Afagh Alavi
Afagh Alavi
University of Social Welfare and Rehabilitation Sciences, Genetics Research Center
Verified email at
Cited by
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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
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
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
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
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
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
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
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
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
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
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
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
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
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
MFSD8 gene mutations; evidence for phenotypic heterogeneity.
KKHR Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M ...
Ophthalmic Genet., 2019
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
Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot–Marie–Tooth patients with TFG mutation
EE Marzieh Khani, Hanieh Taheri, Hosein Shamshiri, Henry Houlden, Stephanie ...
American Journal of Medical Genetics, 2019
A pathogenic homozygous mutation in the pleckstrin homology domain of RASA1 is responsible for familial tricuspid atresia in an Iranian consanguineous family
F Nozari, A., Aghaei-Moghadam, E., Zeinaloo, A., Alavi, A., Firouzabdi, S.G ...
Cell Journal 21 (1), 70-77, 2019
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