Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertility-Reference-Cited by-同舟云学术

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Polymorphisms and haplotypes in VDR gene are associated with female idiopathic infertility

Published:2018-09-17 Issue:2 Volume:23 Page:101-110
ISSN:1464-7273
Container-title:Human Fertility
language:en
Short-container-title:Human Fertility

Author:

Djurovic Jelena¹,Stamenkovic Gorana²,Todorovic Jelena³,Aleksic Natasa¹,Stojkovic Oliver¹

Affiliation:

1. Faculty of Medicine, Institute of Forensic Medicine, University of Belgrade, Belgrade, Serbia;

2. Institute of Biological Research “Siniša Stanković”, University of Belgrade, Belgrade, Serbia;

3. Specialized Medical Practice in the Field of Internal Medicine “Teamed”, Belgrade, Serbia

Funder

Ministry of Education, Science and Technological Development of the Republic of Serbia

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Reproductive Medicine,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14647273.2018.1515503

Reference46 articles.

1. Association between maternal serum 25-hydroxyvitamin D level and pregnancy and neonatal outcomes: systematic review and meta-analysis of observational studies

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association of vitamin D receptor genetic polymorphisms with the risk of infertility: a systematic review and meta-analysis;BMC Pregnancy and Childbirth;2024-05-30

2. Identification of a Single Nucleotide Polymorphism of Vitamin D Receptor (VDR) and Vitamin D Binding Protein (VDBP) Gene and Its Dysregulated Pathway Through VDR-VDBP Interaction Network Analysis in Vitamin D-Deficient Infertile Females;Cureus;2024-03-05

3. Vitamin D Serum Levels and Vitamin D Receptor Genotype in Patients with Parkinson’s Disease;Neuroscience;2023-11

4. Genetic association of vitamin D receptor gene with female infertility;Nucleosides, Nucleotides & Nucleic Acids;2023-07-26

5. Genetic reanalysis of patients with a difference of sex development carrying the NR5A1/SF-1 variant p.Gly146Ala has discovered other likely disease-causing variations;PLOS ONE;2023-07-11

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