Maui Hudson
Biographic Data
| ID | 3615311 |
|---|---|
| NAME | Maui Hudson |
| GIVEN NAMES | Maui |
| FAMILY NAME | Hudson |
| SIGNATURE | HUDSON M |
| AFFILIATIONS | University of Waikato |
| ORCID | 0000-0003-3880-4015 |
| VERIFIED | Yes |
| TOTAL WORKS | 23 |
| TOTAL CITATIONS | 8 |
| AUTHOR COUNT | 23 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2007 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 2 |
Indigenous-led futures in Artificial Intelligence
The entanglement of technoscience and coloniality is increasingly interrogated through Indigenous critiques of science, which challenge its epistemic authority and dominance in policy, governance, and resource management. The push to integrate Indigenous knowledge into research and decision-making frameworks is often seen as a response to equity and Indigenous rights, but it also speaks to the need for more holistic, relational, and contextually …
Exploring the legal, policy, ethical and practical implications of digitisation of botanical and fungal collections
Societal Impact Statement Dried plant and fungal specimens held in collections provide a unique asset to understand the natural world and inform conservation approaches. By creating freely available, digital images of these collections, these specimens can be used by more scientists from around the globe to ask research questions and apply new technologies. We consider the relevant laws, policies and agreements, which are required to ensure this …
Improving visibility for knowledge holders in ethnobiological and ethnopharmacological publications
Navigating the contours of change: What we can learn from mātauranga Māori
Mātauranga Māori and mātauranga whakatere waka are fundamental to revitalising Indigenous communities, strengthening planning for climate change and resilience to climate change impacts. Despite concerns about the risks of climate change to contemporary voyaging, navigators are motivated by their responsibility to maintain and pass on their knowledge of voyaging practices, to raise environmental awareness and to advocate for the environment. Adap…
Aligning policy and practice to implement Care with Fair through Indigenous Peoples’ protocols
Operationalizing the Care and Fair Principles for Indigenous data futures
This discussion emerged from two joint, virtual conference sessions that integrated parallel processes at the Research Data Alliance (RDA): “Operationalising Be FAIR and CARE” ( https://www.rd-alliance.org/operationalising-be-fair-and-care ) and “Implementing the CARE Principles: The CARE-full Process” ( https://www.rd-alliance.org/implementing-care-principles-care-full-process ). The FAIR Data Maturity Model Working Group, hosted by the Research…
Empowering Equitable Data Use Partnerships and Indigenous Data Sovereignties Amid Pandemic Genomics
The COVID-19 pandemic has inequitably impacted Indigenous communities in the United States. In this emergency state that highlighted existing inadequacies in US government and tribal public health infrastructures, many tribal nations contracted with commercial entities and other organization types to conduct rapid diagnostic and antibody testing, often based on proprietary technologies specific to the novel pathogen. They also partnered with publ…
Ethnobiology Phase VI: Decolonizing Institutions, Projects, and Scholarship
Ethnobiology, like many fields, was shaped by early Western imperial efforts to colonize people and lands around the world and extract natural resources. Those legacies and practices persist today and continue to influence the institutions ethnobiologists are a part of, how they carry out research, and their personal beliefs and actions. Various authors have previously outlined five overlapping “phases” of ethnobiology. Here, we argue that ethnob…
The Care Principles for Indigenous Data Governance
Concerns about secondary use of data and limited opportunities for benefit-sharing have focused attention on the tension that Indigenous communities feel between (1) protecting Indigenous rights and interests in Indigenous data (including traditional knowledges) and (2) supporting open data, machine learning, broad data sharing, and big data initiatives. The International Indigenous Data Sovereignty Interest Group (within the Research Data Allian…
Indigenous Genomic Databases: Pragmatic Considerations and Cultural Contexts
The potential to grow genomic knowledge and harness the subsequent clinical benefits has escalated the building of background variant databases (BVDs) for genetic diagnosis across the globe. Alongside the upsurge of this precision medicine, potential benefits have been highlighted for both rare genetic conditions and other diagnoses. However, with the ever-present "genomic divide," Indigenous peoples globally have valid concerns as they endure co…
He Pikinga Waiora: Supporting Māori health organisations to respond to pre-diabetes
Māori health organisations are important actors in systems seeking to improve outcomes and eliminate health inequities. Support from funders and policy makers will be required to build on the strengths of these organisations and to overcome system challenges. To realise improved health outcomes for Māori, the value placed on whānau and community perspectives not only needs to be acknowledged in the implementation of health interventions, health a…
He Pikinga Waiora Implementation Framework: A tool for chronic disease intervention effectiveness in Māori and other indigenous communities
Introduction: Health outcomes for Māori are significantly worse than non-Maori in New Zealand; these inequities mirror those found in indigenous communities elsewhere. Evidence-based interventions with established efficacy may not be effective in indigenous communities without addressing specific implementation challenges. We present an implementation framework for chronic condition interventions for Māori.Theory/Methods: The He Pikinga Waiora Im…
(C)Elsi-us: Reducing Friction with Indigenous Communities in Genomic Research
As government policy settings have become more \nresponsive to aspirations of Indigenous communities and \nresearchers are more sensitive to the concerns of Indigenous communities, the research environment has become more conducive to understanding the cultural implications of genomic research. CELSI-us is a tongue-in-cheek reference to taking the temperature of the relationship between genomic researchers and Indigenous communities. If we create…
Implementation framework for chronic disease intervention effectiveness in Māori and other indigenous communities
BACKGROUND: About 40% of all health burden in New Zealand is due to cancer, cardiovascular disease, and type 2 diabetes/obesity. Outcomes for Māori (indigenous people) are significantly worse than non-Maori; these inequities mirror those found in indigenous communities elsewhere. Evidence-based interventions with established efficacy may not be effective in indigenous communities without addressing specific implementation challenges. We present a…
Whakatipu rawa ma ngā uri whakatipu: Optimising the “Māori” in Māori economic development
One of the great challenges for indigenous and non-indigenous entrepreneurs in the twenty-first century is to move beyond profit maximisation as an acceptable modality for doing business and gravitate towards the concept of socially optimal outcomes, where maximising community well-being and minimising externalities to the natural environment and social justice are paramount. We present findings from a case-study analysis of Māori enterprises tha…
Identifying strategic opportunities for Māori community organisations to respond to pre-diabetes: Building a platform for integrated care to deliver change that matters to communities
The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)
Te Mata Ira—Faces of the Gene: Developing a cultural foundation for biobanking and genomic research involving Māori
Te Mata Ira was a three-year research project (2012–2015) that explored Māori views on genomic research and biobanking for the development of culturally appropriate guidelines. A key component of this process has been to identify Māori concepts that provide cultural reference points for engaging with biobanking and genomic research. These cultural cues provide the basis for describing the cultural logic that underpins engagement in this context i…
Engaging Maori in Biobanking and Genetic Research: Legal, Ethical, and Policy Challenges
Publically funded biobanking initiatives and genetic research should contribute towards reducing inequalities in health by reducing the prevalence and burden of disease. It is essential that Maori and other Indigenous populations share in health gains derived from these activities. The Health Research Council of New Zealand has funded a research project (2012-2015) to identify Maori perspectives on biobanking and genetic research, and to develop …
Enacting Kaitiakitanga: Challenges and Complexities in the Governance and Ownership of Rongoā Research Information
This article explores the tensions one research team has faced in securing appropriate governance or stewardship (which we refer to as kaitiakitanga) of research data. Whilst ethical and regulatory frameworks exist which provide a minimum standard for researchers to meet when working with Māori, what our experience has highlighted is there is currently a "governance" gap in terms of who should hold stewardship of research data collected from Māor…
The art of dialogue with indigenous communities in the new biotechnology world
Te Hau Mihi Ata is a research project that aims to negotiate spaces for and develop processes of dialogue that allow for a deeper level of interaction between mātauranga Māori (Māori indigenous knowledge) and science. Over a two-year period a series of facilitated exchanges or “wānanga” were held focusing on areas of new technology (assisted reproductive technologies, life technologies, and future food technologies) that involved Māori scientists…
Perspectives on the use of embryos in research
This paper explores the epistemological divide between mātauranga Māori (Māori knowledge) and science, and considers which cultural concepts have relevance when considering the use of embryos in research. We argue that empowerment is a necessary precursor for a dialogue process to be effective and to maintain the cultural dignity and confidence of the participants. Negotiating spaces to share ideas, concepts and values between different knowledge…
Think globally, act locally: Collective Consent and the Ethics of Knowledge Production
Ethical review is an integral part of the process of developing research and considering issues associated with the production of knowledge. It is part of a system that primarily legitimises western traditions of inquiry and reinforces western assumptions about knowledge and its benefit to society. Around the world the process of colonisation has excluded indigenous understandings. In New Zealand, Māori (indigenous) knowledge has been similarly m…
Scientific Collaborative Research with Māori Communities: Kaupapa or Kūpapa Māori
The phrase 'for Māori, by Māori, with Māori', synonymous with Kaupapa Māori research, reflects the strong community participatory orientation and aims of this paradigm. Its use has evolved from glib reference and catchphrase, to a 'checklist'/gauge of how well a research project has enacted community participatory principles, and to what extent Māori participation in the research process is meaningful and empowered. Description of research accord…
Scientific Collaborative Research with Māori Communities: Kaupapa or Kūpapa Māori
The phrase 'for Māori, by Māori, with Māori', synonymous with Kaupapa Māori research, reflects the strong community participatory orientation and aims of this paradigm. Its use has evolved from glib reference and catchphrase, to a 'checklist'/gauge of how well a research project has enacted community participatory principles, and to what extent Māori participation in the research process is meaningful and empowered. Description of research accord…
(C)Elsi-us: Reducing Friction with Indigenous Communities in Genomic Research
As government policy settings have become more \nresponsive to aspirations of Indigenous communities and \nresearchers are more sensitive to the concerns of Indigenous communities, the research environment has become more conducive to understanding the cultural implications of genomic research. CELSI-us is a tongue-in-cheek reference to taking the temperature of the relationship between genomic researchers and Indigenous communities. If we create…
Aligning policy and practice to implement Care with Fair through Indigenous Peoples’ protocols
Enacting Kaitiakitanga: Challenges and Complexities in the Governance and Ownership of Rongoā Research Information
This article explores the tensions one research team has faced in securing appropriate governance or stewardship (which we refer to as kaitiakitanga) of research data. Whilst ethical and regulatory frameworks exist which provide a minimum standard for researchers to meet when working with Māori, what our experience has highlighted is there is currently a "governance" gap in terms of who should hold stewardship of research data collected from Māor…
Think globally, act locally: Collective Consent and the Ethics of Knowledge Production
Ethical review is an integral part of the process of developing research and considering issues associated with the production of knowledge. It is part of a system that primarily legitimises western traditions of inquiry and reinforces western assumptions about knowledge and its benefit to society. Around the world the process of colonisation has excluded indigenous understandings. In New Zealand, Māori (indigenous) knowledge has been similarly m…
Scientific Collaborative Research with Māori Communities: Kaupapa or Kūpapa Māori
The phrase 'for Māori, by Māori, with Māori', synonymous with Kaupapa Māori research, reflects the strong community participatory orientation and aims of this paradigm. Its use has evolved from glib reference and catchphrase, to a 'checklist'/gauge of how well a research project has enacted community participatory principles, and to what extent Māori participation in the research process is meaningful and empowered. Description of research accord…
Think globally, act locally: Collective Consent and the Ethics of Knowledge Production
Ethical review is an integral part of the process of developing research and considering issues associated with the production of knowledge. It is part of a system that primarily legitimises western traditions of inquiry and reinforces western assumptions about knowledge and its benefit to society. Around the world the process of colonisation has excluded indigenous understandings. In New Zealand, Māori (indigenous) knowledge has been similarly m…
Perspectives on the use of embryos in research
This paper explores the epistemological divide between mātauranga Māori (Māori knowledge) and science, and considers which cultural concepts have relevance when considering the use of embryos in research. We argue that empowerment is a necessary precursor for a dialogue process to be effective and to maintain the cultural dignity and confidence of the participants. Negotiating spaces to share ideas, concepts and values between different knowledge…
The art of dialogue with indigenous communities in the new biotechnology world
Te Hau Mihi Ata is a research project that aims to negotiate spaces for and develop processes of dialogue that allow for a deeper level of interaction between mātauranga Māori (Māori indigenous knowledge) and science. Over a two-year period a series of facilitated exchanges or “wānanga” were held focusing on areas of new technology (assisted reproductive technologies, life technologies, and future food technologies) that involved Māori scientists…
Enacting Kaitiakitanga: Challenges and Complexities in the Governance and Ownership of Rongoā Research Information
This article explores the tensions one research team has faced in securing appropriate governance or stewardship (which we refer to as kaitiakitanga) of research data. Whilst ethical and regulatory frameworks exist which provide a minimum standard for researchers to meet when working with Māori, what our experience has highlighted is there is currently a "governance" gap in terms of who should hold stewardship of research data collected from Māor…
Engaging Maori in Biobanking and Genetic Research: Legal, Ethical, and Policy Challenges
Publically funded biobanking initiatives and genetic research should contribute towards reducing inequalities in health by reducing the prevalence and burden of disease. It is essential that Maori and other Indigenous populations share in health gains derived from these activities. The Health Research Council of New Zealand has funded a research project (2012-2015) to identify Maori perspectives on biobanking and genetic research, and to develop …
Te Mata Ira—Faces of the Gene: Developing a cultural foundation for biobanking and genomic research involving Māori
Te Mata Ira was a three-year research project (2012–2015) that explored Māori views on genomic research and biobanking for the development of culturally appropriate guidelines. A key component of this process has been to identify Māori concepts that provide cultural reference points for engaging with biobanking and genomic research. These cultural cues provide the basis for describing the cultural logic that underpins engagement in this context i…
Implementation framework for chronic disease intervention effectiveness in Māori and other indigenous communities
BACKGROUND: About 40% of all health burden in New Zealand is due to cancer, cardiovascular disease, and type 2 diabetes/obesity. Outcomes for Māori (indigenous people) are significantly worse than non-Maori; these inequities mirror those found in indigenous communities elsewhere. Evidence-based interventions with established efficacy may not be effective in indigenous communities without addressing specific implementation challenges. We present a…
Whakatipu rawa ma ngā uri whakatipu: Optimising the “Māori” in Māori economic development
One of the great challenges for indigenous and non-indigenous entrepreneurs in the twenty-first century is to move beyond profit maximisation as an acceptable modality for doing business and gravitate towards the concept of socially optimal outcomes, where maximising community well-being and minimising externalities to the natural environment and social justice are paramount. We present findings from a case-study analysis of Māori enterprises tha…
Identifying strategic opportunities for Māori community organisations to respond to pre-diabetes: Building a platform for integrated care to deliver change that matters to communities
The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)
He Pikinga Waiora Implementation Framework: A tool for chronic disease intervention effectiveness in Māori and other indigenous communities
Introduction: Health outcomes for Māori are significantly worse than non-Maori in New Zealand; these inequities mirror those found in indigenous communities elsewhere. Evidence-based interventions with established efficacy may not be effective in indigenous communities without addressing specific implementation challenges. We present an implementation framework for chronic condition interventions for Māori.Theory/Methods: The He Pikinga Waiora Im…
(C)Elsi-us: Reducing Friction with Indigenous Communities in Genomic Research
As government policy settings have become more \nresponsive to aspirations of Indigenous communities and \nresearchers are more sensitive to the concerns of Indigenous communities, the research environment has become more conducive to understanding the cultural implications of genomic research. CELSI-us is a tongue-in-cheek reference to taking the temperature of the relationship between genomic researchers and Indigenous communities. If we create…
He Pikinga Waiora: Supporting Māori health organisations to respond to pre-diabetes
Māori health organisations are important actors in systems seeking to improve outcomes and eliminate health inequities. Support from funders and policy makers will be required to build on the strengths of these organisations and to overcome system challenges. To realise improved health outcomes for Māori, the value placed on whānau and community perspectives not only needs to be acknowledged in the implementation of health interventions, health a…
The Care Principles for Indigenous Data Governance
Concerns about secondary use of data and limited opportunities for benefit-sharing have focused attention on the tension that Indigenous communities feel between (1) protecting Indigenous rights and interests in Indigenous data (including traditional knowledges) and (2) supporting open data, machine learning, broad data sharing, and big data initiatives. The International Indigenous Data Sovereignty Interest Group (within the Research Data Allian…
Indigenous Genomic Databases: Pragmatic Considerations and Cultural Contexts
The potential to grow genomic knowledge and harness the subsequent clinical benefits has escalated the building of background variant databases (BVDs) for genetic diagnosis across the globe. Alongside the upsurge of this precision medicine, potential benefits have been highlighted for both rare genetic conditions and other diagnoses. However, with the ever-present "genomic divide," Indigenous peoples globally have valid concerns as they endure co…
Operationalizing the Care and Fair Principles for Indigenous data futures
This discussion emerged from two joint, virtual conference sessions that integrated parallel processes at the Research Data Alliance (RDA): “Operationalising Be FAIR and CARE” ( https://www.rd-alliance.org/operationalising-be-fair-and-care ) and “Implementing the CARE Principles: The CARE-full Process” ( https://www.rd-alliance.org/implementing-care-principles-care-full-process ). The FAIR Data Maturity Model Working Group, hosted by the Research…
Empowering Equitable Data Use Partnerships and Indigenous Data Sovereignties Amid Pandemic Genomics
The COVID-19 pandemic has inequitably impacted Indigenous communities in the United States. In this emergency state that highlighted existing inadequacies in US government and tribal public health infrastructures, many tribal nations contracted with commercial entities and other organization types to conduct rapid diagnostic and antibody testing, often based on proprietary technologies specific to the novel pathogen. They also partnered with publ…
Ethnobiology Phase VI: Decolonizing Institutions, Projects, and Scholarship
Ethnobiology, like many fields, was shaped by early Western imperial efforts to colonize people and lands around the world and extract natural resources. Those legacies and practices persist today and continue to influence the institutions ethnobiologists are a part of, how they carry out research, and their personal beliefs and actions. Various authors have previously outlined five overlapping “phases” of ethnobiology. Here, we argue that ethnob…
Aligning policy and practice to implement Care with Fair through Indigenous Peoples’ protocols
Navigating the contours of change: What we can learn from mātauranga Māori
Mātauranga Māori and mātauranga whakatere waka are fundamental to revitalising Indigenous communities, strengthening planning for climate change and resilience to climate change impacts. Despite concerns about the risks of climate change to contemporary voyaging, navigators are motivated by their responsibility to maintain and pass on their knowledge of voyaging practices, to raise environmental awareness and to advocate for the environment. Adap…
Indigenous-led futures in Artificial Intelligence
The entanglement of technoscience and coloniality is increasingly interrogated through Indigenous critiques of science, which challenge its epistemic authority and dominance in policy, governance, and resource management. The push to integrate Indigenous knowledge into research and decision-making frameworks is often seen as a response to equity and Indigenous rights, but it also speaks to the need for more holistic, relational, and contextually …
Exploring the legal, policy, ethical and practical implications of digitisation of botanical and fungal collections
Societal Impact Statement Dried plant and fungal specimens held in collections provide a unique asset to understand the natural world and inform conservation approaches. By creating freely available, digital images of these collections, these specimens can be used by more scientists from around the globe to ask research questions and apply new technologies. We consider the relevant laws, policies and agreements, which are required to ensure this …
Improving visibility for knowledge holders in ethnobiological and ethnopharmacological publications
Indigenous (18 works) · Political science (18 works) · Public relations (13 works) · Sociology (13 works) · Indigenous Health, Education, and Rights (10 works) · Biology (9 works) · Computer Science (9 works) · Law (8 works) · Medicine (8 works) · Ecology (7 works)