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Parkinson’s Disease in Saudi Patients: A Genetic Study
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.
Published in PloS one (14.08.2015)
Published in PloS one (14.08.2015)
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Journal Article
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
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.
Published in BMC research notes (07.06.2016)
Published in BMC research notes (07.06.2016)
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Journal Article
Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease
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
Published in Molecular genetics and metabolism reports (01.06.2017)
Published in Molecular genetics and metabolism reports (01.06.2017)
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Journal Article
A New Susceptibility Locus for Myocardial Infarction, Hypertension, Type 2 Diabetes Mellitus, and Dyslipidemia on Chromosome 12q24
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
Published in Disease markers (01.01.2014)
Published in Disease markers (01.01.2014)
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Journal Article
A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits
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
Published in Gene (10.07.2014)
Published in Gene (10.07.2014)
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Journal Article
Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel
Al-Hamed, Mohamed H, Kurdi, Wesam, Alsahan, Nada, Alabdullah, Zainab, Abudraz, Rania, Tulbah, Maha, Alnemer, Maha, Khan, Rubina, Al-Jurayb, Haya, Alahmed, Ahmed, Tahir, Asma I, Khalil, Dania, Edwards, Noel, Al Abdulaziz, Basma, Binhumaid, Faisal S, Majid, Salma, Faquih, Tariq, El-Kalioby, Mohamed, Abouelhoda, Mohamed, Altassan, Nada, Monies, Dorota, Meyer, Brian, Sayer, John A, Albaqumi, Mamdouh
Published in Journal of medical genetics (01.05.2016)
Published in Journal of medical genetics (01.05.2016)
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Journal Article
Thymic Stromal Lymphopoietin (TSLP) gene variant rs1837253 is significantly associated with Asthma prevalence in Pakistani Pashtun women
Afzal, Sibtain, Ramzan, Khushnooda, Khan, Ihsanullah, Ullah, Anhar, Tahir, Asma I, Ramzan, Shaiqa, Ullah, Sajjad, Jamal, Arshad, Absar, Muhammad, Basit, Sulman, Waqar, Ahmed Bilal
Published in Pakistan journal of pharmaceutical sciences (01.11.2020)
Published in Pakistan journal of pharmaceutical sciences (01.11.2020)
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Journal Article
Association of the angiotensinogen gene polymorphism with atherosclerosis and its risk traits in the Saudi population
Al-Najai, Mohammed, Muiya, Paul, Tahir, Asma I, Elhawari, Samar, Gueco, Daisy, Andres, Editha, Mazhar, Nejat, Altassan, Nada, Alshahid, Maie, Dzimiri, Nduna
Published in BMC cardiovascular disorders (11.03.2013)
Published in BMC cardiovascular disorders (11.03.2013)
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Journal Article
The Affymetrix DMET Plus Platform Reveals Unique Distribution of ADME-Related Variants in Ethnic Arabs
Dzimiri, Nduna, Morahan, Grant, Tahir, Asma I., Baz, Batoul, Lykowska-Tarnowska, Agnieszka, Andres, Editha, Muiya, Nzioka P., Nguyen, Cao, Wakil, Salma M., Meyer, Brian F.
Published in Disease markers (01.01.2015)
Published in Disease markers (01.01.2015)
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Journal Article
ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population
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
Published in European journal of medical genetics (01.05.2014)
Published in European journal of medical genetics (01.05.2014)
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Journal Article
Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection
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.
Published in Genes (22.05.2018)
Published in Genes (22.05.2018)
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Journal Article
The 3′-UTR of the adiponectin Q gene harbours susceptibility loci for atherosclerosis and its metabolic risk traits
Muiya, Nzioka, Al-Najai, Mohammed, Tahir, Asma I, Elhawari, Samar, Gueco, Daisy, Andres, Editha, Mazhar, Nejat, Altassan, Nada, Meyer, Brian F, Alshahid, Maie, Dzimiri, Nduna
Published in BMC genetics (13.12.2013)
Published in BMC genetics (13.12.2013)
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Journal Article
A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders
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
Published in Human genomics (12.12.2013)
Published in Human genomics (12.12.2013)
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Journal Article
Variable β-globin haplotypes in Saudi β thalassemia population
Shinwari, Jameela, Alshehri, Tahani, Tahir, Asma I., Jefri, Abdullah Al, AlMomen, Abdulkareem, Bakheet, Dana, AlAnazi, Mohammad, Warsy, Arjumand, Tassan, Nada Al
Published in Open journal of genetics (01.08.2013)
Published in Open journal of genetics (01.08.2013)
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Journal Article
Validation of Ion Torrent TM Inherited Disease Panel with the PGM TM Sequencing Platform for Rapid and Comprehensive Mutation Detection
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
Published in Genes (22.05.2018)
Published in Genes (22.05.2018)
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Journal Article