Search filters

List of works by Zohreh Rahimi

?-Globin gene cluster haplotypes in sickle cell patients from southwest Iran

scientific article published on 24 October 2003

ACE I/D and MMP-7 A-181G variants and the risk of end stage renal disease

scientific article published on March 2017

ACE gene polymorphism and serum ACE activity in Iranians type II diabetic patients with macroalbuminuria

scientific article published on 10 September 2010

ACE insertion/deletion (I/D) polymorphism and diabetic nephropathy.

scientific article

AT2R -1332 G:A polymorphism and diabetic nephropathy in type 2 diabetes mellitus patients

scientific article

Abnormal hemoglobins among Kurdish population of Western Iran: hematological and molecular features

scientific article published on 31 March 2009

An Iranian Child With HbQ-Iran [??75 (EF4) Asp???His]/?????3.7???kb/IVSII.1 G???A

scientific article published in September 2007

Angiotensin converting enzyme insertion/deletion (I/D) (rs4646994) and Vegf polymorphism (+405G/C; rs2010963) in type II diabetic patients: Association with the risk of coronary artery disease

scientific article published on 6 February 2014

Angiotensin type 1 receptor A1166C polymorphism and systemic lupus erythematosus: correlation with cellular immunity and oxidative stress markers.

scientific article

Angiotensin-converting enzyme insertion/deletion (rs106180) and angiotensin type 1 receptor A C (rs106165) genotypes and psoriasis: Correlation with cellular immunity, lipid profile, and oxidative stress markers

scientific article published on 10 October 2018

Association between GSTM1, GSTT1, and GSTP1 variants and the risk of end stage renal disease.

scientific article published on 8 August 2016

Association between apolipoprotein E polymorphism and serum lipid and apolipoprotein levels with Alzheimer's disease

scientific article

Association between apolipoprotein ε4 allele, factor V Leiden, and plasma lipid and lipoprotein levels with sickle cell disease in southern Iran

scientific article published on 7 April 2010

Association between butyrylcholinesterase activity and phenotypes, paraoxonase192 rs662 gene polymorphism and their enzymatic activity with severity of rheumatoid arthritis: Correlation with systemic inflammatory markers and oxidative stress, prelimi

scientific article published in January 2015

Association between cholesteryl ester transfer protein TaqIB variants and risk of coronary artery disease and diabetes mellitus in the population of western Iran.

scientific article

Association between enzymatic and non-enzymatic antioxidant defense mechanism with apolipoprotein E genotypes in Alzheimer disease

scientific article

Association between the -11377 C/G and -11391 G/A polymorphisms of adiponectin gene and adiponectin levels with susceptibility to type 1 and type 2 diabetes mellitus in population from the west of Iran, correlation with lipid profile

scientific article published on 11 September 2018

Association between the cytotoxic T-lymphocyte antigen-4 mutations and the susceptibility to systemic lupus erythematosus; Contribution markers of inflammation and oxidative stress.

scientific article published on 31 October 2016

Association of endothelial nitric oxide synthase gene variant (G894T) with coronary artery disease in Western Iran.

scientific article published on 20 May 2011

Association of matrix metalloproteinase-7A-181G variants with the risk of multiple sclerosis

scientific article published on 01 November 2014

Association of the CYP17 MSP AI (T-34C) and CYP19 codon 39 (Trp/Arg) polymorphisms with susceptibility to acne vulgaris

scientific article published on 28 December 2017

Association of the hypermethylation status of PTEN tumor suppressor gene with the risk of breast cancer among Kurdish population from Western Iran

scientific article published on 29 December 2015

Brain-Derived Neurotrophic Factor Val66Met Polymorphism and Its Synergism with L/S Polymorphism in the Promoter Region of Serotonin Transporter in Bipolar I Disorder Patients in Western Iran

scientific article published on 17 October 2016

Butyrylcholinesterase (BChE) activity is associated with the risk of preeclampsia: influence on lipid and lipoprotein metabolism and oxidative stress ⬇️

scientific article published on May 23, 2013

Butyrylcholinesterase K variant and the APOE-ε4 allele work in synergy to increase the risk of coronary artery disease especially in diabetic patients

scientific article published on 15 August 2009

Butyrylcholinesterase K variants increase the risk of coronary artery disease in the population of western Iran

scientific article published in January 2008

CYP24A1 genetic variants in the vitamin D metabolic pathway are involved in the outcomes of hepatitis C virus infection among high-risk Chinese population

scientific article published on 16 November 2019

Cancer Notification at a Referral Hospital of Kermanshah, Western Iran (2006-2009)

scientific article published on 4 February 2015

Cancer notification at a referral hospital of Kermanshah, Western Iran (2006-2009).

scientific article published on January 2015

Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden

scientific article published on 23 August 2009

Chemerin rs17173608 and vaspin rs2236242 gene variants on the risk of end stage renal disease (ESRD) and correlation with plasma malondialdehyde (MDA) level

scientific article published in November 2018

Co-existence of fatty acids changes in aorta artery and adipose tissue; comparison between CAD and non CAD patients

scientific article published in February 2008

Comparison of fatty acid profiles of aorta and internal mammary arteries in patients with coronary artery disease

scientific article published on 6 March 2006

Concomitant presence of endothelial nitric oxide 894T and angiotensin II-converting enzyme D alleles are associated with diabetic nephropathy in a Kurdish population from Western Iran.

scientific article

Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden.

scientific article published in July 2010

Detection of responsible mutations for beta thalassemia in the Kermanshah Province of Iran using PCR-based techniques

scientific article published on 13 May 2009

Determination of butyrylcholinesterase (BChE) phenotypes to predict the risk of prolonged apnea in persons receiving succinylcholine in the healthy population of western Iran

scientific article published in June 2007

Effect of Acetylcholinesterase and Butyrylcholinesterase on Intrauterine Insemination, Contribution to Inflammations, Oxidative Stress and Antioxidant Status; A Preliminary Report

scientific article published on July 2016

Endothelial Nitric Oxide Synthase (eNOS) 4a/b and G894T Polymorphisms and Susceptibility to Preeclampsia

scientific article published on October 2013

Establishing hematological reference intervals in healthy adults: Ravansar non-communicable disease cohort study, Iran

scientific article published on 23 October 2020

Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran

scientific article

Fatty acid composition of human milk in Western Iran

scientific article

Frequencies of apolipoprotein E polymorphism in a healthy Kurdish population from Kermanshah, Iran

scientific article published in October 2007

Functional Promoter Polymorphisms of MMP-2 C-735T and MMP-9 C-1562T and Their Synergism with MMP-7 A-181G in Multiple Sclerosis

scientific article published on 13 July 2016

Genetic Variants of Pre-microRNAs A-499G(rs3746444) and T-196a2C(rs11614913) with Ulcerative Colitis (UC) and Investigated with Thiopurine-S-Methyltransferase (TPMT) Activity

scientific article published in October 2017

Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran

scientific article published on 18 June 2013

Haplotype analysis of beta thalassemia patients in Western Iran

scientific article published in March 2009

Hb D-Punjab [β 121 (GH4) Glu→Gln]/β0-thalassemia [IVSII.1(G→A)] in two cases from an Iranian family: First report

scientific article published in 2006

Hemospermia: long-term outcome in 165 patients

scientific article published on 5 December 2013

Implications of the genetic epidemiology of globin haplotypes linked to the sickle cell gene in southern Iran

scientific article published in December 2006

Infant With Concomitant Presence of Hernia/Hydrocele and Primary Paratesticular Neuroblastoma

scientific article published in May 2009

Interaction of MTHFR 1298C with ACE D allele augments the risk of diabetic nephropathy in Western Iran.

scientific article published on 23 September 2011

Interaction of eNOS polymorphism with MTHFR variants increase the risk of diabetic nephropathy and its progression in type 2 diabetes mellitus patients

scientific article published on 6 March 2011

Interaction of long noncoding RNA MEG3 with miRNAs: A reciprocal regulation

scientific article published on 19 September 2018

Lack of association between MTHFR C677T and A1298C polymorphisms and risk of childhood acute lymphoblastic leukemia in the Kurdish population from Western Iran.

scientific article

Leukocytosis and alteration of hemoglobin level in patients with severe COVID-19: Association of leukocytosis with mortality

scientific article published on 14 October 2020

MMP-8 C-799T and MMP-8 C+17G polymorphisms in mild and severe preeclampsia: Association between MMP-8 C-799T with susceptibility to severe preeclampsia.

scientific article

MTHFR C677T and eNOS G894T variants in preeclamptic women: Contribution to lipid peroxidation and oxidative stress

scientific article published on 24 October 2012

Matrix metalloproteinase 9 polymorphisms and systemic lupus erythematosus: correlation with systemic inflammatory markers and oxidative stress

scientific article published on 21 November 2014

Matrix metalloproteinase-2 C-735T and its interaction with matrix metalloproteinase-7 A-181G polymorphism are associated with the risk of preeclampsia: influence on total antioxidant capacity and blood pressure

scientific article published on 10 October 2017

Matrix metalloproteinase-2 functional promoter polymorphism G1575A is associated with elevated circulatory MMP-2 levels and increased risk of cardiovascular disease in systemic lupus erythematosus patients.

scientific article published on 9 February 2012

Matrix metalloproteinase-7 A-181G and its interaction with matrix metalloproteinase-9 C-1562T polymorphism in preeclamptic patients: association with malondialdehyde level and severe preeclampsia.

scientific article

Matrix metalloproteinase-9 -1562T allele and its combination with MMP-2 -735 C allele are risk factors for breast cancer

scientific article

Matrix metalloproteinase-9 functional promoter polymorphism 1562C>T increased risk of early-onset coronary artery disease.

scientific article published on 11 May 2011

Mental health problems of young refugees: duration of settlement, risk factors and community-based interventions.

scientific article published on 26 October 2012

Methylentetrahydrofolatereductase (rs1801133) polymorphism and psoriasis: contribution to oxidative stress, lipid peroxidation and correlation with vascular adhesion protein 1, preliminary report

scientific article

Modulation of oxidative and glycolytic skeletal muscle fibers Na+/H+ exchanger1 (NHE1) and Na+/HCO3- co-transporter1 (NBC1) genes and proteins expression in type 2 diabetic rat (Streptozotocin + high fat diet) following long term endurance training.

scientific article published on 20 May 2017

Molecular and hematologic analysis of hemoglobin Q-Iran and hemoglobin Setif in Iranian families.

scientific article

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran

scientific article published in September 2006

NOTCH1, SF3B1, MDM2 and MYD88 mutations in patients with chronic lymphocytic leukemia

NPHP4 variants are associated with pleiotropic heart malformations

scientific article

PPARγ Pro12Ala and C161T polymorphisms in patients with acne vulgaris: Contribution to lipid and lipoprotein profile

scientific article published on 6 November 2017

Paraoxonase (PON1) 55 polymorphism and association with systemic lupus erythematosus

scientific article published on July 9, 2013

Paraoxonase 1 (PON1) 55 polymorphism, lipid profiles and psoriasis

scientific article published in December 2012

Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease

scientific article published on 5 April 2011

Plasma lipids and lipoproteins in children and young adults with major β-thalassemia from western Iran: influence of genotype

scientific article published on 18 November 2010

Plasma lipids in Iranians with sickle cell disease: hypocholesterolemia in sickle cell anemia and increase of HDL-cholesterol in sickle cell trait

scientific article published on 26 September 2005

Preeclampsia and angiotensin converting enzyme (ACE) I/D and angiotensin II type-1 receptor (AT1R) A1166C polymorphisms: association with ACE I/D polymorphism ⬇️

scientific article published on June 19, 2012

Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran

scientific article published on 14 August 2007

Prevalence of iron deficiency anemia among adolescent schoolgirls from Kermanshah, Western Iran.

scientific article published in December 2008

Prevalence of thrombotic risk factors among beta-thalassemia patients from Western Iran

scientific article published on 4 November 2007

Rapid separation of human globin chains in normal and thalassemia patients by RP-HPLC

scientific article published on 5 March 2010

Relationship between serum homovanillic acid, DRD2 C957T (rs6277), and hDAT A559V (rs28364997) polymorphisms and developmental stuttering

scientific article published on 30 August 2018

Serum butyrylcholinesterase activity and phenotype associations with lipid profile in stroke patients

scientific article published on 12 November 2008

Sex steroid hormones and sex hormone binding globulin levels, CYP17 MSP AI (-34T:C) and CYP19 codon 39 (Trp:Arg) variants in children with developmental stuttering

scientific article

Sickle cell disease and venous thromboembolism

scientific article

Sleep Architecture and Hypothalamic-Pituitary-Adrenal Activity in Paradoxical and Psychophysiological Insomnia

scientific article published on 01 November 2018

Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus ⬇️

scientific article published on September 25, 2012

Synergism between apolipoprotein E Ɛ4 allele and paraoxonase (PON1) 55-M allele is associated with risk of systemic lupus erythematosus

scientific article published on 22 December 2017

Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease.

scientific article

Synergistic effects of BuChE non-UU phenotype and paraoxonase (PON1) 55 M allele on the risk of systemic lupus erythematosus: influence on lipid and lipoprotein metabolism and oxidative stress, preliminary report

scientific article published on 7 January 2014

Synergistic effects of angiotensinogen -217 G→A and T704C (M235T) variants on the risk of severe preeclampsia

scientific article published on 23 November 2012

The Association of PPARγ Pro12Ala and C161T Polymorphisms with Polycystic Ovary Syndrome and Their Influence on Lipid and Lipoprotein Profiles.

scientific article published on 18 March 2018

The MMP-2 -735 C Allele is a Risk Factor for Susceptibility to Breast Cancer

scientific article published on 15 August 2014

The Role of Renin Angiotensin Aldosterone System Genes in Diabetic Nephropathy.

scientific article

The T Allele of MTHFR c.C677T and Its Synergism with G (Val 158) Allele of COMT c.G472A Polymorphism Are Associated with the Risk of Bipolar I Disorder

scientific article published on 22 July 2016

The Xmn1 polymorphic site 5' to the (G)gamma gene and its correlation to the (G)gamma:(A)gamma ratio, age at first blood transfusion and clinical features in beta-thalassemia patients from Western Iran.

scientific article

The angiotensin converting enzyme D allele is an independent risk factor for early onset coronary artery disease.

scientific article published on 23 July 2010

The association between GSTT1, M1, and P1 polymorphisms with coronary artery disease in Western Iran.

scientific article published on 16 April 2011

The clinical significance of circulating DSCAM-AS1 in patients with ER-positive breast cancer and construction of its competitive endogenous RNA network

scientific article published on 11 October 2020

The effect of VDR gene polymorphisms and vitamin D level on blood pressure, risk of preeclampsia, gestational age, and body mass index

scientific article published on 11 November 2018

The presence of apolipoprotein ε4 and ε2 alleles augments the risk of coronary artery disease in type 2 diabetic patients

scientific article published in October 2007

The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T among G6PD deficient individuals from Western Iran

scientific article published on 15 February 2009

The serotonin transporter (5-HTTLPR) but not serotonin receptor (5-HT2C Cys23Ser) variant is associated with bipolar I disorder in Kurdish population from Western Iran

scientific article published on 14 January 2015

The β-GLobin Gene Haplotypes Associated With Hb D-Los Angeles [β121(GH4)Glu→Gln] in Western Iran

scientific article published in January 2006

Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden

scientific article

Thrombophilic mutations and susceptibility to preeclapmsia in Western Iran ⬇️

scientific article published on January 1, 2012

eNOS 4a/b polymorphism and its interaction with eNOS G894T variants in type 2 diabetes mellitus: modifying the risk of diabetic nephropathy ⬇️

scientific article published on January 1, 2013

Paulina is supported by:

About Paulina

Help