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Tieteenala 2010 » Lääke- ja terveystieteet » 312 Kliiniset lääketieteet

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Comment on : Development and validation of a novel nomogram for predicting the occurrence of myopia in schoolchildren : A prospective cohort study (2023) Lanca, Carla; et al.; B1
Rare variant analyses across multiethnic cohorts identify novel genes for refractive error (2023) Musolf, Anthony M.; et al.; A1; OA
Associations of Children’s Close Reading Distance and Time Spent Indoors with Myopia, Based on Parental Questionnaire (2022) Pärssinen, Olavi; et al.; A1; OA
Associations of near work time, watching TV, outdoors time, and parents’ myopia with myopia among school children based on 38‐year‐old historical data (2022) Pärssinen, Olavi; et al.; A1; OA
Commonly occurring genetic polymorphisms with a major impact on the risk of nonsyndromic strabismus : replication in a sample from Finland (2022) Plotnikov, Denis; et al.; A1
Early Life Influences on Hearing in Adulthood : a Systematic Review and Two-Step Individual Patient Data Meta-Analysis (2022) Dawes, Piers; et al.; A2; OA
The Effectiveness of Unilateral Cochlear Implantation on Performance-Based and Patient-Reported Outcome Measures in Finnish Recipients (2022) Dietz, Aarno; et al.; A1; OA
Comparison of myopic progression in Finnish and Singaporean children (2021) Pärssinen, Olavi; et al.; A1; OA
Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia (2021) Tideman, J. Willem L.; et al.; A1
Genetic Variants Associated With Human Eye Size Are Distinct From Those Conferring Susceptibility to Myopia (2021) Plotnikov, Denis; et al.; A1; OA