Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experience by Al‐Dewik, Nader, Mohd, Howaida, Al‐Mureikhi, Mariam, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Shahbeck, Noora, El‐Akouri, Karen, Almulla, Mariam, Al Sulaiman, Reem, Musa, Sara, Al‐Marri, Ajayeb Al‐Nabet, Richard, Gabriele, Juusola, Jane, Solomon, Benjamin D., Alkuraya, Fowzan S., Ben‐Omran, Tawfeg

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Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in DCAF17: Report of 58 additional patients from Qatar and literature review by Ali, Rehab, Al‐Dewik, Nader, Mohammed, Shayma, Elfituri, Mahmud, Agouba, Sahar, Musa, Sara, Mahmoud, Laila, Almulla, Mariam, El‐Akouri, Karen, Mohd, Howaida, Bux, Reem, Almulla, Hajer, Othman, Amna, Al‐Mesaifri, Fatma, Shahbeck, Noora, Al‐Muriekhi, Mariam, Khalifa, Amal, Al‐Sulaiman, Reem, Ben‐Omran, Tawfeg

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A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families by Al‐Sulaiman, Reem, Othman, Amna, El‐Akouri, Karen, Fareed, Shehab, AlMulla, Hajer, Sukik, Aseel, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Musa, Sara, Al‐Mulla, Mariam, Ibrahim, Khalid, Mohamed, Khalid, Al‐Nesef, Maryam Ali, Ehlayel, Mohammad, Ben‐Omran, Tawfeg

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Clinical genetics and genomic medicine in Qatar by Al‐Dewik, Nader, Al‐Mureikhi, Mariam, Shahbeck, Noora, Ali, Rehab, Al‐Mesaifri, Fatma, Mahmoud, Laila, Othman, Amna, AlMulla, Mariam, Sulaiman, Reem Al, Musa, Sara, Abdoh, Ghassan, El‐Akouri, Karen, Solomon, Benjamin D., Ben‐Omran, Tawfeg

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Natural history, with clinical, biochemical, and molecular characterization of classical homocystinuria in the Qatari population by Al‐Dewik, Nader, Ali, Alaa, Mahmoud, Yassmin, Shahbeck, Noora, Ali, Rehab, Mahmoud, Laila, Al‐Mureikhi, Mariam, Al‐Mesaifri, Fatma, Musa, Sara, El‐Akouri, Karen, Almulla, Mariam, Al Saadi, Reem, Nasrallah, Gheyath K., Samara, Muthanna, Abdoh, Ghassan, Rifai, Hilal Al, Häberle, Johannes, Thöny, Beat, Kruger, Warren, Blom, Henk J., Ben‐Omran, Tawfeg

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A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients by Musa, Sara, Eyaid, Wafaa, Kamer, Kimberli, Ali, Rehab, Al-Mureikhi, Mariam, Shahbeck, Noora, Al Mesaifri, Fatma, Makhseed, Nawal, Mohamed, Zakkiriah, AlShehhi, Wafaa Ali, Mootha, Vamsi K., Juusola, Jane, Ben-Omran, Tawfeg

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High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders by Yavarna, Tarunashree, Al-Dewik, Nader, Al-Mureikhi, Mariam, Ali, Rehab, Al-Mesaifri, Fatma, Mahmoud, Laila, Shahbeck, Noora, Lakhani, Shenela, AlMulla, Mariam, Nawaz, Zafar, Vitazka, Patrik, Alkuraya, Fowzan S., Ben-Omran, Tawfeg

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Gene therapy for spinal muscular atrophy: the Qatari experience by Ali, Hossamaldein Gaber, Ibrahim, Khalid, Elsaid, Mahmoud Fawzi, Mohamed, Reem Babiker, Abeidah, Mahmoud I. A., Al Rawwas, Azhar Othman, Elshafey, Khaled, Almulla, Hajer, El-Akouri, Karen, Almulla, Mariam, Othman, Amna, Musa, Sara, Al-Mesaifri, Fatma, Ali, Rehab, Shahbeck, Noora, Al-Mureikhi, Mariam, Alsulaiman, Reem, Alkaabi, Saad, Ben-Omran, Tawfeg

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Incorporating Haptic and Olfactory into Surgical Simulation by Halabi, Osama, Al-Mesaifri, Fatma, Al-Ansari, Mariam, Al-Shaabi, Roqaya, Barki, Hichem, Foufou, Sebti

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