Richard Segraves
Lawrence Berkeley National Laboratory(US)University of California, San Francisco(US)GlaxoSmithKline (United States)(US)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Chromosomal and Genetic Variations, Gene expression and cancer classification, Prenatal Screening and Diagnostics, Congenital heart defects research
Most-Cited Works
- → High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays(1998)2,247 cited
- → Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.(1988)1,339 cited
- → Assembly of microarrays for genome-wide measurement of DNA copy number(2001)1,002 cited
- → Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene(2000)597 cited
- → Fully Automatic Quantification of Microarray Image Data(2002)343 cited
- → Breast tumor copy number aberration phenotypes and genomic instability(2006)294 cited