Histology and Molecular Pathology of Pediatric Brain Tumors

Outcome Prediction in Pediatric Medulloblastoma Based on DNA Copy-Number Aberrations of Chromosomes 6q and 17q and theMYCandMYCNLoci

(2009) Stefan Pfister et al.   JOURNAL OF CLINICAL ONCOLOGY

Investigation of chromosome 1q reveals differential expression of members of the S100 family in clinical subgroups of intracranial paediatric ependymoma

(2008) V Rand et al.   BRITISH JOURNAL OF CANCER

Telomere maintenance and dysfunction predict recurrence in paediatric ependymoma

(2008) U Tabori et al.   BRITISH JOURNAL OF CANCER

Correlation between 6q25.3 deletion status and survival in pediatric intracranial ependymomas

(2008) Camelia-Maria Monoranu et al.   CANCER GENETICS AND CYTOGENETICS

Tandem Duplication Producing a Novel OncogenicBRAFFusion Gene Defines the Majority of Pilocytic Astrocytomas

(2008) David T.W. Jones et al.   CANCER RESEARCH

Stepwise accumulation of distinct genomic aberrations in a patient with progressively metastasizing ependymoma

(2008) Till Milde et al.   GENES CHROMOSOMES & CANCER

BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas

(2008) Stefan Pfister et al.   JOURNAL OF CLINICAL INVESTIGATION

Frequent Gains at Chromosome 7q34 Involving BRAF in Pilocytic Astrocytoma

(2008) Eli E. Bar et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Stat Bite: Childhood Cancer Deaths by Site, 2004

(2008)   JNCI-Journal of the National Cancer Institute

Biological background of pediatric medulloblastoma and ependymoma: A review from a translational research perspective

(2008) Judith M. de Bont et al.   NEURO-ONCOLOGY

Multifactorial analysis of predictors of outcome in pediatric intracranial ependymoma

(2008) Lee Ridley et al.   NEURO-ONCOLOGY

High-resolution, dual-platform aCGH analysis reveals frequent HIPK2 amplification and increased expression in pilocytic astrocytomas

(2008) H Deshmukh et al.   ONCOGENE

Integrated Genomics Identifies Five Medulloblastoma Subtypes with Distinct Genetic Profiles, Pathway Signatures and Clinicopathological Features

(2008) Marcel Kool et al.   PLoS One