|
|
Noncoding mutations in neurodevelopmental disorders |
| 1R01MH126933-01A1 |
|
NIMH |
2022 |
|
|
Neural and developmental trajectories of females with autism spectrum disorder |
| 1R01MH127046-01A1 |
|
NIMH |
2022 |
|
|
Cell type signaling specificity of the neurodevelopmental disease-associated DYRK1A kinase |
| 1R01MH127075-01A1 |
|
NIMH |
2022 |
|
|
Novel SETD5-based Molecular Mechanisms and Therapeutic Tools to Understand and Revert Neuronal Dysfunction Associated with Intellectual disability and Autism |
| 1R01MH127077-01A1 |
|
NIMH |
2022 |
|
|
ASH1L mediated transcription networks in autism spectrum disorders |
| 1R01MH127081-01A1 |
|
NIMH |
2022 |
|
|
Autism Caregiver Coaching in Africa |
| 1R01MH127573-01A1 |
|
NIMH |
2022 |
|
|
Elucidating the synaptic interactome of the high risk autism gene ANK2 |
| 1R01MH127848-01A1 |
|
NIMH |
2022 |
|
|
Validating Measures and Unpacking Differences in Service Use for Diverse Children with Autism |
| 1R01MH128275-01A1 |
|
NIMH |
2022 |
|
|
Individualized approaches to determining likelihood of ASD caseness |
| 1R01MH128288-01A1 |
|
NIMH |
2022 |
|
|
Unraveling the Genetic Programs Engaged in ASD Neurons Through Coupled Transcriptomic and Phenotypic Readouts |
| 1R01MH128366-01A1 |
|
NIMH |
2022 |