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    TitleAuthorPublication DatePublisherType
    Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot-Marie-tooth disease: A computational study. Agrahari, Ashish Kumar; Kumar, Amit; R, Siva; Zayed, Hatem; C, George Priya Doss2018ElsevierArticle
    Breast cancer in the GCC countries: A focus on BRCA1/2 and non-BRCA1/2 genes. Rahman, Sumaya; Zayed, Hatem2018ElsevierArticle
    Anaphylaxis triggers in a large tertiary care hospital in Qatar: a retrospective study Abunada, Taghreed; Al-Nesf, Maryam Ali; Thalib, Lukman; Kurdi, Rana; Khalil, Sally; ElKassem, Wessam; Mobayed, Hassan M; Zayed, Hatem... more authors ... less authors2018BMCArticle
    In silico and in vivo models for Qatari-Specific classical homocystinuria as basis for development of novel therapies. Ismail, Hesham M; Krishnamoorthy, Navaneethakrishnan; Al-Dewik, Nader; Zayed, Hatem; Mohamed, Nura A; Giacomo, Valeria Di; Gupta, Sapna; Häberle, Johannes; Thöny, Beat; Blom, Henk J; Kruger, Waren D; Ben-Omran, Tawfeg; Nasrallah, Gheyath K... more authors ... less authors2018WileyArticle
    Structural analysis of missense mutations in galactokinase 1 (GALK1) leading to galactosemia type-2. P, Sneha; Ebrahimi, Elaheh Ahmad; Ghazala, Sara Ahmed; D, Thirumal Kumar; R, Siva; Priya Doss C, George; Zayed, Hatem... more authors ... less authors2018WileyArticle
    Spectrum of mutations of cystic fibrosis in the 22 Arab countries: A systematic review. Al-Sadeq, Duaa; Abunada, Taghreed; Dalloul, Rajaa; Fahad, Sara; Taleb, Sara; Aljassim, Kholoud; Al Hamed, Fatima Alzahra; Zayed, Hatem... more authors ... less authors2018WileyArticle
    Computational approach to unravel the impact of missense mutations of proteins (D2HGDH and IDH2) causing D-2-hydroxyglutaric aciduria 2. Thirumal Kumar, D; Jerushah Emerald, L; George Priya Doss, C; Sneha, P; Siva, R; Charles Emmanuel Jebaraj, W; Zayed, Hatem... more authors ... less authors2018Springer USArticle
    Clinical Exome Sequencing unravels new disease-causing mutations in the myeloproliferative neoplasms: A pilot study in patients from the state of Qatar. Al-Dewik, Nader; Ben-Omran, Tawfeg; Zayed, Hatem; Trujillano, Daniel; Kishore, Shivendra; Rolfs, Arndt; Yassin, Mohamed A... more authors ... less authors2018ElsevierArticle
    Spectrum of mutations of familial hypercholesterolemia in the 22 Arab countries. Alhababi, Dalal; Zayed, Hatem2018ElsevierArticle
    Computational modelling approaches as a potential platform to understand the molecular genetics association between Parkinson's and Gaucher diseases. Thirumal Kumar, D; Eldous, Hend Ghasan; Mahgoub, Zainab Alaa; George Priya Doss, C; Zayed, Hatem2018SpringerArticle
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    Author
    • Zayed, Hatem (12)
    • George Priya Doss, C (3) Thirumal Kumar, D (3) Abunada, Taghreed (2) ... View More
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      Qatar (3) Variant classification (3) adenosine triphosphate (1) Allergy (1) ... View More
    Publication Date
    • 2018 (12)

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