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Matthew R Taylor

University Of Colorado Denver

$5,502,265
Attributed
$8,227,588
Total exposure
5
Grants
3
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 $1.3M · FY200525
$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
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'17
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'20
'21
'22
'23
'24
'25

Funding mix

By agency

NIH$8,227,588 · 5

By mechanism

R01$7,574,447 · 4
K23$653,141 · 1

Top collaborators

Most similar at University Of Colorado Denver

Same institution · by research overlap

Others in their field

Top investigators on “Genes

Research focus

GenesCardiomyopathiesGeneticMutationVariantDesignHeart FailureGenomicsDilated CardiomyopathyGenetic VariantNovel TherapeuticsGenome SequencingResearch PersonnelClinical DataCohortUnited States National Institutes Of HealthRegistriesInnovationCardiac MyocytesBaseHeartPathway InteractionsAffectCardiac

Grant awards (25)

Elucidating the Origin of Sudden Cardiac Death in Dilated Cardiomyopathy: from Phenotype Predictors to Therapeutic Targets$679,139
R01 · FY2025 · HL
Integrative genomic and transcriptomic investigation of human heart failure mechanisms$631,780
R01 · FY2025 · HL · contact PI
Elucidating the Origin of Sudden Cardiac Death in Dilated Cardiomyopathy: from Phenotype Predictors to Therapeutic Targets$22,495
R01 · FY2025 · HL
Elucidating the Origin of Sudden Cardiac Death in Dilated Cardiomyopathy: from Phenotype Predictors to Therapeutic Targets$675,327
R01 · FY2024 · HL
Integrative genomic and transcriptomic investigation of human heart failure mechanisms$624,142
R01 · FY2024 · HL · contact PI
Engineering Cardiac spheroids to study Laminopathies$37,732
R01 · FY2024 · HL
Elucidating the Origin of Sudden Cardiac Death in Dilated Cardiomyopathy: from Phenotype Predictors to Therapeutic Targets$727,280
R01 · FY2023 · HL
Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathy$508,747
R01 · FY2023 · HL
Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathy$510,302
R01 · FY2022 · HL
Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathy$509,525
R01 · FY2021 · HL
Cardiomyocyte phenotype and mechanotransduction in Filamin C gene variants causing arrhythmogenic cardiomyopathy$524,177
R01 · FY2020 · HL
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$410,109
R01 · FY2016 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$429,571
R01 · FY2015 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$391,713
R01 · FY2014 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$37,713
R01 · FY2014 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$20,984
R01 · FY2014 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$385,715
R01 · FY2013 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$39,086
R01 · FY2013 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$384,375
R01 · FY2012 · HL · contact PI
Whole genome DNA sequencing to identify novel genes in dilated cardiomyopathy$24,535
R01 · FY2012 · HL · contact PI
Familial Dilated Cardiomyopathy:Genetic Characterization$130,680
K23 · FY2006 · HL · contact PI
Familial Dilated Cardiomyopathy:Genetic Characterization$130,680
K23 · FY2005 · HL
Familial Dilated Cardiomyopathy:Genetic Characterization$130,661
K23 · FY2004 · HL
Familial Dilated Cardiomyopathy:Genetic Characterization$130,584
K23 · FY2003 · HL
Familial Dilated Cardiomyopathy:Genetic Characterization$130,536
K23 · FY2002 · HL