Myopia 6
What's New
Last Posted: May 04, 2020
- Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort- A Mendelian Randomization Study
X Han et al, JAMA Ophthalmology, April 30, 2020 - Association Between Polygenic Risk Score and Risk of Myopia
NG Mogarrad et al, JAMA Ophthalmology, October 1, 2019 - Genetics of Refraction and Myopia.
Zhang Qingjiong et al. Prog Mol Biol Transl Sci 2015 269-79 - Understanding Images: Seeing Myopia for What it Is- Potentially Treatable
PloS Biologue Blog Post, September 11, 2015 - Advances in the genomics of common eye diseases.
Cooke Bailey Jessica N et al. Hum. Mol. Genet. 2013 Oct 15. (R1) R59-65 - Education influences the role of genetics in myopia.
Verhoeven Virginie J M et al. Eur. J. Epidemiol. 2013 Dec (12) 973-80 - Epidemiology of myopia.
Foster P J et al. Eye (Lond) 2014 Feb (2) 202-8 - Genetic and environmental effects on myopia development and progression.
Goldschmidt E et al. Eye (Lond) 2014 Feb (2) 126-33 - Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future.
Hysi Pirro G et al. Invest. Ophthalmol. Vis. Sci. 2014 May (5) 3344-51 - Genome-wide association study success in ophthalmology.
Mackey David A et al. Curr Opin Ophthalmol 2014 Sep (5) 386-93
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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