Biallelic PTRHD1 Frameshift Variants Associated with Intellectual Disability, Spasticity, and Parkinsonism von Al‐Kasbi, Ghalia, Al‐Saegh, Abeer, Al‐Qassabi, Ahmed, Al‐Jabry, Tariq, Zadjali, Fahad, Al‐Yahyaee, Said, Al‐Maawali, Almundher

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The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families von Al-Kasbi, Ghalia, Al-Murshedi, Fathiya, Al-Kindi, Adila, Al-Hashimi, Nadia, Al-Thihli, Khalid, Al-Saegh, Abeer, Al-Futaisi, Amna, Al-Mamari, Watfa, Al-Asmi, Abdullah, Bruwer, Zandre, Al-Kharusi, Khalsa, Al-Rashdi, Samiya, Zadjali, Fahad, Al-Yahyaee, Said, Al-Maawali, Almundher

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Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene von Hertecant, Jozef L, Ben-Rebeh, Imen, Marah, Muhaned A, Abbas, Thikra, Ayadi, Leila, Ben Salem, Salma, Al-Jasmi, Fatma A, Al-Gazali, Lihadh, Al-Yahyaee, Said A, Ali, Bassam R

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Consanguinity, Endogamy and Inborn Errors of Metabolism in Oman: A Cross-Sectional Study von Al-Thihli, Khalid, Al-Murshedi, Fathiya, Al-Hashmi, Nadia, Al-Mamari, Watfa, Islam, M. Mazharul, Al-Yahyaee, Said A.

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Novel Mutation of GLRA1 in Omani Families With Hyperekplexia and Mild Mental Retardation von Al-Futaisi, Amna Mohammed, MD, Al-Kindi, Mohammed Nasser, BSc, Al-Mawali, Al-Mundher, MD, Koul, Roshan Lal, MD, Al-Adawi, Samir, PhD, Al-Yahyaee, Said Ali, PhD

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Familial Clustering of Type 2 Diabetes among Omanis von Al-Shafaee , Mohammed, Al-Mamari , Ali, Bayoumi , Riad, Al-Sinani , Sawsan, Jaju , Deepali, Al-Abri , Mohammed, Hassan , Mohammed, Al-Hashmi , Khamis, Al-Shafie , Omaima, Woodhouse , Nicholas, Al-Yahyaee , Said, Albarwani , Sulayma, Rizvi , Syed

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Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families von Pei, Weidong, Baron, Heike, Müller-Myhsok, Bertram, Knoblauch, Hans, Ali Al-Yahyaee, Said, Hui, Rutai, Wu, Xigui, Liu, Lisheng, Busjahn, Andreas, Luft, Friedrich C, Schuster, Herbert

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Impaired Fasting Glucose in Omani Adults with no Family History of Type 2 Diabetes von Al-Shafaee , Mohammed, Al-Mamari , Ali, Bayoumi , Riad, Al-Sinani , Sawsan, Jaju , Deepali, Al-Abri , Mohammed, Woodhouse , Nicolas, Al-Hashmi , Khamis, Hassan , Mohammed O, El-Shafie , Omayma, Al-Yahyaee , Said, Albarwani , Sulayma, Rizvi , Syed

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Clinical and molecular analysis of Grebe acromesomelic dysplasia in an Omani family von Al-Yahyaee, Said Ali S., Al-Kindi, Mohammed Nasser, Habbal, Omar, Kumar, Dilip Sankhla

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N-Acetyltransferase Polymorphism Among Northern Sudanese von Al-Yahyaee, Said, Gaffar, Uzma, Al-Ameri, Maryam M., Qureshi, Mansoor, Zadjali, Fahad, Ali, Baderldin H., Bayoumi, Riad

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Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population von Ben-Rebeh, Imen, Hertecant, Jozef L, Al-Jasmi, Fatma A, Aburawi, Hanan E, Al-Yahyaee, Said A, Al-Gazali, Lihadh, Ali, Bassam R

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Lipids-risk categories in Omani type 2 diabetics : impact of the National Cholesterol Educational Program von al-Bahrani, Ali I., Bayyumi, Riyad, al-Yahyaee, Said A.

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Interleukin-1β gene (IL-1B) and interleukin 1 receptor antagonist gene (IL-1RN) polymorphisms and gastric cancer risk in an Omani Arab population von Al-Moundhri, Mansour S., Al-Nabhani, Mariam, Al-Bahrani, Bassim, Burney, Ikram A., Al-Madhani, Ali, Ganguly, Shym S., Al-Yahyaee, Said A., Grant, Christopher S.

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Association of gene variants with susceptibility to type 2diabetes among Omanis von Sawsan Al-Sinani Nicolas Woodhouse Ali Al-Mamari Omaima Al-Shafie Mohammed Al-Shafaee Said Al-Yahyaee Mohammed Hassan Deepali Jaju Khamis Al-Hashmi Mohammed Al-Abri Khalid Al-Rassadi Syed Rizvi Yengo Loic Philippe Froguel Riad Bayoumi

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A potential role of apolipoprotein B in the risk stratification of diabetic patients with dyslipidaemia von Al-Bahrani, Ali I., Bakhiet, Charles S., Bayoumi, Riad A., Al-Yahyaee, Said A.

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Cell Targeting of a Pore-Forming Toxin, CytA δ-Endotoxin from Bacillus thuringiensis Subspecies israelensis, by Conjugating CytA with Anti-Thy 1 Monoclonal Antibodies and Insulin von Al-yahyaee, Said A. S, Ellar, David J

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Apolipoprotein E Polymorphism in Omani Dyslipidemic Patients With and Without Coronary Artery Disease von Al-Yahyaee, Said Ali S., Ganguly, Shyam Sundar, Al-Kindi, Mohammed Nasser, Al-Bahrani, Ali Ihassan

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ApolipoproteinA1-75 G/A (M1-) polymorphism and lipoprotein(a); anti- vs. pro-Atherogenic properties von Albahrani, Ali I, Usher, Jannete J, Alkindi, Mohammed, Marks, Eileen, Ranganath, L, Al-yahyaee, Said

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Apolipoprotein A1 Gene Polymorphisms at the — 75 bp and + 83/84 bp Polymorphic Sites in Healthy Omanis Compared with World Populations von AL-YAHYAEE, SAID ALI S., AL-KINDI, MOHAMMED NASSER, ALBAHRANI, ALI IHSAN

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Isochromosome 9q as a sole anomaly in an Omani boy with acute lymphoblastic leukaemia von Achandira, Udayakumar Muthappa, Pathare, Anil V, Kindi, Salam Al, Dennison, David, Yahyaee, Said Al

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