Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia

Refractive errors, in particular myopia, are a leading cause of morbidity and disability world-wide. Genetic investigation can improve understanding of the molecular mechanisms underlying abnormal eye development and impaired vision. We conducted a meta-analysis of genome-wide association studies in...

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Bibliografiset tiedot
Julkaisussa:Nat Genet
Päätekijät: Hysi, Pirro G., Choquet, Hélène, Khawaja, Anthony P., Wojciechowski, Robert, Tedja, Milly S, Yin, Jie, Simcoe, Mark J., Patasova, Karina, Mahroo, Omar A., Thai, Khanh K, Cumberland, Phillippa M, Melles, Ronald B., Verhoeven, Virginie J.M., Vitart, Veronique, Segre, Ayellet, Stone, Richard A., Wareham, Nick, Hewitt, Alex W, Mackey, David A, Klaver, Caroline CW, MacGregor, Stuart, Khaw, Peng T., Foster, Paul J., Guggenheim, Jeremy A., Rahi, Jugnoo S, Jorgenson, Eric, Hammond, Christopher J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2020
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Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7145443/
https://ncbi.nlm.nih.gov/pubmed/32231278
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-020-0599-0
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