Bashayer Al‐Mubarak

1.1k total citations
19 papers, 797 citations indexed

About

Bashayer Al‐Mubarak is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bashayer Al‐Mubarak has authored 19 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bashayer Al‐Mubarak's work include Genomics, phytochemicals, and oxidative stress (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Bashayer Al‐Mubarak is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (5 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Autism Spectrum Disorder Research (3 papers). Bashayer Al‐Mubarak collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Bashayer Al‐Mubarak's co-authors include Giles E. Hardingham, Karen Bell, Jill H. Fowler, Karen Horsburgh, Paul Baxter, Sudhir Chowdhry, John D. Hayes, David J. A. Wyllie, Siddharthan Chandran and Nada Al Tassan and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Bashayer Al‐Mubarak

19 papers receiving 792 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Bashayer Al‐Mubarak Saudi Arabia 16 474 227 158 111 91 19 797
Céline S. Nicolas France 13 515 1.1× 346 1.5× 138 0.9× 126 1.1× 94 1.0× 23 965
Synthia H. Sun Taiwan 18 301 0.6× 239 1.1× 191 1.2× 103 0.9× 66 0.7× 27 904
Keith Q. Tanis United States 18 350 0.7× 163 0.7× 108 0.7× 186 1.7× 65 0.7× 34 947
Hea Jin Ryu South Korea 21 386 0.8× 294 1.3× 218 1.4× 69 0.6× 54 0.6× 29 912
Jinhee Yang South Korea 13 459 1.0× 300 1.3× 105 0.7× 267 2.4× 69 0.8× 14 824
Edward Beamer Ireland 17 230 0.5× 308 1.4× 160 1.0× 88 0.8× 65 0.7× 22 773
Knut H. Lauritzen Norway 14 599 1.3× 217 1.0× 115 0.7× 303 2.7× 42 0.5× 20 1.0k
Federica Frigerio Italy 12 261 0.6× 497 2.2× 267 1.7× 92 0.8× 54 0.6× 14 993
Yoori Choi South Korea 14 320 0.7× 209 0.9× 186 1.2× 227 2.0× 37 0.4× 31 872
Christophe Crochemore Italy 15 365 0.8× 299 1.3× 146 0.9× 148 1.3× 70 0.8× 16 1.1k

Countries citing papers authored by Bashayer Al‐Mubarak

Since Specialization
Citations

This map shows the geographic impact of Bashayer Al‐Mubarak's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Bashayer Al‐Mubarak with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bashayer Al‐Mubarak more than expected).

Fields of papers citing papers by Bashayer Al‐Mubarak

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bashayer Al‐Mubarak. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Bashayer Al‐Mubarak. The network helps show where Bashayer Al‐Mubarak may publish in the future.

Co-authorship network of co-authors of Bashayer Al‐Mubarak

This figure shows the co-authorship network connecting the top 25 collaborators of Bashayer Al‐Mubarak. A scholar is included among the top collaborators of Bashayer Al‐Mubarak based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Bashayer Al‐Mubarak. Bashayer Al‐Mubarak is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Ghaziuddin, Mohammad, et al.. (2022). Autism and ADHD in the Era of Big Data; An Overview of Digital Resources for Patient, Genetic and Clinical Trials Information. Genes. 13(9). 1551–1551. 2 indexed citations
2.
Al‐Mubarak, Bashayer, et al.. (2022). Globalizing Research toward Diverse Representation in Alzheimer's and Parkinson's Disease. Annals of Neurology. 92(5). 711–714. 1 indexed citations
3.
Al‐Mubarak, Bashayer, Karen Bell, Sudhir Chowdhry, et al.. (2021). Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress. Redox Biology. 47. 102158–102158. 33 indexed citations
4.
Baxter, Paul, Nóra M. Márkus, Owen Dando, et al.. (2021). Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation. Cell Death and Disease. 12(2). 218–218. 19 indexed citations
5.
Al‐Mubarak, Bashayer, Batoul Baz, Dorota Monies, et al.. (2020). Whole exome sequencing in ADHD trios from single and multi-incident families implicates new candidate genes and highlights polygenic transmission. European Journal of Human Genetics. 28(8). 1098–1110. 19 indexed citations
6.
Almohanna, Falah, et al.. (2019). Estimating transfection efficiency in differentiated and undifferentiated neural cells. BMC Research Notes. 12(1). 225–225. 21 indexed citations
7.
Monies, Dorota, Thamer Alkhairallah, Saeed Bohlega, et al.. (2019). Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease. Scientific Reports. 9(1). 3344–3344. 28 indexed citations
8.
Faquih, Tariq, Batoul Baz, Rana F Kattan, et al.. (2018). Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection. Genes. 9(5). 267–267. 8 indexed citations
9.
Al‐Mubarak, Bashayer, Mohamed Abouelhoda, Hesham Aldhalaan, et al.. (2017). Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families. Scientific Reports. 7(1). 5679–5679. 66 indexed citations
10.
Jeans, Alexander, et al.. (2017). Homeostatic Presynaptic Plasticity Is Specifically Regulated by P/Q-type Ca2+ Channels at Mammalian Hippocampal Synapses. Cell Reports. 21(2). 341–350. 18 indexed citations
11.
Bohlega, Saeed, Bashayer Al‐Mubarak, Mohamed Abouelhoda, et al.. (2016). Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families. BMC Research Notes. 9(1). 295–295. 17 indexed citations
12.
Al‐Mubarak, Bashayer, Saeed Bohlega, Thamer Alkhairallah, et al.. (2015). Parkinson’s Disease in Saudi Patients: A Genetic Study. PLoS ONE. 10(8). e0135950–e0135950. 22 indexed citations
13.
Bell, Karen, Bashayer Al‐Mubarak, Sean McKay, et al.. (2015). Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2. Nature Communications. 6(1). 7066–7066. 155 indexed citations
14.
Martel, Marc‐André, Tomás J. Ryan, Karen Bell, et al.. (2012). The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults. Neuron. 74(3). 543–556. 147 indexed citations
15.
Imtiaz, Faiqa, Mohamed S. Rashed, Bashayer Al‐Mubarak, et al.. (2011). Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin. Molecular Genetics and Metabolism. 104(4). 688–690. 16 indexed citations
16.
Imtiaz, Faiqa, Khushnooda Ramzan, Shelley Kennedy, et al.. (2011). A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population. BMC Medical Genetics. 12(1). 91–91. 25 indexed citations
17.
Bell, Karen, Jill H. Fowler, Bashayer Al‐Mubarak, Karen Horsburgh, & Giles E. Hardingham. (2011). Activation of Nrf2-Regulated Glutathione Pathway Genes by Ischemic Preconditioning. Oxidative Medicine and Cellular Longevity. 2011. 1–7. 66 indexed citations
18.
Bell, Karen, Bashayer Al‐Mubarak, Jill H. Fowler, et al.. (2010). Mild oxidative stress activates Nrf2 in astrocytes, which contributes to neuroprotective ischemic preconditioning. Proceedings of the National Academy of Sciences. 108(1). E1–2; author reply E3. 117 indexed citations
19.
Kaya, Namik, Faiqa Imtiaz, Dilek Çolak, et al.. (2008). Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease. Genetics in Medicine. 10(9). 675–684. 17 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Céline S. Nicolas Breakdown of academic impact, for papers by Synthia H. Sun Breakdown of academic impact, for papers by Keith Q. Tanis Breakdown of academic impact, for papers by Hea Jin Ryu Breakdown of academic impact, for papers by Jinhee Yang Breakdown of academic impact, for papers by Edward Beamer Breakdown of academic impact, for papers by Knut H. Lauritzen Breakdown of academic impact, for papers by Federica Frigerio Breakdown of academic impact, for papers by Yoori Choi Breakdown of academic impact, for papers by Christophe Crochemore
Rankless by CCL
2026