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Iman Safari
Iman Safari
Neuroinflammation Unit, BRIC, University of Copenhagen, Denmark
Verified email at bric.ku.dk
Title
Cited by
Cited by
Year
Repeat expansion in C9ORF72 is not a major cause of amyotrophic lateral sclerosis among Iranian patients
A Alavi, S Nafissi, M Rohani, G Shahidi, B Zamani, H Shamshiri, I Safari, ...
Neurobiology of aging 35 (1), 267. e1-267. e7, 2014
422014
Evolution of the SARS-CoV-2 genome and emergence of variants of concern
I Safari, E Elahi
Archives of virology 167 (2), 293-305, 2022
402022
The novel mutation p. Asp251Asn in the β-subunit of succinate-CoA ligase causes encephalomyopathy and elevated succinylcarnitine
E Jaberi, F Chitsazian, G Ali Shahidi, M Rohani, F Sina, I Safari, ...
Journal of human genetics 58 (8), 526-530, 2013
362013
COL18A1 is a candidate eye iridocorneal angle-closure gene in humans
F Suri, S Yazdani, M Chapi, I Safari, P Rasooli, N Daftarian, ...
Human molecular genetics 27 (21), 3772-3786, 2018
342018
Study on SARS-CoV-2 strains in Iran reveals potential contribution of co-infection with and recombination between different strains to the emergence of new strains
P Taghizadeh, S Salehi, A Heshmati, SM Houshmand, K InanlooRahatloo, ...
Virology 562, 63-73, 2021
262021
A possible role for LTBP2 in the etiology of primary angle closure glaucoma
I Safari, S Akbarian, S Yazdani, E Elahi
Journal of Ophthalmic & Vision Research 10 (2), 123, 2015
162015
New evidence on hypoglycemic effect of quinolinic acid in diabetic rats.
MR Dayer, I Safari, MS Dayer
Pakistan Journal of Biological Sciences: PJBS 12 (14), 1025-1030, 2009
162009
ADAM12 is a costimulatory molecule that determines Th1 cell fate and mediates tissue inflammation
Y Liu, R Bockermann, M Hadi, I Safari, B Carrion, M Kveiborg, ...
Cellular & molecular immunology 18 (8), 1904-1919, 2021
152021
The p. Gly61Glu mutation in CYP1B1 affects the extracellular matrix in glaucoma patients
I Safari, F Suri, R Haji-Seyed-Javadi, S Yazdani, E Elahi
Ophthalmic Research 56 (2), 98-103, 2016
122016
Evolution of SARS‐CoV‐2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations
I Safari, K InanlooRahatloo, E Elahi
Journal of Medical Virology 93 (4), 2010-2020, 2021
112021
CHST6 mutations identified in Iranian MCD patients and CHST6 mutations reported worldwide identify targets for gene editing approaches including the CRISPR …
I Safari, A Baradaran-Rafii, S Issazadeh-Navikas, E Elahi
International Ophthalmology 40, 2223-2235, 2020
82020
World‐wide tracking of major SARS‐CoV‐2 genome haplotypes in sequences of June 1 to November 15, 2020 and discovery of rapid expansion of a new haplotype
I Safari, K InanlooRahatloo, E Elahi
Journal of Medical Virology 93 (5), 3251-3256, 2021
52021
Diagnosis of cystathionine beta-synthase deficiency by genetic analysis
F Suri, M Narooie-Nejad, I Safari, H Moazzeni, MR Rohani, A Khajeh, ...
Journal of the Neurological Sciences 347 (1-2), 305-309, 2014
22014
Genetic screening of TGFBI in Iranian patients with TGFBI-associated corneal dystrophies and a meta-analysis of global variation frequencies
R Jozaei, MA Javadi, I Safari, A Moghaddasi, S Feizi, MR Kanavi, S Najafi, ...
Ophthalmic Genetics 43 (4), 496-499, 2022
2022
Ophthalmogenetic Epidemiology in Iran
I Safari, A Moghaddasi, M Yousefpour Marzbali, F Mohammadi, E Elahi, ...
Archives of Persian Ophthalmology 2, 138-170, 2022
2022
Analysis of the Bach2 and HDAC3 Expression in Iranian Patients with Acute Myeloid Leukemia
I Safari, M Nourian, H Naghoosi, A Etemadi, F Zeinali, H Jalaeikhoo, ...
International Journal of Cancer Management 12 (12), 2019
2019
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Articles 1–16