Elahe Elahi

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Topics

Muscular Dystrophy

Dna Damage Response

Respiratory Syndrome Coronavirus

Top Venues

Clinical case reports

Journal of medical virology

Molecular genetics & genomic medicine

Journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease. Clinical case reports 12 (1) (2024)
Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Hamidreza Moazzeni, Hanieh Taheri, Mehdi Sadeghi, Najmeh Salehi, Fereshteh Chitsazian, Elahe Elahi
Identification of UBA1 as the causative gene of an X-linked non-Kennedy spinal-bulbar muscular atrophy. European journal of neurology 29 (12) (2022)
Ensieh Darbari, Hamid Ahmadieh, Narsis Daftarian, Mozhgan Rezaei Kanavi, Fatemeh Suri, Hamideh Sabbaghi, Elahe Elahi
Mutation Screening of Six Exons of ABCA4 in Iranian Stargardt Disease Patients. Journal of ophthalmic & vision research 17 (1) (2022)
Marzieh Khani, Shahriar Nafissi, Hosein Shamshiri, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Identification of RNF13 as cause of recessively inherited ALS in a multi-case pedigree. Journal of medical genetics (2022)
Iman Safari, Elahe Elahi
Evolution of the SARS-CoV-2 genome and emergence of variants of concern. Archives of virology (2021)
Iman Safari, Kolsoum InanlooRahatloo, Elahe Elahi
World-wide tracking of major SARS-CoV-2 genome haplotypes in sequences of June 1 to November 15, 2020 and discovery of rapid expansion of a new haplotype. Journal of medical virology 93 (5) (2021)
Marzieh Khani, Hosein Shamshiri, Farzad Fatehi, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haji Akhoundi, Afagh Alavi, Hamidreza Moazzeni, Hanieh Taheri, Mina Tolou Ghani, Leila Javanparast, Seyyed Saleh Hashemi, Ramona Haji-Seyed-Javadi, Matineh Heidari, Shahriar Nafissi, Elahe Elahi
Description of combined ARHSP/JALS phenotype in some patients with SPG11 mutations. Molecular genetics & genomic medicine 8 (7) (2020)
Hamidreza Moazzeni, Marzieh Khani, Elahe Elahi
Insights into the regulatory molecules involved in glaucoma pathogenesis. American journal of medical genetics. Part C, Seminars in medical genetics 184 (3) (2020)
Iman Safari, Kolsoum InanlooRahatloo, Elahe Elahi
Evolution of SARS-CoV-2 genome from December 2019 to late March 2020: Emerged haplotypes and informative Tag nucleotide variations. Journal of medical virology 93 (4) (2020)
Marzieh Khani, Hanieh Taheri, Hosein Shamshiri, Hamidreza Moazzeni, John Hardy, Jose Tomas Bras, Kolsoum InanlooRahatloo, Afagh Alavi, Shahriar Nafissi, Elahe Elahi
Deep geno- and phenotyping in two consanguineous families with CMT2 reveals HADHA as an unusual disease-causing gene and an intronic variant in GDAP1 as an unusual mutation. Journal of neurology 268 (2) (2020)
Hamidreza Moazzeni, Mohammad Ali Javadi, Danial Asgari, Marzieh Khani, Mohammad Emami, Abolfazl Moghadam, Mahmoud-Reza Panahi-Bazaz, Mehdi Hosseini Tehrani, Farid Karimian, Bagher Hosseini, Tayebeh Nekuie Moghadam, Hossein Hassanpour, Mohammad Taghi Akbari, Elahe Elahi
Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family. The British journal of ophthalmology 104 (11) (2019)