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Effat Farrokhi

Observed names: E Farrokhi, E. Farrokhi, Effat FARROKHI, Effat. Farrokhi, Effate Farrokhi, Farrokhi E, Farrokhi Effat
ORCID: 0000-0002-3068-0719
Observed ORCID: 0000-0002-3068-0719
OpenAlex ID: A5043686301
Effects of Cumin Extract on oxLDL , Paraoxanase 1 Activity , FBS, Total Cholesterol , Triglycerides , HDL-C , LDL-C , Apo A1 , and Apo B in in the Patients with Hypercholesterolemia
2014 · Keihan Ghatreh Samani, Effat Farrokhi · International Journal of Health Sciences · 50
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Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss.
2011 · Ma Tabatabaiefar, F Alasti, et al. · PubMed Central · 42
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Novel mutations in the pejvakin gene are associated with autosomal recessive non‐syndromic hearing loss in Iranian families
2007 · M Hashemzadeh Chaleshtori, MA Simpson, et al. · Clinical Genetics · 34
Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran
2018 · Fatemeh Azadegan-Dehkordi, Tayyebe Bahrami, et al. · Journal of Audiology & Otology · 31
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Familial Colorectal Cancer Type X (FCCTX) and the correlation with various genes—A systematic review
2017 · Mahdieh Nejadtaghi, Hamideh Jafari, et al. · Current Problems in Cancer · 31
Oxidized Low-Density Lipoprotein Increases Bone Sialoprotein Expression in Vascular Smooth Muscle Cells Via Runt-Related Transcription Factor 2
2014 · Effat Farrokhi, Morteza H. Chaleshtori, et al. · The American Journal of the Medical Sciences · 29
DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment
2011 · MA Tabatabaiefar, F Alasti, et al. · Clinical Genetics · 28
Adiponectin inhibits oxidized low density lipoprotein-induced increase in matrix metalloproteinase 9 expression in vascular smooth muscle cells.
2015 · Maryam Saneipour, Keihan Ghatreh-Samani, et al. · PubMed Central · 23
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High carrier frequency of the GJB2 mutation (35delG) in the north of Iran
2007 · Morteza Hashemzadeh Chaleshtori, Effat Farrokhi, et al. · International Journal of Pediatric Otorhinolaryngology · 23
Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3
2012 · Daniz Kooshavar, Mohammad Amin Tabatabaiefar, et al. · International Journal of Pediatric Otorhinolaryngology · 21
Scavenger receptor Class B type I as a potential risk stratification biomarker and therapeutic target in cardiovascular disease
2019 · Reza Sahebi, Seyed Mahdi Hassanian, et al. · Journal of Cellular Physiology · 20
Prevalence and distribution of adhesins and the expression of fibronectin-binding protein (FnbA and FnbB) among Staphylococcus aureus isolates from Shahrekord Hospitals
2019 · Emad Soltani, Effat Farrokhi, et al. · BMC Research Notes · 20
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Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells.
2015 · Effat Farrokhi, Keihan GhatrehSamani, et al. · PubMed Central · 18
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The role and spectrum ofSLC26A4mutations in Iranian patients with autosomal recessive hereditary deafness
2014 · Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, et al. · International Journal of Audiology · 18
A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss
2018 · Fatemeh Azadegan-Dehkordi, Reza Ahmadi, et al. · American Journal of Otolaryngology · 17
Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss
2012 · Nasrin Yazdanpanahi, Morteza Hashemzadeh Chaleshtori, et al. · International Journal of Pediatric Otorhinolaryngology · 16
Effects of Nigella sativa Extracts on the Lipid Profile and Uncoupling Protein-1 Gene Expression in Brown Adipose Tissue of Mice
2018 · Amin Mahmoudi, Keihan Ghatreh Samani, et al. · Advanced Biomedical Research · 15
Compound Heterozygosity for Two NovelSLC26A4Mutations in a Large Iranian Pedigree with Pendred Syndrome
2013 · Nasrin Yazdanpanahi, Mohammad Amin Tabatabaiefar, et al. · Clinical and Experimental Otorhinolaryngology · 15
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Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment
2011 · Mostafa Montazer Zohour, Mohammad Amin Tabatabaiefar, et al. · Genetic Testing and Molecular Biomarkers · 14
The effect of resveratrol on expression of matrix metalloproteinase 9 and its tissue inhibitors in vascular smooth muscle cells.
2018 · Effat Farrokhi, Keihan Ghatreh-Samani, et al. · PubMed Central · 13
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Purslane (Portulaca oleracea) effects on serum paraoxanase-1 activity
2011 · K Gatreh Samani, Effat Farrokhi, et al. · Journal of Shahrekord University of Medical Sciences · 13
Exosomal miRNA‐21‐5p and miRNA‐21‐3p as key biomarkers of myocardial infarction
2024 · Reza Sahebi, Fatemeh Gandomi, et al. · Health Science Reports · 12
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Evaluation of response to hepatitis B vaccine in Iranian 6–18-year-old students
2017 · Alizamen Salehifard Jouneghani, Morteza Hashemzadeh Chaleshtori, et al. · Journal of Research in Medical Sciences · 12
A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame
2011 · Maarten Vanwesemael, Isabelle Schrauwen, et al. · American Journal of Medical Genetics Part A · 12
Molecular Characterization of Iranian Patients with Possible Familial Hypercholesterolemia
2011 · E. Farrokhi, F. Shayesteh, et al. · Indian Journal of Clinical Biochemistry · 12
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Works count: 61
Citation count: 661
H-index: 16
I10-index: 29
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