Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder

Por Shinwari, Jameela M.A., Al Yemni, Eman A.A., Alnaemi, Faten M., Abebe, Dejene, Al-Abdulaziz, Basma S., Al Mubarak, Bashayer R., Ghaziuddin, Mohammad, Al Tassan, Nada A.
Publicado no Psychiatr Genet (2017)

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

Por 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.
Publicado no BMC Res Notes (2016)

Parkinson’s Disease in Saudi Patients: A Genetic Study

Por 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.
Publicado no PLoS One (2015)

Validation of Ion Torrent(TM) Inherited Disease Panel with the PGM(TM) Sequencing Platform for Rapid and Comprehensive Mutation Detection

Por 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.
Publicado no Genes (Basel) (2018)