The application of Deep Learning in Persian Documents Sentiment Analysis von Dastgheib, Mohammad Bagher, Koleini, Sara, Rasti, Farzad

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Persian Text Classification Enhancement by Latent Semantic Space von Dastgheib, Mohammad Bagher, Koleini, Sara

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Design and Implementation of Iranian Digital Object Recognizer (DOR) Phase 1: Persian Articles von Ghane, Mohammad Reza, Koleini, Sara, Dastgheib, Mohammad Bagher

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A Hybrid Accurate Alignment method for large Persian-English corpus construction based on statistical analysis and Lexicon/Persian Word net von Dastgheib, Mohammad Bagher, Fakhrahmad, Seyed Mostafa, Jahromi, Mansour Zolghadri

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The application of Deep Learning in Persian Documents Sentiment Analysis von Mohammad Bagher Dastgheib, Sara Koleini, Farzad Rasti

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Perspell: A New Persian Semantic-Based Spelling Correction System von Dastgheib, Mohammad Bagher, Fakhrahmad, Seyed Mostafa, Jahromi, Mansoor Zolghadri

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A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness von Mohammadi, Sanaz, Jafari Khamirani, Hossein, Baneshi, Maryam, Kamal, Neda, Manoocheri, Jamal, Saffar, Mahsa, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza

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Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature von Khamirani, Hossein Jafari, Zoghi, Sina, Namdar, Zahra Mehdipour, Kamal, Neda, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dastgheib, Seyed Alireza

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Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS von Khamirani, Hossein Jafari, Zoghi, Sina, Sichani, Ali Saber, Dianatpour, Mehdi, Mohammadi, Sanaz, Tabei, Seyed Mohammad Bagher, Dastgheib, Seyed Alireza

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MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family von Zeraatpisheh, Zahra, Sichani, Ali Saber, Kamal, Neda, Khamirani, Hossein Jafari, Zoghi, Sina, Ehsani, Elham, Mohammadi, Sanaz, Tabei, Seyed Sajjad, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Dianatpour, Mehdi

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Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1 von Alavi, Omid, Khamirani, Hossein Jafari, Zoghi, Sina, Feili, Afrooz, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Panahandeh, Seyed Mehdi, Kamali, Majid, Dianatpour, Mehdi

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EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review von Abbasi, Zahra, Jafari Khamirani, Hossein, Tabei, Seyed Mohammad Bagher, Manoochehri, Jamal, Dianatpour, Mehdi, Dastgheib, Seyed Alireza

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Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review von Fazelzadeh Haghighi, Negin, Kamal, Neda, Jafari Khamirani, Hossein, Fazelzadeh Haghighi, Maryam, Dastgheib, Seyed Alireza, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher

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ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review von Kamal, Neda, Khamirani, Hossein Jafari, Mohammadi, Sanaz, Dastgheib, Seyed Alireza, Dianatpour, Mehdi, Tabei, Seyed Mohammad Bagher

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Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1 von Faghihi, Fatemeh, Khamirani, Hossein Jafari, Zoghi, Sina, Kamal, Neda, Yeganeh, Babak Shirazi, Dianatpour, Mehdi, Bagher Tabei, Seyed Mohammad, Dastgheib, Seyed Alireza

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Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder von Mohammadi, Sanaz, Jafari Khamirani, Hossein, Zoghi, Sina, Dastgheib, Seyed Alireza, Tabei, Seyed Mohammad Bagher, Talebzadeh, Mahdieh, Adibi, Mohammad Hossein, Dianatpour, Mehdi

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Phenotype of ST3GAL3 deficient patients: A case and review of the literature von Khamirani, Hossein Jafari, Zoghi, Sina, Faghihi, Fatemeh, Dastgheib, Seyed Alireza, Hassanipour, Hamidreza, Bagher Tabei, Seyed Mohammad, Mohammadi, Sanaz, Masoudi, Marjan, Poorang, Shiva, Ehsani, Elham, Dianatpour, Mehdi

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A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report von Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi

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The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature review von Shafieipour, Negin, Jafari Khamirani, Hossein, Kamal, Neda, Tabei, Seyed Mohammad Bagher, Dianatpour, Mehdi, Dastgheib, Seyed Alireza

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Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report von Manoochehri, Jamal, Dastgheib, Seyed Alireza, Khamirani, Hossein Jafari, Mollaie, Maryam, Sharifi, Zahra, Zoghi, Sina, Tabei, Seyed Mohammad Bagher, Mohammadi, Sanaz, Dehghanian, Fatemeh, Farbod, Zahra, Dianatpour, Mehdi

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