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 (47352)
CDC/NIH Web Information Database (32181)
CDC-Authored Genomics and Precision Health Publications Database (6021)
Precision Health Database (63675)
Tier-Classified Guidelines Database (534)
Pathogen Advanced Molecular Detection Database (26775)
All of Us Reports and Publications Database (673)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226468)
Epigenetic Epidemiology Publications Database (22758)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 25, 2024
. (Total: 63675 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 2298 Records)
Next
Query Trace:
Evidence[original query]>>Original Studies[Product Type]
Family cascade screening for equitable identification of familial hypercholesterolemia: study protocol for a hybrid effectiveness-implementation type III randomized controlled trial.
Christina Johnson et al. Implement Sci 2024 19(1) 30
Similar articles in PubMed
Practice Patterns and Barriers to Vascular Genetic Testing among Vascular Surgeons.
James M Dittman et al. Ann Vasc Surg 2024
Similar articles in PubMed
Prevalence of elevated lipoprotein(a) in cardiac rehabilitation patients - results from a large-scale multicentre registry in Germany.
Christoph Altmann et al. Clin Res Cardiol 2024
Similar articles in PubMed
Association of Obesity with Telomere Length in Human Sperm.
Efthalia Moustakli et al. J Clin Med 2024 13(7)
Similar articles in PubMed
Clinical Utility and Diagnostic Yield of Genetic Testing for Inherited Neuromuscular Disorders in a Single, Large Neuromuscular Center.
Suzahn E Ebert et al. Neurol Clin Pract 2024 14(2) e200268
Similar articles in PubMed
Patient perspectives on pharmacogenomic (PGx) testing for antidepressant prescribing in primary care: a qualitative description study.
Alexandra Cernat et al. J Community Genet 2024
Similar articles in PubMed
Hereditary Cancer Syndrome Carriers: Feeling Left in the Corner.
Celia Diez de Los Rios de la Serna et al. Semin Oncol Nurs 2024 151624
Similar articles in PubMed
Clinical Effectiveness of Newborn Screening for Spinal Muscular Atrophy: A Nonrandomized Controlled Trial.
Oliver Schwartz et al. JAMA Pediatr 2024
Similar articles in PubMed
A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals.
Mariela V Jennings et al. EBioMedicine 2024 105086
Similar articles in PubMed
Susceptibility to Treatment-Resistant Depression Within Families.
Chih-Ming Cheng et al. JAMA Psychiatry 2024
Similar articles in PubMed
Clinical Value of Molecular Targets and FDA-Approved Genome-Targeted Cancer Therapies.
Ariadna Tibau et al. JAMA Oncol 2024
Similar articles in PubMed
Ultrasonographic Fetal Nuchal Translucency Measurements and Cytogenetic Outcomes.
Kara Bellai-Dussault et al. JAMA Netw Open 2024 7(3) e243689
Similar articles in PubMed
Clinician perspectives on policy approaches to genetic risk disclosure in families.
Amicia Phillips et al. Fam Cancer 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
Codesign of Lynch Choices : Using implementation science to create a clinically deliverable patient decision support website to transform cancer genetics care pathways.
Kelly Kohut et al. Psychooncology 2024 33(3) e6330
Similar articles in PubMed
Assessing Students' Knowledge and Attitudes Regarding the Risks and Prevention of Consanguineous Marriage: A Cross-Sectional Online Survey.
Ammar Abdulrahman Jairoun et al. J Multidiscip Healthc 2024 171251-1263
Similar articles in PubMed
Tissue-Based Genomic Testing in Prostate Cancer: 10-Year Analysis of National Trends on the Use of Prolaris, Decipher, ProMark, and Oncotype DX.
Eugenio Bologna et al. Clin Pract 2024 14(2) 508-520
Similar articles in PubMed
Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centre.
D Gareth Evans et al. Fam Cancer 2024
Similar articles in PubMed
Promoting Physical Activity Among Workers for Better Mental Health: An mHealth Intervention With Deep Learning.
Kazuhiro Watanabe et al. J UOEH 2024 46(1) 119-122
Similar articles in PubMed
Improving newborn screening test performance for metachromatic leukodystrophy: Recommendation from a pre-pilot study that identified a late-infantile case for treatment.
Teresa H Y Wu et al. Mol Genet Metab 2024 142(1) 108349
Similar articles in PubMed
The Role of Demographic and Clinical Factors in Germline Mutation Testing for Patients with Primary Hyperparathyroidism.
Patrick T Hangge et al. Ann Surg Oncol 2024
Similar articles in PubMed
Genome-matched treatments and patient outcomes in the Maine Cancer Genomics Initiative (MCGI).
Eric C Anderson et al. NPJ Precis Oncol 2024 8(1) 67
Similar articles in PubMed
Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability.
Lea Urpa et al. Eur J Hum Genet 2024
Similar articles in PubMed
The Finnish Adoptive Family Study of Schizophrenia: differences in somatic diseases and conditions between adoptees with high or low genetic risk for schizophrenia spectrum disorders.
Emma Karjalainen et al. Nord J Psychiatry 2024 1-7
Similar articles in PubMed
Genomic drivers in craniopharyngiomas: Analysis of the AACR project GENIE database.
M Brandon Lehrich et al. Childs Nerv Syst 2024
Similar articles in PubMed
Major Depressive Disorder Prediction Based on Sleep-Wake Disorders Symptoms in US Adolescents: A Machine Learning Approach from National Sleep Research Resource.
Jingsong Luo et al. Psychol Res Behav Manag 2024 17691-703
Similar articles in PubMed
PillHarmonics™: An Orchestrated Pharmacogenetics Medication Clinical Decision Support Service.
Robert H Dolin et al. Appl Clin Inform 2024
Similar articles in PubMed
Impact on costs and outcomes of multi-gene panel testing for advanced solid malignancies: a cost-consequence analysis using linked administrative data.
Alberto Hernando-Calvo et al. EClinicalMedicine 2024 69102443
Similar articles in PubMed
Risk of major adverse liver outcomes among first-degree relatives of individuals with MASLD.
Wen Yang et al. Liver Int 2024
Similar articles in PubMed
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
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 25, 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