Correlation between genetic alteration and long‐term clinical outcome of patients with oligodendroglial tumors, with identification of a consistent region of deletion on chromosome arm 1p

The 1993–94 Généthon human genetic linkage map

1994 • 1,870 citations

Specific Genetic Predictors of Chemotherapeutic Response and Survival in Patients With Anaplastic Oligodendrogliomas

1998 • 1,611 citations

Alterations of Chromosome Arms 1p and 19q as Predictors of Survival in Oligodendrogliomas, Astrocytomas, and Mixed Oligoastrocytomas

2000 • 800 citations

Molecular genetic analysis of oligodendroglial tumors shows preferential allelic deletions on 19q and 1p.

1994 • 595 citations

Cloning of human satellite III DNA: different components are on different chromosomes

1979 • 470 citations

Molecular subtypes of anaplastic oligodendroglioma: implications for patient management at diagnosis.

2001 • 427 citations

Localization of common deletion regions on 1p and 19q in human gliomas and their association with histological subtype

1999 • 380 citations

Shared Allelic Losses on Chromosomes 1p and 19q Suggest a Common Origin of Oligodendroglioma and Oligoastrocytoma

1995 • 348 citations

Successful chemotherapy for recurrent malignant oligodendroglioma

1988 • 346 citations

Molecular Genetic Aspects of Oligodendrogliomas Including Analysis by Comparative Genomic Hybridization

1999 • 274 citations

Frequent replication errors at microsatellite loci in tumors of patients with multiple primary cancers.

1994 • 246 citations

Evidence for a tumor suppressor gene on chromosome 19q associated with human astrocytomas, oligodendrogliomas, and mixed gliomas.

1992 • 212 citations

Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism

1992 • 209 citations

Infrequent p53 gene mutations in medulloblastomas.

1991 • 192 citations

Detection of 1p and 19q Loss in Oligodendroglioma by Quantitative Microsatellite Analysis, a Real-Time Quantitative Polymerase Chain Reaction Assay

2001 • 172 citations

Allelic loss at 1p and 19q frequently occurs in association and may represent early oncogenic events in oligodendroglial tumors

1995 • 164 citations

Pathology and Genetics of Tumours of the Nervous System (World Health Organization Classification of Tumours).

2001 • 151 citations

Histopathological-Molecular Genetic Correlations in Referral Pathologist-Diagnosed Low-Grade “Oligodendroglioma”

2002 • 145 citations

Correlation of histology and molecular genetic analysis of 1p, 19q, 10q, TP53, EGFR, CDK4, and CDKN2A in 91 astrocytic and oligodendroglial tumors.

2002 • 143 citations

Successful chemotherapy for newly diagnosed aggressive oligodendroglioma

1990 • 136 citations

Molecular analysis of chromosomh 1 abnormalities in human gliomas reveals frequent loss of 1p in oligodendroglial tumors

1994 • 136 citations

Multiple Signals Mediate Proliferation, Differentiation, and Survival from the Granulocyte Colony-stimulating Factor Receptor in Myeloid 32D Cells

1999 • 126 citations

Concurrent Hypermethylation of Multiple Genes Is Associated with Grade of Oligodendroglial Tumors

2001 • 122 citations

Concurrent Inactivation of RB1 and TP53 Pathways in Anaplastic Oligodendrogliomas

2001 • 102 citations

Evidence for the involvement of a potential second tumor suppressor gene on chromosome 17 distinct from p53 in malignant astrocytomas.

1992 • 94 citations

Deletion mapping defines different regions in 1p34.2-pter that may harbor genetic information related to human colorectal cancer.

1995 • 90 citations

Analysis of numerical aberrations in specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer

1996 • 89 citations

Mapping of the chromosome 19 q‐arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers

2000 • 85 citations

Identification of Two Distinct Deleted Regions on the Short Arm of Chromosome 1 and Rare Mutation of theCDKN2CGene from 1p32 in Oligodendroglial Tumors

1999 • 85 citations

High-Resolution Analysis of Chromosome Arm 1p Alterations in Meningioma

2000 • 83 citations

Loss of material from chromosome arm 1p during malignant progression of meningioma revealed by fluorescent in Situ hybridization

1998 • 73 citations

Transcriptional inactivation of TP73 expression in oligodendroglial tumors

2002 • 62 citations

Chromosomal imbalances in primary oligodendroglial tumors and their recurrences: clues about malignant progression detected using comparative genomic hybridization

2002 • 48 citations

Human Eukaryotic Initiation Factor EIF2C1 Gene: cDNA Sequence, Genomic Organization, Localization to Chromosomal Bands 1p34–p35, and Expression

1999 • 48 citations

Mutation analysis of the p73 gene in nonastrocytic brain tumours

2001 • 41 citations

A consistent region of deletion on 1p36 in meningiomas

2003 • 41 citations

Frequent deletions of material from chromosome arm 1p in oligodendroglial tumors revealed by double‐target fluorescence in situ hybridization and microsatellite analysis

1995 • 37 citations

PTB-associated splicing factor regulates growth factor-stimulated gene expression in mammalian cells

2002 • 29 citations

Mapping of the chromosome 19 q-arm glioma tumor suppressor gene using fluorescence in situ hybridization and novel microsatellite markers

2000 • 28 citations

Prognostic relevance of TP53 mutations, p53 protein, Ki-67 index and conventional histological grading in oligodendrogliomas.

1999 • 26 citations

High-resolution cytogenetic mapping of the short arm of chromosome 1 with newly isolated 411 cosmid markers by fluorescence in situ hybridization: the precise order of 18 markers on 1p36.1 on prophase chromosomes and “stretched” DNAs

1995 • 25 citations

The DNA-Binding and Transcriptional Activities of MAZ, a Myc-Associated Zinc Finger Protein, Are Regulated by Casein Kinase II

1999 • 22 citations

Structural organization and expression of the mouse gene for Pur‐1, a highly conserved homolog of the human MAZ gene

1999 • 16 citations

The p73 gene is not mutated in oligodendrogliomas which frequently have a deleted region at chromosome 1p36.3.

2000 • 12 citations