-
2
-
-
0141429017
-
Germline BRCA1 mutationsand a basal epithelial phenotype in breast cancer
-
Foulkes WD, Stefansson IM, Chappuis PO, Begin LR, Goffin JR, Wong N, et al. Germline BRCA1 mutationsand a basal epithelial phenotype in breast cancer. J Natl Cancer Inst 2003;95:1482-5.
-
(2003)
J Natl Cancer Inst
, vol.95
, pp. 1482-1485
-
-
Foulkes, W.D.1
Stefansson, I.M.2
Chappuis, P.O.3
Begin, L.R.4
Goffin, J.R.5
Wong, N.6
-
3
-
-
33748939380
-
Distinct patternsof DNAcopynumberalteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer
-
Bergamaschi A, Kim YH, Wang P, Sorlie T, Hernandez-Boussard T, Lonning PE, et al. Distinct patternsof DNAcopynumberalteration are associated with different clinicopathological features and gene-expression subtypes of breast cancer. Genes Chromosomes Cancer 2006;45:1033-40.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 1033-1040
-
-
Bergamaschi, A.1
Kim, Y.H.2
Wang, P.3
Sorlie, T.4
Hernandez-Boussard, T.5
Lonning, P.E.6
-
4
-
-
43749085080
-
Distinctgenomicaberration patternsarefound infamilial breastcancer associated with different immunohistochemical subtypes
-
Melchor L, Honrado E, Garcia MJ, Alvarez S, Palacios J, Osorio A, et al. Distinctgenomicaberration patternsarefound infamilial breastcancer associated with different immunohistochemical subtypes. Oncogene 2008;27:3165-75.
-
(2008)
Oncogene
, vol.27
, pp. 3165-3175
-
-
Melchor, L.1
Honrado, E.2
Garcia, M.J.3
Alvarez, S.4
Palacios, J.5
Osorio, A.6
-
5
-
-
77953123909
-
An integrative genomic and transcriptomic analysis reveals molecular pathways and networks regulated by copy number aberra-tionsin basal-like, HER2 and luminal cancers
-
Natrajan R, Weigelt B, Mackay A, Geyer FC, Grigoriadis A, Tan DS, et al. An integrative genomic and transcriptomic analysis reveals molecular pathways and networks regulated by copy number aberra-tionsin basal-like, HER2 and luminal cancers. Breast Cancer Res Treat 2010;121:575-89.
-
(2010)
Breast Cancer Res Treat
, vol.121
, pp. 575-589
-
-
Natrajan, R.1
Weigelt, B.2
MacKay, A.3
Geyer, F.C.4
Grigoriadis, A.5
Tan, D.S.6
-
6
-
-
84555196106
-
BRCA1 and BRCA2: Different roles in a common pathway of genome protection
-
Roy R, Chun J, Powell SN. BRCA1 and BRCA2: different roles in a common pathway of genome protection. Nat Rev Cancer 2012;12: 68-78.
-
(2012)
Nat Rev Cancer
, vol.12
, pp. 68-78
-
-
Roy, R.1
Chun, J.2
Powell, S.N.3
-
7
-
-
4944229642
-
Hallmarks of 'BRCAness' in sporadic cancers
-
Turner N, Tutt A, Ashworth A. Hallmarks of 'BRCAness' in sporadic cancers. Nat Rev Cancer 2004;4:814-9.
-
(2004)
Nat Rev Cancer
, vol.4
, pp. 814-819
-
-
Turner, N.1
Tutt, A.2
Ashworth, A.3
-
8
-
-
79952253747
-
Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer
-
Gonzalez-Angulo AM, Timms KM, Liu S, Chen H, Litton JK, Potter J, et al. Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer. Clin Cancer Res 2011;17:1082-9.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 1082-1089
-
-
Gonzalez-Angulo, A.M.1
Timms, K.M.2
Liu, S.3
Chen, H.4
Litton, J.K.5
Potter, J.6
-
9
-
-
39749108733
-
High-resolution a CGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer
-
Chin SF, Teschendorff AE, Marioni JC, Wang Y, Barbosa-Morais NL, Thorne NP, et al. High-resolution a CGH and expression profiling identifies a novel genomic subtype of ER negative breast cancer. Genome Biol 2007;8:R215.
-
(2007)
Genome Biol
, vol.8
-
-
Chin, S.F.1
Teschendorff, A.E.2
Marioni, J.C.3
Wang, Y.4
Barbosa-Morais, N.L.5
Thorne, N.P.6
-
10
-
-
78650856888
-
Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes
-
Stefansson OA, Jonasson JG, Johannsson OT, Olafsdottir K, Stei-narsdottir M, Valgeirsdottir S, et al. Genomic profiling of breast tumours in relation to BRCA abnormalities and phenotypes. Breast Cancer Res 2009;11:R47.
-
(2009)
Breast Cancer Res
, vol.11
-
-
Stefansson, O.A.1
Jonasson, J.G.2
Johannsson, O.T.3
Olafsdottir, K.4
Stei-Narsdottir, M.5
Valgeirsdottir, S.6
-
11
-
-
78650026917
-
Genomic signature of BRCA1 deficiency in sporadic basal-like breast tumors
-
Joosse SA, Brandwijk KI, Mulder L, Wesseling J, Hannemann J, Nederlof PM. Genomic signature of BRCA1 deficiency in sporadic basal-like breast tumors. Genes Chromosomes Cancer 2011;50: 71-81.
-
(2011)
Genes Chromosomes Cancer
, vol.50
, pp. 71-81
-
-
Joosse, S.A.1
Brandwijk, K.I.2
Mulder, L.3
Wesseling, J.4
Hannemann, J.5
Nederlof, P.M.6
-
12
-
-
77949908546
-
Efficacy of neoadjuvant Cisplatin in triple-negative breast cancer
-
Silver DP, Richardson AL, Eklund AC, Wang ZC, Szallasi Z, Li Q, et al. Efficacy of neoadjuvant Cisplatin in triple-negative breast cancer. J Clin Oncol 2010;28:1145-53.
-
(2010)
J Clin Oncol
, vol.28
, pp. 1145-1153
-
-
Silver, D.P.1
Richardson, A.L.2
Eklund, A.C.3
Wang, Z.C.4
Szallasi, Z.5
Li, Q.6
-
13
-
-
84856230867
-
Genomic instability in breast and ovarian cancers: Translation into clinical predictive biomarkers
-
Vollebergh MA, Jonkers J, Linn SC. Genomic instability in breast and ovarian cancers: translation into clinical predictive biomarkers. Cel Mol Life Sci 2012;69:223-45.
-
(2012)
Cel Mol Life Sci
, vol.69
, pp. 223-245
-
-
Vollebergh, M.A.1
Jonkers, J.2
Linn, S.C.3
-
14
-
-
80054916858
-
Human BRCA1-associated breast cancer: No increase in numer-ical chromosomal instability compared tosporadictumors
-
Focken T, Steinemann D, Skawran B, Hofmann W, Ahrens P, Arnold N, et al. Human BRCA1-associated breast cancer: no increase in numer-ical chromosomal instability compared tosporadictumors. Cytogenet Genome Res 2011;135:84-92.
-
(2011)
Cytogenet Genome Res
, vol.135
, pp. 84-92
-
-
Focken, T.1
Steinemann, D.2
Skawran, B.3
Hofmann, W.4
Ahrens, P.5
Arnold, N.6
-
15
-
-
33746382920
-
Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors
-
Johannsdottir HK, Jonsson G, Johannesdottir G, Agnarsson BA, Eerola H, Arason A, et al. Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors. Int J Cancer 2006;119:1052-60.
-
(2006)
Int J Cancer
, vol.119
, pp. 1052-1060
-
-
Johannsdottir, H.K.1
Jonsson, G.2
Johannesdottir, G.3
Agnarsson, B.A.4
Eerola, H.5
Arason, A.6
-
16
-
-
0030894785
-
Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations
-
Tirkkonen M, Johannsson O, Agnarsson BA, Olsson H, Ingvarsson S, Karhu R, et al. Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations. Cancer Res 1997;57:1222-7.
-
(1997)
Cancer Res
, vol.57
, pp. 1222-1227
-
-
Tirkkonen, M.1
Johannsson, O.2
Agnarsson, B.A.3
Olsson, H.4
Ingvarsson, S.5
Karhu, R.6
-
17
-
-
0036895886
-
Molecular classification of breast carcinomas by com-parative genomic hybridization: A specific somatic genetic profile for BRCA1 tumors
-
Wessels LF, van Welsem T, Hart AA, van't Veer LJ, Reinders MJ, Nederlof PM. Molecular classification of breast carcinomas by com-parative genomic hybridization: a specific somatic genetic profile for BRCA1 tumors. Cancer Res 2002;62:7110-7.
-
(2002)
Cancer Res
, vol.62
, pp. 7110-7117
-
-
Wessels, L.F.1
Van Welsem, T.2
Hart, A.A.3
Van'T Veer, L.J.4
Reinders, M.J.5
Nederlof, P.M.6
-
18
-
-
79952118064
-
Subtypes of familial breast tumours revealed by expression and copy number profiling
-
Waddell N, Arnold J, Cocciardi S, da Silva L, Marsh A, Riley J, et al. Subtypes of familial breast tumours revealed by expression and copy number profiling. Breast Cancer Res Treat 2010;123: 661-77.
-
(2010)
Breast Cancer Res Treat
, vol.123
, pp. 661-677
-
-
Waddell, N.1
Arnold, J.2
Cocciardi, S.3
Da Silva, L.4
Marsh, A.5
Riley, J.6
-
19
-
-
78149477701
-
Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics
-
Jonsson G, Staaf J, Vallon-Christersson J, Ringner M, Holm K, Hegardt C, et al. Genomic subtypes of breast cancer identified by array-comparative genomic hybridization display distinct molecular and clinical characteristics. Breast Cancer Res 2010;12:R42.
-
(2010)
Breast Cancer Res
, vol.12
-
-
Jonsson, G.1
Staaf, J.2
Vallon-Christersson, J.3
Ringner, M.4
Holm, K.5
Hegardt, C.6
-
20
-
-
70349166545
-
Prediction of BRCA1-association in hereditary non-BRCA1/2 breastcarcinomaswitharray-CGH
-
Joosse SA, van Beers EH, Tielen IH, Horlings H, Peterse JL, Hooger-brugge N, et al. Prediction of BRCA1-association in hereditary non-BRCA1/2 breastcarcinomaswitharray-CGH. Breast Cancer Res Treat 2009;116:479-89.
-
(2009)
Breast Cancer Res Treat
, vol.116
, pp. 479-489
-
-
Joosse, S.A.1
Van Beers, E.H.2
Tielen, I.H.3
Horlings, H.4
Peterse, J.L.5
Hooger-Brugge, N.6
-
21
-
-
79953305446
-
Indicators of homologous recombination deficiency in breast cancer and association with response to neoad-juvant chemotherapy
-
Lips EH, Mulder L, Hannemann J, Laddach N, Vrancken Peeters MT, van de Vijver MJ, et al. Indicators of homologous recombination deficiency in breast cancer and association with response to neoad-juvant chemotherapy. Ann Oncol 2011;22:870-6.
-
(2011)
Ann Oncol
, vol.22
, pp. 870-876
-
-
Lips, E.H.1
Mulder, L.2
Hannemann, J.3
Laddach, N.4
Vrancken Peeters, M.T.5
Van De Vijver, M.J.6
-
22
-
-
79959733228
-
An a CGH classifier derived from BRCA1-mutated breast cancerand benefit of high-dose platinum-based chemotherapy in HER2-negative breast cancer patients
-
Vollebergh MA, Lips EH, Nederlof PM, Wessels LF, Schmidt MK, van Beers EH, et al. An a CGH classifier derived from BRCA1-mutated breast cancerand benefit of high-dose platinum-based chemotherapy in HER2-negative breast cancer patients. Ann Oncol 2011;22: 1561-70.
-
(2011)
Ann Oncol
, vol.22
, pp. 1561-1570
-
-
Vollebergh, M.A.1
Lips, E.H.2
Nederlof, P.M.3
Wessels, L.F.4
Schmidt, M.K.5
Van Beers, E.H.6
-
23
-
-
76249097734
-
Genome Alteration Print (GAP): A tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays
-
Popova T, Manie E, Stoppa-Lyonnet D, Rigaill G, Barillot E, Stern MH. Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays. Genome Biol 2009;10:R128. Available from: http://bioinfo-out.curie.fr/projects/ snp-gap/
-
(2009)
Genome Biol
, vol.10
-
-
Popova Manie, T.E.1
Stoppa-Lyonnet, D.2
Rigaill, G.3
Barillot, E.4
Stern, M.H.5
-
24
-
-
58349094961
-
High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors
-
Manie E, Vincent-Salomon A, Lehmann-Che J, Pierron G, Turpin E, Warcoin M, et al. High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors. Cancer Res 2009;69:663-71.
-
(2009)
Cancer Res
, vol.69
, pp. 663-671
-
-
Manie, E.1
Vincent-Salomon, A.2
Lehmann-Che, J.3
Pierron, G.4
Turpin, E.5
Warcoin, M.6
-
25
-
-
34250208031
-
Identification of typical medullary breast carcinoma as a genomic sub-group of basal-like carcinomas, a heterogeneous new molecular entity
-
Vincent-Salomon A, Gruel N, Lucchesi C, Mac Grogan G, Dendale R, Sigal-Zafrani B, et al. Identification of typical medullary breast carcinoma as a genomic sub-group of basal-like carcinomas, a heterogeneous new molecular entity. Breast Cancer Res 2007; 9:R24.
-
(2007)
Breast Cancer Res
, vol.9
-
-
Vincent-Salomon, A.1
Gruel, N.2
Lucchesi, C.3
Mac Grogan, G.4
Dendale, R.5
Sigal-Zafrani, B.6
-
26
-
-
63849329936
-
Frequent PTEN genomic alterations and activated phosphatidy-linositol 3-kinase pathway in basal-like breast cancer cells
-
Marty B, Maire V, Gravier E, Rigaill G, Vincent-Salomon A, Kappler M, et al. Frequent PTEN genomic alterations and activated phosphatidy-linositol 3-kinase pathway in basal-like breast cancer cells. Breast Cancer Res 2008;10:R101.
-
(2008)
Breast Cancer Res
, vol.10
-
-
Marty, B.1
Maire, V.2
Gravier, E.3
Rigaill, G.4
Vincent-Salomon, A.5
Kappler, M.6
-
27
-
-
84858253707
-
Search for a gene-expression signature of breast cancer local recur-rence in young women
-
Servant N, Bollet MA, Halfwerk H, Bleakley K, Kreike B, Jacob L, et al. Search for a gene-expression signature of breast cancer local recur-rence in young women. Clin Cancer Res 2012;18:1704-15.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 1704-1715
-
-
Servant, N.1
Bollet, M.A.2
Halfwerk, H.3
Bleakley, K.4
Kreike, B.5
Jacob, L.6
-
28
-
-
81255135837
-
Tumor grafts derived from women with breast cancer authentically reflect tumor pathology, growth, metastasis and disease outcomes
-
De Rose YS, Wang G, Lin YC, Bernard PS, Buys SS, Ebbert MT, et al. Tumor grafts derived from women with breast cancer authentically reflect tumor pathology, growth, metastasis and disease outcomes. Nat Med 2011;17:1514-20.
-
(2011)
Nat Med
, vol.17
, pp. 1514-1520
-
-
De Rose, Y.S.1
Wang, G.2
Lin, Y.C.3
Bernard, P.S.4
Buys, S.S.5
Ebbert, M.T.6
-
29
-
-
77957987999
-
Establishment and characterisation of a new breast cancer xenograft obtained from a woman carrying a germline BRCA2 muta-tion
-
De Plater L, Lauge A, Guyader C, Poupon MF, Assayag F, de Cremoux P, et al. Establishment and characterisation of a new breast cancer xenograft obtained from a woman carrying a germline BRCA2 muta-tion. Br J Cancer2010;103:1192-200.
-
(2010)
Br J Cancer
, vol.103
, pp. 1192-1200
-
-
De Plater, L.1
Lauge, A.2
Guyader, C.3
Poupon, M.F.4
Assayag, F.5
De Cremoux, P.6
-
30
-
-
84872608761
-
-
Wellcome Trust Sanger Institute Cancer Genome Project
-
Wellcome Trust Sanger Institute Cancer Genome Project. Available from: http://www.sanger.ac.uk/genetics/CGP
-
-
-
-
31
-
-
72949119310
-
Complex landscapes of somatic rearrangement in human breast cancer genomes
-
Stephens PJ, Mc Bride DJ, Lin ML, Varela I, Pleasance ED, Simpson JT, et al. Complex landscapes of somatic rearrangement in human breast cancer genomes. Nature 2009;462:1005-10.
-
(2009)
Nature
, vol.462
, pp. 1005-1010
-
-
Stephens, P.J.1
Mc Bride, D.J.2
Lin, M.L.3
Varela, I.4
Pleasance, E.D.5
Simpson, J.T.6
-
32
-
-
31544474577
-
BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants
-
Elstrodt F, Hollestelle A, Nagel JH, Gorin M, Wasielewski M, van den Ouweland A, et al. BRCA1 mutation analysis of 41 human breast cancer cell lines reveals three new deleterious mutants. Cancer Res 2006;66:41-5.
-
(2006)
Cancer Res
, vol.66
, pp. 41-45
-
-
Elstrodt, F.1
Hollestelle, A.2
Nagel, J.H.3
Gorin, M.4
Wasielewski, M.5
Van Den Ouweland, A.6
-
33
-
-
77950864281
-
Cp G island methylation affects accessibility of the proximal BRCA1 pro-moter to transcription factors
-
Xu J, Huo D, Chen Y, Nwachukwu C, Collins C, Rowell J, et al. Cp G island methylation affects accessibility of the proximal BRCA1 pro-moter to transcription factors. Breast Cancer Res Treat 2010;120: 593-601.
-
(2010)
Breast Cancer Res Treat
, vol.120
, pp. 593-601
-
-
Xu, J.1
Huo, D.2
Chen, Y.3
Nwachukwu, C.4
Collins, C.5
Rowell, J.6
-
34
-
-
78651330430
-
COSMIC: Mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
-
Forbes SA, Bindal N, Bamford S, Cole C, Kok CY, Beare D, et al. COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer. Nucleic Acids Res 2011;39:D945-50. Available from: http://www.sanger.ac.uk/ genetics/CGP/cosmic/
-
(2011)
Nucleic Acids Res
, vol.39
-
-
Forbes, S.A.1
Bindal, N.2
Bamford, S.3
Cole, C.4
Kok, C.Y.5
Beare, D.6
-
35
-
-
79951788238
-
Enhanced mismatch mutation analysis: Simultaneous detection of point mutations and large scale rearrangements by capillary electrophoresis, application to BRCA1 and BRCA2
-
Houdayer C, Moncoutier V, Champ J, Weber J, Viovy JL, Stoppa-Lyonnet D. Enhanced mismatch mutation analysis: simultaneous detection of point mutations and large scale rearrangements by capillary electrophoresis, application to BRCA1 and BRCA2. Methods Mol Biol 2010;653:147-80.
-
(2010)
Methods Mol Biol
, vol.653
, pp. 147-180
-
-
Houdayer, C.1
Moncoutier, V.2
Champ, J.3
Weber, J.4
Viovy, J.L.5
Stoppa-Lyonnet, D.6
-
36
-
-
84859628102
-
A whole-genome massively parallel sequencing analysis of BRCA1 mutant oestrogen receptor-negative and -positive breast cancers
-
Natrajan R, Mackay A, Lambros MB, Weigelt B, Wilkerson PM, Manie E, et al. A whole-genome massively parallel sequencing analysis of BRCA1 mutant oestrogen receptor-negative and -positive breast cancers. J Pathol 2012;227:29-41.
-
(2012)
J Pathol
, vol.227
, pp. 29-41
-
-
Natrajan, R.1
MacKay, A.2
Lambros, M.B.3
Weigelt, B.4
Wilkerson, P.M.5
Manie, E.6
-
37
-
-
84872608796
-
-
U.S. National Institutes of Health, Bethesda, MD, USA, 1997-2012
-
Rasband WS. Image J, U.S. National Institutes of Health, Bethesda, MD, USA, 1997-2012.Availablefrom: http://imagej.nih.gov/ij/
-
-
-
Rasband, W.S.1
Image, J.2
-
38
-
-
54949156063
-
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios
-
Staaf J, Vallon-Christersson J, Lindgren D, Juliusson G, Rosenquist R, Hoglund M, et al. Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios. BMC Bioinformatics 2008;9:409.
-
(2008)
BMC Bioinformatics
, vol.9
, pp. 409
-
-
Staaf, J.1
Vallon-Christersson, J.2
Lindgren, D.3
Juliusson, G.4
Rosenquist, R.5
Hoglund, M.6
-
39
-
-
59349098193
-
The consequences of tetraploidy and aneu-ploidy
-
Storchova Z, Kuffer C. The consequences of tetraploidy and aneu-ploidy. J Cell Sci 2008;121:3859-66.
-
(2008)
J Cell Sci
, vol.121
, pp. 3859-3866
-
-
Storchova, Z.1
Kuffer, C.2
-
40
-
-
77955603605
-
Genomic architecture characterizes tumor progression paths and fate in breast cancer patients
-
Russnes HG, Vollan HK, Lingjaerde OC, Krasnitz A, Lundin P, Naume B, et al. Genomic architecture characterizes tumor progression paths and fate in breast cancer patients. Sci Transl Med 2010;2:38-47.
-
(2010)
Sci Transl Med
, vol.2
, pp. 38-47
-
-
Russnes, H.G.1
Vollan, H.K.2
Lingjaerde, O.C.3
Krasnitz, A.4
Lundin, P.5
Naume, B.6
-
41
-
-
33845291140
-
Novel patterns of genome rearrangement and their association with survival in breast cancer
-
Hicks J, Krasnitz A, Lakshmi B, Navin NE, Riggs M, Leibu E, et al. Novel patterns of genome rearrangement and their association with survival in breast cancer. Genome Res 2006;16:1465-79.
-
(2006)
Genome Res
, vol.16
, pp. 1465-1479
-
-
Hicks, J.1
Krasnitz, A.2
Lakshmi, B.3
Navin, N.E.4
Riggs, M.5
Leibu, E.6
-
42
-
-
78650959663
-
Massive genomic rearrangement acquired in a single catastrophic event during cancer development
-
Stephens PJ, Greenman CD, Fu B, Yang F, Bignell GR, Mudie LJ, et al. Massive genomic rearrangement acquired in a single catastrophic event during cancer development. Cell 2011;144:27-40.
-
(2011)
Cell
, vol.144
, pp. 27-40
-
-
Stephens, P.J.1
Greenman, C.D.2
Fu, B.3
Yang, F.4
Bignell, G.R.5
Mudie, L.J.6
-
43
-
-
77749331751
-
Global screen in gandext ended nomenclature for 230 aphidicol in-inducible fragile sites, including 61 yet unreported ones
-
Mrasek K, Schoder C, Teichmann AC, Behr K, Franze B, Wilhelm K, et al.Global screen in gandext ended nomenclature for 230 aphidicol in-inducible fragile sites, including 61 yet unreported ones. Int J Oncol 2010;36:929-40.
-
(2010)
Int J Oncol
, vol.36
, pp. 929-940
-
-
Mrasek, K.1
Schoder, C.2
Teichmann, A.C.3
Behr, K.4
Franze, B.5
Wilhelm, K.6
-
44
-
-
78049248432
-
Allele-specific copy number analysis oftumors
-
Van Loo P, Nordgard SH, Lingjaerde OC, Russnes HG, Rye IH, Sun W, et al. Allele-specific copy number analysis oftumors. Proc Natl Acad Sci U S A2010;107:16910-5.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 16910-16915
-
-
Van Loo, P.1
Nordgard, S.H.2
Lingjaerde, O.C.3
Russnes, H.G.4
Rye, I.H.5
Sun, W.6
-
45
-
-
35349024501
-
Network modeling links breast cancer susceptibility and centrosome dysfunction
-
Pujana MA, Han JD, Starita LM, Stevens KN, Tewari M, Ahn JS, et al. Network modeling links breast cancer susceptibility and centrosome dysfunction. Nat Genet 2007;39:1338-49.
-
(2007)
Nat Genet
, vol.39
, pp. 1338-1349
-
-
Pujana, M.A.1
Han, J.D.2
Starita, L.M.3
Stevens, K.N.4
Tewari, M.5
Ahn, J.S.6
-
46
-
-
27144540976
-
Centrosome amplification, chromosome instability and cancer development
-
Fukasawa K. Centrosome amplification, chromosome instability and cancer development. Cancer Lett 2005;230:6-19.
-
(2005)
Cancer Lett
, vol.230
, pp. 6-19
-
-
Fukasawa, K.1
-
47
-
-
77953291328
-
53BP1 loss rescues BRCA1 deficiency and is asso-ciated with triple-negative and BRCA-mutated breast cancers
-
Bouwman P, Aly A, Escandell JM, Pieterse M, Bartkova J, van der Gulden H, et al. 53BP1 loss rescues BRCA1 deficiency and is asso-ciated with triple-negative and BRCA-mutated breast cancers. Nat Struct Mol Biol 2010;17:688-95.
-
(2010)
Nat Struct Mol Biol
, vol.17
, pp. 688-695
-
-
Bouwman, P.1
Aly, A.2
Escandell, J.M.3
Pieterse, M.4
Bartkova, J.5
Van Der Gulden, H.6
-
48
-
-
79551658805
-
Rad52 inactivation is synthetically lethal with BRCA2 deficiency
-
Feng Z, Scott SP, Bussen W, Sharma GG, Guo G, Pandita TK, et al. Rad52 inactivation is synthetically lethal with BRCA2 deficiency. Proc Natl Acad Sci U S A 2011;108:686-91.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 686-691
-
-
Feng, Z.1
Scott, S.P.2
Bussen, W.3
Sharma, G.G.4
Guo, G.5
Pandita, T.K.6
-
49
-
-
39849097680
-
Resistance to therapy caused by intragenic deletion in BRCA2
-
Edwards SL, Brough R, Lord CJ, Natrajan R, Vatcheva R, Levine DA, et al. Resistance to therapy caused by intragenic deletion in BRCA2. Nature 2008;451:1111-5.
-
(2008)
Nature
, vol.451
, pp. 1111-1115
-
-
Edwards, S.L.1
Brough, R.2
Lord, C.J.3
Natrajan, R.4
Vatcheva, R.5
Levine, D.A.6
-
50
-
-
34447298637
-
Genetic epidemiologyof BRCAmutations-familyhistorydetectslessthan50% of the mutation carriers
-
Moller P, Hagen AI, Apold J, Maehle L, Clark N, Fiane B, et al. Genetic epidemiologyof BRCAmutations-familyhistorydetectslessthan50% of the mutation carriers. Eur J Cancer2007;43:1713-7.
-
(2007)
Eur J Cancer
, vol.43
, pp. 1713-1717
-
-
Moller, P.1
Hagen, A.I.2
Apold, J.3
Maehle, L.4
Clark, N.5
Fiane, B.6
-
52
-
-
77955019276
-
Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: A proof-of-concept trial
-
Tutt A, Robson M, Garber JE, Domchek SM, Audeh MW, Weitzel JN, et al. Oral poly(ADP-ribose) polymerase inhibitor olaparib in patients with BRCA1 or BRCA2 mutations and advanced breast cancer: a proof-of-concept trial. Lancet 2010;376:235-44.
-
(2010)
Lancet
, vol.376
, pp. 235-244
-
-
Tutt, A.1
Robson, M.2
Garber, J.E.3
Domchek, S.M.4
Audeh, M.W.5
Weitzel, J.N.6
-
53
-
-
84863010984
-
Phase II, open-label, randomized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhib-itor, and pegylated liposomal doxorubicin in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer
-
Kaye SB, Lubinski J, Matulonis U, Ang JE, Gourley C, Karlan BY, et al. Phase II, open-label, randomized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhib-itor, and pegylated liposomal doxorubicin in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer. J Clin Oncol 2012; 30:372-9.
-
(2012)
J Clin Oncol
, vol.30
, pp. 372-379
-
-
Kaye, S.B.1
Lubinski, J.2
Matulonis, U.3
Ang, J.E.4
Gourley, C.5
Karlan, B.Y.6
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