Genetic etiology of hearing loss in Iran
Babanejad, Mojgan, Beheshtian, Maryam, Jamshidi, Fereshteh, Mohseni, Marzieh, Booth, Kevin T., Kahrizi, Kimia, Najmabadi, Hossein
Published in Human genetics (01.04.2022)
Published in Human genetics (01.04.2022)
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Journal Article
When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)
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
Published in Journal of human genetics (01.07.2020)
Published in Journal of human genetics (01.07.2020)
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Journal Article
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 review
Jamshidi, Fereshteh, Shokouhian, Ebrahim, Mohseni, Marzieh, Kahrizi, Kimia, Najmabadi, Hossein, Babanejad, Mojgan
Published in Molecular genetics & genomic medicine (01.05.2023)
Published in Molecular genetics & genomic medicine (01.05.2023)
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Journal Article
PDZD7 and hearing loss: More than just a modifier
Booth, Kevin T., Azaiez, Hela, Kahrizi, Kimia, Simpson, Allen C., Tollefson, William T.A., Sloan, Christina M., Meyer, Nicole C., Babanejad, Mojgan, Ardalani, Fariba, Arzhangi, Sanaz, Schnieders, Michael J., Najmabadi, Hossein, Smith, Richard J.H.
Published in American journal of medical genetics. Part A (01.12.2015)
Published in American journal of medical genetics. Part A (01.12.2015)
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Journal Article
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in Iran
Babanejad, Mojgan, Fattahi, Zohreh, Bazazzadegan, Niloofar, Nishimura, Carla, Meyer, Nicole, Nikzat, Nooshin, Sohrabi, Elahe, Najmabadi, Amin, Jamali, Peyman, Habibi, Farkhonde, Smith, Richard J.H., Kahrizi, Kimia, Najmabadi, Hossein
Published in American journal of medical genetics. Part A (01.10.2012)
Published in American journal of medical genetics. Part A (01.10.2012)
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Journal Article
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population
Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Faraji Zonooz, Mehrshid, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Mozaffarpour Nouri, Maryam, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Zamanian Najafabadi, Shima, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Sadat Mahdavi, Shokouh, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein
Published in Npj genomic medicine (19.02.2024)
Published in Npj genomic medicine (19.02.2024)
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Journal Article
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population
Fattahi, Zohreh, Shearer, A. Eliot, Babanejad, Mojgan, Bazazzadegan, Niloofar, Almadani, Seyed Navid, Nikzat, Nooshin, Jalalvand, Khadijeh, Arzhangi, Sanaz, Esteghamat, Fatemehsadat, Abtahi, Rezvan, Azadeh, Batool, Smith, Richard J.H., Kahrizi, Kimia, Najmabadi, Hossein
Published in American journal of medical genetics. Part A (01.08.2012)
Published in American journal of medical genetics. Part A (01.08.2012)
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Journal Article
P604: Diagnostic utility of NGS testing in a highly consanguineous population: Findings from 1400+ Iranian patients with Mendelian disorders
Abolhassani, Ayda, Fattahi, Zohreh, Beheshtian, Maryam, Fadaee, Mahsa, Vazehan, Raheleh, Ahangari, Fatemeh, Dehdahsi, Shima, Zonooz, Mehrshid Faraji, Parsimehr, Elham, Kalhor, Zahra, Peymani, Fatemeh, Nouri, Maryam Mozaffarpour, Babanejad, Mojgan, Noudehi, Khadijeh, Fatehi, Fatemeh, Najafabadi, Shima Zamanian, Afroozan, Fariba, Yazdan, Hilda, Bozorgmehr, Bita, Azarkeivan, Azita, Mahdavi, Shokouh Sadat, Nikuei, Pooneh, Fatehi, Farzad, Jamali, Payman, Ashrafi, Mahmoud Reza, Karimzadeh, Parvaneh, Habibi, Haleh, Kahrizi, Kimia, Nafissi, Shahriar, Kariminejad, Ariana, Najmabadi, Hossein
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases
Najafi, Kimia, Gholami, Soheila, Moshtagh, Azadeh, Bazrgar, Masood, Sadatian, Neda, Abbasi, Golemaryam, Rostami, Parvin, Khalili, Soheila, Babanejad, Mojgan, Nourmohammadi, Bahareh, Faramarzi Garous, Negin, Najmabadi, Hossein, Kariminejad, Roxana
Published in Molecular genetics & genomic medicine (01.08.2019)
Published in Molecular genetics & genomic medicine (01.08.2019)
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Journal Article
Association between Cytochrome P450 2 C9 and Vitamin K Epoxide Reductase Complex Subunit 1 Polymorphisms with Warfarin dose among Iranian Patients
Kameli, Reyhaneh, Hasanzad, Mandana, Tahmasebi Fard, Zahra, Babanejad, Mojgan, Imeni, Mahdieh, Feizi Barnaji, Lotfollah, Madadkar, Atoosa, Jamaldini, Seyed Hamid
Published in Research in molecular medicine (01.11.2016)
Published in Research in molecular medicine (01.11.2016)
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Journal Article
Association of polymorphisms at LDLR locus with coronary artery disease independently from lipid profile
Jamaldini, Seyed Hamid, Babanejad, Mojgan, Mozaffari, Reza, Nikzat, Nooshin, Jalalvand, Khadijeh, Badiei, Azadeh, Sanati, Hamidreza, Shakerian, Farshad, Afshari, Mahdi, Kahrizi, Kimia, Najmabadi, Hossein
Published in Acta medica Iranica (2014)
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Published in Acta medica Iranica (2014)
Journal Article
Copy Number Variations in Hereditary Spastic Paraplegia-Related Genes: Evaluation of an Iranian Hereditary Spastic Paraplegia Cohort and Literature Review
Ghasemi, Aida, Sadr, Zahra, Babanejad, Mojgan, Rohani, Mohammad, Alavi, Afagh
Published in Molecular syndromology (01.12.2023)
Published in Molecular syndromology (01.12.2023)
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Journal Article
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran
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
Published in Journal of medical genetics (01.12.2015)
Published in Journal of medical genetics (01.12.2015)
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Journal Article
An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene
Mohseni, Marzieh, Mohammadi, Yusuf, Zare Ashrafi, Farzane, Ghodratpour, Fatemeh, Jalalvand, Khadijeh, Arzhangi, Sanaz, Babanejad, Mojgan, Azizi, Mohammad Hossein, Kahrizi, Kimia, Najmabadi, Hossein
Published in Archives of Iranian medicine (01.03.2023)
Published in Archives of Iranian medicine (01.03.2023)
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Journal Article
Variants in CIB2 cause DFNB48 and not USH1J
Booth, K.T., Kahrizi, K., Babanejad, M., Daghagh, H., Bademci, G., Arzhangi, S., Zareabdollahi, D., Duman, D., El‐Amraoui, A., Tekin, M., Najmabadi, H., Azaiez, H., Smith, R.J.
Published in Clinical genetics (01.04.2018)
Published in Clinical genetics (01.04.2018)
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Journal Article
SLC52A2 mutations cause SCABD2 phenotype: A second report
Babanejad, Mojgan, Adeli, Omid Ali, Nikzat, Nooshin, Beheshtian, Maryam, Azarafra, Hakimeh, Sadeghnia, Farnaz, Mohseni, Marzieh, Najmabadi, Hossein, Kahrizi, Kimia
Published in International journal of pediatric otorhinolaryngology (01.01.2018)
Published in International journal of pediatric otorhinolaryngology (01.01.2018)
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Journal Article
Exome sequencing utility in defining the genetic landscape of hearing loss and novel‐gene discovery in Iran
Mohseni, Marzieh, Babanejad, Mojgan, Booth, Kevin T., Jamali, Payman, Jalalvand, Khadijeh, Davarnia, Behzad, Ardalani, Fariba, Khoshaeen, Atefeh, Arzhangi, Sanaz, Ghodratpour, Fatemeh, Beheshtian, Maryam, Jahanshad, Faezeh, Otukesh, Hasan, Bahrami, Fatemeh, Seifati, Seyed Morteza, Bazazzadegan, Niloofar, Habibi, Farkhonde, Behravan, Hanieh, Mirzaei, Sepide, Keshavarzi, Fatemeh, Nikzat, Nooshin, Mehrjoo, Zohreh, Thiele, Holger, Nothnagel, Michael, Azaiez, Hela, Smith, Richard J., Kahrizi, Kimia, Najmabadi, Hossein
Published in Clinical genetics (01.07.2021)
Published in Clinical genetics (01.07.2021)
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Journal Article
G130V de novo mutation in an Iranian pedigree with nonsyndromic hearing loss without palmoplantar keratoderma
Babanejad, Mojgan, Zarandy, Masoud Motasaddi, Nikzat, Nooshin, Bazazzadegan, Niloofar, Arzhangi, Sanaz, Mohseni, Marzieh, Kahrizi, Kimia, Najmabadi, Hossein
Published in International journal of pediatric otorhinolaryngology (01.11.2019)
Published in International journal of pediatric otorhinolaryngology (01.11.2019)
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Journal Article
C-reactive protein and complement factor H polymorphism interaction in advanced exudative age-related macular degeneration
Soheilian, Roham, Jabbarpour Bonyadi, Mohammad Hossein, Moein, Hamidreza, Babanejad, Mojgan, Ramezani, Alireza, Yaseri, Mehdi, Soheilian, Masoud
Published in International ophthalmology (01.10.2017)
Published in International ophthalmology (01.10.2017)
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Journal Article