Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Khadijeh Jalalvand"'
Autor:
Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi, Michael Nothnagel
Publikováno v:
PLoS Genetics, Vol 15, Iss 9, p e1008385 (2019)
Iran, despite its size, geographic location and past cultural influence, has largely been a blind spot for human population genetic studies. With only sparse genetic information on the Iranian population available, we pursued its genome-wide and geog
Externí odkaz:
https://doaj.org/article/4315684f000740c9942734ccd2e1d473
Autor:
Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi
Publikováno v:
Journal of Rehabilitation, Vol 8, Iss 3, Pp 35-41 (2007)
Objective: Hereditary hearing loss (HHL) is a very common disorder. When inherited in an autosomal recessive manner, it typically presents as an isolated finding. Interestingly and unexpectedly, in spite of extreme heterogeneity, mutations in one gen
Externí odkaz:
https://doaj.org/article/e891523139e44bb594ba117ed736dacc
Autor:
Seyed Hamid Jamaldini, Mojgan Babanejad, Reza Mozaffari, Nooshin Nikzat, Khadijeh Jalalvand, Azadeh Badiei, Hamidreza Sanati, Farshad Shakerian, Mahdi Afshari, Kimia Kahrizi, Hossein Najmabadi
Publikováno v:
Acta Medica Iranica, Vol 52, Iss 5 (2014)
Coronary artery disease (CAD) is the leading cause of mortality in many parts of the world. Genome-wide association studies (GWAS) have identified several genetic variants associated with CAD in Low-density lipoprotein receptor (LDLR) locus. This stu
Externí odkaz:
https://doaj.org/article/79fd04af3bb24427b0fb3bb4a1628908
Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families
Autor:
Ramak Badr, Bahareh Shoja-Saffar, Niloofar Bazzaz-Zadegan, Khadijeh Jalalvand, Kimia Kahrizi, Hossein Najm-Abadi
Publikováno v:
Journal of Rehabilitation, Vol 10, Iss 4, Pp 0-0 (2010)
Objective: Hearing impairment is the most frequent sensorineural defect in 2 forms, syndromic and non–syndromic. The aim of this study is haplotype analysis of seven loci of non–syndromic autosomal recessive hearing loss in Iranian families. Mate
Externí odkaz:
https://doaj.org/article/c8d216d795394ef8bc27827ecbeab8c8
Autor:
Hanieh Behravan, Ahmad Piroozmand, Azam Ghaziasadi, Khadijeh Jalalvand, Mahdieh Koshki, Fatemeh Tavangar, Angila Ataei-Pirkooh, Farid Yousefi, Masoumeh Bayani, Zohreh Fattahi, Hamed Fakhim, Mojtaba Varshochi, Mohammad Khazeni, Zakiye Mokhames, Fariba Shahraki-Sanavi, Reza Malekzadeh, Maryam Beheshtian, Yousef Yahyapour, Seyed Jalal Kiani, Fariba Keramat, Shokouh Ghafari, Behrooz Ataei, Alireza Abdollahi, Afagh Moattari, Fatemeh Keshavarzi, Mohammad Reza Haghshenas, Alireza AnsariMoghaddam, Maryam Azad, Mohammad Hassan Pouriayevali, Mohsen Moghadami, Azarakhsh Azaran, Zohreh Elahi, Farhang Babamahmoodi, Mohamad Soveyzi, Kimia Kahrizi, Hamid Reza Khorram Khorshid, Vahdat Poortahmasebi, Reza Najafipour, Farzane Zare Ashrafi, Akram Ezani, Farid Azizi Jalilian, Mostafa Salehi-Vaziri, Seyed Mohammad Jazayeri, Seyed Mohammad Hashemi-Shahri, Abdolvahab Moradi, Ali Mojtahedi, Fatemeh Ghodratpour, Marzieh Mohseni, Davod Javanmard, Mahsa Tavakoli, Ali Jafarpour, Hossein Najmabadi, Alijan Tabarraei, Alireza Soleimani, Tahmineh Jalali, Elahe Nasri, Mahmood Yaghoubi, Marzieh Kalhor, Farah Bokharaei-Salim, Iman Rezaeiazhar, Masood Ziaee
Publikováno v:
Archives of Iranian Medicine. 25:508-522
SARS-CoV-2 genome surveillance projects provide a good measure of transmission and monitor the circulating SARS-CoV-2 variants at regional and global scales. Iran is one of the most affected countries still involved with the virus circulating in at l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234661a7c997f97453fa3ecb1054d7e1
https://doi.org/10.34172/aim.2022.83
https://doi.org/10.34172/aim.2022.83
Autor:
Gholam Abbas Kaydani, Seyedeh Elham Mortazavi, Seyed Amir Momeni, Talat Mokhtari-Azad, Fatemeh Aghakhani Moghadam, Hanieh Behravan, Mohammad Khazeni, Azarakhsh Azaran, Zakiye Mokhames, Farhad Jeddi, Ebrahim Kord, Seyed Mohammad Hashemi-Shahri, Azam Ghaziasadi, Alijan Tabarraei, Fatemeh Ghodratpour, Masood Ziaee, Ali Jafarpour, Jila Yavarian, Abdolvahab Moradi, Azar Hadadi, Zohreh Fattahi, Hossein Najmabadi, Shokouh Ghafari, Issa Jahanzad, Reza Malekzadeh, Marzieh Mohseni, Farid Yousefi, Shahram Habibzadeh, Seyed Mohammad Jazayeri, Khadijeh Jalalvand, Saber Soltani, Kimia Kahrizi, Alireza Soleimani, Sadegh Ali Azimi, Reza Najafipour, Alireza Abdollahi, Fatemeh Keshavarzi
Publikováno v:
Transboundary and Emerging Diseases
The SARS‐CoV‐2 virus has been rapidly spreading globally since December 2019, triggering a pandemic, soon after its emergence. While Iran was among the first countries confronted with rapid spread of virus in February 2020, no real‐time SARS‐
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c82245f4fea38cae05cc1b94f251910
https://doi.org/10.1111/tbed.14104
https://doi.org/10.1111/tbed.14104
Autor:
Kimia Kahrizi, Fariba Ardalani, Mojdeh Akbari, Mojgan Babanejad, Kevin T. Booth, Hossein Najmabadi, Haleh Habibi, Khadijeh Jalalvand, Nooshin Nikzat, Fatemeh Ghodratpour, Omid Ali Adeli, Marzieh Mohseni, Payman Jamali, Hela Azaiez, Sanaz Arzhangi
Publikováno v:
J Hum Genet
Mutations in the CDC14A (Cell Division-Cycle 14A) gene, which encodes a conserved dual-specificity protein tyrosine phosphatase, have been identified as a cause of autosomal recessive non-syndromic hearing loss (DFNB32) and hearing impairment inferti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0871f42e194feb0aeae554f7d0b00072
https://doi.org/10.1038/s10038-020-0740-z
https://doi.org/10.1038/s10038-020-0740-z
Autor:
Hoda Mehregan, Nooshin Nikzat, Marzieh Mohseni, Kimia Kahrizi, Sussan Banihashemi, Khadijeh Jalalvand, Hossein Najmabadi, Sanaz Arzhangi
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 117:115-126
Objective Hereditary hearing loss is the most common neurosensory disorder in humans caused by myriad mutations in numerous genes. Autosomal recessive nonsyndromic hearing loss (ARNSHL) accounts for 80% of hearing impairments of genetic origin and is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ab4d6c7ba59003be868f155916fc522
https://doi.org/10.1016/j.ijporl.2018.11.025
https://doi.org/10.1016/j.ijporl.2018.11.025
Autor:
Marzieh Mohseni, Kevin T. Booth, Atefeh Khoshaeen, Fatemeh Bahrami, Payman Jamali, Hossein Najmabadi, Niloofar Bazazzadegan, Kimia Kahrizi, Nooshin Nikzat, Farkhonde Habibi, Richard J.H. Smith, Fariba Ardalani, Mojgan Babanejad, Hanieh Behravan, Fatemeh Keshavarzi, Michael Nothnagel, Faezeh Jahanshad, Seyed Morteza Seifati, Fatemeh Ghodratpour, Sanaz Arzhangi, Behzad Davarnia, Zohreh Mehrjoo, Holger Thiele, Khadijeh Jalalvand, Maryam Beheshtian, Hela Azaiez, Sepide Mirzaei, Hasan Otukesh
Publikováno v:
Clin Genet
Hearing loss (HL) is one of the most common sensory defects affecting more than 466 million individuals worldwide. It is clinically and genetically heterogeneous with over 120 genes causing non-syndromic HL identified to date. Here, we performed exom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2652aadda21337130620b09922d67a
https://europepmc.org/articles/PMC8195868/
https://europepmc.org/articles/PMC8195868/
Autor:
Seyed Morteza Seifati, Maryam Beheshtian, Kevin T. Booth, Behzad Davarnia, Faezeh Jahanshad, Farkhonde Habibi, Michael Nothnagel, Atefeh Khoshaeen, Hanieh Behravan, K. Kahrizi, Fatemeh Ghodratpour, Sanaz Arzhangi, Fatemeh Bahrami, Hossein Najmabadi, Payman Jamali, Marzieh Mohseni, Fariba Ardalani, Mojgan Babanejad, Khadijeh Jalalvand, Hela Azaiez, Sepide Mirzaei, Holger Thiele, Zohreh Mehrjoo, Hasan Otukesh, Nooshin Nikzat, Richard J.H. Smith, Fatemeh Keshavarzi, Niloofar Bazazzadegan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c907ed7b80c8ef2500764b3b5e3a683f
https://doi.org/10.1111/cge.13956/v4/response1
https://doi.org/10.1111/cge.13956/v4/response1