← Leaderboards
Taosheng Huang
Children'S Hospital Boston
$4,504,376
Attributed
$4,504,376
Total exposure
8
Grants
6
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. They are the sole PI on all grants (the two match).
Funding over time
peak $778.3K · FY2005–20$1M$750K$500K$250K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
Funding mix
By agency
NIH$4,504,376 · 8
By mechanism
R01$3,994,626 · 5
R21$357,750 · 1
R03$152,000 · 1
M01$0 · 1
Top collaborators
No co-investigators on record.
Others in their field
Top investigators on “Mutation”
- Richard A Gibbs · Baylor College Of Medicine$276,143,183
- David Heimbrook · Leidos Biomedical Research, Inc.$175,834,894
- Randall J Bateman · Washington University$154,391,630
- Eric Martin McDade · Washington University$96,219,353
- Stacey Gabriel · Massachusetts Institute Of Technology$95,141,374
- Tatiana M. Foroud · Indiana Univ-Purdue Univ At Indianapolis$93,475,056
Research focus
MutationMolecularCellsPathogenesisGeneticPathway InteractionsProteinsGenesLeadPlayTranscription FactorTissuesKnock-OutBasePhenotypeMalignant NeoplasmsEmbryoGene ExpressionIn VitroProgramsRecruitment ActivityMitochondrial DysfunctionMitochondriaAffect
Grant awards (24)
Causal Role of Mitochondrial Dysfunctions in Aging by Analyzing an Epigenetic Clock in Patients with Mitochondrial DNA Mutations$159,000
R21 · FY2020 · AG · contact PI
Molecular Mechanism of Biallelic Mutations of FDXR Causing Novel Mitochondriopathy with Optic Atrophy$404,856
R01 · FY2019 · EY · contact PI
Causal Role of Mitochondrial Dysfunctions in Aging by Analyzing an Epigenetic Clock in Patients with Mitochondrial DNA Mutations$198,750
R21 · FY2019 · AG · contact PI
Exploration of the genetic basis and molecular mechanism for paternal mitochondrial DNA inheritance$174,696
R01 · FY2019 · HD · contact PI
Exploration of the genetic basis and molecular mechanism for paternal mitochondrial DNA inheritance$342,084
R01 · FY2018 · HD · contact PI
SLC25A46 mutations cause optic atrophy, axonal neuropathy, and cerebellar neurodegeneration$390,000
R01 · FY2017 · EY · contact PI
SLC25A46 mutations cause optic atrophy, axonal neuropathy, and cerebellar neurodegeneration$390,000
R01 · FY2016 · EY · contact PI
Genetic Studies of Optic Atrophy$177,163
R01 · FY2012 · EY · contact PI
Genetic Studies of Optic Atrophy$336,672
R01 · FY2011 · EY · contact PI
Genetic Studies of Optic Atrophy$353,455
R01 · FY2010 · EY · contact PI
Study on the intracellular Network of TBX3$225,512
R01 · FY2010 · CA · contact PI
Study on the intracellular Network of TBX3$57,659
R01 · FY2010 · CA · contact PI
Genetic Studies of Optic Atrophy$354,072
R01 · FY2009 · EY · contact PI
Study on the intracellular Network of TBX3$226,235
R01 · FY2009 · CA · contact PI
Study on the intracellular Network of TBX3$57,222
R01 · FY2009 · CA · contact PI
Study on the intracellular Network of TBX3$226,875
R01 · FY2008 · CA · contact PI
Study on the intracellular Network of TBX3$50,683
R01 · FY2008 · CA · contact PI
Study on the intracellular Network of TBX3$227,442
R01 · FY2007 · CA · contact PI
Roles of TBX3 and its Isoform, TBX3+2a, in Breast Cancer$76,250
R03 · FY2005 · CA
Roles of TBX3 and its Isoform, TBX3+2a, in Breast Cancer$75,750
R03 · FY2004 · CA
PHENOTYPIC VARIABILITY IN HOLT-ORAM SYNDROME$0
M01 · FY2002 · RR
PHENOTYPIC VARIABILITY IN HOLT-ORAM SYNDROME$0
M01 · FY2001 · RR
PHENOTYPIC VARIABILITY IN HOLT-ORAM SYNDROME$0
M01 · FY2001 · RR
PHENOTYPIC VARIABILITY IN HOLT-ORAM SYNDROME$0
M01 · FY2000 · RR