|
|
Modeling ASD-linked genetic mutations in 3D human brain organoids |
| 5R01MH112940-05 |
|
NIMH |
2022 |
|
|
The Spatiotemporal Landscape of the Human Brain Epitranscriptome |
| 5R01MH117406-05 |
|
NIMH |
2022 |
|
|
Cognitive Genomics as a Window on Neurodevelopment and Psychopathology |
| 5R01MH117646-05 |
|
NIMH |
2022 |
|
|
Construction of the integrated human cortical organoids to investigate neurodevelopmental disorders |
| 5R01MH118344-04 |
|
NIMH |
2022 |
|
|
Investigation of how axon development is disrupted by the autism-causing Timothy syndrome mutation. |
| 5R01MH119157-04 |
|
NIMH |
2022 |
|
|
The influence of common genetic variation on brain overgrowth pathways |
| 5R01MH120125-04 |
|
NIMH |
2022 |
|
|
Connecting 3D genome misfolding to transcriptional silencing in fragile X syndrome |
| 5R01MH120269-04 |
|
NIMH |
2022 |
|
|
TAOK2 Kinase Signaling in Human Neural Stem Cell Development |
| 5R01MH121674-03 |
|
NIMH |
2022 |
|
|
Functional Data Analysis for High-Dimensional Biobehavioral Data |
| 5R01MH122428-03 |
|
NIMH |
2022 |
|
|
Epigenetic Maintenance of Neural Cell Identity |
| 5R01MH122565-02 |
|
NIMH |
2022 |
