Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
About
Public Health Genomics Branch
PHGKB Weekly Horizon Scan
Genomics Precision Health Scan
Advanced Molecular Detection Clips
Non-Genomics Precision Health Scan
CDC-authored Publications Scan
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
All Databases
COVID-19 GPH (47449)
CDC/NIH Web Information Database (32174)
CDC-Authored Genomics and Precision Health Publications Database (5825)
Precision Health Database (63627)
Tier-Classified Guidelines Database (533)
Pathogen Advanced Molecular Detection Database (26729)
All of Us Reports and Publications Database (656)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226303)
Epigenetic Epidemiology Publications Database (22727)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 19, 2024
. (Total: 63627 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 467 Records)
Next
Query Trace:
Disparities[original query]>>Original Studies[Product Type]
Genetic Researchers' Use of and Interest in Research With Diverse Ancestral Groups.
Kaitlyn Jaffe et al. JAMA Netw Open 2024 7(4) e246805
Similar articles in PubMed
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
Similar articles in PubMed
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
Similar articles in PubMed
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
Similar articles in PubMed
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
Similar articles in PubMed
Low Rates of Colorectal Cancer Screening in Our Patients' First-Degree Relatives: Are We Failing Them?
Anyelin Almanzar et al. Dis Colon Rectum 2024
Similar articles in PubMed
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
Similar articles in PubMed
Disparities in Genetic Testing for Neurologic Disorders.
Aaron Baldwin et al. Neurology 2024 102(6) e209161
Similar articles in PubMed
Improving access to exome sequencing in a medically underserved population through the Texome Project
B Vucuolo et al, Genetics in Medicine, February 29, 2024
Generalisable deep learning method for mammographic density prediction across imaging techniques and self-reported race.
Galvin Khara et al. Commun Med (Lond) 2024 4(1) 21
Similar articles in PubMed
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
E Venner et al, Comm Biology, February 19, 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
Similar articles in PubMed
Disparities in OncotypeDx Testing and Subsequent Chemotherapy Receipt by Geography and Socioeconomic Status.
Sarah C Van Alsten et al. Cancer Epidemiol Biomarkers Prev 2024
Similar articles in PubMed
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
Similar articles in PubMed
Risk-management decision-making data from a community-based sample of racially diverse women at high risk of breast cancer: rationale, methods, and sample characteristics of the Daughter Sister Mother Project survey.
Tasleem J Padamsee et al. Breast Cancer Res 2024 26(1) 8
Similar articles in PubMed
'If I knew more… I would feel less worried': Filipino Americans' Attitudes and Knowledge of Genetic Disease, Counseling, and Testing.
Casey R Scherer et al. Public Health Genomics 2024
Similar articles in PubMed
Mediating Factors in the Association of Maternal Educational Level With Pregnancy Outcomes: A Mendelian Randomization Study.
Tormod Rogne et al. JAMA Netw Open 2024 7(1) e2351166
Similar articles in PubMed
Large language models to identify social determinants of health in electronic health records
M Guevera et al, NPJ Digital Medicine, January 11, 2023
Race, Gene Expression Signatures, and Clinical Outcomes of Patients With High-Risk Early Breast Cancer.
Beverly Kyalwazi et al. JAMA Netw Open 2023 6(12) e2349646
Similar articles in PubMed
Online COVID-19 diagnosis prediction using complete blood count: an innovative tool for public health.
Xiaojing Teng et al. BMC Public Health 2023 23(1) 2536
Similar articles in PubMed
Validating racial and ethnic non-bias of artificial intelligence decision support for diagnostic breast ultrasound evaluation.
Clara Koo et al. J Med Imaging (Bellingham) 2023 10(6) 061108
Similar articles in PubMed
Development of a Novel Telemedicine Tool to Reduce Disparities Related to the Identification of Preschool Children with Autism.
Liliana Wagner et al. J Autism Dev Disord 2023
Similar articles in PubMed
Risk of Bias in Chest Radiography Deep Learning Foundation Models.
Ben Glocker et al. Radiol Artif Intell 2023 5(6) e230060
Similar articles in PubMed
Latina immigrants' breast and colon cancer causal attributions: genetics is key.
Katie Fiallos et al. J Community Genet 2023
Similar articles in PubMed
Women's preferences for NIPT as a first-line test in England and France: Challenges for genetic counseling practices.
Adeline Perrot et al. J Genet Couns 2023
Similar articles in PubMed
Pain Frequency and Health Care Utilization Patterns in Women with Sickle Cell Disease Experiencing Menstruation-Associated Pain Crises.
Catherine Segbefia et al. J Womens Health (Larchmt) 2023
Similar articles in PubMed
Perceptions of Nigerian medical students regarding their preparedness for precision medicine: a cross-sectional survey in Lagos, Nigeria.
Chibuzor F Ogamba et al. BMC Med Educ 2023 23(1) 879
Similar articles in PubMed
The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care.
Jason L Vassy et al. Am J Hum Genet 2023 110(11) 1841-1852
Similar articles in PubMed
Patient decisions regarding cancer gene panel testing: An exploratory study.
Margaret M Emmet et al. J Genet Couns 2023
Similar articles in PubMed
Stigma manifestations in cardiomyopathy care impact outcomes for black patients: a qualitative study.
Morgan Wolfgang et al. BMC Cardiovasc Disord 2023 23(1) 553
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
TOP