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HPSC-DERIVED MICROGLIA FOR IN VITRO MODELING OF RETT SYNDROME |
| 1F30MH115616-01 |
GUTTIKONDA, SUDHA R |
NIMH |
2017 |
|
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ALTERED DOPAMINE TRANSPORTER FUNCTION IN AUTISM |
| 1F31MH114316-01 |
AGUILAR, JENNY ISABEL |
NIMH |
2017 |
|
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VOLUME-BASED ANALYSIS OF 6-MONTH INFANT BRAIN MRI FOR AUTISM BIOMARKER IDENTIFICATION AND EARLY DIAGNOSIS |
| 1K01MH109773-01A1 |
WANG, LI |
NIMH |
2017 |
|
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DISTRIBUTION OF CHILD MENTAL HEALTH WORKFORCE AND HEALTH CARE FOR CHILDREN WITH AUTISM |
| 1R01MH112760-01A1 |
YU, HAO |
NIMH |
2017 |
|
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REACTIVATION OF EPIGENETICALLY SILENCED FMR1 AS A THERAPEUTIC APPROACH FOR FRAGILE X SYNDROME |
| 1R01MH113874-01 |
GREEN, MICHAEL R. |
NIMH |
2017 |
|
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GENETIC BASIS OF INHIBITORY COGNITIVE CONTROL AS A DIMENSIONAL CONSTRUCT SPANNING PSYCHIATRIC ILLNESS |
| 1R03MH112032-01A1 |
NURMI, ERIKA L |
NIMH |
2017 |
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WOMEN WITH AUTISM SPECTRUM DISORDERS DURING ADOLESCENCE AND ADULTHOOD: UNIQUE AND COMMON VULNERABILITIES |
| 1R03MH112783-01 |
TAYLOR, JULIE LOUNDS |
NIMH |
2017 |
|
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EPIGENOMIC DYSREGULATION OF NEURODEVELOPMENTAL GENES UNDERLIES AUTISM SPECTRUM DISORDERS |
| 1R21MH114005-01 |
MAUNAKEA, ALIKA KEOLAOKALANI |
NIMH |
2017 |
|
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RAPID, IN VITRO PHENOTYPING OF MONOGENIC NEUROLOGICAL DISORDERS USING CRISPRI AND HIGH-THROUGHPUT ALL-OPTICAL ELECTROPHYSIOLOGY. |
| 1R43MH113447-01A1 |
WERLEY, CHRISTOPHER |
NIMH |
2017 |
|
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CROSS MODAL INTEGRATION OF MOLECULAR AND PHYSIOLOGICAL NETWORKS IN ASD (2/2) |
| 1U01MH115745-01 |
PASCA, SERGIU |
NIMH |
2017 |
