← Leaderboards
Elizabeth M Nolan
Harvard Medical School
$9,339,083
Attributed
$13,362,471
Total exposure
11
Grants
6
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 $2.5M · FY2007–25$5M$3.8M$2.5M$1.3M$0
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$13,362,471 · 11
By mechanism
R01$9,077,248 · 5
DP2$2,512,500 · 1
R21$1,261,931 · 3
R56$399,521 · 1
F32$111,271 · 1
Top collaborators
- Manuela Raffatellu18 shared
- Amanda Gail Oglesby8 shared
Most similar at Harvard Medical School
Same institution · by research overlap
- John J Mekalanos$34,471,043
- William M Wuest$6,242,876
- Steven Joseph Malcolmson$3,134,075
Others in their field
Top investigators on “Pathogen”
- Margaret Juliana McElrath · Fred Hutchinson Cancer Center$343,790,695
- Richard Webby · St. Jude Children'S Research Hospital$265,067,789
- Jeffrey P Krischer · University Of South Florida$130,496,919
- Mark S Klempner · Tufts Medical Center$128,021,180
- Timothy Stedman · American Type Culture Collection$122,230,581
- Adolfo Garcia-Sastre · Icahn School Of Medicine At Mount Sinai$99,962,183
Research focus
PathogenInfectionUptakeGrowthNutrientMetalsEnvironmentIronPathogenic BacteriaDesignProteinsUnited StatesOrganismExpectationSiteInsightMicrobeResearch ProposalsFutureInvestigationAntimicrobialIonsMediatingBase
Grant awards (39)
Harnessing iron acquisition to hinder enterobacterial pathogenesis$635,769
R01 · FY2025 · AI
Bioinorganic Explorations of Host-defense Proteins$314,422
R01 · FY2025 · GM · contact PI
Harnessing iron acquisition to hinder enterobacterial pathogenesis$92,728
R01 · FY2025 · AI
Harnessing iron acquisition to hinder enterobacterial pathogenesis$655,212
R01 · FY2024 · AI
Metallobiochemistry of innate immunity and bacterial physiology$320,529
R01 · FY2024 · GM · contact PI
Bioinorganic Explorations of Host-defense Proteins$314,422
R01 · FY2024 · GM · contact PI
Harnessing iron acquisition to hinder enterobacterial pathogenesis$91,121
R01 · FY2024 · AI
Harnessing iron acquisition to hinder enterobacterial pathogenesis$669,498
R01 · FY2023 · AI
Metallobiochemistry of innate immunity and bacterial physiology$320,529
R01 · FY2023 · GM · contact PI
Bioinorganic Explorations of Host-defense Proteins$314,422
R01 · FY2023 · GM · contact PI
Harnessing iron acquisition to hinder enterobacterial pathogenesis$399,521
R56 · FY2022 · AI
Metallobiochemistry of innate immunity and bacterial physiology$320,529
R01 · FY2022 · GM · contact PI
Bioinorganic Explorations of Host-defense Proteins$314,422
R01 · FY2022 · GM · contact PI
Metallobiochemistry of innate immunity and bacterial physiology$334,304
R01 · FY2021 · GM · contact PI
Antimicrobial activity of Escherichia coli Nissle 1917 microcin M$193,800
R21 · FY2021 · AI
Bioinorganic Explorations of Host-Defense Proteins$272,092
R01 · FY2020 · GM · contact PI
Metallobiochemistry of innate immunity and bacterial physiology$271,261
R01 · FY2020 · GM · contact PI
Antimicrobial activity of Escherichia coli Nissle 1917 microcin M$246,485
R21 · FY2020 · AI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$372,657
R01 · FY2019 · AI
Bioinorganic Explorations of Host-Defense Proteins$273,644
R01 · FY2019 · GM · contact PI
Metallobiochemistry of innate immunity and bacterial physiology$272,173
R01 · FY2019 · GM · contact PI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$373,468
R01 · FY2018 · AI
Metallobiochemistry of innate immunity and bacterial physiology$268,681
R01 · FY2018 · GM · contact PI
Bioinorganic Explorations of Host-Defense Proteins$268,185
R01 · FY2018 · GM · contact PI
Imaging Mobile Zinc Biology$350,721
R01 · FY2017 · GM · contact PI
Metallobiochemistry of innate immunity and bacterial physiology$279,898
R01 · FY2017 · GM · contact PI
Bioinorganic Explorations of Host-Defense Proteins$269,593
R01 · FY2017 · GM · contact PI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$258,094
R01 · FY2017 · AI
Siderophore-based antibiotics: consequences for the microbiota and bacterial pathogens$175,161
R21 · FY2017 · AI · contact PI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$130,293
R01 · FY2017 · AI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$364,603
R01 · FY2016 · AI
Siderophore-based antibiotics: consequences for the microbiota and bacterial pathogens$228,963
R21 · FY2016 · AI · contact PI
Development of siderophore-based vaccines against non-typhoidal Salmonella infection$353,978
R01 · FY2015 · AI
Targeting iron acquisition in Salmonella with siderophore-based immunization$183,880
R21 · FY2015 · AI
Targeting iron acquisition in Salmonella with siderophore-based immunization$233,642
R21 · FY2014 · AI
Antibacterial Peptides and Zinc in Innate Immunity and Mammalian Physiology$2,512,500
DP2 · FY2010 · OD · contact PI
Mechanistic Explorations of Microcin E492m Biosynthesis and Maturation$19,599
F32 · FY2009 · AI · contact PI
Mechanistic Explorations of Microcin E492m Biosynthesis and Maturation$46,826
F32 · FY2008 · AI · contact PI
Mechanistic Explorations of Microcin E492m Biosynthesis and Maturation$44,846
F32 · FY2007 · AI · contact PI