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Genetic etiology of hearing loss in Iran
Author / Creator:Babanejad, Mojgan ; Beheshtian, Maryam ; Jamshidi, Fereshteh ; Mohseni, Marzieh ; Booth, Kevin T. ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Human genetics, 2022-04, Vol.141 (3-4), p.623-631
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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 Iran and literature...
Author / Creator:Jamshidi, Fereshteh ; Shokouhian, Ebrahim ; Mohseni, Marzieh ; Kahrizi, Kimia ; Najmabadi, Hossein ; Babanejad, Mojgan
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2023-05, Vol.11 (5), p.e2168-n/a
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When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
Author / Creator: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
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2020-07, Vol.65 (7), p.609-617
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Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran
Author / Creator:Mohseni, Marzieh ; Ashrafi, Farzane Zare ; Abbaspour Rodbaneh, Ehsan ; Mokabber, Haleh ; Vafaei, Maryam ; Nobakht, Ramiz ; Keshavarzi, Fatemeh ; Arzhangi, Sanaz ; Arish, Sara ; Azar, Zahra Nematollahi ; Kahrizi, Kimia ; Najmabadi, Hossein ; Davarnia, Behzad
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2025-02, Vol.13 (2), p.e70080-n/a
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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
Author / Creator:Fattahi, Zohreh ; Rostami, Parvin ; Najmabadi, Amin ; Mohseni, Marzieh ; Kahrizi, Kimia ; Akbari, Mohammad Reza ; Kariminejad, Ariana ; Najmabadi, Hossein
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2014-07, Vol.59 (7), p.368-375
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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 Sequencing
Author / Creator:Ranjzad, Fariba ; Aghdami, Nasser ; Tara, Ahmad ; Mohseni, Marzieh ; Moghadasali, Reza ; Basiri, Abbas
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Kidney & blood pressure research, 2018-01, Vol.43 (2), p.471-478
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Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2011-10, Vol.478 (7367), p.57-63
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Haplogroup Structure and Genetic Variation Analyses of Mitochondrial Genome SNPs in the Iranian Population
Author / Creator:Ghasemi, Masoumeh ; Mohseni, Marzieh ; Fattahi, Zohreh ; Edizadeh, Masoud ; Beheshtian, Maryam ; Keshavarzi, Fatemeh ; Jalalvand, Khadijeh ; Omrani, Mohammadamin ; Khanbazi, Ali ; Riazalhosseini, Yasser ; Akbari, Mohammad Reza ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2025-03, Vol.28 (3), p.140-148
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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
Author / Creator:Hosseinpour, Maryam ; Ardalani, Fariba ; Mohseni, Marzieh ; Beheshtian, Maryam ; Arzhangi, Sanaz ; Ossareh, Shahrzad ; Najmabadi, Hossein ; Nobakht, Ali ; Kahrizi, Kimia ; Broumand, Behrooz
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2022-09, Vol.25 (9), p.600-608
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Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran
Author / Creator: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
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2015-12, Vol.52 (12), p.823-829
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Distinct genetic variation and heterogeneity of the Iranian population
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2019-09, Vol.15 (9), p.e1008385
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Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment
Author / Creator:Mehregan, Hoda ; Mohseni, Marzieh ; Akbari, Mojdeh ; Jalalvand, Khadijeh ; Arzhangi, Sanaz ; Nikzat, Nooshin ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2019-04, Vol.22 (4), p.189
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An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene
Author / Creator:Mohseni, Marzieh ; Mohammadi, Yusuf ; Zare Ashrafi, Farzane ; Ghodratpour, Fatemeh ; Jalalvand, Khadijeh ; Arzhangi, Sanaz ; Babanejad, Mojgan ; Azizi, Mohammad Hossein ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2023-03, Vol.26 (3), p.176-180
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A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4
Author / Creator: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
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2024-09, Vol.27 (9), p.522-526
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Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups
Author / Creator:Alinaghi, Somayeh ; Mohseni, Marzieh ; Fattahi, Zohreh ; Beheshtian, Maryam ; Ghodratpour, Fatemeh ; Zare Ashrafi, Farzane ; Arzhangi, Sanaz ; Jalalvand, Khadijeh ; Najafipour, Reza ; Khorram Khorshid, Hamid Reza ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2024-02, Vol.27 (2), p.79-88
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Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum
Author / Creator:Taghizadeh, Sara ; Vazehan, Raheleh ; Beheshtian, Maryam ; Sadeghinia, Farnaz ; Fattahi, Zohreh ; Mohseni, Marzieh ; Arzhangi, Sanaz ; Nafissi, Shahriar ; Kariminejad, Ariana ; Najmabadi, Hossein ; Kahrizi, Kimia
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2020-07, Vol.23 (7), p.426-433
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Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism
Author / Creator:Kazemi, Goli ; Peymani, Fatemeh ; Mohseni, Marzieh ; Zare Ashrafi, Farzane ; Arzhangi, Sanaz ; Ardalani, Fariba ; Aghakhani Moghaddam, Fatemeh ; Kahrizi, Kimia ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2020-12, Vol.23 (12), p.842-847
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Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière’s Disease
Author / Creator:Mehrjoo, Zohreh ; Kahrizi, Kimia ; Mohseni, Marzieh ; Akbari, Mojdeh ; Arzhangi, Sanaz ; Jalalvand, Khadijeh ; Najmabadi, Hossein ; Farhadi, Mohammad ; Mohseni, Mohammad ; Asghari, Alimohamad ; Mohebbi, Saleh ; Daneshi, Ahmad
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2020-05, Vol.23 (5), p.319-325
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Impact of Whole Exome Sequencing among Iranian Patients with Autosomal Recessive Retinitis Pigmentosa
Author / Creator:Beheshtian, Maryam ; Rad, Samira Saee ; Babanejad, Mojgan ; Mohseni, Marzieh ; Hashemi, Hassan ; Eshghabadi, Arash ; Hajizadeh, Fedra ; Akbari, Mohammad Reza ; Kahrizi, Kimia ; Esfahani, Mohammad Riazi ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2015-11, Vol.18 (11), p.776
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Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends
Author / Creator:Fattahi, Zohreh ; Mohseni, Marzieh ; Beheshtian, Maryam ; Jafarpour, Ali ; Jalalvand, Khadijeh ; Keshavarzi, Fatemeh ; Behravan, Hanieh ; Ghodratpour, Fatemeh ; Zare Ashrafi, Farzane ; Kalhor, Marzieh ; Azad, Maryam ; Koshki, Mahdieh ; Ghaziasadi, Azam ; Soveyzi, Mohamad ; Abdollahi, Alireza ; Kiani, Seyed Jalal ; Ataei-Pirkooh, Angila ; Rezaeiazhar, Iman ; Bokharaei-Salim, Farah ; Haghshenas, Mohammad Reza ; Babamahmoodi, Farhang ; Mokhames, Zakiye ; Soleimani, Alireza ; Elahi, Zohreh ; Ziaee, Masood ; Javanmard, Davod ; Ghafari, Shokouh ; Ezani, Akram ; Ansari Moghaddam, Alireza ; Shahraki-Sanavi, Fariba ; Hashemi Shahri, Seyed Mohammad ; Azaran, Azarakhsh ; Yousefi, Farid ; Moattari, Afagh ; Moghadami, Mohsen ; Fakhim, Hamed ; Ataei, Behrooz ; Nasri, Elahe ; Poortahmasebi, Vahdat ; Varshochi, Mojtaba ; Mojtahedi, Ali ; Jalilian, Farid ; Khazeni, Mohammad ; Moradi, Abdolvahab ; Tabarraei, Alijan ; Piroozmand, Ahmad ; Yahyapour, Yousef ; Bayani, Masoumeh ; Tavangar, Fatemeh ; Yaghoubi, Mahmood ; Keramat, Fariba ; Tavakoli, Mahsa ; Jalali, Tahmineh ; Pouriayevali, Mohammad Hassan ; Salehi-Vaziri, Mostafa ; Khorram Khorshid, Hamid Reza ; Najafipour, Reza ; Malekzadeh, Reza ; Kahrizi, Kimia ; Jazayeri, Seyed Mohammad ; Najmabadi, Hossein
Publisher:Tehran: Academy of Medical Sciences of I.R. Iran
Journal title:Archives of Iranian medicine, 2022-08, Vol.25 (8), p.508-522
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Genetic etiology of hearing loss in Iran

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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 Iran and literature...

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When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)

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Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran

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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

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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 Sequencing

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders

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Haplogroup Structure and Genetic Variation Analyses of Mitochondrial Genome SNPs in the Iranian Population

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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

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Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

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Distinct genetic variation and heterogeneity of the Iranian population

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Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment

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An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene

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A Village in the Southeastern Region of Iran Harboring the c.716T>A (p.Val239Asp) Mutation in SLC26A4

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Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups

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Molecular Diagnosis of Hereditary Neuropathies by Whole Exome Sequencing and Expanding the Phenotype Spectrum

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Novel Mutation in LARP7 in Two Iranian Consanguineous Families with Syndromic Intellectual Disability and Facial Dysmorphism

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Limbic System Associated Membrane Protein Mutation in an Iranian Family Diagnosed with Ménière’s Disease

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Impact of Whole Exome Sequencing among Iranian Patients with Autosomal Recessive Retinitis Pigmentosa

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Disease Waves of SARS-CoV-2 in Iran Closely Mirror Global Pandemic Trends

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