|
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Disability, diversity and trust in precision medicine research: stakeholders engagement |
| 1 R01 HG010868-01 |
SABATELLO, MAYA |
NHGRI |
2020 |
|
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Optical Genome Mapping (OGM) for Concurrent Genetic and Epigenetic Diagnosis of Inborn Disorders |
| 1 R21 HG011424-01 |
VILAIN, ERIC J |
NHGRI |
2020 |
|
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Feasibility of an Innovative Method to Understand the Dynamics of Choice and Create Diversity in Genomics Research among Older African Americans |
| 1 R21 HG011503-01 |
PASSMORE, SUSAN RACINE |
NHGRI |
2020 |
|
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The X-factor of complex disease: Development, implementation, and extensive application of methods for analysis of the X chromosome in GWA, sequence-based association, and eQTL studies |
| 5R01HG006849-07 |
CLARK, ANDREW G |
NHGRI |
2020 |
|
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GURU: Graduate and Undergraduate Researchers of UCEER |
| 5R25HG010020-03 |
BOTKIN, JEFFREY R |
NHGRI |
2020 |
|
|
Genomics Diversity Summer Program (GDSP) at Stanford |
| 5R25HG010857-02 |
SNYDER, MICHAEL P |
NHGRI |
2020 |
|
|
Subcellular Wireless Axons for in vivo Localized Neuronal Excitation |
| 1 R01 NS105691-01A1 |
KOZAI, TAKASHI DANIEL YOSHIDA |
NINDS |
2020 |
|
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Sur1-Trpm4 regulation of the pro-inflammatory astrocytic secretome in EAE |
| 1 R01 NS107262-01A1 |
GERZANICH, VLADIMIR |
NINDS |
2020 |
|
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Etiology of cognitive decline in Spinocerebellar ataxia type 1 |
| 1 R01 NS109077-01A1 |
CVETANOVIC, MARIJA |
NINDS |
2020 |
|
|
Signaling pathways that modulate neuronal activity |
| 1 R01 NS109476-01A1 |
AILION, MICHAEL |
NINDS |
2020 |
