Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing

Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer

2007 • 5,137 citations

Recurrent Fusion of TMPRSS2 and ETS Transcription Factor Genes in Prostate Cancer

2005 • 3,714 citations

A census of human cancer genes

2004 • 3,190 citations

Patterns of somatic mutation in human cancer genomes

2007 • 2,975 citations

Alu repeats and human genomic diversity

2002 • 1,436 citations

Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome

2007 • 1,150 citations

SSAHA: A Fast Search Method for Large DNA Databases

2001 • 972 citations

A faster circular binary segmentation algorithm for the analysis of array CGH data

2007 • 937 citations

Distinct classes of chromosomal rearrangements create oncogenic ETS gene fusions in prostate cancer

2007 • 829 citations

Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer

2004 • 358 citations

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

2007 • 197 citations

Variant (6;15) translocations in murine plasmacytomas involve a chromosome 15 locus at least 72 kb from the c-myc oncogene.

1985 • 180 citations

Mechanisms of eukaryotic DNA double strand break repair

2006 • 132 citations

Mll partial tandem duplication induces aberrant Hox expression in vivo via specific epigenetic alterations

2006 • 122 citations

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

2003 • 116 citations

The MLL partial tandem duplication in acute myeloid leukaemia

2006 • 102 citations

Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs)

2007 • 96 citations

17q23 amplifications in breast cancer involve the PAT1, RAD51C, PS6K, and SIGma1B genes.

2000 • 94 citations

Characterization of a conserved aphidicolin-sensitive common fragile site at human 4q22 and mouse 6C1: possible association with an inherited disease and cancer

2004 • 93 citations

Array painting reveals a high frequency of balanced translocations in breast cancer cell lines that break in cancer-relevant genes

2007 • 65 citations

NCI series of cell lines: An historical perspective

1996 • 53 citations

Chromosome abnormalities in 10 lung cancer cell lines of the NCI-H series analyzed with spectral karyotyping

2005 • 35 citations

Chimeric transcripts with an open reading frame are generated as a result of translocation to the Pvt‐1 region in mouse B‐cell tumors

1994 • 20 citations

Two reciprocal translocations provide new clues to the high mutability of the Grid2 locus

2005 • 11 citations