Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Fariba, Ardalani"'
Autor:
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Recurrent miscarriages occur in about 5% of couples trying to conceive. In the past decade, the products of miscarriage have been studied using array comparative genomic hybridization (a-CGH). Within the last decade, an association has been
Externí odkaz:
https://doaj.org/article/dfd9e1bd65df4bc1a6c09534993ad5b0
Autor:
Maryam Hosseinpour, Fariba Ardalani, Marzieh Mohseni, Maryam Beheshtian, Sanaz Arzhangi, Shahrzad Ossareh, Hossein Najmabadi, Ali Nobakht, Kimia Kahrizi, Behrooz Broumand
Publikováno v:
Archives of Iranian Medicine. 25:600-608
Background: Autosomal dominant polycystic kidney disease (ADPKD), one of the common inherited disorders in humans, is characterized by the development and enlargement of renal cysts, often leading to end-stage renal disease (ESRD). In this study, Ira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a3778a32e61e7f25ed2f5a30f9ff606
https://doi.org/10.34172/aim.2022.95
https://doi.org/10.34172/aim.2022.95
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, Hossein Najmabadi, Farzane Zare Ashrafi, Sanaz Arzhangi, Goli Kazemi, Marzieh Mohseni, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Fatemeh Peymani
Publikováno v:
Archives of Iranian Medicine. 23:842-847
Background: Recently, we have reported mutations in LARP7 gene, leading to neurodevelopmental disorders (NDDs), the most frequent cause of disability in children with a broad phenotype spectrum and diverse genetic landscape. Methods: Here, we present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e342f34c3e3f94ae9182084fcded167b
https://doi.org/10.34172/aim.2020.112
https://doi.org/10.34172/aim.2020.112
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:
Ariana Kariminejad, Kimia Najafi, Roxana Kariminejad, Hossein Najmabadi, Siavash Ghaderi-Sohi, Zohreh Mehrjoo, Fariba Ardalani
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
Recurrent miscarriages occur in about 5% of couples trying to conceive. In the past decade, the products of miscarriage have been studied using array comparative genomic hybridization (a-CGH). Within the last decade, an association has been proposed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02bd344f6199a2c35c47a3349dd27a92
https://doi.org/10.1038/s41598-021-86309-9
https://doi.org/10.1038/s41598-021-86309-9
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
Autor:
Goli, Kazemi, Fatemeh, Peymani, Marzieh, Mohseni, Farzane, Zare Ashrafi, Sanaz, Arzhangi, Fariba, Ardalani, Fatemeh, Aghakhani Moghaddam, Kimia, Kahrizi, Hossein, Najmabadi
Publikováno v:
Archives of Iranian medicine. 23(12)
Recently, we have reported mutations in LARP7 gene, leading to neurodevelopmental disorders (NDDs), the most frequent cause of disability in children with a broad phenotype spectrum and diverse genetic landscape.Here, we present two Iranian patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e0ae230197f453936efbfe97cdabb3a
https://pubmed.ncbi.nlm.nih.gov/33356342
https://pubmed.ncbi.nlm.nih.gov/33356342
Autor:
Maryam Zarin, Hossein Najmabadi, Azita Azarkeivan, Maghsood Mehri, Fariba Ardalani, Maryam Neishabury
Publikováno v:
Blood cells, moleculesdiseases. 71
Sideroblastic anemias are heterogeneous rare hematological disorders, representing diverse phenotypes. In this study, the genetic cause of congenital, transfusion dependent anemia in four unrelated families consisting of eighteen individuals, with on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::614aae1bae2dbc876dffc67587acf36e
https://pubmed.ncbi.nlm.nih.gov/29499877
https://pubmed.ncbi.nlm.nih.gov/29499877