The Association Between the 5-Hydroxytryptamine Receptor 2A Gene Variants rs6311 and rs6313 and Obstructive Sleep Apnea in the Iranian Kurdish Population-Reference-Cited by-同舟云学术

The Association Between the 5-Hydroxytryptamine Receptor 2A Gene Variants rs6311 and rs6313 and Obstructive Sleep Apnea in the Iranian Kurdish Population

Published:2024-04-01 Issue:4 Volume:28 Page:159-164
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Abdolsamadi Mohammad¹,Rasouli Sharareh¹,Alizadeh Severi Ali¹,Khirehgesh Mohammad Reza²,Safari Fatemeh³,Mahdieh Nejat⁴^ORCID,Khazaie Habibolah⁵,Soleymani Bijan⁶,Akbari Bahman⁵^ORCID

Affiliation:

1. Department of Medical Biotechnology, School of Medicine, Kermanshah University of Medical Science, Kermanshah, Iran.

2. Pharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

3. Diagnostic Laboratory Sciences and Technology Research Center, School of Paramedical Sciences, Shiraz University of Medical Sciences, Shiraz, Iran.

4. Cardiogenetic Research Laboratory, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.

5. Sleep Disorders Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

6. Medical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/gtmb.2023.0272

Reference23 articles.

1. Variability in the 5-HT2A receptor gene is associated with seasonal pattern in major depression

2. Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response

3. 5-HT2a receptor polymorphism gene in bipolar disorder and harm avoidance personality trait

4. A unique serotonin receptor in choroid plexus is linked to phosphatidylinositol turnover.

5. Relationship of obstructive sleep apnea syndrome with the 5-HT2A receptor gene in Brazilian patients

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