Genome-wide association identifies novel ROP risk loci in a multi-ethnic cohort

We conducted a genome-wide association study (GWAS) in a multiethnic cohort of 920 at-risk infants for retinopathy of prematurity (ROP), a major cause of childhood blindness, identifying 2 loci at genome-wide significance level (p<5×10–8) and 7 at suggestive significance (p<5×10–6) for ROP ≥ s...

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Detalles Bibliográficos
Autores principales: Rotter, Jerome, Li, Xiaohui, Owen, Leah A., Taylor, Kent, Ostmo, Susan, Chen, Yii-Der Ida, Coyner, Aaron, Sonmez, Kemal, hartnett, M.Elizabeth, Guo, Xiuqing, Ipp, Eli, Roll, Kathryn, Genter, Pauline, Chan, R.V. Paul, DeAngelis, Margaret, Chiang, Michael, Campbell, J Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246102/
https://www.ncbi.nlm.nih.gov/pubmed/37292936
http://dx.doi.org/10.21203/rs.3.rs-2855404/v1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246102/
https://www.ncbi.nlm.nih.gov/pubmed/37292936
http://dx.doi.org/10.21203/rs.3.rs-2855404/v1

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