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 (47515)
CDC/NIH Web Information Database (32189)
CDC-Authored Genomics and Precision Health Publications Database (5888)
Precision Health Database (63728)
Tier-Classified Guidelines Database (534)
Pathogen Advanced Molecular Detection Database (26775)
All of Us Reports and Publications Database (675)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (226639)
Epigenetic Epidemiology Publications Database (22803)
Release Note
Contact Us
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)
All
Cancer
Diabetes
Economic
Environmental
Equity
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 261 Records)
Next
Query Trace:
HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank.
Mitchell R Lucas et al. BMJ Open 2024 14(3) e081926
Similar articles in PubMed
Early dementia diagnosis: blood proteins reveal at-risk people The results of a large-scale screening study could be used to develop blood tests to diagnose diseases such as Alzheimer’s before symptoms take hold.
M Naddaf, Nature, February 13, 2024
Interest in genetic susceptibility testing and disclosure of AD dementia risk in cognitively normal adults: a survey study.
Lisa Waterink et al. Alzheimers Res Ther 2024 16(1) 1
Similar articles in PubMed
Attitudes toward pre-symptomatic screening for Alzheimer’s dementia in five European countries: a comparison of family members of people with Alzheimer’s dementia versus non-family members
IA Angelidou et al, Frontiers Genetics, December 2023
Association of regular use of ibuprofen and paracetamol, genetic susceptibility, and new-onset dementia in the older population.
Yuanyuan Zhang et al. Gen Hosp Psychiatry 2023 84226-233
Similar articles in PubMed
Emerging diagnostics and therapeutics for Alzheimer disease.
Wade K Self et al. Nat Med 2023
Similar articles in PubMed
Medicaid Enrollment and Service Use Among Adults With Down Syndrome.
Eric Rubenstein et al. JAMA Health Forum 2023 4(8) e232320
Similar articles in PubMed
Proteomics analysis of plasma from middle-aged adults identifies protein markers of dementia risk in later life.
Keenan A Walker et al. Sci Transl Med 2023 15(705) eadf5681
Similar articles in PubMed
Genetic screening for Huntington disease phenocopies in Sweden: A tertiary center case series focused on short tandem repeat (STR) disorders.
Martin Paucar et al. J Neurol Sci 2023 451120707
Similar articles in PubMed
Outreach, Screening, and Randomization of APOE ε4 Carriers into an Alzheimer's Prevention Trial: A global Perspective from the API Generation Program.
T Walsh et al. J Prev Alzheimers Dis 2023 10(3) 453-463
Similar articles in PubMed
Contributions of rare and common variation to early-onset and atypical dementia risk.
Carter A Wright et al. Cold Spring Harb Mol Case Stud 2023
Similar articles in PubMed
Modifiable cardiovascular risk factors and genetics for targeted prevention of dementia.
Ida Juul Rasmussen et al. Eur Heart J 2023
Similar articles in PubMed
Apolipoprotein E (APOE) Haplotypes in Healthy Subjects from Worldwide Macroareas: A Population Genetics Perspective for Cardiovascular Disease, Neurodegeneration, and Dementia.
Paolo Abondio et al. Curr Issues Mol Biol 2023 45(4) 2817-2831
Similar articles in PubMed
How one man's rare Alzheimer’s mutation delayed the onset of disease Genetic resilience found in a person predisposed to early-onset dementia could potentially lead to new treatments.
S Reardon, Nature, May 16, 2023
Evaluation of Plasma Biomarkers for A/T/N Classification of Alzheimer Disease Among Adults of Caribbean Hispanic Ethnicity.
Lawrence S Honig et al. JAMA Netw Open 6(4) e238214
Similar articles in PubMed
Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.
Maximilian Wiesenfarth et al. Brain communications 2023 5(2) fcad087
Similar articles in PubMed
Mediterranean diet adherence is associated with lower dementia risk, independent of genetic predisposition: findings from the UK Biobank prospective cohort study.
Oliver M Shannon et al. BMC medicine 2023 21(1) 81
Similar articles in PubMed
Advancing the Genetics of Lewy Body Disorders with Disease-Modifying Treatments in Mind.
Gilberto Levy et al. Advanced genetics (Hoboken, N.J.) 2023 3(4) 2200011
Similar articles in PubMed
Rationale for the selection of dual primary endpoints in prevention studies of cognitively unimpaired individuals at genetic risk for developing symptoms of Alzheimer's disease.
Angelika Caputo et al. Alzheimer's research & therapy 2023 15(1) 45
Similar articles in PubMed
Genetic propensity for cerebral amyloidosis and risk of mild cognitive impairment and Alzheimer's disease within a cognitive reserve framework.
Niki Mourtzi et al. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023
Similar articles in PubMed
Contributions of rare and common variation to early-onset and atypical dementia risk.
Carter A Wright et al. medRxiv : the preprint server for health sciences 2023
Similar articles in PubMed
Estrogen Receptor Genes, Cognitive Decline, and Alzheimer Disease.
Shahram Oveisgharan et al. Neurology 2023
Similar articles in PubMed
Integrative genetic analysis illuminates ALS heritability and identifies risk genes.
Megat Salim et al. Nature communications 2023 14(1) 342
Similar articles in PubMed
Walking pace, handgrip strength, age, APOE genotypes, and new-onset dementia: the UK Biobank prospective cohort study.
He Panpan et al. Alzheimer's research & therapy 2023 15(1) 9
Similar articles in PubMed
Hormone replacement therapy is associated with improved cognition and larger brain volumes in at-risk APOE4 women: results from the European Prevention of Alzheimer's Disease (EPAD) cohort.
Saleh Rasha N M et al. Alzheimer's research & therapy 2023 15(1) 10
Similar articles in PubMed
Expanding the spectrum of KIF5A mutations-case report of a large kindred with familial ALS and overlapping syndrome.
Dulski JarosLaw et al. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 1-4
Similar articles in PubMed
Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutations.
De Michele Giovanna et al. Acta neurologica Belgica 2023
Similar articles in PubMed
Polygenic resilience score may be sensitive to preclinical Alzheimer's disease changes.
Eissman Jaclyn M et al. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2022 28449-460
Similar articles in PubMed
Alzheimer's disease and related dementias among aging veterans: Examining gene-by-environment interactions with post-traumatic stress disorder and traumatic brain injury.
Logue Mark W et al. Alzheimer's & dementia : the journal of the Alzheimer's Association 2022
Similar articles in PubMed
Transferability of Alzheimer Disease Polygenic Risk Score Across Populations and Its Association With Alzheimer Disease-Related Phenotypes.
Jung Sang-Hyuk et al. JAMA network open 2022 5(12) e2247162
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:
May 01, 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