Nutrition Professionals’ Knowledge Towards Dietary Nitrate in Jeddah, Saudi Arabia: A Cross-Sectional Study von Albathi, Fatmah, Al tassan, Asma, Hadadd, Azizah, Alzahrany, Aljazi, Alqurashi, Hadeel, Basaqr, Reem

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Recessive Mutations in COL25A1 Are a Cause of Congenital Cranial Dysinnervation Disorder von Shinwari, Jameela M.A., Khan, Arif, Awad, Salma, Shinwari, Zakia, Alaiya, Ayodele, Alanazi, Mohamad, Tahir, Asma, Poizat, Coralie, Al Tassan, Nada

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Parkinson's Disease in Saudi Patients: A Genetic Study von Al-Mubarak, Bashayer R, Bohlega, Saeed A, Alkhairallah, Thamer S, Magrashi, Amna I, AlTurki, Maha I, Khalil, Dania S, AlAbdulaziz, Basma S, Abou Al-Shaar, Hussam, Mustafa, Abeer E, Alyemni, Eman A, Alsaffar, Bashayer A, Tahir, Asma I, Al Tassan, Nada A

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Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families von Al-Mubarak, Bashayer, Abouelhoda, Mohamed, Omar, Aisha, AlDhalaan, Hesham, Aldosari, Mohammed, Nester, Michael, Alshamrani, Hussain. A., El-Kalioby, Mohamed, Goljan, Ewa, Albar, Renad, Subhani, Shazia, Tahir, Asma, Asfahani, Sultana, Eskandrani, Alaa, Almusaiab, Ahmed, Magrashi, Amna, Shinwari, Jameela, Monies, Dorota, Al Tassan, Nada

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Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families von Bohlega, Saeed A, Al-Mubarak, Bashayer R, Alyemni, Eman A, Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer E, Khalil, Dania S, Al Haibi, Sara, Abou Al-Shaar, Hussam, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma I, Al Tassan, Nada A

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A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24 von Wakil, Salma M., Muiya, Nzioka P., Tahir, Asma I., al-Najai, Mohammed, Baz, Batoul, Andres, Editha, Mazhar, Nejat, al-Tassan, Nada, Alshahid, Maie, Meyer, Brian F., Dzimiri, Nduna

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Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection von Mustafa, Abeer, Faquih, Tariq, Baz, Batoul, Kattan, Rana, Al-Issa, Abdulelah, Tahir, Asma, Imtiaz, Faiqa, Ramzan, Khushnooda, Al-Sayed, Moeenaldeen, Alowain, Mohammed, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Abouelhoda, Mohamed, Al-Mubarak, Bashayer, Al Tassan, Nada

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A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits von Muiya, Nzioka P., Wakil, Salma, Al-Najai, Mohammed, Tahir, Asma I., Baz, Batoul, Andres, Editha, Al-Boudari, Olyan, Al-Tassan, Nada, Al-Shahid, Maie, Meyer, Brian F., Dzimiri, Nduna

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Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease von Imtiaz, Faiqa, Al-Mostafa, Abeer, Allam, Rabab, Ramzan, Khushnooda, Al-Tassan, Nada, Tahir, Asma I., Al-Numair, Nouf S., Al-Hamed, Mohamed H., Al-Hassnan, Zuhair, Al-Owain, Mohammad, Al-Zaidan, Hamad, Al-Amoudi, Mohammad, Qari, Alya, Balobaid, Ameera, Al-Sayed, Moeenaldeen

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ILDR1 : Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population von Ramzan, Khushnooda, Taibah, Khalid, Tahir, Asma I, Al-Tassan, Nada, Berhan, Amal, Khater, Ahmed M, Al-Hazzaa, Selwa A.F, Al-Owain, Mohammed, Imtiaz, Faiqa

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Validation of Ion Torrent TM Inherited Disease Panel with the PGM TM Sequencing Platform for Rapid and Comprehensive Mutation Detection von Mustafa, Abeer E, Faquih, Tariq, Baz, Batoul, Kattan, Rana, Al-Issa, Abdulelah, Tahir, Asma I, Imtiaz, Faiqa, Ramzan, Khushnooda, Al-Sayed, Moeenaldeen, Alowain, Mohammed, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Abouelhoda, Mohamed, Al-Mubarak, Bashayer R, Al Tassan, Nada A

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A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders von Muiya, Nzioka P, Wakil, Salma M, Tahir, Asma I, Hagos, Samya, Najai, Mohammed, Gueco, Daisy, Al-Tassan, Nada, Andres, Editha, Mazher, Nejat, Meyer, Brian F, Dzimiri, Nduna

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Variable β-globin haplotypes in Saudi β thalassemia population von Shinwari, Jameela, Alshehri, Tahani, Tahir, Asma I., Jefri, Abdullah Al, AlMomen, Abdulkareem, Bakheet, Dana, AlAnazi, Mohammad, Warsy, Arjumand, Tassan, Nada Al

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TP53 genetic alterations in Arab breast cancer patients: Novel mutations, pattern and distribution von AL-QASEM, ABEER J, TOULIMAT, MOHAMED, ELDALI, ABDELMONEIM M, TULBAH, ASMA, AL-YOUSEF, NUJOUD, AL-DAIHAN, SOOAD K, AL-TASSAN, NADA, AL-TWEIGERI, TAHER, ABOUSSEKHRA, ABDELILAH

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MOESM1 of Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families von Bohlega, Saeed, Bashayer Al-Mubarak, Alyemni, Eman, Abouelhoda, Mohamed, Monies, Dorota, Mustafa, Abeer, Khalil, Dania, Haibi, Sara Al, Al-Shaar, Hussam Abou, Faquih, Tariq, El-Kalioby, Mohamed, Tahir, Asma, Tassan, Nada Al

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