Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds
(Posted Apr 25, 2024 9AM)
Impact of Race, Socioeconomic Status, and Geography on Healthcare Outcomes for Children With Sickle Cell Disease in the United States: A Scoping Review
(Posted Apr 19, 2024 10AM)
Family cascade screening for equitable identification of familial hypercholesterolemia: study protocol for a hybrid effectiveness-implementation type III randomized controlled trial
(Posted Apr 19, 2024 10AM)
Genetic Researchers' Use of and Interest in Research With Diverse Ancestral Groups.
(Posted Apr 18, 2024 8AM)
Shirin Ibrahim et al. Atherosclerosis 2024 393117548
Navigating equity in global access to genome therapy expanding access to potentially transformative therapies and benefiting those in need requires global policy changes.
Tsung-Ling Lee et al. Front Genet 2024 151381172
Translational Research and Health Equity: Gene Therapies for Sickle Cell Disease as a Case Study.
Mary A Majumder et al. Ethics Hum Res 2024 46(3) 34-39
Harnessing Artificial Intelligence to Address Oral Health Disparities.
Hawazin W Elani et al. JAMA Health Forum 2024 5(4) e240642
Impact of Race, Socioeconomic Status, and Geography on Healthcare Outcomes for Children With Sickle Cell Disease in the United States: A Scoping Review.
Sameerah Wahab et al. Cureus 2024 16(3) e56089
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Emil K Gustavsson et al. Lancet Neurol 2024
Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID.
Deanna M Green et al. Pediatrics 2024
Population-based BRCA germline mutation screening in the Han Chinese identifies individuals at risk of BRCA mutation-related cancer: experience from a clinical diagnostic center from greater Shanghai area.
Zhiyuan Wu et al. BMC Cancer 2024 24(1) 411
Algor-ethics: charting the ethical path for AI in critical care.
Jonathan Montomoli et al. J Clin Monit Comput 2024
Development and validation of a machine learning model for prediction of type 2 diabetes in patients with mental illness.
Martin Bernstorff et al. Acta Psychiatr Scand 2024
Update on Omicron variant and its threat to vulnerable populations.
Dai Bowen, et al. Public health in practice (Oxford, England) 2024 0 0. 100494
Novel genetic association of the Furin gene polymorphism rs1981458 with COVID-19 severity among Indian populations.
Pandey Rudra Kumar, et al. Scientific reports 2024 0 0. (1) 7822
The impact of comorbidities and economic inequality on COVID-19 mortality in Mexico: a machine learning approach.
Méndez-Astudillo Jorge, et al. Frontiers in big data 2024 0 0. 1298029
Participant flow diagrams for health equity in AI.
Jacob G Ellen et al. J Biomed Inform 2024 152104631
SARS-CoV-2 mutant spectra as variant of concern nurseries: endless variation?
Martínez-González Brenda, et al. Frontiers in microbiology 2024 0 0. 1358258
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
Risk of carditis among adolescents after extending the interdose intervals of BNT162b2.
Min Fan et al. NPJ Vaccines 2024 2 (1) 31
Stacked deep learning approach for efficient SARS-CoV-2 detection in blood samples.
Wang Wu, et al. Artificial intelligence in medicine 2024 0 0. 102767
Machine Learning-Based Decision-Making in Geriatrics: Aging Phenotype Calculator and Survival Prognosis.
Aleksandra Mamchur et al. Aging Dis 2024
Disparities in OncotypeDx Testing and Subsequent Chemotherapy Receipt by Geography and Socioeconomic Status.
Sarah C Van Alsten et al. Cancer Epidemiol Biomarkers Prev 2024
Real-World Trends, Rural-Urban Differences and Socioeconomic Disparities in Utilization of Narrow vs. Broad Next-Generation Sequencing Panels.
Yiqing Zhao et al. Cancer Res Commun 2024
A New-fangled COVID-19 Variant, Eris, Might be the One to Lookout in 2023 or far from Over.
Ray Suman Kumar, et al. Infectious disorders drug targets 2024 0 0.
Advancing Cardiovascular Health Equity Globally Through Digital Technologies.
Oluwabunmi Ogungbe et al. J Am Heart Assoc 2024 13(2) e031237
ACE I/D polymorphism is a risk factor for the clinical severity of COVID-19 in Brazilian male patients.
Almeida Sandro Soares, et al. Molecular biology reports 2024 0 0. (1) 180
Predicting COVID-19 Outcomes: Machine Learning Predictions Across Diverse Datasets.
Panç Kemal, et al. Cureus 2024 0 0. (12) e50932
Using big sequencing data to identify chronic SARS-Coronavirus-2 infections.
Sheri Harari et al. Nat Commun 2024 1 (1) 648
Assessment of ethnic inequalities in diagnostic coding of familial hypercholesterolaemia (FH): A cross-sectional database study in Lambeth, South London.
Mariam Molokhia et al. Atherosclerosis 2023 388117353
Development and assessment of educational materials for spinal muscular atrophy carrier screening in the Plain community.
Carly Eichten et al. J Genet Couns 2024
Reducing Time to Diagnosis of Rare Genetic Diseases in a Medically Underserved Hispanic Population- Lessons Learned for Meaningful Engagement.
Blake Vuocolo et al. Res Sq 2024
Reduction in Breast Cancer Death With Adjuvant Chemotherapy Among US Women According to Race, Ethnicity, and the 21-Gene Recurrence Score.
Hsiao-Ching Huang et al. J Natl Compr Canc Netw 2024 1-14
Trust in prenatal exome sequencing for expectant families facing unexplained fetal anomalies.
Harriet T Rothschild et al. Prenat Diagn 2023
Challenges of Artificial Intelligence in Medicine and Dermatology.
Andrzej Grzybowski et al. Clin Dermatol 2024
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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:Apr 25, 2024
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