← Leaderboards
Jesse M Engreitz
Stanford University
$13,286,146
Attributed
$20,149,945
Total exposure
9
Grants
8
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 $4.9M · FY2018–25$5M$3.8M$2.5M$1.3M$0
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$20,149,945 · 9
By mechanism
UM1$8,717,486 · 1
R01$6,328,596 · 3
R35$2,334,422 · 1
U01$1,469,228 · 1
R00$795,814 · 1
P01$439,599 · 1
Top collaborators
- Thomas None Quertermous5 shared
- Rajat M Gupta3 shared
- Anshul Kundaje3 shared
- Marlene Rabinovitch2 shared
Most similar at Stanford University
Same institution · by research overlap
- Edward S. Boyden$43,934,074
- Amin S Ghabrial$6,601,861
- Thomas None Quertermous$63,279,401
- Lars M Steinmetz$11,858,865
- Claire J Tomlin$2,447,891
Others in their field
Other Emerging Leaders on “Cell Type”
- Evan Z Macosko · Broad Institute, Inc.$36,871,464
- Ethan Dmitrovsky · Leidos Biomedical Research, Inc.$20,250,477
- Thomas Denny · Duke University$19,381,749
- Tomasz Nowakowski · University Of California, San Francisco$18,472,946
- Hemali Phatnani · New York University School Of Medicine$18,358,586
- Rui M. Costa · Columbia University Health Sciences$13,762,381
Research focus
Cell TypeGenesMapsCellsMolecularVariantHuman DiseaseEnhancersGene ExpressionComputer ModelsGenetic VariantUntranslated RnaRegulatory ElementInsightHuman GenomeGeneticBiologicalChromatinGene Expression RegulationGenomeClustered Regularly Interspaced Short Palindromic RepeatsGenomicsAffectCrispr Interference
Grant awards (30)
Stanford Center for Connecting DNA Variants to Function and Phenotype$1,844,885
UM1 · FY2025 · HG · contact PI
Mapping, programming, and correcting gene regulatory sequences for Alagille Syndrome$761,891
R01 · FY2025 · HL · contact PI
Mapping, modeling, and manipulating 3D contacts in vascular cells to connect risk variants to disease genes$693,192
R01 · FY2025 · HL · contact PI
High-throughput cellular genetics to connect noncoding variants to coronary artery disease genes$665,483
R01 · FY2025 · HL
MorPhiC: Constructing a Catalog of Cellular Programs to Identify and Annotate Human Disease Genes$481,992
U01 · FY2025 · HG · contact PI
Scientific Core: Perturb-seq library generation, sequencing, and data analysis$439,599
P01 · FY2025 · HL · contact PI
Stanford Center for Connecting DNA Variants to Function and Phenotype$1,844,885
UM1 · FY2024 · HG · contact PI
Mapping, programming, and correcting gene regulatory sequences for Alagille Syndrome$771,155
R01 · FY2024 · HL · contact PI
Mapping, modeling, and manipulating 3D contacts in vascular cells to connect risk variants to disease genes$679,363
R01 · FY2024 · HL · contact PI
High-throughput cellular genetics to connect noncoding variants to coronary artery disease genes$655,727
R01 · FY2024 · HL
MorPhiC: Constructing a Catalog of Cellular Programs to Identify and Annotate Human Disease Genes$495,232
U01 · FY2024 · HG · contact PI
Mapping enhancer-gene regulation in single cells to connect genetic variants to target genes and cell types$442,022
R35 · FY2024 · HG · contact PI
Stanford Center for Connecting DNA Variants to Function and Phenotype$1,882,535
UM1 · FY2023 · HG · contact PI
Mapping, modeling, and manipulating 3D contacts in vascular cells to connect risk variants to disease genes$693,228
R01 · FY2023 · HL · contact PI
High-throughput cellular genetics to connect noncoding variants to coronary artery disease genes$686,629
R01 · FY2023 · HL
MorPhiC: Constructing a Catalog of Cellular Programs to Identify and Annotate Human Disease Genes$492,004
U01 · FY2023 · HG · contact PI
Mapping enhancer-gene regulation in single cells to connect genetic variants to target genes and cell types$473,100
R35 · FY2023 · HG · contact PI
Stanford Center for Connecting DNA Variants to Function and Phenotype$2,203,614
UM1 · FY2022 · HG · contact PI
Mapping, modeling, and manipulating 3D contacts in vascular cells to connect risk variants to disease genes$721,928
R01 · FY2022 · HL · contact PI
Mapping enhancer-gene regulation in single cells to connect genetic variants to target genes and cell types$473,100
R35 · FY2022 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$241,395
R00 · FY2022 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$19,305
R00 · FY2022 · HG · contact PI
Stanford Center for Connecting DNA Variants to Function and Phenotype$941,567
UM1 · FY2021 · HG · contact PI
Mapping enhancer-gene regulation in single cells to connect genetic variants to target genes and cell types$473,100
R35 · FY2021 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$284,628
R00 · FY2021 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$1,486
R00 · FY2021 · HG · contact PI
Mapping enhancer-gene regulation in single cells to connect genetic variants to target genes and cell types$473,100
R35 · FY2020 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$249,000
R00 · FY2020 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$32,400
K99 · FY2019 · HG · contact PI
Systematic mapping and prediction of gene-enhancer connections$32,400
K99 · FY2018 · HG · contact PI