|
Utilizing Causal X-Linked Intellectual Disability Variants to Gain Insight into the O-GlcNAc Transferase Enzyme |
1F31HD108843-01A1 |
|
NICHD |
2022 |
|
Structural and functional investigations of two lysosomal transporters implicated in developmental disorders |
1F31HD110229-01 |
|
NICHD |
2022 |
|
Illuminating the distribution of extreme evolutionary constraint in the human genome from fetal demise to severe developmental disorders |
1F31HD111109-01 |
|
NICHD |
2022 |
|
Disruption of three-dimensional genome organization as a noncoding mechanism of disease in human developmental disorders |
1K99HD108392-01 |
|
NICHD |
2022 |
|
Suppressing Aneuploidy-associated phenotypes in Down syndrome |
1R01HD107873-01A1 |
|
NICHD |
2022 |
|
Novel computational strategies to deconvolute co-occurring conditions in Down syndrome |
1R01HD109765-01 |
|
NICHD |
2022 |
|
Defining molecular and gene-regulatory dysregulation in Down Syndrome tissues and models |
1R21HD108606-01 |
|
NICHD |
2022 |
|
Molecular basis of congenital disorder of glycosylation type 1N |
1R21HD109719-01 |
|
NICHD |
2022 |
|
Postdoctoral Research in Neurodevelopmental Disorders |
2T32HD040127-21 |
|
NICHD |
2022 |
|
Elevated mitochondrial fusion and function in Down syndrome - Revision - 2 |
3R01HD101006-01S1 |
|
NICHD |
2022 |