Associated Papers
Human melanopsin (OPN4) gene polymorphisms: a systematic review.
Lucio-Enríquez KR et al.
Frontiers in Neuroscience, 2025
Shared and divergent contribution of vitamin A and oxytocin to the aetiology of autism spectrum disorder.
Wang T et al.
Computational and Structural Biotechnology Journal, 2023
38213898 (PubMed )
Supplement: mmc2.xlsx › RIVs_in_VARGs
Case report: A novel missense variant in melanopsin associates with delayed sleep phenotype: Whole genome sequencing study.
Smieszek SP et al.
Frontiers in Genetics, 2022
Exomes of Ductal Luminal Breast Cancer Patients from Southwest Colombia: Gene Mutational Profile and Related Expression Alterations.
Cortes-Urrea C et al.
Biomolecules, 2020
32365829 (PubMed )
Supplement: biomolecules-10-00698-s001.zip › Article-to-BIOMOLECULES_R1_v4Apr2020 › CortesUrreaetal_R1_Supp_Table_S2_339SNPs.xlsx › Tab_S2_339_SNPs_440_alterations
Functional characterisation of naturally occurring mutations in human melanopsin.
Rodgers J et al.
Cellular and Molecular Life Sciences : Cmls, 2018
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