, E.H.7
Li, L.8
Khalil, T.9
Quenneville, L.A.10
Omeroglu, A.11
Poll, A.12
Lepage, P.13
Wong, N.14
Nederlof, P.M.15
Ashworth, A.16
Tonin, P.N.17
Narod, S.A.18
Livingston, D.M.19
Foulkes, W.D.20
more..
-
30
-
-
78650201265
-
PALB2: A novel inactivating mutation in a Italian breast cancer family
-
Balia C, Sensi E, Lombardi G, Roncella M, Bevilacqua G, Caligo MA (2010) PALB2: a novel inactivating mutation in a Italian breast cancer family. Fam Cancer 9:531-536
-
(2010)
Fam Cancer
, vol.9
, pp. 531-536
-
-
Balia, C.1
Sensi, E.2
Lombardi, G.3
Roncella, M.4
Bevilacqua, G.5
Caligo, M.A.6
-
31
-
-
79957608461
-
Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer
-
Hellebrand H, Sutter C, Honisch E, Gross E, Wappenschmidt B, Schem C, Deissler H, Ditsch N, Gress V, Kiechle M, Bartram CR, Schmutzler RK, Niederacher D, Arnold N, Meindl A (2011) Germline mutations in the PALB2 gene are population specific and occur with low frequencies in familial breast cancer. Hum Mutat 32(6):E2176-E2188
-
(2011)
Hum Mutat
, vol.32
, Issue.6
-
-
Hellebrand, H.1
Sutter, C.2
Honisch, E.3
Gross, E.4
Wappenschmidt, B.5
Schem, C.6
Deissler, H.7
Ditsch, N.8
Gress, V.9
Kiechle, M.10
Bartram, C.R.11
Schmutzler, R.K.12
Niederacher, D.13
Arnold, N.14
Meindl, A.15
-
32
-
-
84862776557
-
Rare germline mutations in PALB2 and breast cancer risk: A population-based study
-
WECARE Study Collaborative Group
-
Tischkowitz M, Capanu M, Sabbaghian N, Li L, Liang X, Vallée MP, Tavtigian SV, Concannon P, Foulkes WD, Bernstein L, WECARE Study Collaborative Group, Bernstein JL, Begg CB (2012) Rare germline mutations in PALB2 and breast cancer risk: a population-based study. Hum Mutat 33:674-680
-
(2012)
Hum Mutat
, vol.33
, pp. 674-680
-
-
Tischkowitz, M.1
Capanu, M.2
Sabbaghian, N.3
Li, L.4
Liang, X.5
Vallée, M.P.6
Tavtigian, S.V.7
Concannon, P.8
Foulkes, W.D.9
Bernstein, L.10
Bernstein, J.L.11
Begg, C.B.12
-
33
-
-
65649112112
-
The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype
-
Heikkinen T, Kärkkäinen H, Aaltonen K, Milne RL, Heikkilä P, Aittomäki K, Blomqvist C, Nevanlinna H (2009) The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. Clin Cancer Res 15:3214-3222
-
(2009)
Clin Cancer Res
, vol.15
, pp. 3214-3222
-
-
Heikkinen, T.1
Kärkkäinen, H.2
Aaltonen, K.3
Milne, R.L.4
Heikkilä, P.5
Aittomäki, K.6
Blomqvist, C.7
Nevanlinna, H.8
-
34
-
-
70349969478
-
Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution
-
Shah SP, Morin RD, Khattra J, Prentice L, Pugh T, Burleigh A, Delaney A, Gelmon K, Guliany R, Senz J, Steidl C, Holt RA, Jones S, Sun M, Leung G, Moore R, Severson T, Taylor GA, Teschendorff AE, Tse K, Turashvili G, Varhol R, Warren RL, Watson P, Zhao Y, Caldas C, Huntsman D, Hirst M, Marra MA, Aparicio S (2009) Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution. Nature 461:809-813
-
(2009)
Nature
, vol.461
, pp. 809-813
-
-
Shah, S.P.1
Morin, R.D.2
Khattra, J.3
Prentice, L.4
Pugh, T.5
Burleigh, A.6
Delaney, A.7
Gelmon, K.8
Guliany, R.9
Senz, J.10
Steidl, C.11
Holt, R.A.12
Jones, S.13
Sun, M.14
Leung, G.15
Moore, R.16
Severson, T.17
Taylor, G.A.18
Teschendorff, A.E.19
Tse, K.20
Turashvili, G.21
Varhol, R.22
Warren, R.L.23
Watson, P.24
Zhao, Y.25
Caldas, C.26
Huntsman, D.27
Hirst, M.28
Marra, M.A.29
Aparicio, S.30
more..
-
35
-
-
55749109888
-
Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories?
-
Byrnes GB, Southey MC, Hopper JL (2008) Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories? Breast Cancer Res 10:208
-
(2008)
Breast Cancer Res
, vol.10
, pp. 208
-
-
Byrnes, G.B.1
Southey, M.C.2
Hopper, J.L.3
|