AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report by Mostafa Neissi, Hadideh Mabudi, Javad Mohammadi‐Asl

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The worldwide molecular spectrum and distribution of thalassaemia: a systematic review by Mina Ebrahimi, Javad Mohammadi-Asl, Fakher Rahim

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Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells by Misagh Mohammadi Asl, Javad Mohammadi Asl, Mojgan Naghitorabi

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Retinitis pigmentosa‐1 due to an RP1 mutation in a consanguineous Iranian family: Report of a novel mutation by Mostafa Neissi, Motahareh Sheikh‐Hosseini, Javad Mohammadi‐Asl

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A Novel Disease-Causing ASPA Gene Mutation (c.432+1 G>C) in an Iranian Patient with Canavan Disease: A Case Report by Mostafa Neissi, Motahareh Sheikh-Hosseini, Javad Mohammadi-Asl

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A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss by Mostafa Neissi, Adnan Al-Badran, Javad Mohammadi-Asl

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An intelligent prenatal screening system for the prediction of Trisomy-21 by Amir Jamshidnezhad, Seyed Mohsen Hosseini, Javad Mohammadi-Asl, Mandana Mahmudi

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Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obes... by Fatemeh Haidari, Maryam Asadi, Javad mohammadi-asl, Kambiz Ahmadi-Angali

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Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study by Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi-Birgani, Javad Mohammadi-Asl

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Identification of a novel non-stop mutation in PDE6C gene in an Iranian family with Con-Rod Dystrophy by Shahram Nasiri, Farah Talebi, Javad Mohammadi Asl, Farideh Ghanbari Mardasi

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Do NGS‐based techniques represent a first‐line testing in suspected Duchenne muscular dystrophy? by Seyed Mohammad Hosseini, Nosratollah Alizadeh, Abolfazl Amini, Javad Mohammadi‐Asl

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Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice by Mohammadreza Gholami, Ghasem Saki, Masoud Hemadi, Ali Khodadadi, Javad Mohammadi-asl

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Up-regulation of SNHG5 Expression Level in Patients with Chronic Myeloid Leukemia Compared with Normal Individuals by Zahra Shahpouri-Arani, Mohamad Reza Hajari, Javad Mohammadi-Asl, Najmaldin Saki

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Exome sequencing identified a novel Col6α1 mutation in an Iranian patient with Ullrich congenital muscular dystrophy: a case report by Elaheh Nekouei, Elmira Shokrolahi Yancheshmeh, Javad Mohammadi-Asl, Zafar Maasoumi Moghaddam

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Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family by Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Ali Lashgari, Freidoon Farhadi

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بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز... by Javad Mohammadi-Asl, Arghavan Soleimanizadeh, Hajieh Bibi Shahbazian, Heshmatollah Shahbazian, Neda Golchin

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Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family by Kourosh Riahi, Farideh Ghanbari Mardasi, Farah Talebi, Farzad Jasemi, Javad Mohammadi Asl

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Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder by Neda Golchin, Mohammadreza Hajjari, Reza Azizi Malamiri, Majid Aminzadeh, Javad Mohammadi-asl

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The Diagnostic Value of Gene Expression of FHL1 in the Differential Diagnosis of Papillary Thyroid Carcinoma and Benign Tumors by Javad Mohammadi-Asl, Gholamabbas Dinarvand, Neda Golchin, Nader Saki, Nastran Ranjberi, Iran Rashidi

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Coexistence of P190 BCR/ABL transcript and CALR 52-bp deletion in chronic myeloid leukemia blast crisis: a case report by najmaldin saki, Mohammad Seghatoleslami, Neda Ketabchi, Alireza Ordo, Javad Mohammadi-Asl, Neda Golchin

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