Aida I. Al‐Aqeel

670 total citations
17 papers, 200 citations indexed

About

Aida I. Al‐Aqeel is a scholar working on Clinical Biochemistry, Genetics and Physiology. According to data from OpenAlex, Aida I. Al‐Aqeel has authored 17 papers receiving a total of 200 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Clinical Biochemistry, 7 papers in Genetics and 4 papers in Physiology. Recurrent topics in Aida I. Al‐Aqeel's work include Metabolism and Genetic Disorders (8 papers), Genomics and Rare Diseases (3 papers) and Vitamin D Research Studies (3 papers). Aida I. Al‐Aqeel is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Genomics and Rare Diseases (3 papers) and Vitamin D Research Studies (3 papers). Aida I. Al‐Aqeel collaborates with scholars based in Saudi Arabia, Lebanon and Canada. Aida I. Al‐Aqeel's co-authors include Stephen J. Marx, Pinar T. Ozand, Samia H. Sobki, H. F. DeLuca, Jean M. Prahl, Monique Thomas, Hitoshi Goto, Russell J. Wiese, Howard Jm and Terry Ponich and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Molecular and Cellular Endocrinology.

In The Last Decade

Aida I. Al‐Aqeel

16 papers receiving 189 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aida I. Al‐Aqeel Saudi Arabia 9 68 55 43 35 32 17 200
Shinya Ogasawara Japan 8 33 0.5× 116 2.1× 46 1.1× 14 0.4× 14 0.4× 10 388
Shinji Kitahama Japan 9 47 0.7× 97 1.8× 51 1.2× 9 0.3× 5 0.2× 19 398
M Hamédani Switzerland 8 117 1.7× 34 0.6× 26 0.6× 9 0.3× 7 0.2× 26 278
Hirofumi Makino Japan 6 12 0.2× 71 1.3× 55 1.3× 7 0.2× 21 0.7× 8 382
F. C. Sitzmann Germany 9 19 0.3× 42 0.8× 27 0.6× 18 0.5× 26 0.8× 39 273
Ahmet Sarıcı Türkiye 13 43 0.6× 137 2.5× 14 0.3× 12 0.3× 5 0.2× 40 535
Radhika Susarla United Kingdom 8 126 1.9× 44 0.8× 13 0.3× 8 0.2× 3 0.1× 16 323
Ricky W.K. Law China 10 38 0.6× 88 1.6× 28 0.7× 11 0.3× 9 0.3× 16 459
Kenneth E. Bloom United States 6 51 0.8× 82 1.5× 73 1.7× 31 0.9× 3 0.1× 7 295
YUKIKO YABU Japan 9 58 0.9× 44 0.8× 28 0.7× 10 0.3× 2 0.1× 10 333

Countries citing papers authored by Aida I. Al‐Aqeel

Since Specialization
Citations

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

Fields of papers citing papers by Aida I. Al‐Aqeel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aida I. Al‐Aqeel. 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 Aida I. Al‐Aqeel. The network helps show where Aida I. Al‐Aqeel may publish in the future.

Co-authorship network of co-authors of Aida I. Al‐Aqeel

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

All Works

17 of 17 papers shown
1.
Mohamed, Sarar, W Elsheikh, Aida I. Al‐Aqeel, et al.. (2020). Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. Saudi Medical Journal. 41(7). 703–708. 17 indexed citations
2.
Alhashem, Amal, et al.. (2020). Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis. Saudi Medical Journal. 41(2). 199–202. 4 indexed citations
3.
Nyhan, William L., Georg F. Hoffmann, Aida I. Al‐Aqeel, & Bruce A. Barshop. (2020). Atlas of Inherited Metabolic Diseases. 4 indexed citations
4.
Alhashem, Amal, et al.. (2020). Molecular and clinical characteristics of very long-chain acyl-CoA dehydrogenase deficiency. Saudi Medical Journal. 41(6). 590–596. 2 indexed citations
5.
Al‐Aqeel, Aida I., Claire L. Meek, Judy M.Y. Wong, & Alim P. Mitha. (2015). A novel fusiform aneurysmal model in a rabbit carotid: a combination of pericarotid calcium chloride and elastase incubation. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 42(S1). S12–S12. 1 indexed citations
6.
Kaya, Namik, Dilek Çolak, Albandary AlBakheet, et al.. (2012). Identification of a novel IVD mutation in a consanguineous family with isovaleric acidemia. Gene. 513(2). 297–300. 3 indexed citations
7.
Nyhan, William L., Bruce A. Barshop, & Aida I. Al‐Aqeel. (2011). Atlas of Inherited Metabolic Diseases 3E. 1 indexed citations
8.
Nyhan, William L., Georg F. Hoffmann, Bruce A. Barshop, & Aida I. Al‐Aqeel. (2011). Atlas of Inherited Metabolic Diseases 3E. 9 indexed citations
9.
Al‐Aqeel, Aida I.. (2009). Human cloning, stem cell research. An Islamic perspective.. PubMed. 30(12). 1507–14. 11 indexed citations
10.
Al‐Aqeel, Aida I., et al.. (2008). Preimplantation genetic diagnosis of Morquio disease. Prenatal Diagnosis. 28(10). 900–903. 11 indexed citations
11.
Ponich, Terry, et al.. (2008). Efficacy of Argon Plasma Coagulation Compared with Topical Formalin Application for Chronic Radiation Proctopathy. SHILAP Revista de lepidopterología. 22(2). 129–132. 37 indexed citations
12.
Al‐Aqeel, Aida I., et al.. (2005). Carnitine palmitoyl transferase I deficiency. PubMed. 22(11). 268–271. 4 indexed citations
13.
Al‐Aqeel, Aida I.. (2005). Al-Aqeel Sewairi syndrome, a new autosomal recessive disorder with multicentric osteolysis, nodulosis and arthropathy. The first genetic defect of matrix metalloproteinase 2 gene.. PubMed. 26(1). 24–30. 9 indexed citations
14.
Al‐Aqeel, Aida I.. (2004). COMMON GENETICS AND METABOLIC DISEASES IN SAUDI ARABIA. 9 indexed citations
15.
Al‐Aqeel, Aida I., et al.. (1993). The combined use of intravenous and oral calcium for the treatment of vitamin D dependent rickets type II (VDDRII). Clinical Endocrinology. 39(2). 229–237. 31 indexed citations
16.
Wiese, Russell J., Hitoshi Goto, Jean M. Prahl, et al.. (1993). Vitamin D-dependency rickets type II: truncated vitamin D receptor in three kindreds. Molecular and Cellular Endocrinology. 90(2). 197–201. 43 indexed citations
17.
Al‐Aqeel, Aida I., et al.. (1992). Combined use of intravenous and oral calcium for treatment of vitamin D dependent rickets type II (VDDRII). Pediatric Neurology. 8(5). 352–352. 4 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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