Elsevier,

International Journal of Radiation Oncology Biology Physics, Volume 112, 1 February 2022

Looks at disparities in access to healthcare among Indigenous people.
A Comment on improving the health of Artic Indigenous peoples, in the contexts of SDGs 3, 10, and 15, focusing specifically on the launch of a Lancet Commission that aims to present recommendations for addressing health disparities and key challenges in this community and to identify pathways for change.
Advocacy engagement has been at the forefront of National Cancer Institute (NCI) efforts to advance scientific discoveries and transform medical interventions.
Elsevier, Preventive Medicine, Volume 155, February 2022
Contested racial identity— self-identified race not matching socially-assigned race—may be an indication of experiences with racism.
Study objective: This scoping review was conducted to collate and summarize the published research literature addressing sexual and gender minority care in the emergency department (ED).

Colorectal cancer (CRC) is the third leading cause of cancer-related deaths in the United States.

This Article supports SDGs 3 and 10 by assessing SARS-CoV-2 incidence in six ethnic groups in Amsterdam, and showing that incidence was highest in the largest minority ethnic groups. The findings suggest that prevention measures and vaccination should be especially encouraged in these groups.
Research4Life has been providing free and low-cost access to scientific research in the developing world for 20 years. Read this insightful story about the history of Research4Life, and its new strategy for the future with the aim to help researchers in the developing world fully participate in the global research community. This relates to SDG 4, 10 & 17.
Elsevier,

Med,
Volume 3, Issue 2,
2022,
Pages 93-97,
ISSN 2666-6340

Race and kidney function.
Elsevier,

eBioMedicine, Volume 76, February 2022

This Review supports SDG 3 and 10 by highlighting how genomics research intersects with existing racial and ethnic inequalities and forms of exclusion; there is no universally accepted, consistently applied method for categorising genomic data, which the authors argue is problematic, both from a clinical and scientific perspective, but more fundamentally in terms of the ability of genomics research to achieve the core ethical values of equity and justice.

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