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    Article

    Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

    Achieving a diagnosis for Indigenous people living with a rare, often genetic, disease is crucial for equitable healthcare. The International Rare Disease Research Consortium convened a global Task Force to br...

    Gareth Baynam, Daria Julkowska, Sarah Bowdin, Azure Hermes in Nature Genetics (2024)

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    Article

    Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data

    Addressing Indigenous rights and interests in genetic resources has become increasingly challenging in an open science environment that promotes unrestricted access to genomic data. Although Indigenous experie...

    Maui Hudson, Nanibaa’ A. Garrison, Rogena Sterling in Nature Reviews Genetics (2020)

  3. Article

    Correction to: Native Hawaiian Views on Biobanking

    The original version of this article unfortunately contained a mistake. The name of “Maile Taualii” is now corrected in the author group of this article.

    Maile Taualii, Elise Leimomi Davis, Kathryn L. Braun in Journal of Cancer Education (2020)

  4. Article

    Open Access

    Views on clinical trial recruitment, biospecimen collection, and cancer research: population science from landscapes of the Haudenosaunee (People of the Longhouse)

    Biomedical research in culturally distinct communities is often a challenge. Potential barriers to participation occur because science is presented in a format that lacks cultural acknowledgement. Investigatio...

    Rodney C. Haring, Whitney Ann Henry, Maui Hudson in Journal of Cancer Education (2018)

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    Article

    Native Hawaiian Views on Biobanking

    Genomic science represents a new frontier for health research and will provide important tools for personalizing health care. Biospecimen-based research is an important mechanism for expanding the genomic rese...

    Maile Tauali`i, Elise Leimomi Davis, Kathryn L. Braun in Journal of Cancer Education (2014)