|
|
Exploring the role of genetic structural variation in neuropsychiatric diseases |
| 5F31MH124393-03 |
|
NIMH |
2022 |
|
|
Analysis of Poison Exon Inclusion in Genes Associated with Neurodevelopmental Disorders and Autism Spectrum Disorder |
| 5F31MH126628-02 |
|
NIMH |
2022 |
|
|
Enhancer-targeted correction of haploinsufficient autism risk genes |
| 5F32MH124337-02 |
|
NIMH |
2022 |
|
|
A framework enabling the genomic analysis of psychiatric traits across admixed populations. |
| 5K01MH121659-04 |
|
NIMH |
2022 |
|
|
Generalizing polygenic risk prediction methods across populations for insights into psychiatric disease |
| 5R00MH117229-05 |
|
NIMH |
2022 |
|
|
Early Epigenetic Footprint of Neurological Diseases |
| 5R00MH117393-05 |
|
NIMH |
2022 |
|
|
Novel Statistical methods for DNA Sequencing Data, and applications to Autism. |
| 5R01MH095797-08 |
|
NIMH |
2022 |
|
|
Dissecting neural mechanisms integrating multiple inputs in C.elegans |
| 5R01MH096881-10 |
|
NIMH |
2022 |
|
|
Typical and Pathological Cellular Development of the Human Amygdala |
| 5R01MH097236-10 |
|
NIMH |
2022 |
|
|
Proteogenetics of Autism Spectrum Disorders |
| 5R01MH100175-09 |
|
NIMH |
2022 |
