-
1
-
-
0035960431
-
Familial breast cancer: Collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease
-
Collaborative Group on Hormonal Factors in Breast Cancer
-
Collaborative Group on Hormonal Factors in Breast Cancer: Familial breast cancer: collaborative reanalysis of individual data from 52 epidemiological studies including 58,209 women with breast cancer and 101,986 women without the disease. Lancet 358: 1389-1399, 2001.
-
(2001)
Lancet
, vol.358
, pp. 1389-1399
-
-
-
2
-
-
0038745419
-
Contributions of ATM mutations to familial breast and ovarian cancer
-
Thorstenson YR, Roxas A, Kroiss R, Jenkins MA, Yu KM, Bachrich T, Muhr D, Wayne TL, Chu G, Davis RW, Wagner TM and Oefner PJ: Contributions of ATM mutations to familial breast and ovarian cancer. Cancer Res 63: 3325-3333, 2003.
-
(2003)
Cancer Res
, vol.63
, pp. 3325-3333
-
-
Thorstenson, Y.R.1
Roxas, A.2
Kroiss, R.3
Jenkins, M.A.4
Yu, K.M.5
Bachrich, T.6
Muhr, D.7
Wayne, T.L.8
Chu, G.9
Davis, R.W.10
Wagner, T.M.11
Oefner, P.J.12
-
3
-
-
0037033733
-
A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes
-
Antoniou AC, Pharoah PD, McMullin G, Day NE, Stratton MR, Peto J, Ponder BA and Easton DF: A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes. Br J Cancer 86: 76-83, 2002.
-
(2002)
Br J Cancer
, vol.86
, pp. 76-83
-
-
Antoniou, A.C.1
Pharoah, P.D.2
McMullin, G.3
Day, N.E.4
Stratton, M.R.5
Peto, J.6
Ponder, B.A.7
Easton, D.F.8
-
4
-
-
28244478365
-
Genomic instability and cancer: Networks involved in response to DNA damage
-
Eyfjord JE and Bodvarsdottir SK: Genomic instability and cancer: Networks involved in response to DNA damage. Mutat Res 592: 18-28, 2005.
-
(2005)
Mutat Res
, vol.592
, pp. 18-28
-
-
Eyfjord, J.E.1
Bodvarsdottir, S.K.2
-
5
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanova E, Cooper PR, Nowak NJ, Stumm M, Weemaes CM, Gatti RA, Wilson RK, Digweed M, Rosenthal A, Sperling K, Concannon P and Reis A: Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 93: 467-476, 1998.
-
(1998)
Cell
, vol.93
, pp. 467-476
-
-
Varon, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanova, E.8
Cooper, P.R.9
Nowak, N.J.10
Stumm, M.11
Weemaes, C.M.12
Gatti, R.A.13
Wilson, R.K.14
Digweed, M.15
Rosenthal, A.16
Sperling, K.17
Concannon, P.18
Reis, A.19
-
6
-
-
0033710938
-
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations
-
Varon R, Seemanova E, Chrzanowska K, Hnateyko O, Piekutowska-Abramczuk D, Krajewska-Walasek M, Sykut-Cegielska J, Sperling K and Reis A: Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populations. Eur J Hum Genet 8: 900-902, 2000.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 900-902
-
-
Varon, R.1
Seemanova, E.2
Chrzanowska, K.3
Hnateyko, O.4
Piekutowska-Abramczuk, D.5
Krajewska-Walasek, M.6
Sykut-Cegielska, J.7
Sperling, K.8
Reis, A.9
-
7
-
-
0036836572
-
Mutations and molecular variants of the NBS1 gene in non-Hodgkin's lymphoma
-
Cerosaletti KM, Morrison VA, Sabath DE, Willerford DM and Concannon P: Mutations and molecular variants of the NBS1 gene in non-Hodgkin's lymphoma. Genes Chromosomes Cancer 35: 282-286, 2002.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 282-286
-
-
Cerosaletti, K.M.1
Morrison, V.A.2
Sabath, D.E.3
Willerford, D.M.4
Concannon, P.5
-
8
-
-
0035328489
-
Mutations in the Nijmegen Breakage Syndrome Gene (NBS1) in childhood acute lymphoblastic leukaemia (ALL)
-
Varon R, Reis A, Henze G, Graf v. Einsiedl H, Sperling K and Seeger K: Mutations in the Nijmegen Breakage Syndrome Gene (NBS1) in childhood acute lymphoblastic leukaemia (ALL). Cancer Res 61: 3570-3572, 2001.
-
(2001)
Cancer Res
, vol.61
, pp. 3570-3572
-
-
Varon, R.1
Reis, A.2
Henze, G.3
Graf4
Einsiedl, H.5
Sperling, K.6
Seeger, K.7
-
9
-
-
3042818662
-
Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland
-
Steffen J, Varon R, Mosor M, Maneva G, Maurer M, Stumm M, Nowakowska D, Rubach M, Kosakowska E, Ruka W, Nowecki Z, Rutkowski P, Demkow T, Sadowska M, Bidzinski M, Gawrychowski K and Sperling K: Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. Int J Cancer 111: 67-71, 2004.
-
(2004)
Int J Cancer
, vol.111
, pp. 67-71
-
-
Steffen, J.1
Varon, R.2
Mosor, M.3
Maneva, G.4
Maurer, M.5
Stumm, M.6
Nowakowska, D.7
Rubach, M.8
Kosakowska, E.9
Ruka, W.10
Nowecki, Z.11
Rutkowski, P.12
Demkow, T.13
Sadowska, M.14
Bidzinski, M.15
Gawrychowski, K.16
Sperling, K.17
-
10
-
-
31844434470
-
-
Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, Koltan A, Kuzmicz M, Luszawska-Kutrzeba T, Maciejka-Kapuscinska L, Stolarska M, Stefanska K, Sznurkowska K, Wakulinska A, Wieczorek M, Szczepanski T and Kowalczyk J: Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish paediatric patients with sporadic lymphoid malignancies. Int J Cancer 18: 1269-1274, 2006.
-
Chrzanowska KH, Piekutowska-Abramczuk D, Popowska E, Gladkowska-Dura M, Maldyk J, Syczewska M, Krajewska-Walasek M, Goryluk-Kozakiewicz B, Bubala H, Gadomski A, Gaworczyk A, Kazanowska B, Koltan A, Kuzmicz M, Luszawska-Kutrzeba T, Maciejka-Kapuscinska L, Stolarska M, Stefanska K, Sznurkowska K, Wakulinska A, Wieczorek M, Szczepanski T and Kowalczyk J: Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish paediatric patients with sporadic lymphoid malignancies. Int J Cancer 18: 1269-1274, 2006.
-
-
-
-
11
-
-
0036866797
-
Nijmegen breakage syndrome gene (NBS1) alterations and its protein (nibrin) expression in human ovarian tumours
-
Plisiecka-Halasa J, Dansonka-Mieszkowska A, Rembiszewska A, Bidzinski M, Steffen J and Kupryjanczyk J: Nijmegen breakage syndrome gene (NBS1) alterations and its protein (nibrin) expression in human ovarian tumours. Ann Hum Genet 66: 353-359, 2002.
-
(2002)
Ann Hum Genet
, vol.66
, pp. 353-359
-
-
Plisiecka-Halasa, J.1
Dansonka-Mieszkowska, A.2
Rembiszewska, A.3
Bidzinski, M.4
Steffen, J.5
Kupryjanczyk, J.6
-
12
-
-
17144442945
-
Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin
-
Debniak T, Gorski B, Cybulski C, Jakubowska A, Kurzawski G, Lener M, Mierzejewski M, Masojc B, Medrek K, Kladny J, Zaluga E, Maleszka R, Chosia M and Lubinski J: Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin. Melanoma Res 13: 365-370, 2003.
-
(2003)
Melanoma Res
, vol.13
, pp. 365-370
-
-
Debniak, T.1
Gorski, B.2
Cybulski, C.3
Jakubowska, A.4
Kurzawski, G.5
Lener, M.6
Mierzejewski, M.7
Masojc, B.8
Medrek, K.9
Kladny, J.10
Zaluga, E.11
Maleszka, R.12
Chosia, M.13
Lubinski, J.14
-
13
-
-
10744233070
-
NBS1 is a prostate cancer susceptibility gene
-
Cybulski C, Gorski B, Debniak T, Gliniewicz B, Mierzejewski M, Masojc B, Jakubowska A, Matyjasik J, Zlowocka E, Sikorski A, Narod SA and Lubinski J: NBS1 is a prostate cancer susceptibility gene. Cancer Res 64: 1215-1219, 2004.
-
(2004)
Cancer Res
, vol.64
, pp. 1215-1219
-
-
Cybulski, C.1
Gorski, B.2
Debniak, T.3
Gliniewicz, B.4
Mierzejewski, M.5
Masojc, B.6
Jakubowska, A.7
Matyjasik, J.8
Zlowocka, E.9
Sikorski, A.10
Narod, S.A.11
Lubinski, J.12
-
14
-
-
33745225487
-
Germline mutations 657del5 of the NBS1 gene contribute significantly to the incident of breast cancer in Central Poland
-
Steffen J, Nowakowska D, Niwinska A, Czapczyk D, Kluska A, Piatkowska M, Winiewska A and Paszko Z: Germline mutations 657del5 of the NBS1 gene contribute significantly to the incident of breast cancer in Central Poland. Int J Cancer 119: 472-475, 2006.
-
(2006)
Int J Cancer
, vol.119
, pp. 472-475
-
-
Steffen, J.1
Nowakowska, D.2
Niwinska, A.3
Czapczyk, D.4
Kluska, A.5
Piatkowska, M.6
Winiewska, A.7
Paszko, Z.8
-
15
-
-
33746130359
-
Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukaemia
-
Mosor M, Ziolkowska I, Pernak-Schwarz M, Januszkiewicz-Lewandowska D and Nowak J: Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukaemia. Leukemia 8: 1454-1456, 2006.
-
(2006)
Leukemia
, vol.8
, pp. 1454-1456
-
-
Mosor, M.1
Ziolkowska, I.2
Pernak-Schwarz, M.3
Januszkiewicz-Lewandowska, D.4
Nowak, J.5
-
16
-
-
5044248651
-
First case of aplastic anaemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability
-
Shimada H, Shimizu K, Mimaki S, Sakiyama T, Mori T, Shimasaki N, Yokota J, Nakachi K, Ohta T and Ohki M: First case of aplastic anaemia in a Japanese child with a homozygous missense mutation in the NBS1 gene (I171V) associated with genomic instability. Hum Genet 115: 372-376, 2004.
-
(2004)
Hum Genet
, vol.115
, pp. 372-376
-
-
Shimada, H.1
Shimizu, K.2
Mimaki, S.3
Sakiyama, T.4
Mori, T.5
Shimasaki, N.6
Yokota, J.7
Nakachi, K.8
Ohta, T.9
Ohki, M.10
-
18
-
-
33748852526
-
Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland)
-
Ziolkowska I, Mosor M and Nowak J: Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland). J Appl Genet 47: 269-272, 2006.
-
(2006)
J Appl Genet
, vol.47
, pp. 269-272
-
-
Ziolkowska, I.1
Mosor, M.2
Nowak, J.3
-
19
-
-
21044452905
-
Breast cancer predisposing alleles in Poland
-
Gorski B, Cybulski C, Huzarski T, Byrski T, Gronwald J, Jakubowska A, Stawicka M, Gozdecka-Grodecka S, Szwiec M, Urbanski K, Mitus J, Marczyk E, Dziuba J, Wandzel P, Surdyka D, Haus O, Janiszewska H, Debniak T, Toloczko-Grabarek A, Medrek K, Masojc B, Mierzejewski M, Kowalska E, Narod SA and Lubinski J: Breast cancer predisposing alleles in Poland. Breast Cancer Res Treat 92: 19-24, 2005.
-
(2005)
Breast Cancer Res Treat
, vol.92
, 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..
-
20
-
-
0038505600
-
Germline 657del5 mutation in the NBS1 gene in breast cancer patients
-
Gorski B, Debniak T, Masojc B, Mierzejewski M, Medrek K, Cybulski C, Jakubowska A, Kurzawski G, Chosia M, Scott R and Lubinski J: Germline 657del5 mutation in the NBS1 gene in breast cancer patients. Int J Cancer 106: 379-381, 2003.
-
(2003)
Int J Cancer
, vol.106
, pp. 379-381
-
-
Gorski, B.1
Debniak, T.2
Masojc, B.3
Mierzejewski, M.4
Medrek, K.5
Cybulski, C.6
Jakubowska, A.7
Kurzawski, G.8
Chosia, M.9
Scott, R.10
Lubinski, J.11
-
21
-
-
20044366887
-
NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia
-
Buslov KG, Iyevleva AG, Chekmariova EV, Suspitsin EN, Togo AV, Kuligina ESh, Sokolenko AP, Matsko DE, Turkevich EA, Lazareva YR, Chagunava OL, Bit-Sava EM, Semiglazov VF, Devilee P, Cornelisse C, Hanson KP and Imyanitov EN: NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia. Int J Cancer 114: 585-589, 2005.
-
(2005)
Int J Cancer
, vol.114
, pp. 585-589
-
-
Buslov, K.G.1
Iyevleva, A.G.2
Chekmariova, E.V.3
Suspitsin, E.N.4
Togo, A.V.5
Kuligina, E.S.6
Sokolenko, A.P.7
Matsko, D.E.8
Turkevich, E.A.9
Lazareva, Y.R.10
Chagunava, O.L.11
Bit-Sava, E.M.12
Semiglazov, V.F.13
Devilee, P.14
Cornelisse, C.15
Hanson, K.P.16
Imyanitov, E.N.17
-
22
-
-
0032792820
-
Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: No association with risk of breast cancer
-
Carlomagno F, Chang-Claude J, Dunning AM and Ponder BA: Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer. Genes Chromosomes Cancer 25: 393-395, 1999.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 393-395
-
-
Carlomagno, F.1
Chang-Claude, J.2
Dunning, A.M.3
Ponder, B.A.4
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