Aziza Chedrawi

1.3k total citations
18 papers, 306 citations indexed

About

Aziza Chedrawi is a scholar working on Molecular Biology, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Aziza Chedrawi has authored 18 papers receiving a total of 306 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Psychiatry and Mental health and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Aziza Chedrawi's work include Epilepsy research and treatment (4 papers), Pharmacological Effects and Toxicity Studies (3 papers) and Lysosomal Storage Disorders Research (2 papers). Aziza Chedrawi is often cited by papers focused on Epilepsy research and treatment (4 papers), Pharmacological Effects and Toxicity Studies (3 papers) and Lysosomal Storage Disorders Research (2 papers). Aziza Chedrawi collaborates with scholars based in Saudi Arabia, United States and Germany. Aziza Chedrawi's co-authors include Zuhair N. Al‐Hassnan, Geoffrey Miller, Marvin A. Fishman, Mohammad A. Al–Muhaizea, Nobuyuki Shimozawa, Mohamed S. Rashed, Tomofumi Santa, Minnie Jacob, Osama Y. Al-Dirbashi and Jeffrey L. Noebels and has published in prestigious journals such as Journal of Lipid Research, Gene and Epilepsia.

In The Last Decade

Aziza Chedrawi

17 papers receiving 293 citations

Peers

Aziza Chedrawi

GENET

PHYSI

PMH

Charlotte Thiels Germany

Emma Reid United Kingdom

Hiroko Shimbo Japan

Saad AlShahwan Saudi Arabia

Tessa Wassenberg Netherlands

Mengting Li China

Youjiao Chen China

Hye-Won Hyun South Korea

Sabine Grønborg Denmark

Wenbiao Xiao China

Charlotte Thiels Germany

Aziza Chedrawi

225 ×1.6

46 ×0.6

GENET

22 ×0.4

66 ×1.3

PHYSI

27 ×0.6

PMH

Citations per year, relative to Aziza Chedrawi Aziza Chedrawi (= 1×) peers Charlotte Thiels

Countries citing papers authored by Aziza Chedrawi

Since Specialization

Citations

This map shows the geographic impact of Aziza Chedrawi'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 Aziza Chedrawi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aziza Chedrawi more than expected).

Fields of papers citing papers by Aziza Chedrawi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aziza Chedrawi. 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 Aziza Chedrawi. The network helps show where Aziza Chedrawi may publish in the future.

Co-authorship network of co-authors of Aziza Chedrawi

This figure shows the co-authorship network connecting the top 25 collaborators of Aziza Chedrawi. A scholar is included among the top collaborators of Aziza Chedrawi 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 Aziza Chedrawi. Aziza Chedrawi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Albert, Dimpna C., et al.. (2023). Central pontine myelinolysis and locked‐IN syndrome associated with tacrolimus after pediatric heart transplantation. Pediatric Transplantation. 27(3). e14474–e14474. 1 indexed citations

Alsemari, Abdulaziz, et al.. (2023). Knowledge About Status Epilepticus and Epilepsy; Comparative Study. 6(3). 1 indexed citations

Almass, Rawan, Anoud Albader, Peter Karachunski, et al.. (2020). Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy. Acta Neuropathologica. 139(4). 791–794. 15 indexed citations

Chedrawi, Aziza, et al.. (2020). Beyond a routine blood gas, an easily picked but missed diagnosis of chronic Encephalopathy. International Journal of Pediatrics and Adolescent Medicine. 8(1). 52–54.

Al–Muhaizea, Mohammad A., et al.. (2018). Tuberous sclerosis complex: Clinical spectrum and epilepsy: A retrospective chart review study. Translational Neuroscience. 9(1). 154–160. 10 indexed citations

Garg, Aayushi, et al.. (2015). Subacute encephalitis in a child seropositive for alpha-3 subunit of neuronal nicotinic acetylcholine receptors antibody. Journal of Pediatric Neurology. 12(3). 161–166. 1 indexed citations

Saeed, Muhammad, et al.. (2014). Acute disseminated encephalomyelitis and thrombocytopenia following Epstein-Barr virus infection.. PubMed. 24 Suppl 3. S216–8. 6 indexed citations

Alsemari, Abdulaziz, Faisal Alotaibi, Salah Baz, et al.. (2014). Epilepsy Surgery Series: A Study of 502 Consecutive Patients from a Developing Country. PubMed. 2014. 1–8. 16 indexed citations

Wakil, Salma M., Khushnooda Ramzan, Rana Alomar, et al.. (2013). Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C > T. Gene. 536(1). 217–220. 21 indexed citations

10.

Chedrawi, Aziza, Zuhair N. Al‐Hassnan, Dilek Çolak, et al.. (2011). Novel V97G ASAH1 mutation found in Farber disease patients: Unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system. Brain and Development. 34(5). 400–404. 14 indexed citations

11.

Çolak, Dilek, Hesham Aldhalaan, Michael Nester, et al.. (2010). Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways. Genomics. 97(1). 19–28. 18 indexed citations

12.

Al–Muhaizea, Mohammad A., Zuhair N. Al‐Hassnan, & Aziza Chedrawi. (2009). Variant Late Infantile Neuronal Ceroid Lipofuscinosis (CLN6 Gene) in Saudi Arabia. Pediatric Neurology. 41(1). 74–76. 13 indexed citations

13.

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

14.

Al-Dirbashi, Osama Y., Tomofumi Santa, Mohamed S. Rashed, et al.. (2008). Rapid UPLC-MS/MS method for routine analysis of plasma pristanic, phytanic, and very long chain fatty acid markers of peroxisomal disorders. Journal of Lipid Research. 49(8). 1855–1862. 46 indexed citations

15.

Chedrawi, Aziza, et al.. (2008). Profound Biotinidase Deficiency in a Child With Predominantly Spinal Cord Disease. Journal of Child Neurology. 23(9). 1043–1048. 23 indexed citations

16.

Chedrawi, Aziza, et al.. (2004). Cephalosporin-induced nonconvulsive status epilepticus in a uremic child. Pediatric Neurology. 30(2). 135–139. 16 indexed citations

17.

Heilstedt, Heidi A., Daniel L. Burgess, Aziza Chedrawi, et al.. (2001). Loss of the Potassium Channel β‐Subunit Gene, KCNAB2, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome. Epilepsia. 42(9). 1103–1111. 65 indexed citations

18.

Chedrawi, Aziza, Marvin A. Fishman, & Geoffrey Miller. (2000). Neck-tongue syndrome. Pediatric Neurology. 22(5). 397–399. 23 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.

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