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Abstract
The role of genomic research and medicine in improving health continues to grow significantly, highlighting the need for increased equitable inclusion of diverse populations in genomics. Native Hawaiian and Pacific Islander (NHPI) communities are often missing from these efforts to ensure that the benefits of genomics are accessible to all individuals. In this article, we analyze the qualities of NHPI populations relevant to their inclusion in genomic research and investigate their current representation using data from the genome-wide association studies (GWAS) catalog. A discussion of the barriers NHPI experience regarding participating in research and recommendations to improve NHPI representation in genomic research are also included.
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1 National Institutes of Health, Center for Research on Genomics and Global Health, National Human Genome Research Institute, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165); University of Hawaiʻi at Mānoa, Honolulu, USA (GRID:grid.410445.0) (ISNI:0000 0001 2188 0957); University of Pittsburgh School of Medicine, Pittsburgh, USA (GRID:grid.21925.3d) (ISNI:0000 0004 1936 9000)
2 National Institutes of Health, Center for Research on Genomics and Global Health, National Human Genome Research Institute, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165)
3 National Institutes of Health, Center for Research on Genomics and Global Health, National Human Genome Research Institute, Bethesda, USA (GRID:grid.94365.3d) (ISNI:0000 0001 2297 5165); The George Washington University School of Medicine and Health Sciences, Department of Clinical Research and Leadership, Washington, USA (GRID:grid.253615.6) (ISNI:0000 0004 1936 9510)
4 University of Hawaiʻi at Mānoa, Honolulu, USA (GRID:grid.410445.0) (ISNI:0000 0001 2188 0957)