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)

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)

Genetic spectrum of Saudi Arabian patients with antenatal cystic kidney disease and ciliopathy phenotypes using a targeted renal gene panel

Por 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
Publicado no J Med Genet (2016)