| 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 | 52 | 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 | 31 | 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 | 26 | 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 | 25 | 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 | 18 | 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 | 16 | 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 | 12 | 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 | 11 | 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 | 8 | 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 | 5 | 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 | 5 | 2017 |
| MFSD8 gene mutations; evidence for phenotypic heterogeneity. KKHR Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M ... Ophthalmic Genet., 2019 | 3 | 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 | 3 | 2008 |
| Exclusion of TACSTD2 in an Iranian GDLD pedigree A Alavi, E Elahi, FA Amoli, MH Tehrani Mol Vis 13, 1441-5, 2007 | 3 | 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 | 2 | 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 | 2 | 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 | 2 | 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 | 2 | 2017 |
| Tremor-dominant pantothenate kinase-associated neurodegeneration AF Mohammad Rohani, Gholamali Shahidi, Afagh Alavi, Anthony E. Lang ... Movement Disorders Clinical Practice 1 (-), -, 2017 | 2* | 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 | 2 | 2015 |
elahe elahiUniversity of TehranVerified email at ut.ac.ir
