Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma.
|
Nature
|
2012
|
10.99
|
2
|
Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer.
|
Nat Genet
|
2009
|
10.21
|
3
|
Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma.
|
Cancer Cell
|
2012
|
6.71
|
4
|
Tandem duplication producing a novel oncogenic BRAF fusion gene defines the majority of pilocytic astrocytomas.
|
Cancer Res
|
2008
|
6.44
|
5
|
Intratumor heterogeneity in human glioblastoma reflects cancer evolutionary dynamics.
|
Proc Natl Acad Sci U S A
|
2013
|
5.68
|
6
|
Dissecting the genomic complexity underlying medulloblastoma.
|
Nature
|
2012
|
4.77
|
7
|
Feedback circuit among INK4 tumor suppressors constrains human glioblastoma development.
|
Cancer Cell
|
2008
|
4.71
|
8
|
IDH1 mutations are present in the majority of common adult gliomas but rare in primary glioblastomas.
|
Neuro Oncol
|
2009
|
3.99
|
9
|
Molecular subgroups of medulloblastoma: an international meta-analysis of transcriptome, genetic aberrations, and clinical data of WNT, SHH, Group 3, and Group 4 medulloblastomas.
|
Acta Neuropathol
|
2012
|
3.88
|
10
|
International Society Of Neuropathology--Haarlem consensus guidelines for nervous system tumor classification and grading.
|
Brain Pathol
|
2014
|
3.21
|
11
|
Clonal selection drives genetic divergence of metastatic medulloblastoma.
|
Nature
|
2012
|
2.96
|
12
|
The eEF2 kinase confers resistance to nutrient deprivation by blocking translation elongation.
|
Cell
|
2013
|
2.74
|
13
|
Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas.
|
Cancer Cell
|
2013
|
2.50
|
14
|
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma.
|
Nat Genet
|
2013
|
2.42
|
15
|
Frequent amplification of a chr19q13.41 microRNA polycistron in aggressive primitive neuroectodermal brain tumors.
|
Cancer Cell
|
2009
|
1.92
|
16
|
Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.
|
Acta Neuropathol
|
2011
|
1.90
|
17
|
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
|
Hum Mol Genet
|
2002
|
1.69
|
18
|
Temozolomide versus procarbazine, lomustine, and vincristine in recurrent high-grade glioma.
|
J Clin Oncol
|
2010
|
1.58
|
19
|
Genomic analysis of pilocytic astrocytomas at 0.97 Mb resolution shows an increasing tendency toward chromosomal copy number change with age.
|
J Neuropathol Exp Neurol
|
2006
|
1.54
|
20
|
Upregulating mutations in the TERT promoter commonly occur in adult malignant gliomas and are strongly associated with total 1p19q loss.
|
Acta Neuropathol
|
2013
|
1.53
|
21
|
Replication timing of human chromosome 6.
|
Cell Cycle
|
2005
|
1.52
|
22
|
Frequent promoter hypermethylation and low expression of the MGMT gene in oligodendroglial tumors.
|
Int J Cancer
|
2005
|
1.48
|
23
|
Panel review of anaplastic oligodendroglioma from European Organization For Research and Treatment of Cancer Trial 26951: assessment of consensus in diagnosis, influence of 1p/19q loss, and correlations with outcome.
|
J Neuropathol Exp Neurol
|
2007
|
1.42
|
24
|
Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGH.
|
Oncogene
|
2006
|
1.40
|
25
|
Differential expression of selected histone modifier genes in human solid cancers.
|
BMC Genomics
|
2006
|
1.39
|
26
|
Genetic aberrations leading to MAPK pathway activation mediate oncogene-induced senescence in sporadic pilocytic astrocytomas.
|
Clin Cancer Res
|
2011
|
1.35
|
27
|
Application of array CGH on archival formalin-fixed paraffin-embedded tissues including small numbers of microdissected cells.
|
Lab Invest
|
2006
|
1.35
|
28
|
Genomic profiling identifies discrete deletions associated with translocations in glioblastoma multiforme.
|
Cell Cycle
|
2006
|
1.34
|
29
|
Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis.
|
Genes Chromosomes Cancer
|
2005
|
1.31
|
30
|
Issues of diagnostic review in brain tumor studies: from the Brain Tumor Epidemiology Consortium.
|
Cancer Epidemiol Biomarkers Prev
|
2008
|
1.25
|
31
|
Molecular pathogenesis of astrocytic tumours.
|
J Neurooncol
|
2004
|
1.24
|
32
|
Improved grading and survival prediction of human astrocytic brain tumors by artificial neural network analysis of gene expression microarray data.
|
Mol Cancer Ther
|
2008
|
1.20
|
33
|
Secretory meningiomas are defined by combined KLF4 K409Q and TRAF7 mutations.
|
Acta Neuropathol
|
2013
|
1.15
|
34
|
Clinical significance of EGFR amplification and the aberrant EGFRvIII transcript in conventionally treated astrocytic gliomas.
|
J Mol Med (Berl)
|
2005
|
1.14
|
35
|
LIN28A immunoreactivity is a potent diagnostic marker of embryonal tumor with multilayered rosettes (ETMR).
|
Acta Neuropathol
|
2012
|
1.12
|
36
|
Differential expression and methylation of brain developmental genes define location-specific subsets of pilocytic astrocytoma.
|
Acta Neuropathol
|
2013
|
1.08
|
37
|
AKT1E17K mutations cluster with meningothelial and transitional meningiomas and can be detected by SFRP1 immunohistochemistry.
|
Acta Neuropathol
|
2013
|
1.03
|
38
|
Short postoperative survival for glioblastoma patients with a dysfunctional Rb1 pathway in combination with no wild-type PTEN.
|
Clin Cancer Res
|
2003
|
1.02
|
39
|
MMASS: an optimized array-based method for assessing CpG island methylation.
|
Nucleic Acids Res
|
2006
|
1.00
|
40
|
Characterization of 6q deletions in mature B cell lymphomas and childhood acute lymphoblastic leukemia.
|
Leuk Lymphoma
|
2008
|
0.97
|
41
|
MGMT CpG island is invariably methylated in adult astrocytic and oligodendroglial tumors with IDH1 or IDH2 mutations.
|
Int J Cancer
|
2012
|
0.97
|
42
|
Adult grade II diffuse astrocytomas are genetically distinct from and more aggressive than their paediatric counterparts.
|
Acta Neuropathol
|
2011
|
0.96
|
43
|
Expression of the coxsackie and adenovirus receptor in human astrocytic tumors and xenografts.
|
Int J Cancer
|
2003
|
0.95
|
44
|
High-resolution array-based comparative genomic hybridization of bladder cancers identifies mouse double minute 4 (MDM4) as an amplification target exclusive of MDM2 and TP53.
|
Clin Cancer Res
|
2008
|
0.93
|
45
|
NG2 expression in glioblastoma identifies an actively proliferating population with an aggressive molecular signature.
|
Neuro Oncol
|
2011
|
0.92
|
46
|
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas.
|
Hum Genet
|
2005
|
0.88
|
47
|
BRAF alterations are frequent in cerebellar low-grade astrocytomas with diffuse growth pattern.
|
J Neuropathol Exp Neurol
|
2012
|
0.87
|
48
|
Detailed assessment of copy number alterations revealing homozygous deletions in 1p and 13q in mantle cell lymphoma.
|
Leuk Res
|
2006
|
0.87
|
49
|
Genome-wide analysis of subependymomas shows underlying chromosomal copy number changes involving chromosomes 6, 7, 8 and 14 in a proportion of cases.
|
Brain Pathol
|
2008
|
0.87
|
50
|
Absence of KIAA1549-BRAF fusion in rosette-forming glioneuronal tumors of the fourth ventricle (RGNT).
|
J Neurooncol
|
2012
|
0.87
|
51
|
Distinct patterns of 1p and 19q alterations identify subtypes of human gliomas that have different prognoses.
|
Neuro Oncol
|
2010
|
0.86
|
52
|
Molecular profiling of long-term survivors identifies a subgroup of glioblastoma characterized by chromosome 19/20 co-gain.
|
Acta Neuropathol
|
2015
|
0.86
|
53
|
Amplification of 2p as a genomic marker for transformation in lymphoma.
|
Genes Chromosomes Cancer
|
2014
|
0.83
|
54
|
Chromosome 17 alterations identify good-risk and poor-risk tumors independently of clinical factors in medulloblastoma.
|
Neuro Oncol
|
2011
|
0.82
|
55
|
Allelic gain and amplification on the long arm of chromosome 17 in anaplastic meningiomas.
|
Brain Pathol
|
2002
|
0.82
|
56
|
High-resolution profiling of an 11 Mb segment of human chromosome 22 in sporadic schwannoma using array-CGH.
|
Int J Oncol
|
2003
|
0.80
|
57
|
Novel mechanisms of gene disruption at the medulloblastoma isodicentric 17p11 breakpoint.
|
Genes Chromosomes Cancer
|
2009
|
0.79
|
58
|
Internalisation and retention of EGF-dextran associated radioactivity in transfected Chinese hamster ovary cells expressing the human EGF-receptor.
|
Int J Oncol
|
2002
|
0.78
|