|
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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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GENOMIC SEQUENCING TO AID DIAGNOSIS IN PEDIATRIC AND PRENATAL PRACTICE: EXAMINING CLINICAL UTILITY, ETHICAL IMPLICATIONS, PAYER COVERAGE, AND DATA INTEGRATION IN A DIVERSE POPULATION. |
| 1U01HG009599-01 |
KWOK, PUI-YAN |
NHGRI |
2017 |
|
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HEARING IMPAIRMENT GENETICS STUDIES IN AFRICA (HI-GENES AFRICA) |
| 1U01HG009716-01 |
WONKAM, AMBROISE |
NHGRI |
2017 |
|
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INDIVIDUAL FINDINGS IN GENETIC RESEARCH IN AFRICA (IFGENERA) |
| 1U54HG009790-01 |
WONKAM, AMBROISE |
NHGRI |
2017 |
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EYES OF AFRICA : THE GENETICS OF BLINDNESS |
| 1U54HG009826-01 |
ASHAYE, ADEYINKA O |
NHGRI |
2017 |
