| The subtype of GluN2 C-terminal domain determines the response to excitotoxic insults MA Martel, TJ Ryan, KFS Bell, JH Fowler, A McMahon, B Al-Mubarak, ... Neuron 74 (3), 543-556, 2012 | 209 | 2012 |
| Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2 KFS Bell, B Al-Mubarak, MA Martel, S McKay, N Wheelan, P Hasel, ... Nature communications 6 (1), 7066, 2015 | 178 | 2015 |
| Mild oxidative stress activates Nrf2 in astrocytes, which contributes to neuroprotective ischemic preconditioning KF Bell, B Al-Mubarak, JH Fowler, PS Baxter, K Gupta, T Tsujita, ... Proceedings of the National Academy of Sciences 108 (1), E1-E2, 2011 | 157 | 2011 |
| Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families B Al-Mubarak, M Abouelhoda, A Omar, H AlDhalaan, M Aldosari, ... Scientific reports 7 (1), 5679, 2017 | 96 | 2017 |
| Synaptic NMDAR activity suppresses FOXO1 expression via a cis-acting FOXO binding site: FOXO1 is a FOXO target gene BM Francesc X Soriano & Giles E Hardingham Channels (Austin) 3 (4), 233-239, 2009 | 92* | 2009 |
| Activation of Nrf2-regulated glutathione pathway genes by ischemic preconditioning KFS Bell, JH Fowler, B Al-Mubarak, K Horsburgh, GE Hardingham Oxidative medicine and cellular longevity 2011, 2011 | 88 | 2011 |
| Integrated analysis of whole exome sequencing and copy number evaluation in Parkinson’s disease EA Yemni, D Monies, T Alkhairallah, S Bohlega, M Abouelhoda, ... Scientific Reports 9 (1), 3344, 2019 | 41 | 2019 |
| A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population F Imtiaz, K Taibah, K Ramzan, G Bin-Khamis, S Kennedy, B Al-Mubarak, ... BMC medical genetics 12, 1-6, 2011 | 38 | 2011 |
| Using global team science to identify genetic Parkinson’s disease worldwide EJ Vollstedt, M Kasten, C Klein Annals of neurology 86 (2), 153, 2019 | 31 | 2019 |
| Parkinson’s disease in Saudi patients: a genetic study BR Al-Mubarak, SA Bohlega, TS Alkhairallah, AI Magrashi, MI AlTurki, ... PloS one 10 (8), e0135950, 2015 | 31 | 2015 |
| Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin F Imtiaz, MS Rashed, B Al-Mubarak, R Allam, H El-Karaksy, Z Al-Hassnan, ... Molecular genetics and metabolism 104 (4), 688-690, 2011 | 31 | 2011 |
| Nrf2 target genes can be controlled by neuronal activity in the absence of Nrf2 and astrocytes RF Deighton, NM Márkus, B Al-Mubarak, KFS Bell, S Papadia, PJ Meakin, ... Proceedings of the National Academy of Sciences 111 (18), E1818-E1820, 2014 | 29 | 2014 |
| Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease N Kaya, F Imtiaz, D Colak, M Al-Sayed, A Al-Odaib, F Al-Zahrani, ... Genetics in Medicine 10 (9), 675-684, 2008 | 29 | 2008 |
| Homeostatic presynaptic plasticity is specifically regulated by P/Q-type Ca2+ channels at mammalian hippocampal synapses AF Jeans, FC van Heusden, B Al-Mubarak, Z Padamsey, NJ Emptage Cell reports 21 (2), 341-350, 2017 | 26 | 2017 |
| Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study M Rizig, S Bandres-Ciga, MB Makarious, OO Ojo, PW Crea, OV Abiodun, ... The Lancet Neurology 22 (11), 1015-1025, 2023 | 24 | 2023 |
| Estimating transfection efficiency in differentiated and undifferentiated neural cells AA Alabdullah, B Al-Abdulaziz, H Alsalem, A Magrashi, SM Pulicat, ... BMC research notes 12, 1-7, 2019 | 24 | 2019 |
| Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission BR Al-Mubarak, A Omar, B Baz, B Al-Abdulaziz, AI Magrashi, E Al-Yemni, ... European Journal of Human Genetics 28 (8), 1098-1110, 2020 | 21 | 2020 |
| Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families SA Bohlega, BR Al-Mubarak, EA Alyemni, M Abouelhoda, D Monies, ... BMC research notes 9, 1-7, 2016 | 21 | 2016 |
| Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress BR Al-Mubarak, KFS Bell, S Chowdhry, PJ Meakin, PS Baxter, S McKay, ... Redox biology 47, 102158, 2021 | 20 | 2021 |
| Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort EJ Vollstedt, S Schaake, K Lohmann, S Padmanabhan, A Brice, S Lesage, ... Movement Disorders 38 (2), 286-303, 2023 | 19 | 2023 |
