Now showing items 1-10 of 12
| Title | Author | Publication Date | Publisher | Type |
|---|---|---|---|---|
| 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 Doss | 2018 | Elsevier | Article |
| Breast cancer in the GCC countries: A focus on BRCA1/2 and non-BRCA1/2 genes. | Rahman, Sumaya; Zayed, Hatem | 2018 | Elsevier | Article |
| 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 authors | 2018 | BMC | Article |
| 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 authors | 2018 | Wiley | Article |
| 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 authors | 2018 | Wiley | Article |
| 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 authors | 2018 | Wiley | Article |
| 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 authors | 2018 | Springer US | Article |
| 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 authors | 2018 | Elsevier | Article |
| Spectrum of mutations of familial hypercholesterolemia in the 22 Arab countries. | Alhababi, Dalal; Zayed, Hatem | 2018 | Elsevier | Article |
| 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, Hatem | 2018 | Springer | Article |
