Works by Naeem, Muhammad Asif


Results: 65
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    Mutations in FYCO1 identified in families with congenital cataracts.

    Published in:
    Molecular Vision, 2020, v. 26, p. 334
    By:
    • Iqbal, Hira;
    • Khan, Shahid Y.;
    • Lin Zhou;
    • Irum, Bushra;
    • Ali, Muhammad;
    • Ahmed, Mariya R.;
    • Shahzad, Mohsin;
    • Ali, Muhammad Hassaan;
    • Naeem, Muhammad Asif;
    • Riazuddin, Sheikh;
    • Hejtmancik, J. Fielding;
    • Riazuddin, S. Amer
    Publication type:
    Article
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    Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.

    Published in:
    PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0167562
    By:
    • Irum, Bushra;
    • Khan, Shahid Y.;
    • Ali, Muhammad;
    • Daud, Muhammad;
    • Kabir, Firoz;
    • Rauf, Bushra;
    • Fatima, Fareeha;
    • Iqbal, Hira;
    • Khan, Arif O.;
    • Al Obaisi, Saif;
    • Naeem, Muhammad Asif;
    • Nasir, Idrees A.;
    • Khan, Shaheen N.;
    • Husnain, Tayyab;
    • Riazuddin, Sheikh;
    • Akram, Javed;
    • Eghrari, Allen O.;
    • Riazuddin, S. Amer
    Publication type:
    Article
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    Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.

    Published in:
    PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0162620
    By:
    • Irum, Bushra;
    • Khan, Shahid Y.;
    • Ali, Muhammad;
    • Kaul, Haiba;
    • Kabir, Firoz;
    • Rauf, Bushra;
    • Fatima, Fareeha;
    • Nadeem, Raheela;
    • Khan, Arif O.;
    • Al Obaisi, Saif;
    • Naeem, Muhammad Asif;
    • Nasir, Idrees A.;
    • Khan, Shaheen N.;
    • Husnain, Tayyab;
    • Riazuddin, Sheikh;
    • Akram, Javed;
    • Eghrari, Allen O.;
    • Riazuddin, S. Amer
    Publication type:
    Article
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    A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomes.

    Published in:
    Human Genetics, 2021, v. 140, n. 4, p. 649, doi. 10.1007/s00439-020-02238-z
    By:
    • Ali, Muhammad;
    • Khan, Shahid Y.;
    • Rodrigues, Tony A.;
    • Francisco, Tânia;
    • Jiao, Xiaodong;
    • Qi, Hang;
    • Kabir, Firoz;
    • Irum, Bushra;
    • Rauf, Bushra;
    • Khan, Asma A.;
    • Mehmood, Azra;
    • Naeem, Muhammad Asif;
    • Assir, Muhammad Zaman;
    • Ali, Muhammad Hassaan;
    • Shahzad, Mohsin;
    • Abu-Amero, Khaled K.;
    • Akram, Shehla Javed;
    • Akram, Javed;
    • Riazuddin, Sheikh;
    • Riazuddin, Saima
    Publication type:
    Article
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    Mutations in CERKL and RP1 cause retinitis pigmentosa in Pakistani families.

    Published in:
    Human Genome Variation, 2020, v. 7, n. 1, p. 1, doi. 10.1038/s41439-020-0100-8
    By:
    • Nadeem, Raheela;
    • Kabir, Firoz;
    • Li, Jiali;
    • Gradstein, Libe;
    • Jiao, Xiaodong;
    • Rauf, Bushra;
    • Naeem, Muhammad Asif;
    • Assir, Muhammad Zaman;
    • Riazuddin, Sheikh;
    • Ayyagari, Radha;
    • Hejtmancik, J. Fielding;
    • Riazuddin, S. Amer
    Publication type:
    Article
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    Whole genome sequencing data of multiple individuals of Pakistani descent.

    Published in:
    Scientific Data, 2020, v. 7, n. 1, p. N.PAG, doi. 10.1038/s41597-020-00664-2
    By:
    • Khan, Shahid Y.;
    • Ali, Muhammad;
    • Lee, Mei-Chong W.;
    • Ma, Zhiwei;
    • Biswas, Pooja;
    • Khan, Asma A.;
    • Naeem, Muhammad Asif;
    • Riazuddin, Saima;
    • Riazuddin, Sheikh;
    • Ayyagari, Radha;
    • Hejtmancik, J. Fielding;
    • Riazuddin, S. Amer
    Publication type:
    Article
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