Exploring the genetic basis of essential hypertension: association with AGT gene variants in an Iranian population
This study provides evidence for the involvement of AGT gene variants and haplotypes in the pathogenesis of EH in the Iranian population. These findings highlight the importance of considering genetic factors in the development and management of this prevalent condition.
Authors
- Farzad Hadaegh (ORCID: https://orcid.org/0000-0002-8935-2744)
- Asiyeh Sadat Zahedi (ORCID: https://orcid.org/0000-0001-5184-3460)
- Mohammad Piryaei
- Mahdi Akbarzadeh (ORCID: https://orcid.org/0000-0002-8048-744X)
- Aram Halimi (ORCID: https://orcid.org/0000-0002-7339-4747)
- Amir Abbas Momenan
- Mina Jahangiri (ORCID: https://orcid.org/0000-0001-9119-7571)
- Mehdi Hedayati (ORCID: https://orcid.org/0000-0001-5816-775X)
- Maryam S. Daneshpour (ORCID: https://orcid.org/0000-0003-1525-8672)
- Arash Ghanbarian (ORCID: https://orcid.org/0000-0001-9662-2944)
Institutions
- Tarbiat Modares University (IR)
- Research Institute for Endocrine Sciences (IR)
- Shahid Beheshti University of Medical Sciences (IR)
Publication Details
- Journal
- BMC Genomics
- Published
- 2025-11-28
- DOI
- https://doi.org/10.1186/s12864-025-12369-0
- Primary Topic
- Renin-Angiotensin System Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00