|
Mapping human brain cell type-specific isoform usage in ASD |
1R21MH129817-01 |
|
NIMH |
2022 |
|
Understanding the Genome Maintenance Function of the Fragile X Protein (FMRP) |
1R21MH130812-01 |
|
NIMH |
2022 |
|
Serious mental illness and incarceration: piloting the use of a multi sector linked administrative dataset |
1R34MH128397-01 |
|
NIMH |
2022 |
|
Cortical and subcortical chandelier cell pathophysiology and symptomatology in autism |
2R01MH094681-11 |
|
NIMH |
2022 |
|
Investigation of how axon development is disrupted by the autism-causing Timothy syndrome mutation. |
3R01MH119157-04S1 |
|
NIMH |
2022 |
|
Axonal FMRP in Synaptic Development |
3R01MH126176-02S1 |
|
NIMH |
2022 |
|
Integrated, cell type specific functional genomics analyses of regulatory sequence elements and their dynamic interaction networks in neuropsychiatric brain tissues |
3U01MH116529-04S1 |
|
NIMH |
2022 |
|
The role of autism susceptibility genes in the 16p11.2 locus on the development and function of human stem cell-derived neural cells |
4R00MH119327-03 |
|
NIMH |
2022 |
|
Characterizing human-specific expression of ZP2 in the cerebellum |
5F30MH123074-02 |
|
NIMH |
2022 |
|
Somatic Mosaicism in Neuropsychiatric Disorders |
5F31MH124292-02 |
|
NIMH |
2022 |