The notices it replaced
Its page names no earlier notice: it is new, or it does not say.
Replaced by PAR-25-185.
Who won it before
10 competing awards (new and renewals) from FY2014 to FY2025 under this notice and the notices it replaced: $6,578,113 in first-year total cost, median $650,750.
Most frequent study sections
- Therapeutic Approaches to Genetic Diseases Study Section[TAG]8
- Special Emphasis Panel[ZRG1 MGG-K (02)]1
- Special Emphasis Panel[ZRG1 MGG-L (02)]1
Most frequent institutions
- UNIVERSITY OF PITTSBURGH AT PITTSBURGH2
- CHILDREN'S HOSP OF PHILADELPHIA1
- CHILDREN'S MERCY HOSP (KANSAS CITY, MO)1
- EMORY UNIVERSITY1
- UNIVERSITY OF ALABAMA AT BIRMINGHAM1
| FY | Project | PIs | Institution | First-year cost | Study section |
|---|---|---|---|---|---|
| 2025 | Leveraging whole genome sequencing and functional genomic characterization to improve NSCLP gene discovery1R01DE033908-01A1 | HECHT, JACQUELINE THUFF, CHAD DANIELLETRA, ARIADNE M | UNIVERSITY OF PITTSBURGH AT PITTSBURGH, PA | $645,034 | ZRG1 |
| 2025 | Functional Characterization of Genetic Variants in Rare Disease Associated with Shoc2 scaffold1R01HD118715-01 | GALPERIN, EMILIA | UNIVERSITY OF KENTUCKY, KY | $419,204 | ZRG1 |
| 2024 | Mechanisms of ciliopathy associated structural birth defects1R01HD111399-01A1 | YODER, BRADLEY K. | UNIVERSITY OF ALABAMA AT BIRMINGHAM, AL | $602,956 | TAG |
| 2023 | Evaluating the Impact of Mutations in Distant-Acting Enhancers in Structural Birth Defects1R01HD114353-01 | PENNACCHIO, LEN ALEXANDERVISEL, AXEL | UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB, CA | $816,999 | TAG |
| 2023 | Genomic Risk Variants in Orofacial Clefting: Discovery and Functional Validation1R01DE032319-01 | MARAZITA, MARY L.MURRAY, STEPHEN A | UNIVERSITY OF PITTSBURGH AT PITTSBURGH, PA | $750,143 | TAG |
| 2023 | Functional analysis of ESRP1/2 and CTNND1 gene variants in orofacial cleft1R01DE032332-01 | LIAO, ERIC CHIEN-WEI | CHILDREN'S HOSP OF PHILADELPHIA, PA | $675,857 | TAG |
| 2023 | Multi-organism platform for functional assessment of human birth defect associated genomic variants1R01HD110556-01 | JOHNSON, AARON NKROLL, KRISTEN LORNITZ, DAVID MPAK, STEPHEN CSOLNICAKREZEL, LILIANNA | WASHINGTON UNIVERSITY, MO | $651,149 | TAG |
| 2023 | Screen and functional validation of Pediatric Cardiomyopathy genetic variants in Drosophila1R01HD111480-01 | HAN, ZHE | UNIVERSITY OF MARYLAND BALTIMORE, MD | $650,351 | TAG |
| 2023 | Systematic Identification and Phenotypic Characterization of causal genetic variants in Rare Disease-Associated Birth Defects1R01HD110447-01 | YOUNGER, SCOTT T | CHILDREN'S MERCY HOSP (KANSAS CITY, MO), MO | $641,067 | TAG |
| 2022 | Functional validation of sequence variants affecting neurodevelopmental and craniofacial phenotypes1R56DE031771-01 | CORCES, VICTOR G. | EMORY UNIVERSITY, GA | $725,353 | TAG |
Data: Grants.gov's daily extract and NIH's notice pages and award files, in ScienceGraph release conductgrants-2026-11-09-0.1.0. An award is listed only where NIH's own record names the notice, and a PI only by NIH's profile ID. Grants.gov and NIH do not endorse ScienceDex.