Key Documents
Ronald Davis
- Professor, Biochemistry
- Professor, Genetics
- Member, Bio-X
- Member, Cancer Center
Contact Information
- Academic Offices
Personal Information Email dbowe@stanford.edu
Honors and Awards
- Recipient of, Dickson Prize in Medicine, University of Pittsburgh (2005-2004)
- Lifetime Achievement Award, Genetics Society of America (2004)
- Herbert A. Sober Award, ASBMB/IUBMB (2004)
- Senior Scholar Award in Global Infectious Disease, Ellison Medical Foundation (2002)
- Genetics Society of America Award, Genetics Society of America (1998)
- Biotechnology Research Award, Chiron Corporation (1998)
- Louis S. Rosentiel Award for, Distinguished Work in Basic Medical Research (1992)
- Distinguished Alumni Award, Eastern Illinois University (1984)
- Elected to the, National Academy of Sciences-Genetics (1983)
- Recipient of, United States Steel Award (1981)
- Chaired, Nucleic Acid Gordon Conference (1980)
- Award in Microbiology and Immunology, Eli Lilly and Co. (1976)
- Young Faculty Research Award, Society of the Sigma Xi (1976)
- Teacher-Scholar Grant, Dreyfus (1976)
- EMBO, European Lectureship (1976)
Postdoctoral Advisees
Web Site Links
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industry partners. It is our policy to disclose payments of $5,000 or more, equity valued at $5,000 or more in a publicly traded company, or any equity in a privately held company, to physicians and scientists employed by Stanford University from companies or other commercial entities with which they interact as part of their professional activities.
- Consulting: Affymetrix, CellPoint
- Equity: Affymetrix, CellPoint
Research Interests
We are using Saccharomyces cerevisiae and Human to conduct whole genome analysis projects. The yeast genome sequence has approximately 6,000 genes. We have made a set of haploid and diploid strains (21,000) containing a complete deletion of each gene. In order to facilitate whole genome analysis each deletion is molecularly tagged with a unique 20-mer DNA sequence. This sequence acts as a molecular bar code and makes it easy to identify the presence of each deletion. The mixture of all such tag strains then allows for the analysis of the entire genome with the manipulation of a single culture. During growth under a variety of conditions the loss of a tag indicates the loss of a deletion from the population. The concentration of each tag is determined by PCR amplification of the tags and hybridization to an Affymetrix DNA chip that contains the complement to all of the DNA sequence tags. This approach is being applied to other microorganisms.
We have identified a number of wild isolates of yeast that grow at much higher temperatures than is typical for Saccharomyces cerevisiae and are pathogenic and can kill a mouse. Microarrays have been used to map complex genetic traits such as virulence traits in pathogenic Saccharomyces cerevisiae using hybridization to detect single nucleotide polymorphisms. We have developed a new technology termed Recipical Hemizygosity Scanning that allows the determination of the contribution to the phenotype of all pair wise alleles for the whole genome from 2 independent strains. Using this technology we can map and quantitate all of the alleles in the genome for any complex quantitative trait in a single tube assay. These technologies will allow us to explore allelic contributions in complex mixed culture real environments and to investigate ecology at the genome level.
We are conducting a whole genome analysis (transcriptome and proteome) from blood of Human trauma patients. In this large clinical study we are establishing the standards for clinical genomics. We have developed 2 new technologies, "Molecular Inversion Probes" (MIP) for massive multiplex analysis of SNP and DNA content in Human and, "Mismatch Repair Detection" for discovery of rare Human polymorphisms. Both technologies are being applied to numerous clinical investigations.
Publications
- PLoS Genet. 2009; (10): e1000685
- PLoS Genet. 2009; (6): e1000515
- Hum Mutat. 2009; (2): 228-38
- J Proteome Res. 2009; (1): 290-9
- Genetics. 2009; (1): 185-94
- PLoS Comput Biol. 2009; (4): e1000374
- Genome Res. 2009; (5): 757-69
- Lab Chip. 2009; (10): 1429-34
- Biotechnol Bioeng. 2008; (1): 19-27
- Physiol Genomics. 2008; (2): 190-7
- Clin Chem. 2008; (3): 582-9
- Methods Mol Biol. 2008; 205-20
- Science. 2008; (5874): 362-5
- Proc Natl Acad Sci U S A. 2008; (27): 9296-301
- PLoS Genet. 2008; (7): e1000113
- Nat Chem Biol. 2008; (8): 498-506
- Proc Natl Acad Sci U S A. 2008; (39): 15166-71
- Sens Actuators B Chem. 2008; (1): 79-86
- PLoS One. 2008; (7): e2817
- Proc Natl Acad Sci U S A. 2007; (22): 9387-92
- J Org Chem. 2007; (26): 9875-80
- Nat Protoc. 2007; (11): 2958-74
- PLoS One. 2007; (9): e915
- Cell. 2007; (1): 121-35
- Nat Genet. 2007; (10): 1235-44
- Nat Genet. 2007; (9): 1092-9
- Nat Methods. 2007; (4): 327-9
- Proc Natl Acad Sci U S A. 2007; (15): 6146-51
- PLoS One. 2007; (2): e223
- Nucleic Acids Res. 2007; (7): e47
- J Nat Prod. 2007; (3): 383-90
- Proc Natl Acad Sci U S A. 2007; (5): 1522-7
- Nat Genet. 2007; (2): 199-206
- Proc Natl Acad Sci U S A. 2006; (40): 14773-8
- BMC Bioinformatics. 2006; 500
- Conf Proc IEEE Eng Med Biol Soc. 2006; 1838-41
- Conf Proc IEEE Eng Med Biol Soc. 2006; 1830-3
- PLoS One. 2006; e95
- Genetics. 2006; (1): 511-8
- Proc Natl Acad Sci U S A. 2006; (17): 6466-70
- Proc Natl Acad Sci U S A. 2006; (14): 5320-5
- J Mol Diagn. 2006; (1): 119-27
- Nano Lett. 2006; (11): 2486-92
- Nat Methods. 2006; (8): 601-3
- Cancer Res. 2006; (16): 7910-9
- PLoS Genet. 2006; (7): e115
- Nat Biotechnol. 2006; (9): 1112-3
- Biochem Biophys Res Commun. 2006; (2): 689-96
- Genetics. 2005; (4): 1915-25
- Mol Cell Proteomics. 2005; (5): 700-9
- Proc Natl Acad Sci U S A. 2005; (41): 14717-22
- PLoS Genet. 2005; (2): e24
- Nano Lett. 2005; (2): 403-7
- J Forensic Sci. 2005; (5): 1109-13
- Proc Natl Acad Sci U S A. 2005; (22): 7952-7
- Biophys Chem. 2005; (3): 175-85
- Proc Natl Acad Sci U S A. 2005; (4): 1092-7
- Nat Genet. 2005; (12): 1333-40
- Proc Natl Acad Sci U S A. 2004; (30): 11046-51
- Proc Natl Acad Sci U S A. 2004; (19): 7329-34
- Dev Cell. 2004; (1): 133-44
- Proc Natl Acad Sci U S A. 2004; (3): 793-8
- Nucleic Acids Res. 2004; (21): e166
- PLoS Biol. 2004; (12): e427
- Nat Biotechnol. 2003; (6): 673-8
- Cancer Res. 2003; (12): 3325-33
- Hum Mutat. 2003; (3): 214-21
- J Virol Methods. 2003; (2): 171-6
- Nature. 2002; (6896): 387-91
- Nat Genet. 2002; (4): 400-4
- Proc Natl Acad Sci U S A. 2002; (13): 8778-83
- Science. 2002; (5590): 2270-5
- Nature. 2002; (6906): 534-7
- Biotechniques. 2002; (4): 788, 790, 792 passim
- Proc Natl Acad Sci U S A. 2002; (24): 15530-5
- Nucleic Acids Res. 2002; (7): e31
- BMC Genet. 2002; 2
- Nature. 2002; (6878): 326-30
- Proc Natl Acad Sci U S A. 2001; (22): 12608-13
- Proc Natl Acad Sci U S A. 2001; (17): 9883-8
- Am J Hum Genet. 2001; (2): 396-412
- Nat Genet. 2001; (1): 48-54
- Nucleic Acids Res. 2000; (1): 102-3
- Proc Natl Acad Sci U S A. 2000; (26): 14433-7
- Novartis Found Symp. 2000; 105-9; discussion 109-11
- Proc Natl Acad Sci U S A. 2000; (13): 7354-9
- Nat Genet. 2000; (3): 358-61
- Biotechnol Genet Eng Rev. 2000; 109-46
- Parasitology. 1999; S73-80
- Nat Genet. 1999; (2): 203-7
- Science. 1999; (5429): 901-6
- Methods Enzymol. 1999; 3-18
- Genome Res. 1999; (5): 457-62
- Nat Genet. 1999; (4): 385-9
- Proc Natl Acad Sci U S A. 1999; (1): 61-6
- Nature. 1999; (6723): 152-6
- Nat Genet. 1999; (3): 278-83
- J Mol Biol. 1999; (2): 437-45
- J Mol Biol. 1999; (2): 417-35
- J Nucl Med. 1999; (1): 184-91
- Proc Natl Acad Sci U S A. 1999; (7): 3796-800
- Genome Res. 1998; (8): 848-55
- Science. 1998; (5380): 1194-7
- Proc Natl Acad Sci U S A. 1998; (7): 3752-7
- Trends Biotechnol. 1998; (7): 301-6
- Mol Cell. 1998; (1): 65-73
- Curr Opin Genet Dev. 1997; (6): 771-6
- Proc Natl Acad Sci U S A. 1997; (24): 13057-62
- Genome Res. 1997; (10): 996-1005
- Proc Natl Acad Sci U S A. 1997; (17): 8945-7
- J Clin Microbiol. 1997; (7): 1822-8
- Nature. 1997; (6632 Suppl): 78-81
- Proc Natl Acad Sci U S A. 1997; (6): 2150-5
- Nucleic Acids Res. 1996; (20): 3879-86
- Nat Genet. 1996; (4): 450-6
- Genetics. 1996; (4): 1387-97
- Proc Natl Acad Sci U S A. 1996; (20): 10614-9
- Proc Natl Acad Sci U S A. 1995; (17): 7912-5
- Science. 1995; (5235): 467-70
- Biotechniques. 1995; (4): 625-6
- Infect Immun. 1995; (2): 478-85
- Proc Natl Acad Sci U S A. 1994; (18): 8393-7
- Science. 1994; (5184): 436-9
- Infect Immun. 1994; (12): 5447-55
- Gene. 1994; (1): 63-8
- Science. 1994; (5164): 1458-60
- Genetics. 1994; (4): 1261-9
- Mol Gen Genet. 1994; (6): 653-7
- Genetics. 1993; (2): 287-96
- Genes Dev. 1993; (6): 974-85
- Genes Dev. 1993; (3): 367-79
- Proc Natl Acad Sci U S A. 1993; (2): 452-6
- J Mol Biol. 1992; (1): 38-53
- Proc Natl Acad Sci U S A. 1992; (23): 11589-93
- Science. 1992; (5089): 1773-5
- Proc Natl Acad Sci U S A. 1992; (9): 3894-8
- Yeast. 1991 Aug-Sep; (6): 607-8
- J Biol Chem. 1991; (16): 10112-21
- Proc Natl Acad Sci U S A. 1991; (23): 10421-5
- Nucleic Acids Res. 1991; (10): 2781
- Science. 1990; (4946): 1077-9
- J Biol Chem. 1990; (12): 6916-20
- Cell. 1990; (3): 437-46
- Cell. 1990; (3): 357-64
- Genes Dev. 1990; (2): 157-66
- Cell. 1989; (5): 857-67
- Proc Natl Acad Sci U S A. 1989; (15): 5898-902
- Mol Cell Biol. 1989; (6): 2544-50
- Proc Natl Acad Sci U S A. 1989; (10): 3689-93
- Genes Dev. 1989; (2): 185-97
- Ann N Y Acad Sci. 1989; 104-17
- Mol Cell Biol. 1988; (10): 4370-80
- Proc Natl Acad Sci U S A. 1988; (16): 6027-31
- Proc Natl Acad Sci U S A. 1988; (14): 5006-10
- Science. 1988; (4859): 1669-72
- Mol Cell Biol. 1988; (4): 1469-73
- Gene. 1988; (2): 303-12
- Nucleic Acids Res. 1987; (19): 7865-76
- Mol Cell Biol. 1987; (9): 3268-76
- Mol Cell Biol. 1987; (8): 2783-93
- Proc Natl Acad Sci U S A. 1987; (15): 5202-5206
- Proc Natl Acad Sci U S A. 1986; (21): 8073-8076
- Proc Natl Acad Sci U S A. 1986; (15): 5372-5376