JPX and LINC00641 ncRNAs expression in prostate tissue: a case-control study by Roshanak S Sajjadi, Mohammad Hossein Modarressi, Mohammad Amin Tabatabaiefar

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Bisulfite treatment of CG-rich track of trinucleotide repeat expansion disorder: Make the sequence less CG rich by Zahra Joz Abbasalian, Hossein Khanahmad, Mohammad Amin Tabatabaiefar

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WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family by Mahnaz Norouzi, Mohammad Shafiei, Zeinab Abdollahi, Paniz Miar, Hamid Galehdari, Mohammad Hasan Emami, Mehrdad Zeinalian, Mohammad Amin Tabatabaiefar, Mohammad Amin Tabatabaiefar

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Implementation and Optimization of Annotation and Interpretation Step of Next-Generation Sequencing Data for Non-Syndromic Autosomal Recessive Hearing Loss by Mehdi Shahhoseini, Newsha Molavi, Mohammad Amin Tabatabaiefar, Mohammadreza Sehhati

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X‐linked mental retardation‐hypotonic facies syndrome: Exome sequencing identifies novel clinical characteristics associated with c.5182G>C mutation in the ATRX gene by Fatemeh Shakarami, Mehdi Jahani, Zahra Nouri, Mohammad Amin Tabatabaiefar

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Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran by Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI

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Using classification and K-means methods to predict breast cancer recurrence in gene expression data by Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar, Ali Haji Gholami, Mohammad Sattari

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Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report by Mosa Arghand Dargahi, Mohammad Amin Tabatabaiefar, Shervin Taslimi, Zakaria Zakariaei

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Lynch-like Syndrome and its Molecular Approaches: A Brief Report and Literature Review by Zeinab Abdollahi, Mohammad Amin Tabatabaiefar, Mohammad Hassan Emami, Mehrdad Zeinalian

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Bilateral Dislocation of Temporomandibular Joint Induced by Haloperidol Following Suicide Attempt: A Case Report by Zakaria Zakariaei, Shervin Taslimi, Mohammad Amin Tabatabaiefar, Mosa Arghand Dargahi

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A 15;15 Translocation in a couple with Repeated Abortions: Case report by Aazam Ahmadi shadmehri, Javad Tavakkoly Bazzaz, Mojtaba Darbouy, Mohammad Amin Tabatabaiefar

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Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science? by Zahra Mohammadi, Arezou Karamzadeh, Mohammad Amin Tabatabaiefar, Hossein Khanahmad, Laleh Shariati

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Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent by Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj

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Sequence-identification of Candida species isolated from candidemia by Naeimeh Fathi, Rasoul Mohammadi, Mohammad Amin Tabatabaiefar, Mohammad Ghahri, Seyedeh Zahra Sadrossadati

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Genotyping of carbapenem resistant Acinetobacter baumannii isolated from tracheal tube discharge of hospitalized patients in intensive care units, Ahvaz, Iran by Saeed Shoja, Mojtaba Moosavian, Amir Peymani, Mohammad-Amin Tabatabaiefar, Soodabeh Rostami, Nasim Ebrahimi

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New Variants in the CDH1 Gene in Iranian Families with Hereditary Diffuse Gastric Cancer by Majid Kheirollahi, Maryam Saneipour, Mohammad Amin Tabatabaiefar, Mehrdad Zeinalian, Mohammad Minakari, Abbas Moridnia

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A Homozygous Nonsense Variant in UVSSA Causes UV-sensitive Syndrome from Very Large Kindred: The First Report from Iran by Azam Ahmadi Shadmehri, Fahimeh Akbarian, Azadeh Rahimi, Mohammad Reza Pourreza, Mohammad Amin Tabatabaiefar

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The Importance of SNPs at miRNA Binding Sites as Biomarkers of Gastric and Colorectal Cancers: A Systematic Review by Fatemeh Hajibabaie, Navid Abedpoor, Nazanin Assareh, Mohammad Amin Tabatabaiefar, Laleh Shariati, Ali Zarrabi

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تجزیه و تحلیل پیوستگی ژنتیکی لوکوس‌های DFNB40 و DFNB48 در خانواده‌هایی با ناشنوایی غیر سندرمی مغلوب اتوزومی از استان‌های غربی کشور... by Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour, Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori

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Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper by Mohammad Reza Pourreza, Hannane Mohammadi, Ladan Sadeghian, Samira Asgharzadeh, Mohammadreza Sehhati, Mohammad Amin Tabatabaiefar

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