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The molecular roles of RFX3 in neurodevelopment and Autism Spectrum disorder |
1F30MH128995-01A1 |
|
NIMH |
2022 |
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Defining the gene regulatory roles of non-coding variants in the pathogenesis of autism |
1F31MH131380-01 |
|
NIMH |
2022 |
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Discovery of genetic modifiers of PTEN-ASD severity in a library of genetically diverse iPSC lines |
1K01MH131856-01 |
|
NIMH |
2022 |
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Noncoding mutations in neurodevelopmental disorders |
1R01MH126933-01A1 |
|
NIMH |
2022 |
|
Unraveling the Genetic Programs Engaged in ASD Neurons Through Coupled Transcriptomic and Phenotypic Readouts |
1R01MH128366-01A1 |
|
NIMH |
2022 |
|
2/4 The Autism Sequencing Consortium: Discovering autism risk genes and how they impact core features of the disorder |
1R01MH129722-01 |
|
NIMH |
2022 |
|
1/4 - The Autism Sequencing Consortium: Discovering autism risk genes and how they impact core features of the disorder |
1R01MH129724-01 |
|
NIMH |
2022 |
|
3/4 The Autism Sequencing Consortium: Discovering autism risk genes and how they impact core features of the disorder |
1R01MH129725-01 |
|
NIMH |
2022 |
|
4/4 - The Autism Sequencing Consortium: Discovering autism risk genes and how they impact core features of the disorder |
1R01MH129751-01 |
|
NIMH |
2022 |
|
Autism Disparities Conference Series: Building Capacity for the Next Generation of Diverse Scholars Addressing the Translational Pipeline |
1R13MH130112-01 |
|
NIMH |
2022 |