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] Evaluation of Genetic Markers as Instruments for Mendelian Randomization Studies on Vitamin D
[PMID 22649517] Polymorphisms related to the serum 25-hydroxyvitamin d level and risk of myocardial infarction, diabetes, cancer and mortality. The tromsø study
[PMID 20541252] Common genetic determinants of vitamin D insufficiency: a genome-wide association study.
[PMID 22701574] Instrumental variable estimation of the causal effect of plasma 25-hydroxy-vitamin D on colorectal cancer risk: a mendelian randomization analysis
[PMID 23377224] Genetic Variation in the Vitamin D Pathway in Relation to Risk of Prostate Cancer - Results from Breast and Prostate Cancer Cohort Consortium (BPC3)
[PMID 23924835] Genetic variant in vitamin D binding protein is associated with serum 25-hydroxyvitamin D and vitamin D insufficiency in southern Chinese
[PMID 22740028] An exploratory analysis of common genetic variants in the vitamin D pathway including genome-wide associated variants in relation to glioma risk and outcome.
[PMID 26448018] Variants in Vitamin D Binding Protein Gene Are Associated With Gestational Diabetes Mellitus