Genetics of intellectual disability in consanguineous families von Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Herwig, Ralf, Hosseini, Masoumeh, Oppitz, Cornelia, Abedini, Seyedeh Sedigheh, Suckow, Vanessa, Larti, Farzaneh, Beheshtian, Maryam, Lipkowitz, Bettina, Akhtarkhavari, Tara, Mehvari, Sepideh, Otto, Sabine, Mohseni, Marzieh, Arzhangi, Sanaz, Jamali, Payman, Mojahedi, Faezeh, Taghdiri, Maryam, Papari, Elaheh, Soltani Banavandi, Mohammad Javad, Akbari, Saeide, Tonekaboni, Seyed Hassan, Dehghani, Hossein, Ebrahimpour, Mohammad Reza, Bader, Ingrid, Davarnia, Behzad, Cohen, Monika, Khodaei, Hossein, Albrecht, Beate, Azimi, Sarah, Zirn, Birgit, Bastami, Milad, Wieczorek, Dagmar, Bahrami, Gholamreza, Keleman, Krystyna, Vahid, Leila Nouri, Tzschach, Andreas, Gärtner, Jutta, Gillessen-Kaesbach, Gabriele, Varaghchi, Jamileh Rezazadeh, Timmermann, Bernd, Pourfatemi, Fatemeh, Jankhah, Aria, Chen, Wei, Nikuei, Pooneh, Kalscheuer, Vera M., Oladnabi, Morteza, Wienker, Thomas F., Ropers, Hans-Hilger, Najmabadi, Hossein

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WDR81 Gene Silencing Can Reduce Exosome Levels in Human U87-MG Glioblastoma Cells von Tadayoni nia, Amin, Bazi, Zahra, Khosravi, Ayyoob, Oladnabi, Morteza

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Serum soluble Fas ligand is a severity and mortality prognostic marker for COVID-19 patients von Saleki, Kiarash, Shirzad, Moein, Javanian, Mostafa, Mohammadkhani, Sheyda, Alijani, Mohammad Hossein, Miri, Niloufarsadat, Oladnabi, Morteza, Azadmehr, Abbas

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Distinct genetic variation and heterogeneity of the Iranian population von Mehrjoo, Zohreh, Fattahi, Zohreh, Beheshtian, Maryam, Mohseni, Marzieh, Poustchi, Hossein, Ardalani, Fariba, Jalalvand, Khadijeh, Arzhangi, Sanaz, Mohammadi, Zahra, Khoshbakht, Shahrouz, Najafi, Farid, Nikuei, Pooneh, Haddadi, Mohammad, Zohrehvand, Elham, Oladnabi, Morteza, Mohammadzadeh, Akbar, Jafari, Mandana Hadi, Akhtarkhavari, Tara, Gooshki, Ehsan Shamsi, Haghdoost, Aliakbar, Najafipour, Reza, Niestroj, Lisa-Marie, Helwing, Barbara, Gossmann, Yasmina, Toliat, Mohammad Reza, Malekzadeh, Reza, Nürnberg, Peter, Kahrizi, Kimia, Najmabadi, Hossein, Nothnagel, Michael

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In silico analysis of mutation spectrum of Ehlers-Danlos, osteogenesis imperfecta, and cutis laxa overlapping phenotypes in Iranian population von Khosravi, Teymoor, Naghipoor, Karim, Vaghefi, Fatemeh, Falahati, Ali Mohammad, Oladnabi, Morteza

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Cannabinoid CB2 Receptor Functional Variation (Q63R) Is Associated with Multiple Sclerosis in Iranian Subjects von Tahamtan, Alireza, Rezaiy, Shahrzad, Samadizadeh, Saeed, Moradi, Abdolvahab, Tabarraei, Alijan, Javid, Naeme, Oladnabi, Morteza, Naeimi, Mohammad Hosein

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Niosome-encapsulated auraptene reduced the mRNA expression of VEGF-A and PDGFs genes in human retina-derived RPE cell line von Vahidi, Akram, Khosravi, Teymoor, Dastaviz, Farzad, Sheikh Arabi, Mehdi, Khosravi, Ayyoob, Oladnabi, Morteza

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The role of miRNAs and lncRNAs in neurofibromatosis type 1 von Khosravi, Teymoor, Oladnabi, Morteza

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Impact of umbelliprenin-containing niosome nanoparticles on VEGF-A and CTGF genes expression in retinal pigment epithelium cells von Dastaviz, Farzad, Vahidi, Akram, Khosravi, Teymoor, Khosravi, Ayyoob, Sheikh Arabi, Mehdi, Bagheri, Abouzar, Rashidi, Mohsen, Oladnabi, Morteza

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Hearing Loss Among Families with 2 and More Affected Members in Golestan Province, Iran: A Cross-Sectional Study of 320 Families von Sudani, Zainab M. Al, Khosravi, Teymoor, Oladnabi, Morteza

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A Rare Combination of Compound Heterozygous Mutations in the PAH Gene in Three Unrelated Consanguineous Iranian Families with Classical Phenylketonuria von Rahimzadeh, Arian, Khosravi, Teymoor, Motallebi, Farzaneh, Al Sudani, Zainab M, Vaghefi, Fatemeh, Kowsari, Ali, Oladnabi, Morteza

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Toll-Like Receptor (TLR)-9 rs352140 Polymorphism is an Immunopathology Protective Factor in Parkinson's Disease in the Northern Iranian Population von Miri, Niloufar Sadat, Saadat, Payam, Azadmehr, Abbas, Oladnabi, Morteza, Daraei, Abdolreza

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Extremely low frequency-pulsed electromagnetic fields affect proangiogenic-related gene expression in retinal pigment epithelial cells von Oladnabi, Morteza, Bagheri, Abouzar, Rezaei Kanavi, Mozhgan, Azadmehr, Abbas, Kianmehr, Anvarsadat

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Correlation between ELF-PEMF exposure and Human RPE Cell Proliferation, Apoptosis and Gene Expression von Oladnabi, Morteza, Mishan, Mohammad Amir, Rezaeikanavi, Mozhgan, Zargari, Mehryar, Sadeghi, Rouhallah Najjar, Bagheri, Abouzar

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Variants in Intron 4 of PD-1 Gene are Associated with the Susceptibility to SLE in an Iranian Population von Khanjari, Yousef, Oladnabi, Morteza, Abdollahi, Nafiseh, Heidari, Ahmad, Mohammadi, Saeed, Tabarraei, Alijan

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A Comparative Analysis of Gene Expression Profile in Liver and Esophageal Cancer using Expressed Sequence Tags von Ramezani, Mahboobeh, Shamsabadi, Fatemeh, Oladnabi, Morteza

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Emerging SARS-Cov-2 Infection in a Rapidly Changing World von Dorgaleleh, Saeed, Miri, Niloufar Sadat, Hajimohammadi, Zahra, hosravi-bachehmir, Farzaneh, Vahidi, Akram, Oladnabi, Morteza

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The Role of Genetic Counseling in the Prevention of Intellectual Disability and Deafness: Two Common Disabilities in Iran von Fatemeh Shahraki, Morteza Oladnabi

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The Molecular Pathogenesis, Diagnostic Criteria, Symptoms, Clinical Manifestations, and Gene-Based Therapeutic Approaches in Neurofibromatosis von Fatemeh Shahraki, Morteza Oladnabi

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Whole exome sequencing identifies a novel variant in the COL12A1 gene in a family with Ullrich congenital muscular dystrophy 2 von Naghipoor, Karim, Khosravi, Teymoor, Oladnabi, Morteza

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