Marwan Nashabat

691 total citations
25 papers, 422 citations indexed

About

Marwan Nashabat is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Marwan Nashabat has authored 25 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 8 papers in Genetics. Recurrent topics in Marwan Nashabat's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (5 papers) and Folate and B Vitamins Research (5 papers). Marwan Nashabat is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (5 papers) and Folate and B Vitamins Research (5 papers). Marwan Nashabat collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Marwan Nashabat's co-authors include Majid Alfadhel, Brahim Tabarki, Khalid Hundallah, Muhammad Umair, Waleed Altwaijri, Fuad Al Mutairi, Mohammed Al‐Owain, Fowzan S. Alkuraya, Ahmed Alfares and Ahmed Al‐Rumayyan and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Scientific Reports.

In The Last Decade

Marwan Nashabat

25 papers receiving 421 citations

Peers

Marwan Nashabat

GENET

RHEUM

NEURO

Sietske H. Kevelam Netherlands

Deborah L. Renaud United States

Chupong Ittiwut Thailand

Johan Van Hove United States

Anna Wedell Sweden

Ahmed Alfares Saudi Arabia

Annette Bley Germany

Natsuko Arai‐Ichinoi Japan

Khalid Al‐Thihli Oman

Aisha Al‐Shamsi United Arab Emirates

Sietske H. Kevelam Netherlands

Marwan Nashabat

283 ×1.2

86 ×0.7

83 ×0.8

GENET

33 ×0.5

RHEUM

100 ×1.9

NEURO

Citations per year, relative to Marwan Nashabat Marwan Nashabat (= 1×) peers Sietske H. Kevelam

Countries citing papers authored by Marwan Nashabat

Since Specialization

Citations

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

Fields of papers citing papers by Marwan Nashabat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marwan Nashabat

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

All Works

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20 of 20 papers shown

Alfadhel, Majid, Marwan Nashabat, Ahmed Alfares, et al.. (2021). Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial. Orphanet Journal of Rare Diseases. 16(1). 422–422. 18 indexed citations

Tabarki, Brahim, et al.. (2021). Inherited Metabolic Causes of Stroke in Children: Mechanisms, Types, and Management. Frontiers in Neurology. 12. 633119–633119. 7 indexed citations

Umair, Muhammad, Muhammad Farooq Khan, Marwan Nashabat, et al.. (2021). Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish. Frontiers in Cell and Developmental Biology. 9. 736960–736960. 12 indexed citations

Barhoumi, Tlili, Abdulaziz Asiri, Marwan Nashabat, et al.. (2021). A homozygous nonsense mutation in DCBLD2 is a candidate cause of developmental delay, dysmorphic features and restrictive cardiomyopathy. Scientific Reports. 11(1). 12861–12861. 11 indexed citations

Alghamdi, Malak, Khalid Alhasan, Marwan Nashabat, et al.. (2020). Diversity of Phenotype and Genetic Etiology of 23 Cystinuria Saudi Patients: A Retrospective Study. Frontiers in Pediatrics. 8. 569389–569389. 9 indexed citations

Bhat, Javaid Akhter, Marwan Nashabat, Yusra Alyafee, et al.. (2020). A Missense Mutation in the UGDH Gene Is Associated With Developmental Delay and Axial Hypotonia. Frontiers in Pediatrics. 8. 71–71. 18 indexed citations

Asiri, Abdulaziz, Muhammad Umair, Yusra Alyafee, et al.. (2020). Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay. Annals of Clinical and Translational Neurology. 7(6). 956–964. 16 indexed citations

Alfadhel, Majid, et al.. (2020). Clinical presentation of seven patients with Methylenetetrahydrofolate reductase deficiency. Molecular Genetics and Metabolism Reports. 25. 100644–100644. 6 indexed citations

Nashabat, Marwan, Waleed Altwaijri, Khalid Hundallah, et al.. (2019). The landscape of early infantile epileptic encephalopathy in a consanguineous population. Seizure. 69. 154–172. 38 indexed citations

10.

Nashabat, Marwan, Fuad Al Mutairi, Wafaa Eyaid, et al.. (2019). Evaluation of long-term effectiveness of the use of carglumic acid in patients with propionic acidemia (PA) or methylmalonic acidemia (MMA): study protocol for a randomized controlled trial. BMC Pediatrics. 19(1). 195–195. 9 indexed citations

11.

Barhoumi, Tlili, Marwan Nashabat, Mohamed Boudjelal, et al.. (2019). Delta Like-1 Gene Mutation: A Novel Cause of Congenital Vertebral Malformation. Frontiers in Genetics. 10. 534–534. 18 indexed citations

12.

Alfadhel, Majid, Muhammad Umair, Bader Almuzzaini, et al.. (2019). Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening. Annals of Clinical and Translational Neurology. 6(10). 2097–2103. 39 indexed citations

13.

Nashabat, Marwan, Sultan Al‐Khenaizan, & Majid Alfadhel. (2018). Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations. Therapeutics and Clinical Risk Management. Volume 14. 225–229. 9 indexed citations

14.

Nashabat, Marwan, et al.. (2017). Pulmonary hypertension and vasculopathy in incontinentia pigmenti: a case report. Therapeutics and Clinical Risk Management. Volume 13. 629–634. 5 indexed citations

15.

Nashabat, Marwan, Majid Alfadhel, Ali Alasmari, et al.. (2017). Clinical, Biochemical, and Molecular Features in 37 Saudi Patients with Very Long Chain Acyl CoA Dehydrogenase Deficiency. JIMD Reports. 40. 47–53. 16 indexed citations

16.

Nashabat, Marwan, et al.. (2017). Delineation of cystinuria in Saudi Arabia: A case series. BMC Nephrology. 18(1). 50–50. 4 indexed citations

17.

Alfadhel, Majid, Marwan Nashabat, Muhammad Talal Alrifai, et al.. (2017). Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases. European Journal of Paediatric Neurology. 22(1). 46–55. 22 indexed citations

18.

Alfadhel, Majid, et al.. (2017). Mitochondrial iron-sulfur cluster biogenesis from molecular understanding to clinical disease. Neurosciences. 22(1). 4–13. 21 indexed citations

19.

Mutairi, Fuad Al, Majid Alfadhel, Marwan Nashabat, et al.. (2017). Phenotypic and Molecular Spectrum of Aicardi-Goutières Syndrome: A Study of 24 Patients. Pediatric Neurology. 78. 35–40. 35 indexed citations

20.

Alfadhel, Majid, Marwan Nashabat, Ahmed Alfares, et al.. (2016). Mutation in SLC6A9 encoding a glycine transporter causes a novel form of non-ketotic hyperglycinemia in humans. Human Genetics. 135(11). 1263–1268. 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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