-
1
-
-
41149137119
-
Localized infant neuroblastomas often show spontaneous regression: Results of the prospective trials NB95-S and NB97
-
Hero, B. et al. Localized infant neuroblastomas often show spontaneous regression: Results of the prospective trials NB95-S and NB97. J. Clin. Oncol. 26, 1504-1510 (2008).
-
(2008)
J. Clin. Oncol
, vol.26
, pp. 1504-1510
-
-
Hero, B.1
-
2
-
-
84876430459
-
Children's Oncology Group's 2013 blueprint for research: Neuroblastoma
-
Park, J.R. et al. Children's Oncology Group's 2013 blueprint for research: Neuroblastoma. Pediatr. Blood Cancer 60, 985-993 (2013).
-
(2013)
Pediatr. Blood Cancer
, vol.60
, pp. 985-993
-
-
Park, J.R.1
-
3
-
-
79551628428
-
Treatment and outcomes of patients with relapsed, high-risk neuroblastoma: Results of German trials
-
Simon, T. et al. Treatment and outcomes of patients with relapsed, high-risk neuroblastoma: Results of German trials. Pediatr. Blood Cancer 56, 578-583 (2011).
-
(2011)
Pediatr. Blood Cancer
, vol.56
, pp. 578-583
-
-
Simon, T.1
-
4
-
-
77953523121
-
Recent advances in neuroblastoma
-
Maris, J.M. Recent advances in neuroblastoma. N. Engl. J. Med. 362, 2202-2211 (2010).
-
(2010)
N. Engl. J. Med
, vol.362
, pp. 2202-2211
-
-
Maris, J.M.1
-
5
-
-
58249093955
-
The International Neuroblastoma Risk Group (INRG) classification system: An INRG Task Force report
-
Cohn, S.L. et al. The International Neuroblastoma Risk Group (INRG) classification system: An INRG Task Force report. J. Clin. Oncol. 27, 289-297 (2009).
-
(2009)
J. Clin. Oncol
, vol.27
, pp. 289-297
-
-
Cohn, S.L.1
-
6
-
-
0033600283
-
Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma
-
Bown, N. et al. Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma. N. Engl. J. Med. 340, 1954-1961 (1999).
-
(1999)
N. Engl. J. Med
, vol.340
, pp. 1954-1961
-
-
Bown, N.1
-
7
-
-
28144453057
-
Chromosome 1p and 11q deletions and outcome in neuroblastoma
-
Attiyeh, E.F. et al. Chromosome 1p and 11q deletions and outcome in neuroblastoma. N. Engl. J. Med. 353, 2243-2253 (2005).
-
(2005)
N. Engl. J. Med
, vol.353
, pp. 2243-2253
-
-
Attiyeh, E.F.1
-
8
-
-
0022388606
-
Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas
-
Seeger, R.C. et al. Association of multiple copies of the N-myc oncogene with rapid progression of neuroblastomas. N. Engl. J. Med. 313, 1111-1116 (1985).
-
(1985)
N. Engl. J. Med
, vol.313
, pp. 1111-1116
-
-
Seeger, R.C.1
-
9
-
-
13344275864
-
Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma
-
Caron, H. et al. Allelic loss of chromosome 1p as a predictor of unfavorable outcome in patients with neuroblastoma. N. Engl. J. Med. 334, 225-230 (1996).
-
(1996)
N. Engl. J. Med
, vol.334
, pp. 225-230
-
-
Caron, H.1
-
10
-
-
84858248558
-
Association of age at diagnosis and genetic mutations in patients with neuroblastoma
-
Cheung, N.K. et al. Association of age at diagnosis and genetic mutations in patients with neuroblastoma. J. Am. Med. Assoc. 307, 1062-1071 (2012).
-
(2012)
J. Am. Med. Assoc
, vol.307
, pp. 1062-1071
-
-
Cheung, N.K.1
-
11
-
-
84859216598
-
Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes
-
Molenaar, J.J. et al. Sequencing of neuroblastoma identifies chromothripsis and defects in neuritogenesis genes. Nature 483, 589-593 (2012).
-
(2012)
Nature
, vol.483
, pp. 589-593
-
-
Molenaar, J.J.1
-
12
-
-
84874664731
-
The genetic landscape of high-risk neuroblastoma
-
Pugh, T.J. et al. The genetic landscape of high-risk neuroblastoma. Nat. Genet. 45, 279-284 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 279-284
-
-
Pugh, T.J.1
-
13
-
-
84871982155
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
-
Sausen, M. et al. Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma. Nat. Genet. 45, 12-17 (2013).
-
(2013)
Nat. Genet
, vol.45
, pp. 12-17
-
-
Sausen, M.1
-
14
-
-
60549088714
-
Radiolabeled metaiodobenzylguanidine for imaging and therapy of neuroblastoma
-
Taggart, D., Dubois, S. & Matthay, K.K. Radiolabeled metaiodobenzylguanidine for imaging and therapy of neuroblastoma. Q. J. Nucl. Med. Mol. Imaging 52, 403-418 (2008).
-
(2008)
Q. J. Nucl. Med. Mol. Imaging
, vol.52
, pp. 403-418
-
-
Taggart, D.1
Dubois, S.2
Matthay, K.K.3
-
15
-
-
84906819212
-
Emergence of new ALK mutations at relapse of neuroblastoma
-
Schleiermacher, G. et al. Emergence of new ALK mutations at relapse of neuroblastoma. J. Clin. Oncol. 32, 2727-2734 (2014).
-
(2014)
J. Clin. Oncol
, vol.32
, pp. 2727-2734
-
-
Schleiermacher, G.1
-
16
-
-
84860782006
-
Absolute quantification of somatic DNA alterations in human cancer
-
Carter, S.L. et al. Absolute quantification of somatic DNA alterations in human cancer. Nat. Biotechnol. 30, 413-421 (2012).
-
(2012)
Nat. Biotechnol
, vol.30
, pp. 413-421
-
-
Carter, S.L.1
-
17
-
-
78549262724
-
Patientoriented gene set analysis for cancer mutation data
-
Boca, S.M., Kinzler, K.W., Velculescu, V.E., Vogelstein, B. & Parmigiani, G. Patientoriented gene set analysis for cancer mutation data. Genome Biol. 11, R112 (2010).
-
(2010)
Genome Biol
, vol.11
, pp. R112
-
-
Boca, S.M.1
Kinzler, K.W.2
Velculescu, V.E.3
Vogelstein, B.4
Parmigiani, G.5
-
18
-
-
1542515338
-
A census of human cancer genes
-
Futreal, P.A. et al. A census of human cancer genes. Nat. Rev. Cancer 4, 177-183 (2004).
-
(2004)
Nat. Rev. Cancer
, vol.4
, pp. 177-183
-
-
Futreal, P.A.1
-
19
-
-
84912059340
-
ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma
-
Bresler, S.C. et al. ALK mutations confer differential oncogenic activation and sensitivity to ALK inhibition therapy in neuroblastoma. Cancer Cell 26, 682-694 (2014).
-
(2014)
Cancer Cell
, vol.26
, pp. 682-694
-
-
Bresler, S.C.1
-
20
-
-
77955038485
-
NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome
-
Hölzel, M. et al. NF1 is a tumor suppressor in neuroblastoma that determines retinoic acid response and disease outcome. Cell 142, 218-229 (2010).
-
(2010)
Cell
, vol.142
, pp. 218-229
-
-
Hölzel, M.1
-
21
-
-
31544452561
-
Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease
-
Tartaglia, M. et al. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Am. J. Hum. Genet. 78, 279-290 (2006).
-
(2006)
Am. J. Hum. Genet
, vol.78
, pp. 279-290
-
-
Tartaglia, M.1
-
22
-
-
76749166680
-
High frequency of p53/MDM2/p14ARF pathway abnormalities in relapsed neuroblastoma
-
Carr-Wilkinson, J. et al. High frequency of p53/MDM2/p14ARF pathway abnormalities in relapsed neuroblastoma. Clin. Cancer Res. 16, 1108-1118 (2010).
-
(2010)
Clin. Cancer Res
, vol.16
, pp. 1108-1118
-
-
Carr-Wilkinson, J.1
-
23
-
-
84859187259
-
Systematic identification of genomic markers of drug sensitivity in cancer cells
-
Garnett, M.J. et al. Systematic identification of genomic markers of drug sensitivity in cancer cells. Nature 483, 570-575 (2012).
-
(2012)
Nature
, vol.483
, pp. 570-575
-
-
Garnett, M.J.1
-
24
-
-
77955477995
-
Accumulation of segmental alterations determines progression in neuroblastoma
-
Schleiermacher, G. et al. Accumulation of segmental alterations determines progression in neuroblastoma. J. Clin. Oncol. 28, 3122-3130 (2010).
-
(2010)
J. Clin. Oncol
, vol.28
, pp. 3122-3130
-
-
Schleiermacher, G.1
-
25
-
-
84874102335
-
Evolution and impact of subclonal mutations in chronic lymphocytic leukemia
-
Landau, D.A. et al. Evolution and impact of subclonal mutations in chronic lymphocytic leukemia. Cell 152, 714-726 (2013).
-
(2013)
Cell
, vol.152
, pp. 714-726
-
-
Landau, D.A.1
-
26
-
-
84923341318
-
Increased MAPK reactivation in early resistance to dabrafenib/trametinib combination therapy of BRAF-mutant metastatic melanoma
-
Long, G.V. Increased MAPK reactivation in early resistance to dabrafenib/trametinib combination therapy of BRAF-mutant metastatic melanoma. Nat. Commun. 5, 5694 (2014).
-
(2014)
Nat. Commun
, vol.5
, pp. 5694
-
-
Long, G.V.1
-
27
-
-
54049120220
-
Activating mutations in ALK provide a therapeutic target in neuroblastoma
-
George, R.E. et al. Activating mutations in ALK provide a therapeutic target in neuroblastoma. Nature 455, 975-978 (2008).
-
(2008)
Nature
, vol.455
, pp. 975-978
-
-
George, R.E.1
-
28
-
-
84876966952
-
Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: A Children's Oncology Group phase 1 consortium study
-
Mossé, Y.P. et al. Safety and activity of crizotinib for paediatric patients with refractory solid tumours or anaplastic large-cell lymphoma: A Children's Oncology Group phase 1 consortium study. Lancet Oncol. 14, 472-480 (2013).
-
(2013)
Lancet Oncol
, vol.14
, pp. 472-480
-
-
Mossé, Y.P.1
-
29
-
-
84863753157
-
The ALKF1174L mutation potentiates the oncogenic activity of MYCN in neuroblastoma
-
Berry, T. et al. The ALKF1174L mutation potentiates the oncogenic activity of MYCN in neuroblastoma. Cancer Cell 22, 117-130 (2012).
-
(2012)
Cancer Cell
, vol.22
, pp. 117-130
-
-
Berry, T.1
-
30
-
-
84908011214
-
Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALK-mutated neuroblastoma
-
Moore, N.F. et al. Molecular rationale for the use of PI3K/AKT/mTOR pathway inhibitors in combination with crizotinib in ALK-mutated neuroblastoma. Oncotarget 5, 8737-8749 (2014).
-
(2014)
Oncotarget
, vol.5
, pp. 8737-8749
-
-
Moore, N.F.1
-
31
-
-
74949138753
-
Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays
-
Drmanac, R. et al. Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays. Science 327, 78-81 (2010).
-
(2010)
Science
, vol.327
, pp. 78-81
-
-
Drmanac, R.1
-
32
-
-
84922572688
-
Sequenza: Allele-specific copy number and mutation profiles from tumor sequencing data
-
Favero, F. et al. Sequenza: Allele-specific copy number and mutation profiles from tumor sequencing data. Ann. Oncol. 26, 64-70 (2015).
-
(2015)
Ann. Oncol
, vol.26
, pp. 64-70
-
-
Favero, F.1
-
33
-
-
69649109364
-
Circos: An information aesthetic for comparative genomics
-
Krzywinski, M. et al. Circos: An information aesthetic for comparative genomics. Genome Res. 19, 1639-1645 (2009).
-
(2009)
Genome Res
, vol.19
, pp. 1639-1645
-
-
Krzywinski, M.1
-
34
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li, H. & Durbin, R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25, 1754-1760 (2009).
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
35
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna, A. et al. The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20, 1297-1303 (2010).
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
-
36
-
-
84874025843
-
Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples
-
Cibulskis, K. et al. Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. Nat. Biotechnol. 31, 213-219 (2013).
-
(2013)
Nat. Biotechnol
, vol.31
, pp. 213-219
-
-
Cibulskis, K.1
-
37
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang, K., Li, M. & Hakonarson, H. ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 38, e164 (2010).
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
38
-
-
84975795680
-
An integrated map of genetic variation from 1, 092 human genomes
-
1000 Genomes Project Consortium.
-
1000 Genomes Project Consortium. An integrated map of genetic variation from 1, 092 human genomes. Nature 491, 56-65 (2012).
-
(2012)
Nature
, vol.491
, pp. 56-65
-
-
-
39
-
-
84866440781
-
DELLY: Structural variant discovery by integrated paired-end and split-read analysis
-
Rausch, T. et al. DELLY: Structural variant discovery by integrated paired-end and split-read analysis. Bioinformatics 28, i333-i339 (2012).
-
(2012)
Bioinformatics
, vol.28
, pp. i333-i339
-
-
Rausch, T.1
-
40
-
-
84860782006
-
Absolute quantification of somatic DNA alterations in human cancer
-
Carter, S.L. et al. Absolute quantification of somatic DNA alterations in human cancer. Nat. Biotechnol. 30, 413-421 (2012).
-
(2012)
Nat. Biotechnol
, vol.30
, pp. 413-421
-
-
Carter, S.L.1
-
41
-
-
84897954204
-
PyClone: Statistical inference of clonal population structure in cancer
-
Roth, A. et al. PyClone: Statistical inference of clonal population structure in cancer. Nat. Methods 11, 396-398 (2014).
-
(2014)
Nat. Methods
, vol.11
, pp. 396-398
-
-
Roth, A.1
-
42
-
-
84858707750
-
Targeted BIRC5 silencing using YM155 causes cell death in neuroblastoma cells with low ABCB1 expression
-
Lamers, F. et al. Targeted BIRC5 silencing using YM155 causes cell death in neuroblastoma cells with low ABCB1 expression. Eur. J. Cancer 48, 763-771 (2012).
-
(2012)
Eur. J. Cancer
, vol.48
, pp. 763-771
-
-
Lamers, F.1
-
43
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
Gnirke, A. et al. Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nat. Biotechnol. 27, 182-189 (2009).
-
(2009)
Nat. Biotechnol
, vol.27
, pp. 182-189
-
-
Gnirke, A.1
|