Genetic etiology of hearing loss in Iran von Babanejad, Mojgan, Beheshtian, Maryam, Jamshidi, Fereshteh, Mohseni, Marzieh, Booth, Kevin T., Kahrizi, Kimia, Najmabadi, Hossein

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When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS) von Mohseni, Marzieh, Akbari, Mojdeh, Booth, Kevin T, Babanejad, Mojgan, Azaiez, Hela, Ardalani, Fariba, Arzhangi, Sanaz, Jalalvand, Khadijeh, Nikzat, Nooshin, Ghodratpour, Fatemeh, Jamali, Payman, Adeli, Omid Ali, Habibi, Haleh, Kahrizi, Kimia, Najmabadi, Hossein

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Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in... von Jamshidi, Fereshteh, Shokouhian, Ebrahim, Mohseni, Marzieh, Kahrizi, Kimia, Najmabadi, Hossein, Babanejad, Mojgan

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Mutation profile of BBS genes in Iranian patients with Bardet-Biedl syndrome: genetic characterization and report of nine novel mutations in five BBS genes von Fattahi, Zohreh, Rostami, Parvin, Najmabadi, Amin, Mohseni, Marzieh, Kahrizi, Kimia, Akbari, Mohammad Reza, Kariminejad, Ariana, Najmabadi, Hossein

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Correlation Between Internet Addiction and General Health in Students of Qom University of Medical Sciences in 2018 von Yousefi, Sadegh, Mohseni, Marzieh, Biderafsh, Azam, Shoghi, Hamed, Shafiei, Seyed Ali

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Identification of Three Novel Frameshift Mutations in the PKD1 Gene in Iranian Families with Autosomal Dominant Polycystic Kidney Disease Using Efficient Targeted Next-Generation S... von Ranjzad, Fariba, Aghdami, Nasser, Tara, Ahmad, Mohseni, Marzieh, Moghadasali, Reza, Basiri, Abbas

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Investigation of the Relationship Between a Genetic Polymorphism in ACTN3 and Elite Sport Performance Among Iranian Soccer Players von Honarpour, Asal, Mohseni, Marzieh, Ghavidel Hajiagha, Siamak, Irani, Shiva, Najmabadi, Hossein

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Microstructure, magnetic and microwave absorptive behavior of doped W-type hexaferrite nanoparticles prepared by co-precipitation method von Gordani, Gholam Reza, Mohseni, Marzieh, Ghasemi, Ali, Hosseini, Sayed Rahman

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GJB2 mutations: Passage through Iran von Najmabadi, Hossein, Nishimura, Carla, Kahrizi, Kimia, Riazalhosseini, Yasser, Malekpour, Mahdi, Daneshi, Ahmad, Farhadi, Mohammad, Mohseni, Marzieh, Mahdieh, Nejat, Ebrahimi, Ahmad, Bazazzadegan, Niloofar, Naghavi, Anoosh, Avenarius, Matthew, Arzhangi, Sanaz, Smith, Richard J.H.

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Iranome: A catalog of genomic variations in the Iranian population von Fattahi, Zohreh, Beheshtian, Maryam, Mohseni, Marzieh, Poustchi, Hossein, Sellars, Erin, Nezhadi, Sayyed Hossein, Amini, Amir, Arzhangi, Sanaz, Jalalvand, Khadijeh, Jamali, Peyman, Mohammadi, Zahra, Davarnia, Behzad, Nikuei, Pooneh, Oladnabi, Morteza, Mohammadzadeh, Akbar, Zohrehvand, Elham, Nejatizadeh, Azim, Shekari, Mohammad, Bagherzadeh, Maryam, Shamsi‐Gooshki, Ehsan, Börno, Stefan, Timmermann, Bernd, Haghdoost, Aliakbar, Najafipour, Reza, Khorram Khorshid, Hamid Reza, Kahrizi, Kimia, Malekzadeh, Reza, Akbari, Mohammad R., Najmabadi, Hossein

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders von Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman, Zecha, Agnes, Mohseni, Marzieh, Püttmann, Lucia, Vahid, Leyla Nouri, Jensen, Corinna, Moheb, Lia Abbasi, Bienek, Melanie, Larti, Farzaneh, Mueller, Ines, Weissmann, Robert, Darvish, Hossein, Wrogemann, Klaus, Hadavi, Valeh, Lipkowitz, Bettina, Esmaeeli-Nieh, Sahar, Wieczorek, Dagmar, Kariminejad, Roxana, Firouzabadi, Saghar Ghasemi, Cohen, Monika, Fattahi, Zohreh, Rost, Imma, Mojahedi, Faezeh, Hertzberg, Christoph, Dehghan, Atefeh, Rajab, Anna, Banavandi, Mohammad Javad Soltani, Hoffer, Julia, Falah, Masoumeh, Musante, Luciana, Kalscheuer, Vera, Ullmann, Reinhard, Kuss, Andreas Walter, Tzschach, Andreas, Kahrizi, Kimia, Ropers, H. Hilger

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A Frameshift Variant in ANKRD24 Implicates Its Role in Human Non‐Syndromic Hearing Loss von Kazemi, Negar, Rezvani Rezvandeh, Raziye, Zare Ashrafi, Farzane, Shokouhian, Ebrahim, Edizadeh, Masoud, Booth, Kevin T. A., Kahrizi, Kimia, Najmabadi, Hossein, Mohseni, Marzieh

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Targeted Next Generation Sequencing Revealed Novel Variants in the PKD1 and PKD2 Genes of Iranian Patients with Autosomal Dominant Polycystic Kidney Disease von Hosseinpour, Maryam, Ardalani, Fariba, Mohseni, Marzieh, Beheshtian, Maryam, Arzhangi, Sanaz, Ossareh, Shahrzad, Najmabadi, Hossein, Nobakht, Ali, Kahrizi, Kimia, Broumand, Behrooz

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Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran von Sloan-Heggen, Christina M, Babanejad, Mojgan, Beheshtian, Maryam, Simpson, Allen C, Booth, Kevin T, Ardalani, Fariba, Frees, Kathy L, Mohseni, Marzieh, Mozafari, Reza, Mehrjoo, Zohreh, Jamali, Leila, Vaziri, Saeideh, Akhtarkhavari, Tara, Bazazzadegan, Niloofar, Nikzat, Nooshin, Arzhangi, Sanaz, Sabbagh, Farahnaz, Otukesh, Hasan, Seifati, Seyed Morteza, Khodaei, Hossein, Taghdiri, Maryam, Meyer, Nicole C, Daneshi, Ahmad, Farhadi, Mohammad, Kahrizi, Kimia, Smith, Richard JH, Azaiez, Hela, Najmabadi, Hossein

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Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients von Mehvari, Sepideh, Karimian Fathi, Nahid, Saki, Sara, Asadnezhad, Maryam, Arzhangi, Sanaz, Ghodratpour, Fatemeh, Mohseni, Marzieh, Zare Ashrafi, Farzane, Sadeghian, Saeed, Boroumand, Mohammadali, Shokohizadeh, Fatemeh, Rostami, Elham, Boroumand, Rahnama, Najafipour, Reza, Malekzadeh, Reza, Riazalhosseini, Yasser, Akbari, Mohammadreza, Lathrop, Mark, Najmabadi, Hossein, Hosseini, Kaveh, Kahrizi, Kimia

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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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Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss von Mehregan, Hoda, Mohseni, Marzieh, Jalalvand, Khadijeh, Arzhangi, Sanaz, Nikzat, Nooshin, Banihashemi, Sussan, Kahrizi, Kimia, Najmabadi, Hossein

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Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment von Mehregan, Hoda, Mohseni, Marzieh, Akbari, Mojdeh, Jalalvand, Khadijeh, Arzhangi, Sanaz, Nikzat, Nooshin, Kahrizi, Kimia, Najmabadi, Hossein

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An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene von Mohseni, Marzieh, Mohammadi, Yusuf, Zare Ashrafi, Farzane, Ghodratpour, Fatemeh, Jalalvand, Khadijeh, Arzhangi, Sanaz, Babanejad, Mojgan, Azizi, Mohammad Hossein, Kahrizi, Kimia, Najmabadi, Hossein

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A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4 von Zare Ashrafi, Farzane, Dorgaleleh, Saeed, Rezvani Rezvandeh, Raziye, Kazemi, Negar, Azizi, Nasrin, Edizadeh, Masoud, Azizi, Mohammad Hossein, Kahrizi, Kimia, Najmabadi, Hossein, Najafipour, Reza, Mohseni, Marzieh

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