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Afagh Alavi
Afagh Alavi
University of Social Welfare and Rehabilitation Sciences, Genetics Research Center
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Contributions of MYOC and CYP1B1 mutations to JOAG
B Bayat, S Yazdani, A Alavi, M Chiani, F Chitsazian, BK Tusi, F Suri, ...
Molecular vision 14, 508, 2008
752008
Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients
A Alavi, S Nafissi, M Rohani, B Zamani, B Sedighi, H Shamshiri, JB Fan, ...
Neurobiology of aging 34 (5), 1516. e1-1516. e8, 2013
462013
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
The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
AA Pashaei M, Rahimi Bidgoli MM, Zare-Abdollahi D, Najmabadi H, Haji-Seyed ...
J Assist Reprod Genet., 2020
402020
PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation
MA Dezfouli, A Alavi, M Rohani, M Rezvani, T Nekuie, B Klotzle, ...
Movement Disorders 28 (2), 228-231, 2013
392013
Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients
A Alavi, E Elahi, MH Tehrani, FA Amoli, MA Javadi, N Rafati, M Chiani, ...
Investigative ophthalmology & visual science 48 (10), 4490-4497, 2007
272007
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
Manifestation of diffuse yellowish keratoderma on the palms and soles in autosomal recessive congenital ichthyosis patients may be indicative of mutations in NIPAL4
A Alavi, MM Shahshahani, B Klotzle, JB FAN, M Ronaghi, E Elahi
The Journal of dermatology 39 (4), 375-381, 2012
222012
Identification of mutation in NPC2 by exome sequencing results in diagnosis of Niemann–Pick disease type C
A Alavi, S Nafissi, H Shamshiri, MM Nejad, E Elahi
Molecular genetics and metabolism 110 (1-2), 139-144, 2013
212013
Clinical spectrum in multiple families with primary COQ10 deficiency
SSHDZAMKBAVSAKIRFDFNFMRA Alavi
American Journal of Medical Genetics Part A, 2021
192021
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
KKHR Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M ...
Ophthalmic Genet., 2019
182019
A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family
A Nozari, E Aghaei-Moghadam, A Zeinaloo, R Mollazadeh, MT Majnoon, ...
Gene 659, 160-167, 2018
172018
LGMD2E is the most common type of sarcoglycanopathies in the Iranian population
A Alavi, S Esmaeili, Y Nilipour, S Nafissi, SH Tonekaboni, G Zamani, ...
Journal of Neurogenetics, 161-169, 2017
172017
HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry
EE Afagh Alavi, Hosein Shamshiri, Shahriar Nafissi, Marzieh Khani, Brandy ...
Neurobiology of Aging 36 (3), 1606.e1–1606.e7, 2015
172015
Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families
M Pashaei, A Davarzani, R Hajati, B Zamani, S Nafissi, F Larti, Y Nilipour, ...
Journal of neurogenetics 35 (2), 84-94, 2021
152021
Identification of let-7f and miR-338 as plasma-based biomarkers for sporadic amyotrophic lateral sclerosis using meta-analysis and empirical validation.
ZB Daneshafrooz N, Joghataei MT, Mehdizadeh M, Alavi A, Barati M, Panahi B ...
Sci Rep. 12 (1), 1373, 2022
142022
Action myoclonus and seizure in Kufor‐Rakeb syndrome
M Rohani, AE Lang, F Sina, E Elahi, A Fasano, J Hardy, J Bras, A Alavi
Movement Disorders Clinical Practice 5 (2), 195-199, 2018
132018
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
J Alonso-Pérez, L González-Quereda, C Bruno, C Panicucci, A Alavi, ...
Brain 145 (2), 596-606, 2022
122022
CAPN1 and hereditary spastic paraplegia: a novel variant in an Iranian family and overview of the genotype-phenotype correlation
MM Rahimi Bidgoli, L Javanparast, M Rohani, H Najmabadi, B Zamani, ...
International Journal of Neuroscience 131 (10), 962-974, 2021
122021
Identification of novel TFG mutation in HMSN-P pedigree: Emphasis on variable clinical presentations
M Khani, H Shamshiri, A Alavi, S Nafissi, E Elahi
Journal of the Neurological Sciences 369, 318-323, 2016
122016
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Articles 1–20