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23 Projects
Fiscal Year: Active ProjectsOpportunity Number: RFA-HG-20-037; RFA-HG-20-036; RFA-HG-25-002; RFA-HG-25-003; RFA-HG-25-004; RFA-HG-23-032; RFA-HG-23-033; RFA-HG-23-048
TActProjectYearSubPrincipal Investigator(s)/ Project Leader(s)OrganizationFiscal YearAdmin ICFunding ICFY Total Cost by ICSimilar Projects
Facilitating the Implementation of Population-wide Genomic Screening across Diverse Populations and Settings (FOCUS)
1TfR01ActfHG013851Projectf01YearfMEDICAL UNIVERSITY OF SOUTH CAROLINA2024NHGRI
NCI
NHGRI
$386,000
$370,716
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Translating the Clinical Knowledge of Mendelian Diseases to Real-world EHR Data to Improve Identification of Undiagnosed Patients
5TfR01ActfHG012657Projectf03YearfVANDERBILT UNIVERSITY MEDICAL CENTER2024NHGRI
NHGRI
$730,538
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Genomic medicine and gene function implementation for an underserved population
5TfR01ActfHG011795Projectf04YearfBAYLOR COLLEGE OF MEDICINE2024NHGRI
NHGRI
$942,969
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Age-based genomic screening in newborns, infants, and children: a novel paradigm in public health genomics
5TfR01ActfHG012271Projectf03YearfUNIV OF NORTH CAROLINA CHAPEL HILL2024NHGRI
NHGRI
$880,318
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Age-based genomic screening in newborns, infants, and children: a novel paradigm in public health genomics
3TfR01ActfHG012271Projectf03S1YearfUNIV OF NORTH CAROLINA CHAPEL HILL2024NHGRI
NHGRI
$89,095
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Navigating Online Patient Experiences of Genomic Medicine: Identifying and Overcoming Obstacles for African American Communities
5TfR21ActfHG011802Projectf02YearfBOSTON CHILDREN'S HOSPITAL2022NHGRI
NHGRI
$292,975
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Integrative Analyses of Clinical Pharmacogenetic Data to Prevent Hospital Readmission in Real-World Health Systems
5TfR21ActfHG013413Projectf02YearfENDEAVOR HEALTH CLINICAL OPERATIONS2025NHGRI
NHGRI
$300,811
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Clinical Expansion of Precision Medicine in the Emergency Department
1TfR01ActfHG013416Projectf01A1YearfUNIVERSITY OF FLORIDA2024NHGRI
NHGRI
$672,525
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Preemptive pharmacogenetic testing in medically underserved populations
5TfR01ActfHG011800Projectf04YearfUNIVERSITY OF FLORIDA2024NHGRI
NHGRI
$830,531
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MAGNET: MAKING GENOMICS ACCESSIBLE FOR NEWBORNS IN TEXAS
1TfR01ActfHG013428Projectf01A1YearfBAYLOR COLLEGE OF MEDICINE2024NHGRI
NHGRI
$705,600
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RESCUE: Rare Disease Detection and Escalation Support via a Learning Health System
5TfR01ActfHG012655Projectf03YearfCOLUMBIA UNIVERSITY HEALTH SCIENCES2024NHGRI
NHGRI
$1,003,342
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African Rare Diseases Initiative (ARDI): Advancing Genomic Medicine through rare diseases research in Africa
5TfR01ActfHG012284Projectf02YearfCENTRE DE GENETIQUE HUMAINE2024NHGRI
NHGRI
$628,907
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Calypso: a web software system supporting team-based, longitudinal genomic diagnostic care
5TfR01ActfHG012286Projectf04YearfUNIVERSITY OF UTAH2025NHGRI
NHGRI
$803,674
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Using Behavioral Economics and Implementation Science to Advance the Use of Genomic Medicine Utilizing an EHR Infrastructure across a Diverse Health System
5TfR01ActfHG012670Projectf03YearfUNIVERSITY OF PENNSYLVANIA2024NHGRI
NHGRI
$790,117
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Deploying a genomic-medicine risk assessment model for diverse primary care populations and settings
5TfR01ActfHG011794Projectf04YearfDUKE UNIVERSITY2024NHGRI
NHGRI
$704,127
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Rational Integration of Polygenic Risk Scores (RIPS)
5TfR01ActfHG012262Projectf04YearfVANDERBILT UNIVERSITY MEDICAL CENTER2025NHGRI
NHGRI
$790,943
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BUILDING THE EVIDENCE BASE FOR APPROPRIATE AND EFFICIENT IMPLEMENTATION OF EMERGING GENOMIC TESTS FOR DISEASE MANAGEMENT AND SCREENING
5TfR01ActfHG011792Projectf04YearfUNIVERSITY OF CALIFORNIA, SAN FRANCISCO2024NHGRI
NHGRI
$918,686
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Toward DNA Sequencing as a Primary Newborn Screen for Treatable Disorders not Amenable to Current Screening
5TfR21ActfHG011805Projectf02YearfUNIVERSITY OF CALIFORNIA, SAN FRANCISCO2022NHGRI
NHGRI
$323,000
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Let's Talk: Overcoming barriers to the uptake of cascade screening through a stakeholder-informed online intervention
1TfR21ActfHG013417Projectf01YearfUNIV OF NORTH CAROLINA CHAPEL HILL2024NHGRI
NHGRI
$575,098
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Advancing the implementation of variant-level functional data into clinical databases and clinical practice
5TfR01ActfHG013025Projectf03YearfUNIVERSITY OF WASHINGTON2025NHGRI
NHGRI
$715,577
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Fair Phenotype Annotation and Genomic Reinterpretation
5TfR01ActfHG013031Projectf02YearfCOLUMBIA UNIVERSITY HEALTH SCIENCES2024NHGRI
NHGRI
$880,069
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Real-time genetic diagnosis at the point of care
5TfR01ActfHG011799Projectf04YearfGEISINGER CLINIC2024NHGRI
NHGRI
$902,661
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VIGOR: Virtual Genome Center for Infant Health
5TfR01ActfHG011798Projectf04YearfBOSTON CHILDREN'S HOSPITAL2024NHGRI
NHGRI
$1,027,589
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