| 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 | 56 | 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 | 34 | 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 | 30 | 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 | 29 | 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 | 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 | 17 | 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 | 13 | 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 | 11 | 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 | 11 | 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 | 10 | 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 | 10 | 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 | 6 | 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 | 6 | 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 | 6 | 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 | 5 | 2020 |
| MFSD8 gene mutations; evidence for phenotypic heterogeneity. KKHR Zare-Abdollahi D, Bushehri A, Alavi A, Dehghani A, Mousavi-Mirkala M ... Ophthalmic Genet., 2019 | 4 | 2019 |
| Tremor-dominant pantothenate kinase-associated neurodegeneration AF Mohammad Rohani, Gholamali Shahidi, Afagh Alavi, Anthony E. Lang ... Movement Disorders Clinical Practice 1 (-), -, 2017 | 4* | 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 | 4 | 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 | 3 | 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 | 3* | 2019 |
elahe elahiUniversity of TehranVerified email at ut.ac.ir
