Search Results - Jabbarpour, Neda

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  1. 1
    Identification of Two Novel Pathogenic Variants of the ATM Gene in the Iranian-Azeri Turkish Ethnic Group by Applying Whole Exome Sequencing

    Identification of Two Novel Pathogenic Variants of the ATM Gene in the Iranian-Azeri Turkish Ethnic Group by Applying Whole Exome Sequencing by Amandi, Amir-Reza Dalal, Jabbarpour, Neda, Shiva, Shadi, Bonyadi, Mortaza

    Published in Current genomics
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  2. 2
    A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity

    A novel loss of function mutation in the PHD domain of the RAG2 gene, affecting zinc-binding affinity by Jabbarpour, Neda, Bonyadi, Mortaza, Sadeghi, Leila

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  3. 3
    Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation

    Giant axonal neuropathy: a rare inherited neuropathy with a novel mutation by Poorshiri, Bita, Jabbarpour, Neda, Barzegar, Mohammad, Bonyadi, Mortaza, Ebadi, Zakiyeh

    Published in Neurogenetics
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  4. 4
    Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder

    Identification and bioinformatics analysis of a novel variant in the HERC2 gene in a patient with intellectual developmental disorder by Asghari Sarfaraz, Asal, Jabbarpour, Neda, Bonyadi, Mortaza, Khalaj-Kondory, Mohammad

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  5. 5
    Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion

    Identification of a novel mutation in the HACD1 gene in an Iranian family with autosomal recessive congenital myopathy, with fibre-type disproportion by Jabbarpour, Neda, Poorshiri, Bita, Saei, Hassan, Barzegar, Mohammad, Bonyadi, Mortaza

    Published in Journal of genetics
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  6. 6
    Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract

    Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract by Jabbarpour, Neda, Saei, Hassan, Jabbarpoor Bonyadi, Mohammad Hossein, Bonyadi, Mortaza

    Published in Ophthalmic genetics
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  7. 7
    Effects of voluntary, involuntary exercise and sertraline on anxiety, social and cognitive behavior in female rat model of post-traumatic stress disorder

    Effects of voluntary, involuntary exercise and sertraline on anxiety, social and cognitive behavior in female rat model of post-traumatic stress disorder by Sheikhzadeh Hesari, Farzam, Ebrahimiasl, Sarieh, Zakeri-Milani, Parvin, Honarmand, Haneieh, Hamdollahi Dashkasan, Mahdi, Jabbarpour, Neda

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  8. 8
    Identification of a de novo, Novel Pathogenic Variant in the Splice Region of the SOX10 Gene in an Iranian Azeri Turkish Family with Waardenburg Syndrome

    Identification of a de novo, Novel Pathogenic Variant in the Splice Region of the SOX10 Gene in an Iranian Azeri Turkish Family with Waardenburg Syndrome by Roudbari, Faranak, Dallal Amandi, Amir-Reza, Bonyadi, Mortaza, Sadeghi, Leyla, Jabbarpour, Neda

    Published in Molecular syndromology
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  9. 9
    Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract

    Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract by Jabbarpour, Neda, Saei, Hassan, Jabbarpoor Bonyadi, Mohammad Hossein, Bonyadi, Mortaza

    Published in Ophthalmic Genetics
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  10. 10
    Association of CFI p.Gly119Arg gene polymorphism with age-related macular degeneration (AMD) disease in the population living in Tehran

    Association of CFI p.Gly119Arg gene polymorphism with age-related macular degeneration (AMD) disease in the population living in Tehran by Neda Norouzi, Mortaza Bonyadi, Esmaeil Babaei, Mohammad Hossein Jabbarpour Bonyadi

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