Abbas Parsian
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Explore the profile of Abbas Parsian including associated specialties, affiliations and a list of published articles.
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28
Citations
534
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Recent Articles
1.
Zhang H, Grant B, Hodgkinson C, Ruan W, Kerridge B, Huang B, et al.
Mol Psychiatry
. 2021 Nov;
27(3):1742-1753.
PMID: 34759357
Substance use disorders (SUDs) are moderately to highly heritable and are in part cross-transmitted genetically, as observed in twin and family studies. We performed exome-focused genotyping to examine the cross-transmission...
2.
Rahimi Z, Ahmadi R, Vaisi-Raygani A, Rahimi Z, Bahrehmand F, Parsian A
J Matern Fetal Neonatal Med
. 2013 May;
26(16):1590-4.
PMID: 23650977
Objective: To determine the butyrylcholinesterase (BChE) activity and phenotypes in preeclampsia and its possible association with lipid and lipoprotein metabolism and oxidative stress in preeclamptic women. Methods: In a case-control...
3.
Rahimi Z, Nourozi-Rad R, Rahimi Z, Parsian A
Hum Genomics
. 2012 Nov;
6:20.
PMID: 23157875
Background: The present study was conducted to investigate the possible outcome of interaction between endothelial nitric oxide (NOS3) G894T and cholesteryl ester transfer TaqIB variants on the risk of coronary...
4.
Rahimi Z, Malek-Khosravi S, Rahimi Z, Jalilvand F, Parsian A
Clin Biochem
. 2012 Oct;
46(1-2):143-7.
PMID: 23103710
Objectives: We aimed to investigate the association between methylenetetrahydrofolate reductase (MTHFR) C677T and endothelial nitric oxide synthase (eNOS) G894T polymorphisms with lipid peroxidation, total antioxidant capacity (TAC) and the risk...
5.
Rahimi Z, Rahimi Z, Mozafari H, Parsian A
J Renin Angiotensin Aldosterone Syst
. 2012 Jun;
14(2):174-80.
PMID: 22719026
Background: The aim of the present study was to investigate the association between angiotensin converting enzyme (ACE) insertion/deletion (I/D) and angiotensin II type-1 receptor (AT1R) A1166C polymorphisms with the risk...
6.
Malek-Khosravi S, Rahimi Z, Rahimi Z, Jalilvand F, Parsian A
J Thromb Thrombolysis
. 2011 Nov;
33(1):109-15.
PMID: 22068545
The aim of the present study was to investigate the frequency and the possible association between thrombophilic mutations of factor V Leiden (FVL) and prothrombin G20210A with preeclampsia among Kurdish...
7.
Rahimi Z, Vaisi-Raygani A, Rahimi Z, Parsian A
Nephrology (Carlton)
. 2011 Oct;
17(2):175-81.
PMID: 22026967
Aim: The present study investigated the influence of insertion (I)/deletion (D) polymorphism of the angiotensin II-converting enzyme (ACE) gene in combination with endothelial nitric oxide (eNOS) G894T polymorphism on the...
8.
Azhar M, Rahimi Z, Vaisi-Raygani A, Akramipour R, Madani H, Rahimi Z, et al.
Genet Test Mol Biomarkers
. 2011 Oct;
16(3):198-202.
PMID: 22017305
Aims: Polymorphism in genes involved in folate metabolism may influence the susceptibility to acute lymphoblastic leukemia (ALL). The aim of the present study was to determine the role of the...
9.
Rahimi Z, Parsian A
Mediterr J Hematol Infect Dis
. 2011 Jun;
3(1):e2011024.
PMID: 21713075
Hemoglobin S in homozygous state or in combination with one of the structural variants of Hb D-Punjab, Hb O-Arab, Hb C or β-thalassemia mutation results in sickle cell disease (SCD)...
10.
Rahimi Z, Nourozi-Rad R, Vaisi-Raygani A, Saidi M, Rahimi Z, Ahmadi R, et al.
Genet Test Mol Biomarkers
. 2011 Jun;
15(11):813-9.
PMID: 21689002
Aims: To shed light on the previously inconsistent results about the association of cholesteryl ester transfer protein TaqIB (CETP TaqIB) variants, high-density lipoprotein cholesterol (HDL-C) levels, and the risk of...