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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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Public Health Genomics Branch
PHGKB Weekly Horizon Scan
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CDC/NIH Web Information Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC/NIH Web Information Database
CDC/NIH Information Database|Search|PHGKB
Last data update: Sep 03, 2024
. (Total: 8777 Documents)
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Records 1-30 (of 6333 Records)
CDC/NIH Web Information
Public Health Genetics, Gene Therapy, and Duchenne Muscular Dystrophy
CDC Webinar, December 18, 2023
We Screen Newborns Don’t We? Progress in DNA-based Population Screening
Video presentations, CDC and Precision Public Health Network webinar, May 18, 2023
We Screen Newborns Don’t We? Progress in DNA-based Population Screening
CDC Public Health Genomics Webinar, May 18, 2023,
Rare Disease Day at NIH 2023
NIH, December 2022
From Guthrie to Genomes: The Continued Evolution of Newborn Screening
A Gaviglio et al, CDC Blog Post, August 15, 2022
From Guthrie to Genomes: Expanding Bioinformatic Capabilities in Newborn Screening Programs
A Gaviglio et al, CDC Blog Post, March 21, 2022
Bespoke Gene Therapy Consortium
NIH, October 2021
NIH, FDA and 15 private organizations join forces to increase effective gene therapies for rare diseases
NIH press release, October 27, 2021
Muscular Dystrophy
CDC, 2021
Rare Diseases Registry Program (RaDaR)
NIH, July 2021
PaVe-GT: Collaborative NIH Effort Aimed at Creating a Gene Therapy Playbook, Making Rare Disease Treatments More Accessible
NIH NCATS, November 30, 2020
Rare Diseases and COVID-19
CDC COVID-19 Genomics and Precision Health Portal, August 2020
NIH-supported research survey to examine impact of COVID-19 on rare diseases community
NIH, May 7, 2020
Encouraging News for Kids with Neurofibromatosis Type 1
NIH Director's Blog, March 24, 2020
NCATS Rare Diseases Are Not Rare! 2020 Challenge Details
NCATS, March 2020
Novel lab-on-a-chip blood tests could greatly expand newborn exams for rare diseases
NHLBI, February 27, 2020
Rare Disease Day 2020
NIH, February 28, 2020
One Little Girl’s Story Highlights the Promise of Precision Medicine
F Collins, NIH director's blog, October 23, 2019
Assessing Gene-Environment Interactions in the Study of Rare Diseases
CDC Webinar, August 21, 2019
Rare Diseases Public Health Genomics Knowledge Base
CDC Office of Public Health Genomics , 2019
About Rare Cancers
NCI Information, 2019
Thoughts from the Front Lines of Rare Disease Research
NIH Directors Blog, February 28, 2019
Nitisinone increases melanin in people with albinism
NIH News Release, February 20, 2019
Rare Diseases Are Not Rare!
C Austin, NIH, February 2019
DEAF1-associated disorders
From NCATS Genetic and Rare Diseases Information Center
Hemochromatosis type 5
From NCATS Genetic and Rare Diseases Information Center
Autosomal Dominant Tubulointerstitial Kidney Disease, REN-Related
From NCATS Genetic and Rare Diseases Information Center
Jackhammer esophagus
From NCATS Genetic and Rare Diseases Information Center
Papular epidermal nevi with skyline basal cell layers syndrome
From NCATS Genetic and Rare Diseases Information Center
Plasmacytoma
From NCATS Genetic and Rare Diseases Information Center
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Page last reviewed:
Feb 1, 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
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