|
The molecular roles of RFX3 in neurodevelopment and Autism Spectrum disorder |
1F30MH128995-01A1 |
|
NIMH |
2022 |
|
Defining the gene regulatory roles of non-coding variants in the pathogenesis of autism |
1F31MH131380-01 |
|
NIMH |
2022 |
|
Single-molecule Investigation of the Interaction Between MeCP2 and Chromatin |
1F31MH132306-01 |
|
NIMH |
2022 |
|
Discovery of genetic modifiers of PTEN-ASD severity in a library of genetically diverse iPSC lines |
1K01MH131856-01 |
|
NIMH |
2022 |
|
Machine Learning for Precision Treatments in Schizophrenia |
1K23MH129628-01A1 |
|
NIMH |
2022 |
|
Tourette Syndrome genetics and neuroimaging international collaborative study |
1R01MH126213-01A1 |
|
NIMH |
2022 |
|
Noncoding mutations in neurodevelopmental disorders |
1R01MH126933-01A1 |
|
NIMH |
2022 |
|
Identification of metabolic alterations during cortical development in a human cellular model for 22q11.2 deletion syndrome |
1R01MH128352-01 |
|
NIMH |
2022 |
|
Unraveling the Genetic Programs Engaged in ASD Neurons Through Coupled Transcriptomic and Phenotypic Readouts |
1R01MH128366-01A1 |
|
NIMH |
2022 |
|
Estimating The Fraction of Variance Explained by Genetics and Neuroanatomy in Neuropsychiatric Conditions |
1R01MH128923-01A1 |
|
NIMH |
2022 |