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Dan R Littman

New York University School Of Medicine

$30,444,906
Attributed
$38,669,892
Total exposure
15
Grants
12
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 $7.9M · FY200525
$10M$7.5M$5M$2.5M$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$38,669,892 · 15

By mechanism

R01$23,055,694 · 7
RC4$4,838,627 · 1
RC2$3,994,224 · 1
R37$3,310,727 · 1
P01$1,990,942 · 1
S10$496,855 · 1

Top collaborators

Most similar at New York University School Of Medicine

Same institution · by research overlap

Others in their field

Top investigators on “Cells

Research focus

CellsAutoimmune DiseasesT-LymphocyteGenesInflammatoryIntestinesMutationImmune SystemCytokineResponsePathway InteractionsCell Differentiation ProcessGeneticInflammationImmune ResponseImmuneTissuesCell TypeMediatingGene ExpressionIn VivoIn VitroGenetic TranscriptionMicrobial

Grant awards (65)

Multiscale genome engineering to map cis-regulatory variants in human and mouse$1,118,730
R01 · FY2025 · HG
Mechanism of microbiota-mediated potentiation of checkpoint blockade efficacy in lung cancer$572,168
R01 · FY2025 · CA · contact PI
Determinants of induced Treg and inflammatory Th17 cell balance in response to potentially pathogenic microbiota$505,444
R01 · FY2025 · AI · contact PI
Multiscale genome engineering to map cis-regulatory variants in human and mouse$1,082,024
R01 · FY2024 · HG
Mechanism of microbiota-mediated potentiation of checkpoint blockade efficacy in lung cancer$543,560
R01 · FY2024 · CA · contact PI
Determinants of induced Treg and inflammatory Th17 cell balance in response to potentially pathogenic microbiota$521,077
R01 · FY2024 · AI · contact PI
Multiscale genome engineering to map cis-regulatory variants in human and mouse$1,133,309
R01 · FY2023 · HG
Mechanism of microbiota-mediated potentiation of checkpoint blockade efficacy in lung cancer$560,724
R01 · FY2023 · CA · contact PI
Determinants of induced Treg and inflammatory Th17 cell balance in response to potentially pathogenic microbiota$521,077
R01 · FY2023 · AI · contact PI
Mechanism of microbiota-mediated potentiation of checkpoint blockade efficacy in lung cancer$560,724
R01 · FY2022 · CA · contact PI
Determinants of induced Treg and inflammatory Th17 cell balance in response to potentially pathogenic microbiota$521,077
R01 · FY2022 · AI · contact PI
Mechanism of microbiota-mediated potentiation of checkpoint blockade efficacy in lung cancer$572,168
R01 · FY2021 · CA · contact PI
Determinants of induced Treg and inflammatory Th17 cell balance in response to potentially pathogenic microbiota$521,077
R01 · FY2021 · AI · contact PI
Roles of DDX5 and its associated long non-coding RNAs in RORgt-mediated host immune system functions$536,329
R01 · FY2020 · AI · contact PI
Roles of nucleoporins in RORgammat-dependent immune functions$423,750
R01 · FY2020 · AI · contact PI
Roles of DDX5 and its associated long non-coding RNAs in RORgt-mediated host immune system functions$536,329
R01 · FY2019 · AI · contact PI
Roles of nucleoporins in RORgammat-dependent immune functions$423,750
R01 · FY2019 · AI · contact PI
A network model of the gut host-microbe ecosystem in Inflammatory Bowel Disease$636,092
R01 · FY2018 · DK · contact PI
Roles of DDX5 and its associated long non-coding RNAs in RORgt-mediated host immune system functions$536,329
R01 · FY2018 · AI · contact PI
Roles of nucleoporins in RORgammat-dependent immune functions$423,750
R01 · FY2018 · AI · contact PI
A network model of the gut host-microbe ecosystem in Inflammatory Bowel Disease$636,092
R01 · FY2017 · DK · contact PI
Roles of DDX5 and its associated long non-coding RNAs in RORgt-mediated host immune system functions$536,329
R01 · FY2017 · AI · contact PI
Roles of nucleoporins in RORgammat-dependent immune functions$423,750
R01 · FY2017 · AI · contact PI
A transcriptional network analysis of Tr1 cells$416,064
P01 · FY2017 · NS · contact PI
A network model of the gut host-microbe ecosystem in Inflammatory Bowel Disease$636,092
R01 · FY2016 · DK · contact PI
Roles of DDX5 and its associated long non-coding RNAs in RORgt-mediated host immune system functions$536,329
R01 · FY2016 · AI · contact PI
Roles of nucleoporins in RORgammat-dependent immune functions$423,750
R01 · FY2016 · AI · contact PI
A transcriptional network analysis of Tr1 cells$416,065
P01 · FY2016 · NS · contact PI
A network model of the gut host-microbe ecosystem in Inflammatory Bowel Disease$631,837
R01 · FY2015 · DK · contact PI
A transcriptional network analysis of Tr1 cells$416,068
P01 · FY2015 · NS · contact PI
A network model of the gut host-microbe ecosystem in Inflammatory Bowel Disease$631,590
R01 · FY2014 · DK · contact PI
A transcriptional network analysis of Tr1 cells$374,129
P01 · FY2014 · NS · contact PI
Ligands and cofactors required for RORgt function in the immune system$389,248
R01 · FY2013 · AI · contact PI
A transcriptional network analysis of Tr1 cells$368,616
P01 · FY2013 · NS · contact PI
Ligands and Cofactors Required for RORgt Function in the Immune System$133,105
R01 · FY2013 · AI · contact PI
Elucidation of the transcriptional network underlying the Th17 lineage program$107,541
RC4 · FY2013 · AI · contact PI
Ligands and cofactors required for RORgt function in the immune system$414,092
R01 · FY2012 · AI · contact PI
Ligands and cofactors required for RORgt function in the immune system$414,092
R01 · FY2011 · AI · contact PI
Dendritic Cell Restriction and Innate Immune Sensing of HIV Infection$209,138
R21 · FY2011 · AI · contact PI
Elucidation of the transcriptional network underlying the Th17 lineage program.$4,731,086
RC4 · FY2010 · AI · contact PI
Role of oral and intestinal microbiota in Rheumatoid Arthritis$1,998,164
RC2 · FY2010 · AR
Role of ROR??t in the transcriptional regulatory network underlying Th17 lineage$495,241
RC1 · FY2010 · AI · contact PI
Ligands and cofactors required for RORgt function in the immune system$418,275
R01 · FY2010 · AI · contact PI
Dendritic Cell Restriction and Innate Immune Sensing of HIV Infection$253,500
R21 · FY2010 · AI · contact PI
Role of oral and intestinal microbiota in Rheumatoid Arthritis$1,996,060
RC2 · FY2009 · AR
Ligands and cofactors required for RORgt function in the immune system$422,709
R01 · FY2009 · AI · contact PI
Murine Model System for HIV Pathogenesis$526,866
R01 · FY2008 · AI · contact PI
Screen for Small Molecule Compounds that Modulate the Transcriptional Activity of$24,944
R03 · FY2008 · DA · contact PI
Murine Model System for HIV Pathogenesis$521,428
R01 · FY2007 · AI · contact PI
Cellular Factors Required for HIV Entry$400,606
R37 · FY2007 · AI · contact PI
Murine Model System for HIV Pathogenesis$521,358
R01 · FY2006 · AI · contact PI
Cellular Factors Required for HIV Entry$412,571
R37 · FY2006 · AI · contact PI
Murine Model System for HIV Pathogenesis$518,355
R01 · FY2005 · AI
Cellular Factors Required for HIV Entry$422,500
R37 · FY2005 · AI
Murine Model System for HIV Pathogenesis$503,260
R01 · FY2004 · AI
Cellular Factors Required for HIV Entry$422,500
R37 · FY2004 · AI
Cellular Factors Required for HIV Entry$421,771
R37 · FY2003 · AI
MURINE MODEL SYSTEM FOR HIV PATHOGENESIS$409,456
R01 · FY2003 · AI
Acquisition of High Speed Cell Sorter$496,855
S10 · FY2002 · RR
MURINE MODEL SYSTEM FOR HIV PATHOGENESIS$397,530
R01 · FY2002 · AI
CELLULAR FACTORS REQUIRED FOR HIV ENTRY$364,515
R37 · FY2002 · AI
MURINE MODEL SYSTEM FOR HIV PATHOGENESIS$385,953
R01 · FY2001 · AI
CELLULAR FACTORS REQUIRED FOR HIV ENTRY$343,588
R37 · FY2001 · AI
CELLULAR FACTORS REQUIRED FOR HIV ENTRY$522,676
R37 · FY2000 · AI
MURINE MODEL SYSTEM FOR HIV PATHOGENESIS$374,710
R01 · FY2000 · AI