Advancing diagnosis and research for rare genetic diseases in indigenous peoples

Baynam, Gareth; Julkowska, Daria; Bowdin, Sarah; Hermes, Azure; McMaster, Christopher R.; Prichep, Elissa; Richer, Etienne; Van der Westhuizen, Francois H.; Repetto, Gabriela M.; Malherbe, Helen L.; Reichardt, Juergen K.V.; Arbour, Laura; Hudson, Maui; Du Plessis, Kelly; Haendel, Melissa; Wilcox, Phillip; Lynch, Sally Ann; Rind, Shamir; Easteal, Simon; Estivill, Xavier; Caron, Nadine; Chongo, Meck; Thomas, Yarlalu; Letinturier, Mary Catherine V.; Vorster, Barend Christiaan

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dc.contributor.author	Baynam, Gareth
dc.contributor.author	Julkowska, Daria
dc.contributor.author	Bowdin, Sarah
dc.contributor.author	Hermes, Azure
dc.contributor.author	McMaster, Christopher R.
dc.contributor.author	Prichep, Elissa
dc.contributor.author	Richer, Etienne
dc.contributor.author	Van der Westhuizen, Francois H.
dc.contributor.author	Repetto, Gabriela M.
dc.contributor.author	Malherbe, Helen L.
dc.contributor.author	Reichardt, Juergen K.V.
dc.contributor.author	Arbour, Laura
dc.contributor.author	Hudson, Maui
dc.contributor.author	Du Plessis, Kelly
dc.contributor.author	Haendel, Melissa
dc.contributor.author	Wilcox, Phillip
dc.contributor.author	Lynch, Sally Ann
dc.contributor.author	Rind, Shamir
dc.contributor.author	Easteal, Simon
dc.contributor.author	Estivill, Xavier
dc.contributor.author	Caron, Nadine
dc.contributor.author	Chongo, Meck
dc.contributor.author	Thomas, Yarlalu
dc.contributor.author	Letinturier, Mary Catherine V.
dc.contributor.author	Vorster, Barend Christiaan
dc.date.accessioned	2024-07-03T05:23:16Z
dc.date.issued	2024-02
dc.description.abstract	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 bridge the gap in diagnosing Indigenous rare diseases, and identify solutions to tackle the health inequity faced by Indigenous people.	en_US
dc.description.department	Biochemistry	en_US
dc.description.department	Genetics	en_US
dc.description.department	Microbiology and Plant Pathology	en_US
dc.description.embargo	2024-08-08
dc.description.librarian	hj2024	en_US
dc.description.sdg	SDG-03:Good heatlh and well-being	en_US
dc.description.sdg	SDG-10:Reduces inequalities	en_US
dc.description.sponsorship	The IRDiRC Indigenous Population Task Force was supported by the Scientific Secretariat of IRDiRC, funded by the European Union through the European Joint Programme on Rare Disease (EJP RD) under the European Union’s Horizon 2020 Research and Innovation Programme.	en_US
dc.description.uri	https://www.nature.com/ng	en_US
dc.identifier.citation	Baynam, G., Julkowska, D., Bowdin, S. et al. Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nature Genetics 56, 189–193 (2024). https://doi.org/10.1038/s41588-023-01642-1.	en_US
dc.identifier.issn	1061-4036 (print)
dc.identifier.issn	1546-1718 (online)
dc.identifier.other	10.1038/s41588-023-01642-1
dc.identifier.uri	http://hdl.handle.net/2263/96770
dc.language.iso	en	en_US
dc.publisher	Nature Research	en_US
dc.rights	© 2024, The Author(s), under exclusive licence to Springer Nature America, Inc.	en_US
dc.subject	Genetic services	en_US
dc.subject	Genetics research	en_US
dc.subject	Indigenous people	en_US
dc.subject	Healthcare	en_US
dc.subject	Rare diseases	en_US
dc.subject	Genetic diseases	en_US
dc.subject	SDG-03: Good health and well-being	en_US
dc.subject	Indigenous rare diseases	en_US
dc.subject	Health inequity	en_US
dc.subject	SDG-10: Reduced inequalities	en_US
dc.title	Advancing diagnosis and research for rare genetic diseases in indigenous peoples	en_US
dc.type	Postprint Article	en_US