Saad AlShahwan

2.0k total citations
22 papers, 520 citations indexed

About

Saad AlShahwan is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, Saad AlShahwan has authored 22 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Neurology and 6 papers in Clinical Biochemistry. Recurrent topics in Saad AlShahwan's work include Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Saad AlShahwan is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Mitochondrial Function and Pathology (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Saad AlShahwan collaborates with scholars based in Saudi Arabia, United States and Türkiye. Saad AlShahwan's co-authors include Brahim Tabarki, Amal Alhashem, Erika Fernández‐Vizarra, Pio D’Adamo, P Goffrini, Massimo Zeviani, Eman Bakhsh, Paolo Gasparini, Paolo Mereghetti and Ileana Ferrero and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Saad AlShahwan

21 papers receiving 509 citations

Peers

Saad AlShahwan

NEURO

GENET

CMN

Johann Penzien Germany

Alfonso Oyarzábal Spain

Ángela Arias Spain

Thilo Kaehne Germany

M. Pineda Spain

Mercedes Casado Spain

María Teresa García‐Silva Spain

K Naess Sweden

Maria Stella Vari Italy

Emma Reid United Kingdom

Johann Penzien Germany

Saad AlShahwan

268 ×1.0

184 ×1.2

143 ×1.5

NEURO

72 ×1.1

GENET

106 ×1.8

CMN

Citations per year, relative to Saad AlShahwan Saad AlShahwan (= 1×) peers Johann Penzien

Countries citing papers authored by Saad AlShahwan

Since Specialization

Citations

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

Fields of papers citing papers by Saad AlShahwan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saad AlShahwan

This figure shows the co-authorship network connecting the top 25 collaborators of Saad AlShahwan. A scholar is included among the top collaborators of Saad AlShahwan 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 Saad AlShahwan. Saad AlShahwan 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

Thabet, Farah, et al.. (2024). Bi-allelic variants in HCRT cause autosomal recessive narcolepsy. Neurogenetics. 25(2). 79–83.

Alhashem, Amal, et al.. (2018). Novel Homozygous Mutation of the AIMP1 Gene: A Milder Neuroimaging Phenotype With Preservation of the Deep White Matter. Pediatric Neurology. 91. 57–61. 7 indexed citations

Alhashem, Amal, Eissa Faqeih, Majid Alfadhel, et al.. (2017). Congenital disorders of glycosylation: The Saudi experience. American Journal of Medical Genetics Part A. 173(10). 2614–2621. 29 indexed citations

AlShahwan, Saad, et al.. (2017). Sepiapterin reductase deficiency: Report of 5 new cases. European Journal of Paediatric Neurology. 21(3). 583–586. 9 indexed citations

Alhashem, Amal, et al.. (2017). Recessive AFG3L2 Mutation Causes Progressive Microcephaly, Early Onset Seizures, Spasticity, and Basal Ganglia Involvement. Pediatric Neurology. 71. 24–28. 16 indexed citations

Tabarki, Brahim, Amal Alhashem, Saad AlShahwan, et al.. (2015). Severe CNS involvement in WWOX mutations: Description of five new cases. American Journal of Medical Genetics Part A. 167(12). 3209–3213. 28 indexed citations

Tabarki, Brahim, et al.. (2015). Treatment of biotin-responsive basal ganglia disease: Open comparative study between the combination of biotin plus thiamine versus thiamine alone. European Journal of Paediatric Neurology. 19(5). 547–552. 40 indexed citations

Alhashem, Amal, Anas M. Alazami, Kalthoum Tlili, et al.. (2015). Further Delineation of the ALG9-CDG Phenotype. JIMD Reports. 27. 107–112. 18 indexed citations

Tabarki, Brahim, et al.. (2013). Bilateral External Ophthalmoplegia in Biotin-Responsive Basal Ganglia Disease. The Journal of Pediatrics. 162(6). 1291–1292. 4 indexed citations

10.

Fernández‐Vizarra, Erika, Saad AlShahwan, Eman Bakhsh, et al.. (2008). Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase. The American Journal of Human Genetics. 82(6). 1281–1289. 143 indexed citations

11.

Sass, Jörn Oliver, Florence Jobard, Meral Topçu, et al.. (2008). L‐2‐Hydroxyglutaric aciduria: Identification of ten novel mutations in theL2HGDHgene. Journal of Inherited Metabolic Disease. 31(S2). 275–279. 17 indexed citations

12.

Rashed, Mohamed S., Amal Saadallah, Zuhair Rahbeeni, et al.. (2004). Determination of urinary S‐sulphocysteine, xanthine and hypoxanthine by liquid chromatography–electrospray tandem mass spectrometry. Biomedical Chromatography. 19(3). 223–230. 34 indexed citations

13.

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

14.

Aljumah, Mohammed, Ramanath Majumdar, Saad Al‐Rajeh, et al.. (2003). Molecular analysis of the spinal muscular atrophy and neuronal apoptosis inhibitory protein genes in Saudi patients with spinal muscular atrophy.. PubMed. 24(10). 1052–4. 16 indexed citations

15.

Aljumah, Mohammed, Ramanath Majumdar, Saad Al‐Rajeh, et al.. (2002). Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.. PubMed. 23(12). 1478–82. 14 indexed citations

16.

AlShahwan, Saad, et al.. (1995). Familial Congenital Hemiparesis. Journal of Child Neurology. 10(5). 413–414. 3 indexed citations

17.

Anderson, Leigh C., et al.. (1995). Reading-induced absence seizures. Neurology. 45(8). 1623–1624. 9 indexed citations

18.

AlShahwan, Saad, et al.. (1994). Hemisomatic spasms in children. Neurology. 44(7). 1332–1332. 36 indexed citations

19.

AlShahwan, Saad, et al.. (1993). Choroido‐cerebral calcification syndrome with retardation. Neurology. 43(11). 2387–2387. 1 indexed citations

20.

Singh, Balbir, et al.. (1992). Cerebrochoroidal syndrome. Pediatric Neurology. 8(5). 347–347. 1 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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