Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.

doi:10.1210/jc.2017-00682

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.

The Journal of clinical endocrinology and metabolism - 1 Aug 2017

Moon Rebecca J, Harvey Nicholas C, Cooper Cyrus, D'Angelo Stefania, Curtis Elizabeth M, Crozier Sarah R, Barton Sheila J, Robinson Sian M, Godfrey Keith M, Graham Nikki J, Holloway John W, Bishop Nicholas J, Kennedy Stephen, Papageorghiou Aris T, Schoenmakers Inez, Fraser Robert, Gandhi Saurabh V, Prentice Ann, Inskip Hazel M, Javaid M Kassim

Abstract excerpt

Context: Single-nucleotide polymorphisms (SNPs) in genes related to vitamin D metabolism have been associated with serum 25-hydroxyvitamin D [25(OH)D] concentration, but these relationships have not been examined following antenatal cholecalciferol supplementation. Objective: To determine whether SNPs in DHCR7, CYP2R1, CYP24A1, and GC are associated with the response to gestational cholecalciferol...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cholecalciferol

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cholestanetriol 26-Monooxygenase

Share to Cytochrome P450 Family 2

Share to Oxidoreductases Acting on CH-CH Group Donors

Share to Vitamin D-Binding Protein

Share to Vitamin D Deficiency

Share to Vitamin D3 24-Hydroxylase

Share to Vitamins

Source

Open in PubMed Open full text

Identifiers

PMID: 28575224
DOI: 10.1210/jc.2017-00682
PMCID: PMC5546866

Genes

DHCR7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Response to Antenatal Cholecalciferol Supplementation Is Associated With Common Vitamin D-Related Genetic Variants.PMID 28575224Read ↗

Maternal and Fetal Genetic Variation in Vitamin D Metabolism and Umbilical Cord Blood 25-Hydroxyvitamin D.Semantic proximity Read ↗

Fetal and Maternal Genetic Variants Influencing Neonatal Vitamin D Status.Semantic proximity Read ↗

SNP rs11185644 of RXRA gene is identified for dose-response variability to vitamin D3 supplementation: a randomized clinical trial.Semantic proximity Read ↗

Genetic Variants Influencing Individual Vitamin D StatusSemantic proximity Read ↗

The Role of Polymorphisms in Vitamin D-Related Genes in Response to Vitamin D Supplementation.Semantic proximity Read ↗

Common variants in CYP2R1 and GC genes predict vitamin D concentrations in healthy Danish children and adults.Semantic proximity Read ↗

Maternal VDR variants rather than 25-hydroxyvitamin D concentration during early pregnancy are associated with type 1 diabetes in the offspring.Semantic proximity Read ↗

Genetic variants in CYP2R1, CYP24A1, and VDR modify the efficacy of vitamin D3 supplementation for increasing serum 25-hydroxyvitamin D levels in a randomized controlled trial.Semantic proximity Read ↗

Determinants of vitamin D status: focus on genetic variations.Semantic proximity Read ↗

Genetic control of serum 25(OH)D levels and its association with ethnicity.Semantic proximity Read ↗

Genetic Variation in CYP2R1 and GC Genes Associated With Vitamin D Deficiency Status.Semantic proximity Read ↗

Single nucleotide polymorphisms in the vitamin D pathway associating with circulating concentrations of vitamin D metabolites and non-skeletal health outcomes: Review of genetic association studies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.