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Stephen Montgomery
Stanford University
$23,593,399
Attributed
$49,427,041
Total exposure
9
Grants
7
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 $10.3M · FY2015–25$20M$15M$10M$5M$0
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$49,427,041 · 9
By mechanism
U01$22,534,482 · 2
U24$16,901,456 · 1
R01$9,682,303 · 5
R03$308,800 · 1
Top collaborators
- Anshul Kundaje12 shared
- Michael P Snyder9 shared
- Matthew Thomas Wheeler6 shared
- Jonathan Adam Bernstein5 shared
- Thomas J Montine5 shared
- Manuel A Rivas5 shared
Most similar at Stanford University
Same institution · by research overlap
- Laramie Duncan$2,522,903
- Anshul Kundaje$16,927,829
- Manuel A Rivas$2,174,080
- Iain M Johnstone$10,221,358
- Anandi Krishnan$1,190,205
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
VariantAlzheimer&AposGeneticGenesFunctional GenomicsData SetGenotype-Tissue Expression ProjectCommunitiesCellsGenomicsMapsPublic Health RelevanceTissuesChromatinResourcesAllelesGenetic VariantLinkPhenotypeAtac-SeqEpigenomicsWhole GenomeReporterCohort
Grant awards (38)
Stanford Mendelian Genomics Research Center$2,781,357
U01 · FY2025 · HG · contact PI
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologies$1,622,284
U01 · FY2025 · AG
Identifying causal genetic variants and molecular mechanisms impacting mental health$523,574
R01 · FY2025 · MH · contact PI
Integrating 4DN data to identify functional rare variants in UDN and GTEx$308,800
R03 · FY2025 · OD · contact PI
Stanford MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$272,001
U24 · FY2025 · DK
Stanford Mendelian Genomics Research Center$2,778,468
U01 · FY2024 · HG · contact PI
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologies$1,655,392
U01 · FY2024 · AG
Stanford MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$885,999
U24 · FY2024 · DK
Mapping Molecular and Phenotypic Interactions in Alzheimers Disease$696,367
R01 · FY2024 · AG · contact PI
Identifying causal genetic variants and molecular mechanisms impacting mental health$615,969
R01 · FY2024 · MH · contact PI
Stanford Mendelian Genomics Research Center$154,400
U01 · FY2024 · HG · contact PI
Stanford Mendelian Genomics Research Center$2,838,036
U01 · FY2023 · HG · contact PI
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologies$1,660,007
U01 · FY2023 · AG
Mapping Molecular and Phenotypic Interactions in Alzheimers Disease$735,792
R01 · FY2023 · AG · contact PI
Identifying causal genetic variants and molecular mechanisms impacting mental health$615,969
R01 · FY2023 · MH · contact PI
Stanford Mendelian Genomics Research Center$2,840,303
U01 · FY2022 · HG · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$2,736,699
U24 · FY2022 · DK
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologies$1,669,192
U01 · FY2022 · AG
Mapping Molecular and Phenotypic Interactions in Alzheimers Disease$735,792
R01 · FY2022 · AG · contact PI
Identifying causal genetic variants and molecular mechanisms impacting mental health$616,220
R01 · FY2022 · MH · contact PI
SOFTWARE FOR LARGE-SCALE INFERENCE OF THE GENETICS OF LIFESTYLE MEASURES, BIOMARKERS, AND COMMON AND RARE DISEASES$392,500
R01 · FY2022 · HG · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$4,020,046
U24 · FY2021 · DK
Stanford Mendelian Genomics Research Center$2,836,860
U01 · FY2021 · HG · contact PI
Multi-omic functional assessment of novel AD variants using high-throughput and single-cell technologies$1,698,183
U01 · FY2021 · AG
Mapping Molecular and Phenotypic Interactions in Alzheimers Disease$735,792
R01 · FY2021 · AG · contact PI
Identifying causal genetic variants and molecular mechanisms impacting mental health$618,007
R01 · FY2021 · MH · contact PI
SOFTWARE FOR LARGE-SCALE INFERENCE OF THE GENETICS OF LIFESTYLE MEASURES, BIOMARKERS, AND COMMON AND RARE DISEASES$392,500
R01 · FY2021 · HG · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$4,481,145
U24 · FY2020 · DK
Mapping Molecular and Phenotypic Interactions in Alzheimers Disease$735,792
R01 · FY2020 · AG · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$2,529,956
U24 · FY2019 · DK
Integrative multi-omics in whole genome studies of HLBS disorders$440,919
R01 · FY2019 · HL · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$1,734,178
U24 · FY2018 · DK
Integrative multi-omics in whole genome studies of HLBS disorders$440,919
R01 · FY2018 · HL · contact PI
Predicting causal non-coding variants in a founder population$454,272
R01 · FY2017 · HG · contact PI
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$157,976
U24 · FY2017 · DK
Stanford/Salk MoTrPAC Site for Genomes, Epigenomes and Transcriptomes$83,456
U24 · FY2017 · DK
Predicting causal non-coding variants in a founder population$454,272
R01 · FY2016 · HG · contact PI
Predicting causal non-coding variants in a founder population$477,647
R01 · FY2015 · HG · contact PI