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CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v8.8)
PHGKB
About
Public Health Genomics Branch
Genomics and Precision Health Update
Genomics (A-Z)
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
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Implementation Science PHGKB
Neurological Disorders PHGKB
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Primary Immune Deficiency Diseases PHGKB
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Reproductive and Child Health PHGKB
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(Current Edition)
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(Current Edition)
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(Current Edition)
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COVID-19 GPH (46611)
CDC/NIH Web Information Database (31913)
CDC-Authored Genomics and Precision Health Publications Database (4776)
Precision Health Database (62224)
Tier-Classified Guidelines Database (530)
Pathogen Advanced Molecular Detection Database (25875)
All of Us Reports and Publications Database (531)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (223516)
Epigenetic Epidemiology Publications Database (22119)
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CDC/NIH Web Information Database|Home|PHGKB
CDC/NIH Web Information Database
CDC/NIH Information Database|Search|PHGKB
Reproductive and Child Health
Last data update: Dec 01, 2023
. (Total: 8775 Documents)
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Records 1-30 (of 262 Records)
CDC/NIH Web Information
Public Health Genetics, Gene Therapy, and Duchenne Muscular Dystrophy
CDC Webinar, December 18, 2023
Newborn Screening Is a Lifesaver
CDC, July 2023
Community Counts: Understanding Hemophilia and Other Bleeding Disorders through Public Health Surveillance
CDC webinar, August 24, 2023
Fragile X Syndrome – Moving Research FORWARD
CDC, July 2023
Improving Identification of Tic Disorders
CDC, June 2023
Emerging Trends in Gene Therapy: Thalassemia as a Case Study
CDC Seminar— June 22, 2023, 2:00–3:00 PM ET
Risk Factors and Causes for Tourette Syndrome
CDC, 2023
A Parent’s Guide to Genetics and Hearing Loss
CDC, 2023
What is Autism Spectrum Disorder?
CDC, 2023
Sickle Cell Data Collection Program
CDC, March 2023
Birth Defects Research and Tracking
CDC, March 2023
Implementation of Population-Based Genetic Testing of Newborn Infants for Prediction of Hearing Loss in Ontario, Canada
CDC Webinar, April 19, 2023
Population Screening for Rare Pathogenic Variants as the Low Hanging Fruit for Public Health Genomics Across the Lifespan
MJ Khoury, CDC Blog Post, February 13, 2023
Transcript for Vital Signs Telebriefing: Children with sickle cell anemia are at risk for stroke and other complications
CDC, October 2022
From Guthrie to Genomes: The Continued Evolution of Newborn Screening
A Gaviglio et al, CDC Blog Post, August 15, 2022
Fragile X syndrome: Learning what families need, one person at a time.
CDC, July 2022
Population Genomic Screening is Here: We Need Evidence on Health Impact and Optimal Implementation
MJ Khoury et al, CDC Blog Post, June 21, 2022
Can’t Stop, Won’t Stop: The Resiliency of Newborn Screening Programs during the COVID-19 Pandemic
A Gaviglio, CDC Blog Post, June 14, 2022
Breaking Down Barriers to ED Care for People with SCD
CDC, May 2022
Facts About Hereditary Hemorrhagic Telangiectasia
CDC, June 2022
Using Pharmacogenomics to Better Understand the Role of Selected Medications and Birth Defect Risk
M Jenkins et al, CDC Blog Post, April 12, 2022
Precision Public Health in Action: Enhancing models to predict risk of adverse treatment outcomes in people with hemophilia
CJ Bean et al, CDC Blog Post, March 29, 2022
From Guthrie to Genomes: Expanding Bioinformatic Capabilities in Newborn Screening Programs
A Gaviglio et al, CDC Blog Post, March 21, 2022
Disease of the Week: Hemophilia
CDC, March 2022
5 Things to Know About Heart Defects
CDC, February 2022
Precision Public Health in Action: New CDC Pilot Projects Integrating Human Genomics into Public Health Surveillance and Applied Research
M Clyne et al, CDC Blog Post, February 14, 2022
Awareness of Birth Defects Across the Lifespan
CDC, January 3, 2022
V-safe and Registry Monitoring People Who Report Pregnancy
CDC, December 7, 2021
Real Stories from People Living with Hemophilia – Carrie
CDC, November 2021
Real Stories from People Living with Sickle Cell Disease: Rae Blaylark
CDC, November 2021
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Page last reviewed:
Oct 1, 2023
Page last updated:
Dec 01, 2023
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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