Whole Exome Sequencing Reveals Multiple Mutations in Uncommon Genes of Familial Hypercholesterolaemia von Athar, Mohammad, Al-Allaf, Faisal Ahmed, Alnouri, Fahad, Taher, Mohiuddin Mohammed, Bouazzaoui, Abdellatif, Bogari, Neda Mustafa, Elbjeirami, Wafa Mohammed, Faidah, Hani Saleh, Abduljaleel, Zainularifeen

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Influence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome von Bogari, Neda M, Naffadi, Hind Mansour, Babalghith, Ahmad O., Azher, Zohor Asaad, Abumansour, Iman Sabri, Melibary, Ehab M., Qattan, Muneera, Alluhaibi, Amaal M., Amin, Amr A, Bogari, Mustafa, Bogari, Dema Neda, Obaid, Rami, Allam, Reem M

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Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population von Bogari, Neda M., Aljohani, Ashwag, Dannoun, Anas, Elkhateeb, Osama, Porqueddu, Masimo, Amin, Amr A., Bogari, Dema N., Taher, Mohiuddin M., Buba, Faruk, Allam, Reem M., Bogari, Mustafa N., Alamanni, Francesco

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Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema von Bogari, Neda M., Amin, Amr A., Rayes, Husni H., Abdelmotelb, Ahmed, Al-Allaf, Faisal A., Dannoun, Anas, Al-Amodi, Hiba S., Sedayo, Anas A., Almalk, Hilal, Moulana, Amna, Balkhair, Rania, Jambi, Fatma, Madani, Fakhriah, Abutalib, Mwafaq, Taher, Mohiuddin M., Bouazzaoui, Abdellatif, Aljohani, Ashwag, Bogari, Mustafa N., G.K., Udaya Raja, Fawzy, Ahmed, Alharbi, Khalid Khalaf, Ali Khan, Imran

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