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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 01, 2024
. (Total: 63728 Documents since 2012)
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Genetic Research within Indigenous Communities: Engagement Opportunities and Pathways Forward
Global health systems strengthening: FIGO's strategic view on reducing maternal and newborn mortality worldwide.
Jezid Miranda et al. Int J Gynaecol Obstet 2024
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Inequity of genetic screening: DNA tests fail non-white families more often
Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds
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
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Genetic Researchers' Use of and Interest in Research With Diverse Ancestral Groups.
Kaitlyn Jaffe et al. JAMA Netw Open 2024 7(4) e246805
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Oncologists' perceptions of tumor genomic profiling and barriers to communicating secondary hereditary risks to African American cancer patients.
Michael J Hall et al. BMC Cancer 2024 24(1) 412
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Socioecologic Factors and Racial Differences in Breast Cancer Multigene Prognostic Scores in US Women.
Ashwini Z Parab et al. JAMA Netw Open 2024 7(4) e244862
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Universal Exome Sequencing in Critically Ill Adults: A Diagnostic Yield of 25% and Race-Based Disparities in Access to Genetic Testing.
Jessica Gold et al. medRxiv 2024
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Iowa Newborn Screening Program Experience with Hemoglobinopathy Screening over the Last Two Decades and Its Increasing Global Relevance.
Ryan Jilek et al. Int J Neonatal Screen 2024 10(1)
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Barriers and Unequal Access to Timely Molecular Testing Results: Addressing the Inequities in Cancer Care Delays across Canada.
Stephanie Snow et al. Curr Oncol 2024 31(3) 1359-1375
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Birth Prevalence of Sickle Cell Disease and County-Level Social Vulnerability - Sickle Cell Data Collection Program, 11 States, 2016-2020.
Mariam Kayle et al. MMWR Morb Mortal Wkly Rep 2024 73(12) 248-254
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Overcoming barriers to single-cell RNA sequencing adoption in low- and middle-income countries
TB Serebour et al, EJHG, April 2, 2024
Low Rates of Colorectal Cancer Screening in Our Patients' First-Degree Relatives: Are We Failing Them?
Anyelin Almanzar et al. Dis Colon Rectum 2024
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Accessibility, availability and common practices regarding genetic testing for epilepsy across Europe: A survey of the European Reference Network EpiCARE.
Maria T Papadopoulou et al. Epilepsia Open 2024
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Physical signs and atherosclerotic cardiovascular disease in familial hypercholesterolemia: the HELLAS-FH Registry.
Loukianos S Rallidis et al. J Cardiovasc Med (Hagerstown) 2024
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[Cystic fibrosis in Morroco : what do words mean without action ?].
Naima Amenzoui et al. Rev Med Liege 2024 79(3) 175-180
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Disparities in Genetic Testing for Neurologic Disorders.
Aaron Baldwin et al. Neurology 2024 102(6) e209161
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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
Improving access to exome sequencing in a medically underserved population through the Texome Project
B Vucuolo et al, Genetics in Medicine, February 29, 2024
Researchers optimize genetic tests for diverse populations to tackle health disparities
NIH, February 2024
Compassion and equity-focused clinical genomics training for health professional learners.
Taylor J Berninger et al. J Genet Couns 2024
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The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
E Venner et al, Comm Biology, February 19, 2024
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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Overcoming barriers to equitable genomic healthcare
KM Girisha, EJHG, February 13, 2024
Racial and ethnic disparities in genomic testing among lung cancer patients: a systematic review.
Clare Meernik et al. J Natl Cancer Inst 2024
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From intention to action: Assessing need and creating a JEDI toolkit for individuals teaching cancer genetics curriculum.
Jamie Paysour et al. J Genet Couns 2024
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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
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Disparities in genetic testing for breast cancer among black and Hispanic women in the United States.
Oludamilola Olufosoye et al. Clin Imaging 2024 107110066
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Disparities in OncotypeDx Testing and Subsequent Chemotherapy Receipt by Geography and Socioeconomic Status.
Sarah C Van Alsten et al. Cancer Epidemiol Biomarkers Prev 2024
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 01, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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