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Maui Hudson

Researcher at University of Waikato

Publications -  45
Citations -  1048

Maui Hudson is an academic researcher from University of Waikato. The author has contributed to research in topics: Indigenous & Medicine. The author has an hindex of 14, co-authored 39 publications receiving 542 citations.

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The CARE Principles for Indigenous Data Governance

TL;DR: The goal is that stewards and other users of Indigenous data will ‘Be FAIR and CARE’ and the Principles complement the existing data-centric approach represented in the ‘FAIR Guiding Principles for scientific data management and stewardship’ (Findable, Accessible, Interoperable, Reusable).
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Implementation framework for chronic disease intervention effectiveness in Māori and other indigenous communities.

TL;DR: The He Pikinga Waiora Implementation Framework appears to be well suited to advance implementation science for indigenous communities in general and Māori in particular and has promise as a policy and planning tool to evaluate and design effective interventions for chronic disease prevention in indigenous communities.
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Operationalizing the CARE and FAIR Principles for Indigenous data futures.

TL;DR: The CARE Principles for Indigenous Data Governance (CARE) as discussed by the authors is a set of principles for data governance in big data, open data, and open science, which is based on FAIR principles for scientific data.
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The Treaty of Waitangi and Research Ethics in Aotearoa

TL;DR: In this article, the authors suggest a revised interpretation of the Treaty of Waitangi principles to incorporate the range of ethical issues that Māori have expressed as important, such as respect for their indigenous rights, control over research processes and reciprocity within research relationships.
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Engaging Māori in biobanking and genomic research: a model for biobanks to guide culturally informed governance, operational, and community engagement activities.

TL;DR: The He Tangata Kei Tua model provides a framework for considering cultural values in relation to other community or indigenous contexts and will be useful for biobanks, researchers, ethics committee members, and those who engage in consultation or advice about biobanking in local, regional, national, or international settings.