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Mehrnoosh Khodaeian
Mehrnoosh Khodaeian
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Cited by
Cited by
Year
Association between genetic variants and diabetes mellitus in Iranian populations: a systematic review of observational studies
M Khodaeian, S Enayati, O Tabatabaei-Malazy, MM Amoli
Journal of diabetes research 2015 (1), 585917, 2015
772015
Effect of vitamins C and E on insulin resistance in diabetes: a meta‐analysis study
M Khodaeian, O Tabatabaei‐Malazy, M Qorbani, F Farzadfar, P Amini, ...
European journal of clinical investigation 45 (11), 1161-1174, 2015
512015
Polymorphisms of antioxidant genes as a target for diabetes management
O Tabatabaei-Malazy, M Khodaeian, F Bitarafan, B Larijani, MM Amoli
International journal of molecular and cellular medicine 6 (3), 135, 2017
362017
Effects of 50 Hz electromagnetic fields on the histology, apoptosis, and expression of c-Fos and β-Catenin on the livers of preincubated white leghorn chicken …
MS Lahijani, S Farivar, M Khodaeian
Electromagnetic Biology and Medicine 30 (3), 158-169, 2011
222011
Prevalence and genotype distribution of human papillomavirus infection among 12 076 Iranian women
F Bitarafan, MR Hekmat, M Khodaeian, E Razmara, T Ashrafganjoei, ...
International Journal of Infectious Diseases 111, 295-302, 2021
112021
Influence of antioxidants' gene variants on risk of diabetes mellitus and its complications: a systematic review.
F Bitarafan, M Khodaeian, O Tabatabaei-Malazy, MM Amoli
Minerva endocrinologica 44 (3), 310-325, 2017
112017
Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family
F Bitarafan, M Khodaeian, E Amjadi Sardehaei, FZ Darvishi, N Almadani, ...
Molecular and Cellular Pediatrics 8, 1-8, 2021
92021
A novel missense variant in the LMNB2 gene causes progressive myoclonus epilepsy
F Soleimanipour, E Razmara, F Rahbarizadeh, E Fallahi, M Khodaeian, ...
Acta Neurologica Belgica, 1-9, 2021
62021
Kabuki syndrome: identification of two novel variants in KMT2D and KDM6A
M Khodaeian, E Jafarinia, F Bitarafan, S Shafeii, N Almadani, ...
Molecular Syndromology 12 (2), 118-126, 2021
52021
Molecular investigation of WFS1 gene exon 8 in Iranian patients with Wolfram syndrome
R Abbasi, F Bitarafan, M Khodaeian, A Ebrahim-Habibi, F Abbasi, ...
International Journal of Diabetes in Developing Countries 36, 75-80, 2016
52016
Withdrawal reasons of randomized controlled trials on type 2 diabetes: a systematic review
S Mohseni, O Tabatabaei-Malazy, M Peimani, HS Ejtahed, M Khodaeian, ...
DARU Journal of Pharmaceutical Sciences 29, 39-50, 2021
32021
Compound Heterozygous Mutations in PNKP Gene in an Iranian Child with Microcephaly, Seizures, and Developmental Delay
F Bitarafan, M Khodaeian, N Almadani, A Kalhor, EA Sardehaei, ...
Fetal and Pediatric Pathology 40 (2), 174-180, 2021
32021
Three Novel Variants identified in FBN1 and TGFBR2 in seven Iranian families with suspected Marfan syndrome
F Bitarafan, E Razmara, M Khodaeian, M Keramatipour, A Kalhor, ...
Molecular Genetics & Genomic Medicine 8 (8), e1274, 2020
32020
Association between genetic variants and obesity in Iranian population
MO TABATABAEI, M Khodaeian, MM Amoli
Iranian Journal of Public Health 43 (1), 71-82, 2014
22014
Reporting a novel growth hormone receptor gene variant in an Iranian consanguineous pedigree with Laron syndrome: a case report
F Bitarafan, M Khodaeian, F Garrousi, R Khalesi, D Ghazi Nader, B Karimi, ...
BMC Endocrine Disorders 23 (1), 155, 2023
12023
Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage
M Khodaeian, F Bitarafan, F Garrousi, EA Sardehie, N Pak, ...
Journal of Clinical Laboratory Analysis 37 (21-22), e24983, 2023
2023
Meta-analysis of the anti-oxidative and anti-inflammatory effects of hypoglycaemic plant-derived medicines
B Azizi, S Mohseni, O Tabatabaei-Malazy, F Esmaeili, M Khodaeian, ...
Inflammopharmacology 31 (5), 2521-2539, 2023
2023
Targeted Next-Generation Sequencing identifies two novel CFTR gene mutations in Iranian patients with Cystic Fibrosis
AR Bitaraf, F Bitarafan, M Khodaeian, M Garshasbi
EUROPEAN JOURNAL OF HUMAN GENETICS 26, 857-857, 2018
2018
Ps-83: Mutations Detection in Patients with Wolfram Syndrome from Iran
M Khodaeian, HR Sh, F Abbasi, MM Amoli
IJFS-Int J Fertil Steril 16 (Suppl 1), 2014
2014
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Articles 1–19