← Leaderboards
Luca Pinello
Dana-Farber Cancer Inst
$6,835,504
Attributed
$14,529,208
Total exposure
6
Grants
4
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 $3.5M · FY2015–25$5M$3.8M$2.5M$1.3M$0
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$14,529,208 · 6
By mechanism
UM1$8,671,281 · 1
R35$2,555,210 · 1
R01$1,553,510 · 1
U01$856,513 · 1
R00$746,999 · 1
K99$145,695 · 1
Top collaborators
- Daniel Evan Bauer8 shared
- Richard I Sherwood5 shared
- Guillaume Lettre4 shared
- Danilo Pellin1 shared
Most similar at Dana-Farber Cancer Inst
Same institution · by research overlap
- Peter Campbell$932,920
- Nathanael Schiander Gray$36,761,550
- Pietro Genovese$5,128,749
- Jens G Lohr$2,586,070
- Mehmet Kemal Samur$259,753
Others in their field
Top investigators on “Variant”
- Richard A Gibbs · Baylor College Of Medicine$367,607,426
- Richard K. Wilson · Washington University$295,336,569
- Stacey Gabriel · Massachusetts Institute Of Technology$169,231,712
- David Heimbrook · Leidos Biomedical Research, Inc.$125,120,179
- Heidi L Rehm · Broad Institute, Inc.$96,250,516
- Margaret A Pericak-Vance · Doheny Eye Institute$83,999,609
Research focus
VariantGenomeGenetic VariantCommunitiesPhenotypeLinkGenome Wide Association StudyGene ExpressionTraitGeneticCellsClustered Regularly Interspaced Short Palindromic RepeatsGenetic VariationData SetGenome EditingGenesElementsComputing MethodologiesComplexHuman DiseaseCellular AssayChromatinDissectionCrispr/Cas Technology
Grant awards (18)
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing$1,890,246
UM1 · FY2025 · HG · contact PI
Robust verification of genetic variant-associated candidate off-target sites$856,513
U01 · FY2025 · AI
Computational tools for precision genome editing$751,289
R01 · FY2025 · HG
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing$1,890,246
UM1 · FY2024 · HG · contact PI
Computational tools for precision genome editing$802,221
R01 · FY2024 · HG
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing$1,928,820
UM1 · FY2023 · HG · contact PI
Multiscale exploration of the functional non-coding genome$507,642
R35 · FY2023 · HG · contact PI
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing$1,928,820
UM1 · FY2022 · HG · contact PI
Multiscale exploration of the functional non-coding genome$507,642
R35 · FY2022 · HG · contact PI
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing$1,033,149
UM1 · FY2021 · HG · contact PI
Multiscale exploration of the functional non-coding genome$507,642
R35 · FY2021 · HG · contact PI
Multiscale exploration of the functional non-coding genome$507,642
R35 · FY2020 · HG · contact PI
Multiscale exploration of the functional non-coding genome$524,642
R35 · FY2019 · HG · contact PI
Discovering disease-causal variants by linking genetic and epigenetic variation$249,000
R00 · FY2019 · HG · contact PI
Discovering disease-causal variants by linking genetic and epigenetic variation$249,000
R00 · FY2018 · HG · contact PI
Discovering disease-causal variants by linking genetic and epigenetic variation$248,999
R00 · FY2017 · HG · contact PI
Discovering disease-causal variants by linking genetic and epigenetic variation$42,497
K99 · FY2016 · HG · contact PI
Discovering disease-causal variants by linking genetic and epigenetic variation$103,198
K99 · FY2015 · HG · contact PI