← Leaderboards
Peter White
Research Inst Nationwide Children'S Hosp
$1,725,496
Attributed
$3,843,737
Total exposure
4
Grants
1
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 $695.6K · FY2010–25$1M$750K$500K$250K$0
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$3,843,737 · 4
By mechanism
R01$2,678,237 · 1
R21$665,500 · 2
S10$500,000 · 1
Top collaborators
- Vidu Garg6 shared
- Kim Lewis Mcbride4 shared
- Bimal Pankaj Chaudhari1 shared
Most similar at Research Inst Nationwide Children'S Hosp
Same institution · by research overlap
- Vidu Garg$10,712,827
- Bimal Pankaj Chaudhari$217,250
Others in their field
Top investigators on “Genomics”
- Eric S Lander · Whitehead Institute For Biomedical Res$790,826,794
- Richard A Gibbs · Baylor College Of Medicine$661,700,875
- Richard K. Wilson · Washington University$497,388,134
- Leonard Freedman · Leidos Biomedical Research, Inc.$405,398,682
- David Heimbrook · Leidos Biomedical Research, Inc.$333,649,126
- Stacey Gabriel · Massachusetts Institute Of Technology$331,896,891
Research focus
GenomicsChildTechnologyGenomeGenome SequencingDiagnosisChildhoodGenetic VariantVariantWeightDatabasesNational Heart, Lung, And Blood InstituteGeneticBioinformaticsSegregationExomeCohortGenetic Predisposition To DiseaseGenesGene ExpressionCongenital AbnormalityCardiovascular SystemCellsAffect
Grant awards (8)
NeoGx-III: Interpretable Machine Learning with Integrated Analysis of Maternal & Infant Electronic Medical Records for Unbiased Prediction of Need for Genome Sequencing in Level III NICUs$434,500
R21 · FY2025 · HD
A Multi-omic approach towards improving candidate gene identification and variant prioritization in patients with congenital heart disease$115,500
R21 · FY2023 · HL
A Multi-omic approach towards improving candidate gene identification and variant prioritization in patients with congenital heart disease$115,500
R21 · FY2022 · HL
Exome sequencing and functional studies in familial CHD$649,481
R01 · FY2015 · HL
Exome sequencing and functional studies in familial CHD$664,040
R01 · FY2014 · HL
Exome sequencing and functional studies in familial CHD$669,080
R01 · FY2013 · HL
Exome sequencing and functional studies in familial CHD$695,636
R01 · FY2012 · HL
Acquisition of an Illumina Genome Analyzer for The Research Institute$500,000
S10 · FY2010 · RR · contact PI