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Christopher D Porada

Wake Forest University Health Sciences

$6,964,841
Attributed
$12,933,031
Total exposure
7
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 $1.8M · FY200525
$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25

Funding mix

By agency

NIH$12,933,031 · 7

By mechanism

R01$12,163,513 · 6
U01$769,518 · 1

Top collaborators

Most similar at Wake Forest University Health Sciences

Same institution · by research overlap

Others in their field

Top investigators on “Cells

Research focus

CellsImmuneSheepLifeVectorAnimal ModelGene TherapyHemophilia ABirthTransgenesProteinsF8 GeneInheritedDoseIncidencePre-ClinicalTreatment EfficacyGenetic DiseasesProductionPrenatalAdultSafetyCurative TreatmentsEngraftment

Grant awards (25)

Targeted conditioning to maximize prenatal HSC engraftment for SCD$665,070
R01 · FY2025 · HL
Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia A$652,874
R01 · FY2025 · HL
Using human liver tissue equivalents to optimize AAV-mediated GT and better define age-related clinical risks$383,800
R01 · FY2025 · HL
Targeted conditioning to maximize prenatal HSC engraftment for SCD$662,949
R01 · FY2024 · HL
Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia A$648,076
R01 · FY2024 · HL
Using human liver tissue equivalents to optimize AAV-mediated GT and better define age-related clinical risks$383,921
R01 · FY2024 · HL
Targeted conditioning to maximize prenatal HSC engraftment for SCD$716,640
R01 · FY2023 · HL
Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia A$673,905
R01 · FY2023 · HL
Using human liver tissue equivalents to optimize AAV-mediated GT and better define age-related clinical risks$397,789
R01 · FY2023 · HL
Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia A$707,639
R01 · FY2022 · HL
Prenatal Cell and Gene Therapy for Hemophilia A$698,903
R01 · FY2020 · HL
cGMP Manufacture Of FVIII-Expressing Placental Cells For Hemophilia A$383,839
U01 · FY2020 · HL
Prenatal Cell and Gene Therapy for Hemophilia A$692,734
R01 · FY2019 · HL
Postnatal Cell-Based Therapies for Hemophilia A$577,601
R01 · FY2019 · HL
cGMP Manufacture Of FVIII-Expressing Placental Cells For Hemophilia A$385,679
U01 · FY2019 · HL
Prenatal Cell and Gene Therapy for Hemophilia A$675,825
R01 · FY2018 · HL
Postnatal Cell-Based Therapies for Hemophilia A$577,601
R01 · FY2018 · HL
Prenatal Cell and Gene Therapy for Hemophilia A$746,740
R01 · FY2017 · HL
Postnatal Cell-Based Therapies for Hemophilia A$606,184
R01 · FY2017 · HL
Postnatal Cell-Based Therapies for Hemophilia A$698,612
R01 · FY2016 · HL
In Utero Gene Therapy$191,150
R01 · FY2006 · HD · contact PI
In Utero Gene Therapy$195,750
R01 · FY2005 · HD
In Utero Gene Therapy$195,750
R01 · FY2004 · HD
In Utero Gene Therapy$195,750
R01 · FY2003 · HD
In Utero Gene Therapy$218,250
R01 · FY2002 · HD