|
Characterizing human-specific expression of ZP2 in the cerebellum |
1 F30 MH123074-01A1 |
CHERSKOV, ADRIANA |
NIMH |
2021 |
|
Functional genomic investigation of complement signaling in the human brain |
1 F30 MH125523-01A1 |
KIM, MINSOO |
NIMH |
2021 |
|
Somatic Mosaicism in Neuropsychiatric Disorders |
1 F31 MH124292-01A1 |
MAURY, EDUARDO ANTONIO |
NIMH |
2021 |
|
Analysis of Poison Exon Inclusion in Genes Associated with Neurodevelopmental Disorders and Autism Spectrum Disorder |
1 F31 MH126628-01 |
FELKER, STEPHANIE ANN |
NIMH |
2021 |
|
Enhancer-targeted correction of haploinsufficient autism risk genes |
1 F32 MH124337-01A1 |
CHEN, GEORGE TSUN-TE |
NIMH |
2021 |
|
Epigenetic Maintenance of Neural Cell Identity |
1 R01 MH122565-01A1 |
BELL, OLIVER |
NIMH |
2021 |
|
Functional convergence following disruption of diverse genes associated with neurodevelopmental disorders |
1 R01 MH123155-01A1 |
BRENNAND, KRISTEN JENNIFER |
NIMH |
2021 |
|
Maternal health in pregnancy and autism risk - genetic and non-genetic mechanisms |
1 R01 MH124817-01 |
JANECKA, MAGDALENA |
NIMH |
2021 |
|
Fine-Mapping Genome-Wide Associated Loci using Multi-omics Data to Identify Mechanisms Affecting Serious Mental Illness |
1 R01 MH125235-01 |
MACDONALD, MATTHEW L |
NIMH |
2021 |
|
Multiethnic genomic epigenomic and transcriptomic fine-mapping and functional validation analysis of schizophrenia and bipolar disorder risk loci |
1 R01 MH125246-01 |
ROUSSOS, PANAGIOTIS |
NIMH |
2021 |