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Manuel L. Gonzalez-Garay

Researcher at University of Arizona

Publications -  47
Citations -  14617

Manuel L. Gonzalez-Garay is an academic researcher from University of Arizona. The author has contributed to research in topics: Gene & Chinese hamster ovary cell. The author has an hindex of 23, co-authored 46 publications receiving 13374 citations. Previous affiliations of Manuel L. Gonzalez-Garay include University of Texas at Austin & Universidad Autónoma de Nuevo León.

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Comprehensive genomic characterization defines human glioblastoma genes and core pathways

Roger E. McLendon, +233 more
- 23 Oct 2008 - 
TL;DR: The interim integrative analysis of DNA copy number, gene expression and DNA methylation aberrations in 206 glioblastomas reveals a link between MGMT promoter methylation and a hypermutator phenotype consequent to mismatch repair deficiency in treated gliobeasts, demonstrating that it can rapidly expand knowledge of the molecular basis of cancer.
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Somatic mutations affect key pathways in lung adenocarcinoma

Li Ding, +96 more
- 23 Oct 2008 - 
TL;DR: Somatic mutations in primary lung adenocarcinoma for several tumour suppressor genes involved in other cancers and for sequence changes in PTPRD as well as the frequently deleted gene LRP1B are found.
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Genome sequence of the Brown Norway rat yields insights into mammalian evolution

Richard A. Gibbs, +242 more
- 01 Apr 2004 - 
TL;DR: This first comprehensive analysis of the genome sequence of the Brown Norway (BN) rat strain is reported, which is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution.
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The genome of the sea urchin Strongylocentrotus purpuratus.

Erica Sodergren, +246 more
- 10 Nov 2006 - 
TL;DR: The sequence and analysis of the 814-megabase genome of the sea urchin Strongylocentrotus purpuratus is reported, a model for developmental and systems biology and yields insights into the evolution of deuterostomes.
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An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.

Catherine A. Brownstein, +210 more
- 25 Mar 2014 - 
TL;DR: The CLARITY Challenge provides a comprehensive assessment of current practices for using genome sequencing to diagnose and report genetic diseases and reveals a general convergence of practices on most elements of the analysis and interpretation process.