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NIH funding notice PA-11-085

Genetic Susceptibility & Variability of Human Structural Birth Defects (R01)

Closed on January 2, 2014.

Posted
December 22, 2010
Close date
January 2, 2014
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: $891,550 in first-year total cost, median $445,775.

Most frequent study sections

  1. Genetics of Health and Disease Study Section[GHD]2

Most frequent institutions

  1. CINCINNATI CHILDRENS HOSP MED CTR1
  2. UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON1
Competing awards under PA-11-085 and the notices it replaced
FYProjectPIsInstitutionFirst-year costStudy section
2014Creating a Myelomeningocele Exome Variant Map1R01HD073434-01A1AU, KIT SINGUNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON, TX$488,554GHD
2014Forward Genetic Analysis of Congenital Defects in Cortical Circuits and Structure1R01NS085023-01A1STOTTMANN, ROLF WCINCINNATI CHILDRENS HOSP MED CTR, OH$402,996GHD

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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PA-11-085: Genetic Susceptibility & Variability of Human Structural Birth Defects (R01) | ScienceDex | ConductScience