CDC-Authored Genomics and Precision Health Publications Database
Last data update: Dec 01, 2023. (Total: 4776 publications since 2011)
Query Trace: Rare diseases[original query] |
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Common Challenges and Identified Solutions for State Newborn Screening Programs during COVID-19 Pandemic.
Simon D , Broadbridge E , Baker M , Gaviglio A , Gruber D , Piper KN , Tavakoli NP , Sullivan J , Kennedy A . Int J Neonatal Screen 2022 8 (1) ![]() |
American Academy of Optometry Microbial Keratitis Think Tank.
Szczotka-Flynn LB , Shovlin JP , Schnider CM , Caffery BE , Alfonso EC , Carnt NA , Chalmers RL , Collier S , Jacobs DS , Joslin CE , Kroken AR , Lakkis C , Pearlman E , Schein OD , Stapleton F , Tu E , Willcox MDP . Optom Vis Sci 2021 98 (3) 182-198 |
Challenges and Opportunities for Communication about the Role of Genomics in Public Health.
Allen CG , Green RF , Bowen S , Dotson WD , Yu W , Khoury MJ . Public Health Genomics 2021 24 1-7 |
The need for a next-generation public health response to rare diseases.
Valdez Rodolfo, Grosse Scott D, Khoury Muin J. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Oct . Genetics in medicine : official journal of the American College of Medical Genetics 2016 Oct |
The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study.
Karaceper Maria D, Chakraborty Pranesh, Coyle Doug, Wilson Kumanan, Kronick Jonathan B, Hawken Steven, Davies Christine, Brownell Marni, Dodds Linda, Feigenbaum Annette, Fell Deshayne B, Grosse Scott D, Guttmann Astrid, Laberge Anne-Marie, Mhanni Aizeddin, Miller Fiona A, Mitchell John J, Nakhla Meranda, Prasad Chitra, Rockman-Greenberg Cheryl, Sparkes Rebecca, Wilson Brenda J, Potter Beth K, . Orphanet journal of rare diseases 2016 Feb 1112 . Orphanet journal of rare diseases 2016 Feb 1112 |
Public Health and Rare Diseases: Oxymoron No More.
Valdez Rodolfo, Ouyang Lijing, Bolen Julie. Preventing chronic disease 2016 Jan 13E05 . Preventing chronic disease 2016 Jan 13E05 |
Evaluation of the validity and utility of genetic testing for rare diseases.
Grosse Scott D, Kalman Lisa, Khoury Muin J. Advances in experimental medicine and biology 2010 686115-31 . Advances in experimental medicine and biology 2010 686115-31 |
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- Page last updated:Dec 01, 2023
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