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Sara Kathryn Young-Baird
Henry M. Jackson Fdn For The Adv Mil/Med
$1,111,471
Attributed
$1,111,471
Total exposure
3
Grants
3
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. They are the sole PI on all grants (the two match).
Funding over time
peak $372.9K · FY2017–25$500K$375K$250K$125K$0
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$1,111,471 · 3
By mechanism
R00$738,591 · 1
R35$372,880 · 1
FI2$0 · 1
Top collaborators
No co-investigators on record.
Most similar at Henry M. Jackson Fdn For The Adv Mil/Med
Same institution · by research overlap
- Barrington G Burnett$2,776,928
- Thomas Flagg$975,941
Others in their field
Other Emerging Leaders on “Gene Expression”
- Evan Z Macosko · Broad Institute, Inc.$35,121,158
- Ethan Dmitrovsky · Leidos Biomedical Research, Inc.$26,358,801
- Benjamin E Deverman · Broad Institute, Inc.$16,920,984
- Tomasz Nowakowski · University Of California, San Francisco$15,628,426
- Stacey Lynn Clardy · Utah State Higher Education System--University Of Utah$15,093,619
- Crystal Mackall · Children'S Hosp Of Philadelphia$14,040,300
Research focus
Gene ExpressionImpairmentTranslationsMessenger RnaPeptide Initiation FactorsGuanosine TriphosphateProtein BiosynthesisMehmo SyndromeLinkMemberGenesInitiator CodonGenerationsEpilepsyHuman DiseaseInduced Pluripotent Stem CellGenome-WideCharacteristicsBiological Adaptation To StressElectrophysiology (Science)DiagnosisCrispr/Cas TechnologyExperimental StudyAcronyms
Grant awards (5)
Regulation of protein synthesis during cellular stress$372,880
R35 · FY2025 · GM · contact PI
Molecular analysis of MEHMO syndrome mutations in translation factor eIF2$242,564
R00 · FY2024 · HD · contact PI
Molecular analysis of MEHMO syndrome mutations in translation factor eIF2$247,028
R00 · FY2023 · HD · contact PI
Molecular analysis of MEHMO syndrome mutations in translation factor eIF2$248,999
R00 · FY2022 · HD · contact PI
Molecular analysis of MEHMO syndrome: Translational profiling of stem cells and derived neurons from patients with mutations in translation factor eIF2γ$0
FI2 · FY2017 · GM · contact PI