Afagh Alavi
Afagh Alavi
University of Social Welfare and Rehabilitation Sciences, Genetics Research Center
Verified email at
TitleCited byYear
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
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
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
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
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
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
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
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
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
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
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
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
KKHR Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M ...
Ophthalmic Genet., 2019
Mutation screening of TGFBI in two Iranian Avellino corneal dystrophy pedigrees
A Alavi, E Elahi, M Rahmati‐Kamel, F Karimian, M Rezaei‐Kanavi
Clinical & experimental ophthalmology 36 (1), 26-30, 2008
Exclusion of TACSTD2 in an Iranian GDLD pedigree
A Alavi, E Elahi, FA Amoli, MH Tehrani
Mol Vis 13, 1441-5, 2007
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
Genotype and phenotype analysis of 43 Iranian facioscapulohumeral muscular dystrophy patients; Evidence for anticipation
A Alavi, S Esmaeili, S Nafissi, K Kahrizi, H Najmabadi
Neuromuscular Disorders 28 (4), 303-314, 2018
Pantothenate kinase-associated neurodegeneration mimicking Tourette syndrome: a case report and review of the literature
M Rohani, A Fasano, AE Lang, B Zamani, L Javanparast, MMR Bidgoli, ...
Neurological Sciences 39, 1797-1800, 2018
Mutations in C19orf12 and intronic repeat expansions in C9orf72 not observed in Iranian Parkinson's disease patients
A Alavi, MM Nejad, G Shahidi, E Elahi
Neurobiology of aging 54, 214. e11-214. e12, 2017
Tremor-dominant pantothenate kinase-associated neurodegeneration
AF Mohammad Rohani, Gholamali Shahidi, Afagh Alavi, Anthony E. Lang ...
Movement Disorders Clinical Practice 1 (-), -, 2017
Observation of c. 260A> G mutation in superoxide dismutase 1 that causes p. Asn86Ser in Iranian amyotrophic lateral sclerosis patient and absence of genotype/phenotype correlation
M Khani, A Alavi, S Nafissi, E Elahi
Iranian journal of neurology 14 (3), 152, 2015
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