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Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children
Author(s) -
Anders Kämpe,
Maria Enlund-Cerullo,
Saara Valkama,
Elisa HolmlundSuila,
Jenni Rosendahl,
Helena Hautaalus,
Minna Pekkinen,
Sture Andersson,
O Mäkitie
Publication year - 2020
Publication title -
yearbook of pediatric endocrinology
Language(s) - English
Resource type - Journals
eISSN - 1662-4009
pISSN - 1662-3991
DOI - 10.1530/ey.17.5.6
Subject(s) - vitamin d and neurology , genome wide association study , vitamin d binding protein , mendelian randomization , vitamin d deficiency , genetic association , haplotype , 1000 genomes project , expression quantitative trait loci , biology , candidate gene , imputation (statistics) , genotype , medicine , quantitative computed tomography , endocrinology , genetics , single nucleotide polymorphism , gene , bone density , genetic variants , osteoporosis , machine learning , missing data , computer science

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