|
Investigating a novel mechanism underlying prefrontal cortex dysfunction in autism and intellectual disability |
1F30MH127800-01A1 |
|
NIMH |
2022 |
|
The Role of the ASD Risk Gene CHD8 in Neural Development |
1F30MH132282-01 |
|
NIMH |
2022 |
|
Mechanisms underlying impaired hippocampal physiology in Fragile X Syndrome |
1F31MH127933-01A1 |
|
NIMH |
2022 |
|
Cell type signaling specificity of the neurodevelopmental disease-associated DYRK1A kinase |
1R01MH127075-01A1 |
|
NIMH |
2022 |
|
ASH1L mediated transcription networks in autism spectrum disorders |
1R01MH127081-01A1 |
|
NIMH |
2022 |
|
Elucidating the synaptic interactome of the high risk autism gene ANK2 |
1R01MH127848-01A1 |
|
NIMH |
2022 |
|
Investigating mechanisms underlying impaired social and spatial cognition in rodent models of Fragile X syndrome |
1R01MH131317-01 |
|
NIMH |
2022 |
|
Neurodevelopmental Disorder Risk Gene Regulation of Intrinsic Membrane Excitability: A Rheostat that Tunes Dendritic Morphogenesis to Regulate Circuit Assembly During Development |
1R01MH131788-01 |
|
NIMH |
2022 |
|
Molecular Mechanisms of Developmental Spine Remodeling |
2R56MH113280-06A1 |
|
NIMH |
2022 |
|
Characterizing patient-specific TBR1 mutations: Understanding a master regulator of autism risk. |
3R01MH113926-05S1 |
|
NIMH |
2022 |