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 (47463)
CDC/NIH Web Information Database (32208)
CDC-Authored Genomics and Precision Health Publications Database (6094)
Precision Health Database (63881)
Tier-Classified Guidelines Database (535)
Pathogen Advanced Molecular Detection Database (26916)
All of Us Reports and Publications Database (698)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (227294)
Epigenetic Epidemiology Publications Database (22886)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Cancer
Last data update: May 18, 2024
. (Total: 63881 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 - 9 (of 9 Records)
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
GPNMB confers risk for Parkinson's disease through interaction with α-synuclein.
Diaz-Ortiz Maria E et al. Science (New York, N.Y.) 2022 377(6608) eabk0637
Similar articles in PubMed
Morbidity, risk of cancer and mortality in 3,645 HFE mutations carriers.
Hagström Hannes et al. Liver international : official journal of the International Association for the Study of the Liver 2021 Jan
Similar articles in PubMed
Somatic mutations in LRRK2 identify a subset of invasive mammary carcinomas associated with high mutation burden.
Parrilla Castellar Edgardo R et al. The American journal of pathology 2020 Sep
Similar articles in PubMed
Direct-To-Consumer Genetic Testing: Is the Public Ready for Simple, At-Home DNA Tests to Detect Disease Risk?
Bates Mary et al. IEEE pulse 9(6) 11-14
Similar articles in PubMed
Mendelian Randomization Studies of Coffee and Caffeine Consumption.
Cornelis Marilyn C et al. Nutrients 2018 Sep 10(10)
Similar articles in PubMed
Decoding Your DNA: What to Consider Before Genetic Testing
K Hobson, US News, September, 2018
What Personal Genome Testing Can and Can't Do-The limitations of personal genome service testing
M Shermer, Scientific American, August 2018
Clinicians' attitudes toward general screening of the Ashkenazi-Jewish population for prevalent founder BRCA1/2 and LRRK2 mutations.
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 18, 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