Works matching AU Fattahi, Zohreh

Results: 39
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    Iranome: A catalog of genomic variations in the Iranian population.

    Published in:
    Human Mutation, 2019, v. 40, n. 11, p. 1968, doi. 10.1002/humu.23880
    By:
    • 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
    Publication type:
    Article
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    Identification of disease‐causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.

    Published in:
    Clinical Genetics, 2019, v. 95, n. 6, p. 718, doi. 10.1111/cge.13549
    By:
    • Beheshtian, Maryam;
    • Fattahi, Zohreh;
    • Fadaee, Mahsa;
    • Vazehan, Raheleh;
    • Jamali, Payman;
    • Parsimehr, Elham;
    • Kamgar, Mahboubeh;
    • Zonooz, Mehrshid Faraji;
    • Mahdavi, Shokouh Sadat;
    • Kalhor, Zahra;
    • Arzhangi, Sanaz;
    • Abedini, Seyedeh Sedigheh;
    • Kermani, Farahnaz Sabbagh;
    • Mojahedi, Faezeh;
    • Kalscheuer, Vera M.;
    • Ropers, Hans‐Hilger.;
    • Kariminejad, Ariana;
    • Najmabadi, Hossein;
    • Kahrizi, Kimia
    Publication type:
    Article
    9

    Effect of inbreeding on intellectual disability revisited by trio sequencing.

    Published in:
    Clinical Genetics, 2019, v. 95, n. 1, p. 151, doi. 10.1111/cge.13463
    By:
    • Kahrizi, Kimia;
    • Hosseini, Masoumeh;
    • Fattahi, Zohreh;
    • Beheshtian, Maryam;
    • Mohseni, Marzieh;
    • Mehvari, Sepideh;
    • Mehrjoo, Zohreh;
    • Akhtarkhavari, Tara;
    • Ghaderi, Zhila;
    • Rahimi, Maryam;
    • Arzhangi, Sanaz;
    • Falahat Chian, Milad;
    • Sadeghinia, Farnaz;
    • Najmabadi, Hossein;
    • Pourfatemi, Fatemeh;
    • Mojahedi, Faezeh;
    • Khodaie‐Ardakani, Mohammad‐Reza;
    • Najafipour, Reza;
    • Hu, Hao;
    • Kalscheuer, Vera M.
    Publication type:
    Article
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    Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.

    Published in:
    American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 8, p. 1857, doi. 10.1002/ajmg.a.34411
    By:
    • 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
    Publication type:
    Article
    13

    ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences.

    Published in:
    2022
    By:
    • Sumathipala, Dulika;
    • Strømme, Petter;
    • Fattahi, Zohreh;
    • Lüders, Torben;
    • Sheng, Ying;
    • Kahrizi, Kimia;
    • Einarsen, Ingunn Holm;
    • Sloan, Jennifer L;
    • Najmabadi, Hossein;
    • van den Heuvel, Lambert;
    • Wevers, Ron A;
    • Guerrero-Castillo, Sergio;
    • Mørkrid, Lars;
    • Valayannopoulos, Vassili;
    • Backe, Paul Hoff;
    • Venditti, Charles P;
    • Karnebeek, Clara D van;
    • Nilsen, Hilde;
    • Frengen, Eirik;
    • Misceo, Doriana
    Publication type:
    journal article
    14

    CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability.

    Published in:
    American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2018, v. 177, n. 8, p. 691, doi. 10.1002/ajmg.b.32648
    By:
    • Kazeminasab, Somayeh;
    • Taskiran, Ibrahim Ihsan;
    • Fattahi, Zohreh;
    • Bazazzadegan, Niloofar;
    • Hosseini, Masoumeh;
    • Rahimi, Maryam;
    • Oladnabi, Morteza;
    • Haddadi, Mohammad;
    • Celik, Arzu;
    • Ropers, Hans‐Hilger;
    • Najmabadi, Hossein;
    • Kahrizi, Kimia
    Publication type:
    Article
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    SARS-CoV-2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions.

    Published in:
    Transboundary & Emerging Diseases, 2022, v. 69, n. 3, p. 1375, doi. 10.1111/tbed.14104
    By:
    • Fattahi, Zohreh;
    • Mohseni, Marzieh;
    • Jalalvand, Khadijeh;
    • Moghadam, Fatemeh Aghakhani;
    • Ghaziasadi, Azam;
    • Keshavarzi, Fatemeh;
    • Yavarian, Jila;
    • Jafarpour, Ali;
    • Mortazavi, Seyedeh Elham;
    • Ghodratpour, Fatemeh;
    • Behravan, Hanieh;
    • Khazeni, Mohammad;
    • Momeni, Seyed Amir;
    • Jahanzad, Issa;
    • Moradi, Abdolvahab;
    • Tabarraei, Alijan;
    • Azimi, Sadegh Ali;
    • Kord, Ebrahim;
    • Hashemi-Shahri, Seyed Mohammad;
    • Azaran, Azarakhsh
    Publication type:
    Article
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    Genetic Analysis of 27 Y-STR Haplotypes in 11 Iranian Ethnic Groups.

    Published in:
    Archives of Iranian Medicine (AIM), 2024, v. 27, n. 2, p. 79, doi. 10.34172/aim.2024.13
    By:
    • 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
    Publication type:
    Article
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    Implementation of an In-House Platform for Rapid Screening of SARS-CoV-2 Genome Variations.

    Published in:
    Archives of Iranian Medicine (AIM), 2023, v. 26, n. 2, p. 69, doi. 10.34172/aim.2023.12
    By:
    • Ashrafi, Farzane Zare;
    • Mohseni, Marzieh;
    • Beheshtian, Maryam;
    • Fattahi, Zohreh;
    • Ghodratpour, Fatemeh;
    • Keshavarzi, Fatemeh;
    • Behravan, Hanieh;
    • Kalhor, Marzieh;
    • Jalalvand, Khadijeh;
    • Azad, Maryam;
    • Koshki, Mahdieh;
    • Jafarpour, Ali;
    • Ghaziasadi, Azam;
    • Abdollahi, Alireza;
    • Kiani, Seyed Jalal;
    • Ataei-Pirkooh, Angila;
    • Azhar, Iman Rezaei;
    • Bokharaei-Salim, Farah;
    • Haghshenas, Mohammad Reza;
    • Babamahmoodi, Farhang
    Publication type:
    Article
    25

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

    Published in:
    Archives of Iranian Medicine (AIM), 2022, v. 25, n. 8, p. 508, doi. 10.34172/aim.2022.83
    By:
    • Fattahi, Zohreh;
    • Mohseni, Marzieh;
    • Beheshtian, Maryam;
    • Jafarpour, Ali;
    • Jalalvand, Khadijeh;
    • Keshavarzi, Fatemeh;
    • Behravan, Hanieh;
    • Ghodratpour, Fatemeh;
    • Ashrafi, Farzane Zare;
    • 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
    Publication type:
    Article
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    De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.

    Published in:
    Archives of Iranian Medicine (AIM), 2017, v. 20, n. 9, p. 617
    By:
    • Edizadeh, Masoud;
    • Vazehan, Raheleh;
    • Javadi, Fatemeh;
    • Dehdahsi, Shima;
    • Fadaee, Mahsa;
    • Zonooz, Mehrshid Faraji;
    • Parsimehr, Elham;
    • Ahangari, Fatemeh;
    • Abolhassani, Ayda;
    • Kalhor, Zahra;
    • Fattahi, Zohreh;
    • Beheshtian, Maryam;
    • Kariminejad, Ariana;
    • Akbari, Mohammad Reza;
    • Najmabadi, Hossein;
    • Nafissi, Shariar
    Publication type:
    Article
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    Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability.

    Published in:
    Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01158-w
    By:
    • Sheikh, Taimoor I.;
    • Vasli, Nasim;
    • Pastore, Stephen;
    • Kharizi, Kimia;
    • Harripaul, Ricardo;
    • Fattahi, Zohreh;
    • Pande, Shruti;
    • Naeem, Farooq;
    • Hussain, Abrar;
    • Mir, Asif;
    • Islam, Omar;
    • Girisha, Katta Mohan;
    • Irfan, Muhammad;
    • Ayub, Muhammad;
    • Schwarzer, Christoph;
    • Najmabadi, Hossein;
    • Shukla, Anju;
    • Sladky, Valentina C.;
    • Braun, Vincent Zoran;
    • Garcia-Carpio, Irmina
    Publication type:
    Article
    34

    SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

    Published in:
    Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-45933-5
    By:
    • Nashabat, Marwan;
    • Nabavizadeh, Nasrinsadat;
    • Saraçoğlu, Hilal Pırıl;
    • Sarıbaş, Burak;
    • Avcı, Şahin;
    • Börklü, Esra;
    • Beillard, Emmanuel;
    • Yılmaz, Elanur;
    • Uygur, Seyide Ecesu;
    • Kayhan, Cavit Kerem;
    • Bosco, Luca;
    • Eren, Zeynep Bengi;
    • Steindl, Katharina;
    • Richter, Manuela Friederike;
    • Bademci, Guney;
    • Rauch, Anita;
    • Fattahi, Zohreh;
    • Valentino, Maria Lucia;
    • Connolly, Anne M.;
    • Bahr, Angela
    Publication type:
    Article
    35

    Did the GJB2 35delG mutation originate in Iran?

    Published in:
    American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 10, p. 2453, doi. 10.1002/ajmg.a.34225
    By:
    • Norouzi, Vahideh;
    • Azizi, Hiva;
    • Fattahi, Zohreh;
    • Esteghamat, Fatemehsadat;
    • Bazazzadegan, Niloofar;
    • Nishimura, Carla;
    • Nikzat, Nooshin;
    • Jalalvand, Khadijeh;
    • Kahrizi, Kimia;
    • Smith, Richard. J. H.;
    • Najmabadi, Hossein
    Publication type:
    Article
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    Distinct genetic variation and heterogeneity of the Iranian population.

    Published in:
    PLoS Genetics, 2019, v. 15, n. 9, p. 1, doi. 10.1371/journal.pgen.1008385
    By:
    • 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
    Publication type:
    Article
    38

    Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.

    Published in:
    NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0
    By:
    • 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
    Publication type:
    Article
    39

    Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.

    Published in:
    NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00393-0
    By:
    • 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
    Publication type:
    Article