Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic Ancestry Groups in Biomedical Publications
G Feero et al, JAMA, March 12, 2024 (Posted Mar 12, 2024 0PM)
Improving access to exome sequencing in a medically underserved population through the Texome Project
B Vucuolo et al, Genetics in Medicine, February 29, 2024 (Posted Mar 03, 2024 10AM)
Researchers optimize genetic tests for diverse populations to tackle health disparities
NIH, February 2024 (Posted Mar 01, 2024 0PM)
A call for increased inclusivity and global representation in pharmacogenetic testing.
April Kennedy et al. NPJ Genom Med 2024 2 (1) 13 (Posted Feb 23, 2024 3PM)
Ezeilo Chidimma Ogechukwu, et al. Journal of occupational and environmental medicine 2024 0 0.
Artificial intelligence (AI) or augmented intelligence? How big data and AI are transforming healthcare: Challenges and opportunities.
K Moodley et al. S Afr Med J 2024 114(1) 22-26
Genetic counselors' and community clinicians' implementation and perceived barriers to informed consent during pre-test counseling for hereditary cancer risk.
Alexandra Capasso et al. J Genet Couns 2024
Development of a Social Risk Score in the Electronic Health Record to Identify Social Needs Among Underserved Populations: Retrospective Study.
Elham Hatef et al. JMIR Form Res 2024 8e54732
Disparities in Genetic Testing for Neurologic Disorders.
Aaron Baldwin et al. Neurology 2024 102(6) e209161
Taking the risk. A systematic review of ethical reasons and moral arguments in the clinical use of polygenic risk scores.
Lara Andreoli et al. Am J Med Genet A 2024 e63584
Artificial Intelligence in Pediatrics: Learning to Walk Together.
Kaan Can Demirbas et al. Turk Arch Pediatr 2024 59(2) 121-130
Social and demographic factors associated with receipt of a COVID-19 vaccine initial booster dose and with interval between primary series completion and initial booster dose uptake among persons aged ≥ 12 years, United States, August 2021-October 2022.
Meng Lu, et al. Vaccine 2024 0 0.
The descriptive epidemiology of pre-omicron SARS-CoV-2 breakthrough infections and severe outcomes in Manitoba, Canada.
Shaw Souradet Y, et al. Frontiers in epidemiology 2024 0 0. 1248847
Molecular characterization of SARS-CoV-2 Omicron clade and clinical presentation in children.
Scutari Rossana, et al. Scientific reports 2024 0 0. (1) 5325
Telemedicine-Enhanced Lung Cancer Screening Using Mobile Computed Tomography Unit with Remote Artificial Intelligence Assistance in Underserved Communities: Initial Results of a Population Cohort Study in Western China.
Wenjuan Tao et al. Telemed J E Health 2024
Next-generation treatments: Immunotherapy and advanced therapies for COVID-19.
Arevalo-Romero Jenny Andrea, et al. Heliyon 2024 0 0. (5) e26423
A survey on awareness, knowledge and preferences toward genetic testing among the United States general public.
Shahariar Mohammed Fahim et al. Per Med 2024
Efficacy of Community Health Worker-Delivered Family Health History-Based Breast Cancer Education and Services Among Chinese Americans.
Bertille Assoumou et al. J Cancer Educ 2024
Utilizing cost-effective portable equipment to enhance COVID-19 variant tracking both on-site and at a large scale.
Sung Yong Park et al. J Clin Microbiol 2024 2 e0155823
The Science of Precision Prevention: Research Opportunities and Clinical Applications to Reduce Cardiovascular Health Disparities.
Thomas A Pearson et al. JACC Adv 2024 3(1)
The next chapter for Africa's genomic initiatives
P Adepoujo, Lancet Id, March 2024
Compassion and equity-focused clinical genomics training for health professional learners.
Taylor J Berninger et al. J Genet Couns 2024
Patient Perceptions on the Advancement of Noninvasive Prenatal Testing for Sickle Cell Disease among Black Women in the United States.
Shameka P Thomas et al. AJOB Empir Bioeth 2024 1-10
Implementation of rapid genomic sequencing in safety-net neonatal intensive care units: protocol for the VIrtual GenOme CenteR (VIGOR) proof-of-concept study.
Alissa M D'Gama et al. BMJ Open 2024 14(2) e080529
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About Health Equity PHGKB
Health Equity PHGKB is an online, continuously updated, searchable database of genomics and precision health information and publications relevant to health equity...more
Content Summary
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:Mar 27, 2024
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