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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 |
|
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THE CONTRIBUTION FOLATE AND VITAMIN B12 GENES TO DISEASE. |
| 1ZIAHG000167-17 |
BRODY, LAWRENCE |
NHGRI |
2016 |
|
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GENETIC ANALYSIS OF ATTENTION DEFICIT HYPERACTIVITY DISORDER |
| 1ZIAHG000175-17 |
MUENKE, MAXIMILIAN |
NHGRI |
2016 |
|
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INTERVENTIONS IN GENETIC COUNSELING |
| 1ZIAHG200317-13 |
BIESECKER, BARBARA BOWLES |
NHGRI |
2016 |
|
|
INVESTIGATIONS OF METHYLMALONIC ACIDEMIA AND RELATED DISORDERS |
| 1ZIAHG200318-13 |
VENDITTI, CHARLES P |
NHGRI |
2016 |
