Baynam, GarethJulkowska, DariaBowdin, SarahHermes, AzureMcMaster, ChristopherPrichep, ElissaRicher, ÉtienneVan der Westhuizen, FrancoisRepetto, GabrielaMalherbe, HelenReichardt, JuergenArbour, LauraHudson, MauiDu Plessis, KellyHaendel, MelissaWilcox, PhillipLynch, SallyRind, ShamirEasteal, SimonEstivill, XavierCaron, NadineChongo, MeckThomas, YarlaluLetinturier, MaryVorster. Barend2025-01-092025-01-092024Baynam G, Julkowska D, Bowdin S, Hermes A, McMaster CR, Prichep E, Richer É, van der Westhuizen FH, Repetto GM, Malherbe H, Reichardt JKV, Arbour L, Hudson M, du Plessis K, Haendel M, Wilcox P, Lynch SA, Rind S, Easteal S, Estivill X, Caron N, Chongo M, Thomas Y, Letinturier MCV, Vorster BC. Advancing diagnosis and research for rare genetic diseases in Indigenous peoples. Nat Genet. 2024 Feb;56(2):189-193. doi: 10.1038/s41588-023-01642-1https://hdl.handle.net/11447/9605Achieving 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.enArticlehttps://doi.org/10.1038/s41588-023-01642-1