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NIH funding notice PAR-16-061

Natural History of Disorders Identifiable by Screening of Newborns (R01)

Closed on January 24, 2018.

Posted
December 11, 2015
Close date
January 24, 2018
Activity codes
Not stated on the notice page
Institutes taking part
Not stated on the notice page

Read the notice on Grants.gov · NIH Guide page

The notices it replaced

Its page was not saved, so the notices it replaced are not known.

Who won it before

2 competing awards (new and renewals) from FY2014 to FY2025 under this notice and the notices it replaced: $1,237,117 in first-year total cost, median $618,559.

Most frequent study sections

  1. Special Emphasis Panel[ZRG1 GGG-B (50)]2

Most frequent institutions

  1. UNIVERSITY OF COLORADO DENVER1
  2. WASHINGTON STATE UNIVERSITY1
Competing awards under PAR-16-061 and the notices it replaced
FYProjectPIsInstitutionFirst-year costStudy section
2018Natural History of Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD), a Heritable Disorder of GABA Metabolism1R01HD091142-01A1GIBSON, K MICHAELWASHINGTON STATE UNIVERSITY, WA$686,980ZRG1
2017The eXtraordinarY Babies Study: Natural History of Health and Neurodevelopment in Infants and Young Children with Sex Chromosome Trisomy1R01HD091251-01A1TARTAGLIA, NICOLE RENEEUNIVERSITY OF COLORADO DENVER, CO$550,137ZRG1

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.

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PAR-16-061: Natural History of Disorders Identifiable by Screening of Newborns (R01) | ScienceDex | ConductScience