Exome sequencing in high and low fetal haemoglobin Arab–Indian haplotype sickle cell disease von Alnafie, Awatif N., Alateeq, Suad A., Al‐Muhanna, Fahad A., Alsulaiman, Ahmed M., Alfarhan, Mohammed, Buali, Waleed, Vatte, Chitti Babu, Cyrus, Cyril, Keating, Brendan, Al‐Ali, Amein K., Steinberg, Martin H

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Sickle cell disease in the Eastern Province of Saudi Arabia: Clinical and laboratory features von Al‐Ali, Amein K., Alsulaiman, Ahmed, Alfarhan, Mohammed, Safaya, Surinder, Vatte, Chitti Babu, Albuali, Waleed M., Qutub, Hatem O., Alzahrani, Alhusain J., Milton, Jacqueline N., Steinberg, Martin H.

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Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population von AbdulAzeez, Sayed, Al-Nafie, Awatif N, Al-Shehri, Abdullah, Borgio, J Francis, Baranova, Ekaterina V, Al-Madan, Mohammed S, Al-Ali, Rudaynah A, Al-Muhanna, Fahad, Al-Ali, Abdullah, Al-Mansori, Mohammed, Ibrahim, Mohammed Fakhry, Asselbergs, Folkert W, Keating, Brendan, Koeleman, Bobby P C, Al-Ali, Amein K

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Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign von Alsultan, Abdulrahman, Alabdulaali, Mohammed K., Griffin, Paula J., AlSuliman, Ahmed M., Ghabbour, Hazem A., Sebastiani, Paola, Albuali, Waleed H., Al‐Ali, Amein K., Chui, David H. K., Steinberg, Martin H.

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Gut microbiota analyses of inflammatory bowel diseases from a representative Saudi population von Alsulaiman, Raed M, Al-Quorain, Abdulaziz A, Al-Muhanna, Fahad A, Piotrowski, Stanley, Kurdi, Ezzeddin A, Vatte, Chittibabu, Alquorain, Ahmed A, Alfaraj, Noorah H, Alrezuk, Abdulaziz M, Robinson, Fred, Dowdell, Alexa K, Alamri, Turki A, Hamilton, Lauren, Lad, Hetal, Gao, Hui, Gandla, Divya, Keating, Brendan J, Meng, Ryan, Piening, Brian, Al-Ali, Amein K

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Lack of MERS coronavirus neutralizing antibodies in humans, eastern province, Saudi Arabia von Gierer, Stefanie, Hofmann-Winkler, Heike, Albuali, Waleed H, Bertram, Stephanie, Al-Rubaish, Abdullah M, Yousef, Abdullah A, Al-Nafaie, Awatif N, Al-Ali, Amein K, Obeid, Obeid E, Alkharsah, Khaled R, Pöhlmann, Stefan

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Comparative and molecular analysis of MRSA isolates from infection sites and carrier colonization sites von Alkharsah, Khaled R, Rehman, Suriya, Alkhamis, Fatimah, Alnimr, Amani, Diab, Asim, Al-Ali, Amein K

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Whole-exome sequencing of a Saudi epilepsy cohort reveals association signals in known and potentially novel loci von Al Anazi, Abdulrahman H, Ammar, Ahmed S, Al-Hajj, Mahmoud, Cyrus, Cyril, Aljaafari, Danah, Khoda, Iname, Abdelfatah, Ahmed K, Alsulaiman, Abdullah A, Alanazi, Firas, Alanazi, Rawan, Gandla, Divya, Lad, Hetal, Barayan, Samar, Keating, Brendan J, Al-Ali, Amein K

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Uncovering myocardial infarction genetic signatures using GWAS exploration in Saudi and European cohorts von Al-Ali, Amein K., Al-Rubaish, Abdullah M., Alali, Rudaynah A., Almansori, Mohammed S., Al-Jumaan, Mohammed A., Alshehri, Abdullah M., Al-Madan, Mohammed S., Vatte, ChittiBabu, Cherlin, Tess, Young, Sylvia, Verma, Shefali S., Morahan, Grant, Koeleman, Bobby P. C., Keating, Brendan J.

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Gut microbiota analyses of Saudi populations for type 2 diabetes-related phenotypes reveals significant association von Al-Muhanna, Fahad A, Dowdell, Alexa K, Al Eleq, Abdulmohsen H, Albaker, Waleed I, Brooks, Andrew W, Al-Sultan, Ali I, Al-Rubaish, Abdullah M, Alkharsah, Khaled R, Sulaiman, Raed M, Al-Quorain, Abdulaziz A, Cyrus, Cyril, Alali, Rudaynah A, Vatte, Chittibabu, Robinson, Fred L, Zhou, Xin, Snyder, Michael P, Almuhanna, Afnan F, Keating, Brendan J, Piening, Brian D, Al-Ali, Amein K

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A phased SNP-based classification of sickle cell anemia HBB haplotypes von Shaikho, Elmutaz M, Farrell, John J, Alsultan, Abdulrahman, Qutub, Hatem, Al-Ali, Amein K, Figueiredo, Maria Stella, Chui, David H K, Farrer, Lindsay A, Murphy, George J, Mostoslavsky, Gustavo, Sebastiani, Paola, Steinberg, Martin H

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Elevated plasma level of the glycolysis byproduct methylglyoxal on admission is an independent biomarker of mortality in ICU COVID-19 patients von Alomar, Fadhel A., Alshakhs, Marai N., Abohelaika, Salah, Almarzouk, Hassan M., Almualim, Mohammed, Al-Ali, Amein K., Al-Muhanna, Fahad, Alomar, Mohammed F., Alhaddad, Mousa J., Almulaify, Mohammed S., Alessa, Faisal S., Alsalman, Ahmed S., Alaswad, Ahmed, Bidasee, Sean R., Alsaad, Hassan A., Alali, Rudaynah A., AlSheikh, Mona H., Akhtar, Mohammed S., Al Mohaini, Mohammed, Alsalman, Abdulkhaliq J., Alturaifi, Hussain, Bidasee, Keshore R.

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Association of MBL2 Gene Polymorphism with Dental Caries in Saudi Children von Alyousef, Yousef M., Borgio, J. Francis, AbdulAzeez, Sayed, Al-Masoud, Naif, Al-Ali, Ali A., Al-Shwaimi, Emad, Al-Ali, Amein K.

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Oral microbiota analyses of paediatric Saudi population reveals signatures of dental caries von Alyousef, Yousef M, Piotrowski, Stanley, Alonaizan, Faisal A, Alsulaiman, Ahmed, Alali, Ali A, Almasood, Naif N, Vatte, Chittibabu, Hamilton, Lauren, Gandla, Divya, Lad, Hetal, Robinson, Fred L, Cyrus, Cyril, Meng, Ryan C, Dowdell, Alexa, Piening, Brian, Keating, Brendan J, Al-Ali, Amein K

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Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA2 in β-thalassaemia carriers von Cyrus, Cyril, Vatte, Chittibabu, Chathoth, Shahanas, Sayed, Abdul Azeez, Borgio, J. Francis, Alrubaish, Mohammed Abdullah, Alfalah, Rawan, Alsaikhan, Jana, Ali, Amein K. Al

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Influence of vitamin D levels on bone mineral density and osteoporosis von Sadat-Ali, Mir, Al Elq, Abdulmohsen H, Al-Turki, Haifa A, Al-Mulhim, Fathma A, Al-Ali, Amein K

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A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia von Vathipadiekal, Vinod, Farrell, John J., Wang, Shuai, Edward, Heather L., Shappell, Heather, Al‐Rubaish, A.M., Al‐Muhanna, Fahad, Naserullah, Z., Alsuliman, A., Qutub, Hatem Othman, Simkin, Irene, Farrer, Lindsay A., Jiang, Zhihua, Luo, Hong‐Yuan, Huang, Shengwen, Mostoslavsky, Gustavo, Murphy, George J., Patra, Pradeep K., Chui, David H.K., Alsultan, Abdulrahman, Al‐Ali, Amein K., Sebastiani, Paola, Steinberg, Martin H.

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Genome-wide copy number variant screening of Saudi schizophrenia patients reveals larger deletions in cases versus controls von Abumadini, Mahdi S, Al Ghamdi, Kholoud S, Alqahtani, Abdullah H, Almedallah, Dana K, Callans, Lauren, Jarad, Jumanah A, Cyrus, Cyril, Koeleman, Bobby P C, Keating, Brendan J, Pankratz, Nathan, Al-Ali, Amein K

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The role of MicroRNA as a potential diagnostic and prognostic biomarker for cerebral aneurysms von Al-Jehani, Hosam M, Turkistani, Alaa N, Alrayes, Majd M, AlHamid, May A, AlShamikh, Arwa S, Al Sadah, Zhra M, Alabbas, Faisal M, Cyrus, Cyril, Al-Ali, Amein K

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Tyrosine kinase domain mutations of EGFR gene in head and neck squamous cell carcinoma von Vatte, Chittibabu, Al Amri, Ali M, Cyrus, Cyril, Chathoth, Shahanas, Acharya, Sadananda, Hashim, Tariq Mohammad, Al Ali, Zhara, Alshreadah, Saleh Tawfeeq, Alsayyah, Ahmed, Al-Ali, Amein K

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