Bashayer Al‐Mubarak

1.1k citations

19 papers · 797 indexed · h-index 16

Impact in

Biological Psychiatry top 10%
- Tryptophan and brain disorders
Neurology top 5%
- Neuroinflammation and Neurodegeneration Mechanisms
- Parkinson's Disease Mechanisms and Treatments

Papers in ⓘ

Neurology 4
- Parkinson's Disease Mechanisms and Treatments 2
Developmental Neuroscience 2

Co-authors: Giles E. Hardingham (6 shared papers)Karen Bell (5 shared papers)Karen Horsburgh (3 shared papers)Jill H. Fowler (3 shared papers)Paul Baxter (4 shared papers)Sudhir Chowdhry (3 shared papers)John D. Hayes (3 shared papers)David J. A. Wyllie (2 shared papers)
Journals: Scientific Reports (2 papers)Genes (2 papers)Proceedings of the National Academy of Sciences (1 paper)Molecular Genetics and Metabolism (1 paper)Nature Communications (1 paper)
Partner nations: Saudi Arabia United Kingdom United States

In The Last Decade

Bashayer Al‐Mubarak

19 papers receiving 792 citations

Peers

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-authors

The 25 scholars most cited alongside Bashayer Al‐Mubarak, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bashayer Al‐Mubarak Line = papers co-authored together Bashayer Al‐Mubarak links everyone, so they are left out of the graph.

All Works

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19 of 19 papers shown

#	Work
1	Neuronal development is promoted by weakened intrinsic antioxidant defences due to epigenetic repression of Nrf2 Nature Communications ·Karen Bell, Bashayer Al‐Mubarak, Marc-André Martel, Sean McKay, Nicola Wheelan, Philip Hasel, Nóra M. Márkus, Paul Baxter, Ruth F. Deighton, Andrea Serio, Bilada Bilican, Sudhir Chowdhry, Paul J. Meakin, Michael L.J. Ashford, David J. A. Wyllie, Robert H. Scannevin, Siddharthan Chandran, John D. Hayes, Giles E. Hardingham	2015	155
2	The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults Neuron ·Marc‐André Martel, Tomás J. Ryan, Karen Bell, Jill H. Fowler, Aoife McMahon, Bashayer Al‐Mubarak, Noboru H. Komiyama, Karen Horsburgh, Peter C. Kind, Seth G. N. Grant, David J. A. Wyllie, Giles E. Hardingham	2012	147
3	Mild oxidative stress activates Nrf2 in astrocytes, which contributes to neuroprotective ischemic preconditioning Proceedings of the National Academy of Sciences ·Karen Bell, Bashayer Al‐Mubarak, Jill H. Fowler, Paul Baxter, Kunal Gupta, Tadayuki Tsujita, Sudhir Chowdhry, Rickie Patani, Siddharthan Chandran, Karen Horsburgh, John D. Hayes, Giles E. Hardingham	2010	117
4	Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families Scientific Reports ·Bashayer Al‐Mubarak, Mohamed Abouelhoda, Aisha Omar, Hesham Aldhalaan, Mohammed S. Al‐Dosari, Michael Nester, Hussain Al-Shamrani, Mohamed El-Kalioby, Ewa Goljan, Renad Albar, Shazia Subhani, Asma I. Tahir, Sultana M. Asfahani, Alaa Eskandrani, Ahmed Almusaiab, Amna Magrashi, Jameela Shinwari, Dorota Monies, Nada Al Tassan	2017	66
5	Activation of Nrf2-Regulated Glutathione Pathway Genes by Ischemic Preconditioning Oxidative Medicine and Cellular Longevity ·Karen Bell, Jill H. Fowler, Bashayer Al‐Mubarak, Karen Horsburgh, Giles E. Hardingham	2011	66
6	Non-canonical Keap1-independent activation of Nrf2 in astrocytes by mild oxidative stress Redox Biology ·Bashayer Al‐Mubarak, Karen Bell, Sudhir Chowdhry, Paul J. Meakin, Paul Baxter, Sean McKay, Owen Dando, Michael L.J. Ashford, Irina G. Gazaryan, John D. Hayes, Giles E. Hardingham	2021	33
7	Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson’s Disease Scientific Reports ·Eman A.A. Al Yemni, Dorota Monies, Thamer Alkhairallah, Saeed Bohlega, Mohamed Abouelhoda, Amna Magrashi, Abeer E. Mustafa, Basma Al-Abdulaziz, Mohamed H. Al‐Hamed, Batoul Baz, Ewa Goljan, Renad Albar, Amjad Jabaan, Tariq Faquih, Shazia Subhani, Wafa Ali Eltayb, Jameela Shinwari, Bashayer Al‐Mubarak, Nada Al Tassan	2019	28
8	A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population BMC Medical Genetics ·Faiqa Imtiaz, Khalid Taibah, Khushnooda Ramzan, Ghada BinKhamis, Shelley Kennedy, Bashayer Al‐Mubarak, Daniah Trabzuni, Rabab Allam, Abeer Al‐Mostafa, Sameera Sogaty, Abdulmoneem H Al-Shaikh, Saeed S Bamukhayyar, Brian F. Meyer, Mohammed Al‐Owain	2011	25
9	Parkinson’s Disease in Saudi Patients: A Genetic Study PLoS ONE ·Bashayer Al‐Mubarak, Saeed Bohlega, Thamer Alkhairallah, Amna Magrashi, Maha I. AlTurki, Dania S. Khalil, Basma Al-Abdulaziz, Hussam Abou‐Al‐Shaar, Abeer E. Mustafa, Eman A. Alyemni, Bashayer A. Alsaffar, Asma I. Tahir, Nada Al Tassan	2015	22
10	Estimating transfection efficiency in differentiated and undifferentiated neural cells BMC Research Notes ·Abeer A. Alabdullah, Basma Al-Abdulaziz, Hanan Alsalem, Amna Magrashi, Subramanian Manogaran Pulicat, Amer Almzroua, Falah Almohanna, Abdullah M. Assiri, Nada Al Tassan, Bashayer Al‐Mubarak	2019	21
11	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 ·Bashayer Al‐Mubarak, Aisha Omar, Batoul Baz, Basma Al-Abdulaziz, Amna Magrashi, Eman A. Alyemni, Amjad Jabaan, Dorota Monies, Mohamed Abouelhoda, Dejene Abebe, Mohammad Ghaziuddin, Nada Al Tassan	2020	19
12	Targeted de-repression of neuronal Nrf2 inhibits α-synuclein accumulation Cell Death and Disease ·Paul Baxter, Nóra M. Márkus, Owen Dando, Xin He, Bashayer Al‐Mubarak, Jing Qiu, Giles E. Hardingham	2021	19
13	Homeostatic Presynaptic Plasticity Is Specifically Regulated by P/Q-type Ca2+ Channels at Mammalian Hippocampal Synapses Cell Reports ·Alexander Jeans, Fran C. van Heusden, Bashayer Al‐Mubarak, Zahid Padamsey, Nigel J. Emptage	2017	18
14	Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease Genetics in Medicine ·Namik Kaya, Faiqa Imtiaz, Dilek Çolak, Moeenaldeen AlSayed, Ali Al‐Odaib, Fatma Alzahrani, Bashayer Al‐Mubarak, Mohammad Al-Owain, Hesham Aldhalaan, Aziza Chedrawi, Zuhair N. Al‐Hassnan, Serdar Coşkun, Nadia Sakati, Pinar T. Ozand, Brian F. Meyer	2008	17
15	Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families BMC Research Notes ·Saeed Bohlega, Bashayer Al‐Mubarak, Eman A. Alyemni, Mohamed Abouelhoda, Dorota Monies, Abeer E. Mustafa, Dania S. Khalil, Sara Al Haibi, Hussam Abou‐Al‐Shaar, Tariq Faquih, Mohamed El-Kalioby, Asma I. Tahir, Nada Al Tassan	2016	17
16	Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin Molecular Genetics and Metabolism ·Faiqa Imtiaz, Mohamed S. Rashed, Bashayer Al‐Mubarak, Rabab Allam, Hanaa El-Karaksy, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Hamad Alzaidan, Zuhair Rahbeeni, Alya Qari, Brian F. Meyer, Moeen Al-Sayed	2011	16
17	Validation of Ion TorrentTM Inherited Disease Panel with the PGMTM Sequencing Platform for Rapid and Comprehensive Mutation Detection Genes ·Abeer E. Mustafa, Tariq Faquih, Batoul Baz, Rana F Kattan, Abdulelah AlIssa, Asma I. Tahir, Faiqa Imtiaz, Khushnooda Ramzan, Moeenaldeen AlSayed, Mohammed Al‐Owain, Zuhair N. Al‐Hassnan, Hamad Alzaidan, Mohamed Abouelhoda, Bashayer Al‐Mubarak, Nada Al Tassan	2018	8
18	Autism and ADHD in the Era of Big Data; An Overview of Digital Resources for Patient, Genetic and Clinical Trials Information Genes ·Faris M. Abomelha, Hesham Aldhalaan, Mohammad Ghaziuddin, Nada Al Tassan, Bashayer Al‐Mubarak	2022	2
19	Globalizing Research toward Diverse Representation in Alzheimer's and Parkinson's Disease Annals of Neurology ·Bashayer Al‐Mubarak, Mohamed Ahmed Nour, Artur Francisco Schumacher Schuh, Sara Bandrés‐Ciga	2022	1

About Bashayer Al‐Mubarak

Bashayer Al‐Mubarak is a scholar working on Neurology, Developmental Neuroscience, Biological Psychiatry, Clinical Biochemistry and Behavioral Neuroscience, having authored 19 papers that have together received 797 indexed citations. Recurring topics across this work include Genomics, phytochemicals, and oxidative stress (5 papers), Autism Spectrum Disorder Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Metabolism and Genetic Disorders (2 papers), Parkinson's Disease Mechanisms and Treatments (2 papers), CRISPR and Genetic Engineering (2 papers), Nuclear Receptors and Signaling (2 papers) and Attention Deficit Hyperactivity Disorder (2 papers). The work is most often cited by research in Biological Psychiatry (48 citations), Neurology (158 citations), Developmental Neuroscience (67 citations), Cellular and Molecular Neuroscience (227 citations) and Molecular Biology (474 citations). Bashayer Al‐Mubarak has collaborated with scholars based in Saudi Arabia, United Kingdom and United States. Frequent co-authors include Giles E. Hardingham, Karen Bell, Karen Horsburgh, Jill H. Fowler, Paul Baxter, Sudhir Chowdhry, John D. Hayes, David J. A. Wyllie, Siddharthan Chandran and Nada Al Tassan. Their work appears in journals such as Scientific Reports, Genes, Proceedings of the National Academy of Sciences, Molecular Genetics and Metabolism and Nature Communications.

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.

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