Autism and ADHD in the Era of Big Data; An Overview of Digital Resources for Patient, Genetic and Clinical Trials Information

por Abomelha, Faris M., AlDhalaan, Hesham, Ghaziuddin, Mohammad, Al-Tassan, Nada A., Al-Mubarak, Bashayer R.
Publicado 2022

Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation

por Baxter, Paul S., Márkus, Nóra M., Dando, Owen, He, Xin, Al-Mubarak, Bashayer R., Qiu, Jing, Hardingham, Giles E.
Publicado 2021

PTPA variants and the risk for Parkinson’s disease in diverse ancestry populations

por Ostrožovičová, Miriam, Mecheri, Yasser, Al-Mubarak, Bashayer R, Al-Tassan, Nada, Makarious, Mary B, Periñan, Maria Teresa, Bandres-Ciga, Sara
Publicado 2023

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 2017

Estimating transfection efficiency in differentiated and undifferentiated neural cells

por Alabdullah, Abeer A., Al-Abdulaziz, Basma, Alsalem, Hanan, Magrashi, Amna, Pulicat, Subramanian M., Almzroua, Amer A., Almohanna, Falah, Assiri, Abdullah Mohamed, Al Tassan, Nada A., Al-Mubarak, Bashayer R.
Publicado 2019

Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission

por Al-Mubarak, Bashayer R., Omar, Aisha, Baz, Batoul, Al-Abdulaziz, Basma, Magrashi, Amna I., Al-Yemni, Eman, Jabaan, Amjad, Monies, Dorota, Abouelhoda, Mohamed, Abebe, Dejene, Ghaziuddin, Mohammad, Al-Tassan, Nada A.
Publicado 2020

Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress

por Al-Mubarak, Bashayer R., Bell, Karen F.S., Chowdhry, Sudhir, Meakin, Paul J., Baxter, Paul S., McKay, Sean, Dando, Owen, Ashford, Michael L.J., Gazaryan, Irina, Hayes, John D., Hardingham, Giles E.
Publicado 2021

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 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 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 2018