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Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers

Data up to Jan 2025

Published2008
Citations304
References44

Total Citations Per Year

Abstract

References (44)

Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles

2005 • 44,461 citations

Human Breast Cancer: Correlation of Relapse and Survival with Amplification of the HER-2/ neu Oncogene

1987 • 11,429 citations

PTEN , a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate Cancer

1997 • 4,753 citations

Cancer genes and the pathways they control

2004 • 4,172 citations

The Consensus Coding Sequences of Human Breast and Colorectal Cancers

2006 • 3,040 citations

Patterns of somatic mutation in human cancer genomes

2007 • 2,975 citations

A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types

1994 • 2,821 citations

Identification of a candidate tumour suppressor gene, MMAC1, at chromosome 10q23.3 that is mutated in multiple advanced cancers

1997 • 2,746 citations

The Genomic Landscapes of Human Breast and Colorectal Cancers

2007 • 2,716 citations

Large-Scale Copy Number Polymorphism in the Human Genome

2004 • 2,542 citations

DPC4 , A Candidate Tumor Suppressor Gene at Human Chromosome 18q21.1

1996 • 2,320 citations

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

2007 • 1,760 citations

Characterizing the cancer genome in lung adenocarcinoma

2007 • 1,110 citations

Comparative lesion sequencing provides insights into tumor evolution

2008 • 791 citations

Role of the p16 tumor suppressor gene in cancer.

1998 • 710 citations

A high-resolution survey of deletion polymorphism in the human genome

2005 • 664 citations

Frequency of homozygous deletion at p16/CDKN2 in primary human tumours

1995 • 653 citations

Diabetes and obesity: the twin epidemics

2006 • 641 citations

Amplification of endogenous myc-related DNA sequences in a human myeloid leukaemia cell line

1982 • 630 citations

Array comparative genomic hybridization and its applications in cancer

2005 • 583 citations

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

2006 • 512 citations

Whole-genome genotyping with the single-base extension assay

2005 • 362 citations

Homozygous Deletions and Chromosome Amplifications in Human Lung Carcinomas Revealed by Single Nucleotide Polymorphism Array Analysis

2005 • 340 citations

Pathway Mapping Tools for Analysis of High Content Data

2006 • 257 citations

Topoisomerase IIα Gene Amplification Predicts Favorable Treatment Response to Tailored and Dose-Escalated Anthracycline-Based Adjuvant Chemotherapy in HER-2/neu–Amplified Breast Cancer: Scandinavian Breast Group Trial 9401

2006 • 247 citations

Genome-Wide Loss of Heterozygosity and Copy Number Analysis in Melanoma Using High-Density Single-Nucleotide Polymorphism Arrays

2007 • 228 citations

Digital karyotyping

2002 • 219 citations

Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution

2007 • 197 citations

Three Classes of Genes Mutated In Colorectal Cancers with Chromosomal Instability

2004 • 189 citations

Mapping the Cancer Genome

2007 • 188 citations

Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies.

2007 • 174 citations

Amplification and overexpression of topoisomerase IIalpha predict response to anthracycline-based therapy in locally advanced breast cancer.

2002 • 174 citations

Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays

2007 • 154 citations

High‐resolution genomic and expression analyses of copy number alterations in breast tumors

2008 • 151 citations

PCDH8, the human homolog of PAPC, is a candidate tumor suppressor of breast cancer

2008 • 131 citations

End-sequence profiling: Sequence-based analysis of aberrant genomes

2003 • 116 citations

Genetic alterations in cancer as a result of breakage at fragile sites

2003 • 99 citations

Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome

2008 • 85 citations

Homozygous deletion scanning of the lung cancer genome at a 100‐kb resolution

2007 • 61 citations

Emerging DNA sequencing technologies for human genomic medicine

2008 • 60 citations

The Power of Riboswitches

2007 • 51 citations

Mutational analysis of gene families in human cancer

2004 • 49 citations

Targeting the absence: Homozygous DNA deletions as immutable signposts for cancer therapy

2007 • 37 citations

Digital karyotyping

2007 • 23 citations

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Integrated analysis of homozygous deletions, focal amplifications, and sequence… (2008) – Proceedings of the National Academy of Sciences | Metascience Observatory Explorer