-
1
-
-
78049398107
-
Distant metastasis occurs late during the genetic evolution of pancreatic cancer
-
Yachida S, Jones S, Bozic I, Antal T, Leary R, et al. (2010) Distant metastasis occurs late during the genetic evolution of pancreatic cancer. Nature 467: 1114-1117.
-
(2010)
Nature
, vol.467
, pp. 1114-1117
-
-
Yachida, S.1
Jones, S.2
Bozic, I.3
Antal, T.4
Leary, R.5
-
2
-
-
78049380554
-
The patterns and dynamics of genomic instability in metastatic pancreatic cancer
-
Campbell PJ, Yachida S, Mudie LJ, Stephens PJ, Pleasance ED, et al. (2010) The patterns and dynamics of genomic instability in metastatic pancreatic cancer. Nature 467: 1109-1113.
-
(2010)
Nature
, vol.467
, pp. 1109-1113
-
-
Campbell, P.J.1
Yachida, S.2
Mudie, L.J.3
Stephens, P.J.4
Pleasance, E.D.5
-
3
-
-
79953766940
-
Tumour evolution inferred by single-cell sequencing
-
Navin N, Kendall J, Troge J, Andrews P, Rodgers L, et al. (2011) Tumour evolution inferred by single-cell sequencing. Nature 472: 90-94.
-
(2011)
Nature
, vol.472
, pp. 90-94
-
-
Navin, N.1
Kendall, J.2
Troge, J.3
Andrews, P.4
Rodgers, L.5
-
4
-
-
74949101897
-
Inferring tumor progression from genomic heterogeneity
-
Navin N, Krasnitz A, Rodgers L, Cook K, Meth J, et al. (2010) Inferring tumor progression from genomic heterogeneity. Genome Res 20: 68-80.
-
(2010)
Genome Res
, vol.20
, pp. 68-80
-
-
Navin, N.1
Krasnitz, A.2
Rodgers, L.3
Cook, K.4
Meth, J.5
-
5
-
-
77955635233
-
Cancer statistics, 2010
-
Jemal A, Siegel R, Xu J, Ward E, (2010) Cancer statistics, 2010. CA Cancer J Clin 60: 277-300.
-
(2010)
CA Cancer J Clin
, vol.60
, pp. 277-300
-
-
Jemal, A.1
Siegel, R.2
Xu, J.3
Ward, E.4
-
6
-
-
33747163982
-
Recurrent glioblastoma multiforme: a review of natural history and management options
-
Hou LC, Veeravagu A, Hsu AR, Tse VC, (2006) Recurrent glioblastoma multiforme: a review of natural history and management options. Neurosurg Focus 20: E5.
-
(2006)
Neurosurg Focus
, vol.20
-
-
Hou, L.C.1
Veeravagu, A.2
Hsu, A.R.3
Tse, V.C.4
-
7
-
-
77749338221
-
Recent advances in therapy for glioblastoma
-
Clarke J, Butowski N, Chang S, (2010) Recent advances in therapy for glioblastoma. Arch Neurol 67: 279-283.
-
(2010)
Arch Neurol
, vol.67
, pp. 279-283
-
-
Clarke, J.1
Butowski, N.2
Chang, S.3
-
8
-
-
68149165608
-
Treatment options for recurrent glioblastoma: pitfalls and future trends
-
Franceschi E, Tosoni A, Bartolini S, Mazzocchi V, Fioravanti A, et al. (2009) Treatment options for recurrent glioblastoma: pitfalls and future trends. Expert Rev Anticancer Ther 9: 613-619.
-
(2009)
Expert Rev Anticancer Ther
, vol.9
, pp. 613-619
-
-
Franceschi, E.1
Tosoni, A.2
Bartolini, S.3
Mazzocchi, V.4
Fioravanti, A.5
-
9
-
-
20044366163
-
Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma
-
Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, et al. (2005) Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 352: 987-996.
-
(2005)
N Engl J Med
, vol.352
, pp. 987-996
-
-
Stupp, R.1
Mason, W.P.2
van den Bent, M.J.3
Weller, M.4
Fisher, B.5
-
10
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
Cancer Genome Atlas Research Network
-
Cancer Genome Atlas Research Network (2008) Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 455: 1061-1068.
-
(2008)
Nature
, vol.455
, pp. 1061-1068
-
-
-
11
-
-
52949127312
-
An integrated genomic analysis of human glioblastoma multiforme
-
Parsons DW, Jones S, Zhang X, Lin JC, Leary RJ, et al. (2008) An integrated genomic analysis of human glioblastoma multiforme. Science 321: 1807-1812.
-
(2008)
Science
, vol.321
, pp. 1807-1812
-
-
Parsons, D.W.1
Jones, S.2
Zhang, X.3
Lin, J.C.4
Leary, R.J.5
-
12
-
-
77956838065
-
Advances in understanding cancer genomes through second-generation sequencing
-
Meyerson M, Gabriel S, Getz G, (2010) Advances in understanding cancer genomes through second-generation sequencing. Nat Rev Genet 11: 685-696.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 685-696
-
-
Meyerson, M.1
Gabriel, S.2
Getz, G.3
-
13
-
-
33745926178
-
Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing
-
Thomas RK, Nickerson E, Simons JF, Jänne PA, Tengs T, et al. (2006) Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing. Nat Med 12: 852-855.
-
(2006)
Nat Med
, vol.12
, pp. 852-855
-
-
Thomas, R.K.1
Nickerson, E.2
Simons, J.F.3
Jänne, P.A.4
Tengs, T.5
-
14
-
-
70449711757
-
Genetic alterations and signaling pathways in the evolution of gliomas
-
Ohgaki H, Kleihues P, (2009) Genetic alterations and signaling pathways in the evolution of gliomas. Cancer Sci 100: 2235-2241.
-
(2009)
Cancer Sci
, vol.100
, pp. 2235-2241
-
-
Ohgaki, H.1
Kleihues, P.2
-
15
-
-
34250877865
-
Genetic pathways to primary and secondary glioblastoma
-
Ohgaki H, Kleihues P, (2007) Genetic pathways to primary and secondary glioblastoma. Am J Pathol 170: 1445-1453.
-
(2007)
Am J Pathol
, vol.170
, pp. 1445-1453
-
-
Ohgaki, H.1
Kleihues, P.2
-
16
-
-
73649123907
-
Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1
-
Verhaak RG, Hoadley KA, Purdom E, Wang V, Qi Y, et al. (2010) Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. Cancer Cell 17: 98-110.
-
(2010)
Cancer Cell
, vol.17
, pp. 98-110
-
-
Verhaak, R.G.1
Hoadley, K.A.2
Purdom, E.3
Wang, V.4
Qi, Y.5
-
17
-
-
0030920610
-
Sequence mapping by electronic PCR
-
Schuler GD, (1997) Sequence mapping by electronic PCR. Genome Res 7: 541-550.
-
(1997)
Genome Res
, vol.7
, pp. 541-550
-
-
Schuler, G.D.1
-
18
-
-
55549097836
-
Mapping short DNA sequencing reads and calling variants using mapping quality scores
-
Li H, Ruan J, Durbin R, (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 18: 1851-1858.
-
(2008)
Genome Res
, vol.18
, pp. 1851-1858
-
-
Li, H.1
Ruan, J.2
Durbin, R.3
-
19
-
-
77957799874
-
Allele-specific expression of TGFBR1 in colon cancer patients
-
Tomsic J, Guda K, Liyanarachchi S, Hampel H, Natale L, et al. (2010) Allele-specific expression of TGFBR1 in colon cancer patients. Carcinogenesis 31: 1800-1804.
-
(2010)
Carcinogenesis
, vol.31
, pp. 1800-1804
-
-
Tomsic, J.1
Guda, K.2
Liyanarachchi, S.3
Hampel, H.4
Natale, L.5
-
20
-
-
67449152486
-
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients
-
Guda K, Natale L, Lutterbaugh J, Wiesner GL, Lewis S, et al. (2009) Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients. Cancer Res 69: 4959-4961.
-
(2009)
Cancer Res
, vol.69
, pp. 4959-4961
-
-
Guda, K.1
Natale, L.2
Lutterbaugh, J.3
Wiesner, G.L.4
Lewis, S.5
-
21
-
-
77954380684
-
Comparison of Sanger sequencing, pyrosequencing, and melting curve analysis for the detection of KRAS mutations: diagnostic and clinical implications
-
Tsiatis AC, Norris-Kirby A, Rich RG, Hafez MJ, Gocke CD, et al. (2010) Comparison of Sanger sequencing, pyrosequencing, and melting curve analysis for the detection of KRAS mutations: diagnostic and clinical implications. J Mol Diagn 12: 425-432.
-
(2010)
J Mol Diagn
, vol.12
, pp. 425-432
-
-
Tsiatis, A.C.1
Norris-Kirby, A.2
Rich, R.G.3
Hafez, M.J.4
Gocke, C.D.5
-
22
-
-
73949129820
-
The Catalogue of Somatic Mutations in Cancer (COSMIC)
-
Unit 10.11
-
Forbes SA, Bhamra G, Bamford S, Dawson E, Kok C, et al. (2010) The Catalogue of Somatic Mutations in Cancer (COSMIC). Curr Protoc Hum Genet Chapter 10: Unit 10.11.
-
(2010)
Curr Protoc Hum Genet Chapter
, vol.10
-
-
Forbes, S.A.1
Bhamra, G.2
Bamford, S.3
Dawson, E.4
Kok, C.5
-
23
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
International HapMap Consortium
-
International HapMap Consortium (2007) A second generation human haplotype map of over 3.1 million SNPs. Nature 449: 851-861.
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
-
24
-
-
0036119504
-
Accounting for human polymorphisms predicted to affect protein function
-
Ng PC, Henikoff S, (2002) Accounting for human polymorphisms predicted to affect protein function. Genome Res 12: 436-446.
-
(2002)
Genome Res
, vol.12
, pp. 436-446
-
-
Ng, P.C.1
Henikoff, S.2
-
25
-
-
33846650692
-
Distinguishing cancer-associated missense mutations from common polymorphisms
-
Kaminker JS, Zhang Y, Waugh A, Haverty PM, Peters B, et al. (2007) Distinguishing cancer-associated missense mutations from common polymorphisms. Cancer Res 67: 465-473.
-
(2007)
Cancer Res
, vol.67
, pp. 465-473
-
-
Kaminker, J.S.1
Zhang, Y.2
Waugh, A.3
Haverty, P.M.4
Peters, B.5
-
26
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, et al. (2010) A method and server for predicting damaging missense mutations. Nat Methods 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
-
27
-
-
67349257845
-
Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer
-
Liu W, Laitinen S, Khan S, Vihinen M, Kowalski J, et al. (2009) Copy number analysis indicates monoclonal origin of lethal metastatic prostate cancer. Nat Med 15: 559-565.
-
(2009)
Nat Med
, vol.15
, pp. 559-565
-
-
Liu, W.1
Laitinen, S.2
Khan, S.3
Vihinen, M.4
Kowalski, J.5
-
28
-
-
77955562856
-
Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes
-
Li M, Schönberg A, Schaefer M, Schroeder R, Nasidze I, et al. (2010) Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes. Am J Hum Genet 87: 237-249.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 237-249
-
-
Li, M.1
Schönberg, A.2
Schaefer, M.3
Schroeder, R.4
Nasidze, I.5
|