← Leaderboards
Eric T. Kool
Stanford University
$24,920,252
Attributed
$25,152,752
Total exposure
18
Grants
11
Lead (contact PI)
Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants.
Funding over time
peak $1.4M · FY2005–25$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$25,152,752 · 18
By mechanism
R01$21,421,922 · 12
R35$2,353,448 · 1
S10$500,000 · 1
R21$472,382 · 2
R43$405,000 · 2
Top collaborators
- Lucian Orbai2 shared
- Arash Ash Alizadeh1 shared
Most similar at Stanford University
Same institution · by research overlap
- Joseph C Wu$80,370,369
- Feng Zhang$30,715,029
- Karlene A Cimprich$14,496,208
- Mark A Kay$46,920,488
- Lei Stanley Qi$14,888,989
Others in their field
Top investigators on “Cells”
- Lawrence Corey · Fred Hutchinson Cancer Center$536,344,731
- Barton F Haynes · Duke University$457,457,619
- David Heimbrook · Leidos Biomedical Research, Inc.$454,789,509
- Glenda E Gray · Wits Health Consortium (Pty), Ltd$299,104,942
- Dennis R. Burton · Scripps Research Institute$278,781,854
- Mary M Horowitz · Medical College Of Wisconsin$237,383,608
Research focus
CellsMolecularBiologicalDesignBaseProteinsImageStructureFluorescenceLabelBiologyToxic EffectReagentNucleotidesChemistryPathway InteractionsNucleic AcidsPropertyRepairedTissuesPermeabilitySmall MoleculeComplexClinically Relevant
Grant awards (83)
Transcriptome Analysis with RNA-Reactive Probes$623,371
R35 · FY2025 · GM · contact PI
Transcriptome Analysis with RNA-Reactive Probes$623,371
R35 · FY2024 · GM · contact PI
Measuring and Modulating DNA Damage Surveillance Pathways$463,803
R01 · FY2024 · CA · contact PI
Transcriptome Analysis with RNA-Reactive Probes$12,184
R35 · FY2024 · GM · contact PI
Transcriptome Analysis with RNA-Reactive Probes$623,371
R35 · FY2023 · GM · contact PI
Measuring and Modulating DNA Damage Surveillance Pathways$478,442
R01 · FY2023 · CA · contact PI
Transcriptome Analysis with RNA-Reactive Probes$45,832
R35 · FY2023 · GM · contact PI
Measuring and Modulating DNA Damage Surveillance Pathways$467,789
R01 · FY2022 · CA · contact PI
Transcriptome Analysis with RNA-Reactive Probes$425,319
R35 · FY2022 · GM · contact PI
Covalent Profiling of RNA Targets and Off-targets$376,023
R01 · FY2022 · GM · contact PI
Measuring and Modulating DNA Damage Surveillance Pathways$477,636
R01 · FY2021 · CA · contact PI
Covalent Profiling of RNA Targets and Off-targets$378,023
R01 · FY2021 · GM · contact PI
Probing the Transcriptome with Multifunctional Acylation Chemistry$319,854
R01 · FY2021 · GM · contact PI
Measuring and Modulating Oxidative DNA Damage Surveillance Pathways$493,411
R01 · FY2020 · CA · contact PI
Covalent Profiling of RNA Targets and Off-targets$379,964
R01 · FY2020 · GM · contact PI
Probing the Transcriptome with Multifunctional Acylation Chemistry$318,684
R01 · FY2020 · GM · contact PI
Measuring and Modulating Oxidative DNA Damage Surveillance Pathways$479,612
R01 · FY2019 · CA · contact PI
Probing the Transcriptome with Multifunctional Acylation Chemistry$382,014
R01 · FY2019 · GM · contact PI
Covalent Profiling of RNA Targets and Off-targets$347,105
R01 · FY2019 · GM · contact PI
Measuring and Modulating Oxidative DNA Damage Surveillance Pathways$428,963
R01 · FY2018 · CA · contact PI
Probing the Transcriptome with Multifunctional Acylation Chemistry$316,518
R01 · FY2018 · GM · contact PI
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular Contexts$304,658
R01 · FY2018 · GM · contact PI
Measuring and Modulating Oxidative DNA Damage Surveillance Pathways$429,953
R01 · FY2017 · CA · contact PI
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular Contexts$304,667
R01 · FY2017 · GM · contact PI
DNA-carbon Assemblies for Multispectral Imaging$303,533
R01 · FY2017 · GM · contact PI
Reversible Reagents for Next-Gen Biomolecule and Tissue Preservation$225,000
R43 · FY2017 · ES
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular Contexts$304,620
R01 · FY2016 · GM · contact PI
DNA-carbon Assemblies for Multispectral Imaging$302,405
R01 · FY2016 · GM · contact PI
Templated Chemistry for RNA Analysis$302,206
R01 · FY2016 · GM · contact PI
DNA-carbon Assemblies for Multispectral Imaging$320,378
R01 · FY2015 · GM · contact PI
Highly Reactive Hydrazone Chemistry: Orthogonal Modification in Cellular Contexts$319,588
R01 · FY2015 · GM · contact PI
Templated Chemistry for RNA Analysis$301,407
R01 · FY2015 · GM · contact PI
Rescuing Nucleic Acids from Formalin Damage in Cancer Specimens$180,000
R43 · FY2015 · CA
Templated Chemistry for RNA Analysis$300,631
R01 · FY2014 · GM · contact PI
DNA-carbon Assemblies for Multispectral Imaging$300,249
R01 · FY2014 · GM · contact PI
Templated Chemistry for RNA Analysis$299,879
R01 · FY2013 · GM · contact PI
Probing Nucleotide Recognition in the Genetic Information Pathway$307,417
R01 · FY2012 · GM · contact PI
Probing Nucleotide Recognition in the Genetic Information Pathway$307,826
R01 · FY2011 · GM · contact PI
RNA-Templated Chemistry for Cellular Genetic Imaging$289,593
R01 · FY2011 · GM · contact PI
Oligomeric Fluorescent Reporters on a DNA Scaffold$284,012
R01 · FY2011 · GM · contact PI
Probing Nucleotide Recognition in the Genetic Information Pathway$311,337
R01 · FY2010 · GM · contact PI
RNA-Templated Chemistry for Cellular Genetic Imaging$292,794
R01 · FY2010 · GM · contact PI
Oligomeric Fluorescent Reporters on a DNA Scaffold$287,168
R01 · FY2010 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOULBE HELIX$95,615
R01 · FY2010 · GM · contact PI
Probing Nucleotide Recognition in the Genetic Information Pathway$314,875
R01 · FY2009 · GM · contact PI
RNA-Templated Chemistry for Cellular Genetic Imaging$296,023
R01 · FY2009 · GM · contact PI
Oligomeric Fluorescent Reporters on a DNA Scaffold$290,349
R01 · FY2009 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOULBE HELIX$280,021
R01 · FY2009 · GM · contact PI
RNA-Templated Chemistry for Cellular Genetic Imaging$296,287
R01 · FY2008 · GM · contact PI
Oligomeric Fluorescent Reporters on a DNA Scaffold$290,622
R01 · FY2008 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOULBE HELIX$279,293
R01 · FY2008 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOULBE HELIX$51,009
R01 · FY2008 · GM · contact PI
NUCLEOBASE SHAPE MIMICS AS BIOMOLECULAR PROBES$286,964
R01 · FY2007 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOUBLE HELIX$278,586
R01 · FY2007 · GM · contact PI
CHEMICAL AND BIOLOGICAL MIMICRY OF TELOMERASE$273,663
R01 · FY2007 · GM · contact PI
NUCLEOBASE SHAPE MIMICS AS BIOMOLECULAR PROBES$296,340
R01 · FY2006 · GM · contact PI
RE-ENGINEERING THE DIAMETER OF THE DOULBE HELIX$286,200
R01 · FY2006 · GM · contact PI
CHEMICAL AND BIOLOGICAL MIMICRY OF TELOMERASE$282,550
R01 · FY2006 · GM · contact PI
AUTOLIGATION PROBES FOR HIGHLY SELECTIVE RNA IMAGING$266,878
R01 · FY2006 · GM · contact PI
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLD$266,878
R01 · FY2006 · GM · contact PI
NUCLEOBASE SHAPE MIMICS AS BIOMOLECULAR PROBES$304,260
R01 · FY2005 · GM
CHEMICAL AND BIOLOGICAL MIMICRY OF TELOMERASE$290,050
R01 · FY2005 · GM
AUTOLIGATION PROBES FOR HIGHLY SELECTIVE RNA IMAGING$273,300
R01 · FY2005 · GM
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLD$273,300
R01 · FY2005 · GM
NUCLEOBASE SHAPE MIMICS AS BIOMOLECULAR PROBES$305,008
R01 · FY2004 · GM
CHEMICAL AND BIOLOGICAL MIMICRY OF TELOMERASE$290,714
R01 · FY2004 · GM
AUTOLIGATION PROBES FOR HIGHLY SELECTIVE RNA IMAGING$273,300
R01 · FY2004 · GM
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLD$273,300
R01 · FY2004 · GM
RE-ENGINEERING THE DIAMETER OF THE DOUBLE HELIX$239,617
R01 · FY2004 · GM
AUTOLIGATION PROBES FOR HIGHLY SELECTIVE RNA IMAGING$272,482
R01 · FY2003 · GM
POLYFLUOROPHORES ASSEMBLED ON A DNA SCAFFOLD$271,389
R01 · FY2003 · GM
RE-ENGINEERING THE DIAMETER OF THE DOUBLE HELIX$239,617
R01 · FY2003 · GM
NONPOLAR NUCLEOSIDE ISOSTERES AS BIOMOLECULAR PROBES$218,960
R01 · FY2003 · EB
PURCHASE OF A VARIAN INOVA 600 MHz NMR SPECTROMETER$500,000
S10 · FY2002 · RR
RE-ENGINEERING THE DIAMETER OF THE DOUBLE HELIX$239,617
R01 · FY2002 · GM
NONPOLAR NUCLEOSIDE ISOSTERES AS BIOMOLECULAR PROBES$218,960
R01 · FY2002 · GM
NOVEL PROBE TOPOLOGIES IN BIOMEDICAL DIAGNOSTICS$120,000
R21 · FY2002 · RR
NONPOLAR NUCLEOSIDE ISOSTERES AS BIOMOLECULAR PROBES$268,785
R01 · FY2001 · GM
RE-ENGINEERING THE DIAMETER OF THE DOUBLE HELIX$239,617
R01 · FY2001 · GM
NOVEL PROBE TOPOLOGIES IN BIOMEDICAL DIAGNOSTICS$120,000
R21 · FY2001 · RR
AUTOLIGATION PROBES AS CANCER DIAGNOSTICS$115,691
R21 · FY2001 · GM
NONPOLAR NUCLEOSIDE ISOSTERES AS BIOMOLECULAR PROBES$215,331
R01 · FY2000 · GM
AUTOLIGATION PROBES AS CANCER DIAGNOSTICS$116,691
R21 · FY2000 · GM