Works by Najafipour, Reza


Results: 44
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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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    The PTRHD1 Mutation in Intellectual Disability.

    Published in:
    Archives of Iranian Medicine (AIM), 2021, v. 24, n. 10, p. 747, doi. 10.34172/aim.2021.110
    By:
    • Cheraghi, Sara;
    • Moghbelinejad, Sahar;
    • Najmabadi, Hossein;
    • Kahrizi, Kimia;
    • Najafipour, Reza
    Publication type:
    Article
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    Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.

    Published in:
    Clinical Genetics, 2024, v. 105, n. 6, p. 611, doi. 10.1111/cge.14491
    By:
    • Mehvari, Sepideh;
    • Karimian Fathi, Nahid;
    • Saki, Sara;
    • Asadnezhad, Maryam;
    • Arzhangi, Sanaz;
    • Ghodratpour, Fatemeh;
    • Mohseni, Marzieh;
    • Zare Ashrafi, Farzane;
    • Sadeghian, Saeed;
    • Boroumand, Mohammadali;
    • Shokohizadeh, Fatemeh;
    • Rostami, Elham;
    • Boroumand, Rahnama;
    • Najafipour, Reza;
    • Malekzadeh, Reza;
    • Riazalhosseini, Yasser;
    • Akbari, Mohammadreza;
    • Lathrop, Mark;
    • Najmabadi, Hossein;
    • Hosseini, Kaveh
    Publication type:
    Article
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    Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

    Published in:
    Human Molecular Genetics, 2015, v. 24, n. 20, p. 5697, doi. 10.1093/hmg/ddv286
    By:
    • Heidari, Abolfazl;
    • Chanakan Tongsook;
    • Najafipour, Reza;
    • Musante, Luciana;
    • Vasli, Nasim;
    • Garshasbi, Masoud;
    • Hao Hu;
    • Mittal, Kirti;
    • McNaughton, Amy J. M.;
    • Sritharan, Kumudesh;
    • Hudson, Melissa;
    • Stehr, Henning;
    • Talebi, Saeid;
    • Moradi, Mohammad;
    • Darvish, Hossein;
    • Rafiq, Muhammad Arshad;
    • Mozhdehipanah, Hossein;
    • Rashidinejad, Ali;
    • Samiei, Shahram;
    • Ghadami, Mohsen
    Publication type:
    Article
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    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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