1. Impact of Whole Exome Sequencing among Iranian Patients with Autosomal Recessive Retinitis Pigmentosa

Maryam Beheshtian, Samira Saee Rad, Mojgan Babanejad, Marzieh Mohseni, Hassan Hashemi, Arash Eshghabadi, Fedra Hajizadeh, Mohammad Reza Akbari, Kimia Kahrizi, Mohammad Riazi Esfahani*, Hossein Najmabadi*

Arch Iran Med. 2015;18(11): 0.

PMID: 26497376 Scopus ID: 84944741309

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Review

2. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review

Maryam Beheshtian, Mojgan Babanejad, Hela Azaiez, Niloofar Bazazzadegan, Diana Kolbe, Christina Sloan-Heggen, Sanaz Arzhangi, Kevin Booth, Marzieh Mohseni, Kathy Frees, Mohammad Hossein Azizi, Ahmad Daneshi, Kimia Kahrizi, Richard JH Smith, Hossein Najmabadi

Arch Iran Med. 2016;19(10): 0.

PMID: 27743438 Scopus ID: 85047586224

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Case Report

3. An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene

Marzieh Mohseni , Yusuf Mohammadi , Farzane Zare Ashrafi, Fatemeh Ghodratpour, Khadijeh Jalalvand, Sanaz Arzhangi, Mojgan Babanejad, Mohammad Hossein Azizi, Kimia Kahrizi, Hossein Najmabadi*

Arch Iran Med. 2023;26(3): 176-180. doi: 10.34172/aim.2023.27

PMCID: PMC10685723 PMID: 37543941

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A Monthly Peer-Reviewed Medical Journal Published by the Academy of Medical Sciences of the I.R. Iran; Indexed in PubMed/MEDLINE, ISI Web of Science, EMBASE, SCOPUS, CINHAL, PASCAL, CSA, SID, ISSN: Print 1029-2977, Online 1735-3947.The impact factor of Archives of Iranian Medicine according to Journal Citation Reports® (JCR®) 2016 is 1.20.