GGrantIndex
← Leaderboards

Andrew Ben Stergachis

University Of Washington

$7,149,667
Attributed
$14,579,825
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 $5.4M · FY201225
$10M$7.5M$5M$2.5M$0
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25

Funding mix

By agency

NIH$14,579,825 · 6

By mechanism

UM1$8,410,614 · 1
R01$2,335,740 · 1
DP5$1,943,750 · 1
U01$1,418,806 · 1
T32$352,091 · 1
F30$118,824 · 1

Top collaborators

Most similar at University Of Washington

Same institution · by research overlap

Others in their field

Top investigators on “Genomics

Research focus

GenomicsVariantGenetic VariantGenesHuman DiseaseSamplingEpigenetic ProcessGeneticGenomeChromatinHuman GeneticsAreaSingle Nucleotide PolymorphismMedical GeneticsComplexPatternResourcesWhole GenomeNucleotidesGenetic VariationGenomic MedicinePathogenicityData SetCommunities

Grant awards (17)

'Mosaicism in Human Tissues, from Telomere to Telomere to RFA-22-013: "Somatic Mosaicism across Human Tissues Program: Genome Characterization Centers."$2,999,999
UM1 · FY2025 · DA
Advancing the implementation of variant-level functional data into clinical databases and clinical practice$715,577
R01 · FY2025 · HG
Medical Genetics Postdoctoral Fellowship$352,091
T32 · FY2025 · GM · contact PI
'Mosaicism in Human Tissues, from Telomere to Telomere to RFA-22-013: "Somatic Mosaicism across Human Tissues Program: Genome Characterization Centers."$2,750,000
UM1 · FY2024 · DA
Tooling for accurately studying the epigenome along the human pangenome reference$1,418,806
U01 · FY2024 · HG · contact PI
Advancing the implementation of variant-level functional data into clinical databases and clinical practice$793,971
R01 · FY2024 · HG
Investigating the contribution of non-coding genetic variation to rare disorders$388,750
DP5 · FY2024 · OD · contact PI
'Mosaicism in Human Tissues, from Telomere to Telomere to RFA-22-013: "Somatic Mosaicism across Human Tissues Program: Genome Characterization Centers."$2,499,999
UM1 · FY2023 · DA
Advancing the implementation of variant-level functional data into clinical databases and clinical practice$826,192
R01 · FY2023 · HG
Investigating the contribution of non-coding genetic variation to rare disorders$388,750
DP5 · FY2023 · OD · contact PI
Somatic Mosaicism across Human Tissues Program: Genome Characterization Centers (GCC SMaHT)$160,616
UM1 · FY2023 · DA
Investigating the contribution of non-coding genetic variation to rare disorders$388,750
DP5 · FY2022 · OD · contact PI
Investigating the contribution of non-coding genetic variation to rare disorders$388,750
DP5 · FY2021 · OD · contact PI
Investigating the contribution of non-coding genetic variation to rare disorders$388,750
DP5 · FY2020 · OD · contact PI
Inter-individual epigenetic variation in hematopoietic progenitor cells$47,676
F30 · FY2014 · DK · contact PI
Inter-individual epigenetic variation in hematopoietic progenitor cells$36,019
F30 · FY2013 · DK · contact PI
Inter-individual epigenetic variation in hematopoietic progenitor cells$35,129
F30 · FY2012 · DK · contact PI