Abdulrahman Alswaid

3.1k total citations
29 papers, 1.1k citations indexed

About

Abdulrahman Alswaid is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Abdulrahman Alswaid has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 5 papers in Clinical Biochemistry. Recurrent topics in Abdulrahman Alswaid's work include Connective tissue disorders research (6 papers), Metabolism and Genetic Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Abdulrahman Alswaid is often cited by papers focused on Connective tissue disorders research (6 papers), Metabolism and Genetic Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Abdulrahman Alswaid collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Abdulrahman Alswaid's co-authors include Mohammed Al Balwi, André Mégarbané, Laurence Faivre, Arnold Münnich, Valérie Cormier‐Daire, Hélène Dollfus, Yves Alembik, Peter H. Byers, Shawna M. Pyott and David R. Eyre and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Atherosclerosis.

In The Last Decade

Abdulrahman Alswaid

27 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Abdulrahman Alswaid Saudi Arabia 16 698 509 195 159 155 29 1.1k
Ariana Kariminejad Iran 21 715 1.0× 756 1.5× 66 0.3× 127 0.8× 284 1.8× 100 1.5k
Luitgard M. Neumann Germany 20 1.0k 1.5× 708 1.4× 170 0.9× 97 0.6× 189 1.2× 46 1.7k
Nara Sobreira United States 19 671 1.0× 690 1.4× 128 0.7× 101 0.6× 86 0.6× 61 1.3k
Nursel Elçioğlu Türkiye 19 1.3k 1.9× 1.2k 2.4× 95 0.5× 145 0.9× 195 1.3× 70 2.0k
Sanjeev S. Bhaskar United Kingdom 20 609 0.9× 1.1k 2.2× 120 0.6× 155 1.0× 84 0.5× 31 1.6k
Céline Huber France 21 1.2k 1.7× 1.2k 2.4× 161 0.8× 104 0.7× 252 1.6× 49 1.9k
Anas M. Alazami Saudi Arabia 22 584 0.8× 857 1.7× 95 0.5× 129 0.8× 100 0.6× 55 1.5k
Jill Urquhart United Kingdom 23 519 0.7× 1.3k 2.6× 120 0.6× 203 1.3× 195 1.3× 48 1.9k
James O’Sullivan United Kingdom 22 510 0.7× 1.4k 2.7× 166 0.9× 198 1.2× 141 0.9× 40 2.0k
Monika Goś Poland 19 331 0.5× 769 1.5× 91 0.5× 114 0.7× 94 0.6× 49 1.2k

Countries citing papers authored by Abdulrahman Alswaid

Since Specialization
Citations

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

Fields of papers citing papers by Abdulrahman Alswaid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdulrahman Alswaid

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

All Works

20 of 20 papers shown
1.
Almannai, Mohammed, Abdulrahman Alswaid, Wafaa Eyaid, et al.. (2024). Consanguinity and Occurrence of Monogenic Diseases in a Single Tertiary Centre in Riyadh, Saudi Arabia: A 2 Years Cross-Sectional Study. The Application of Clinical Genetics. Volume 17. 151–158.
2.
Alharbi, Wardah, Lamia Alsubaie, Abdulrahman Alswaid, et al.. (2022). The variant artificial intelligence easy scoring (VARIES) system. Computers in Biology and Medicine. 145. 105492–105492. 2 indexed citations
3.
Eissa, Mariam Al, Lamia Alsubaie, Abdulrahman Alswaid, et al.. (2021). Genetic carrier screening for disorders included in newborn screening in the Saudi population. SHILAP Revista de lepidopterología. 4(2). 70–75. 7 indexed citations
4.
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
5.
Alsubaie, Lamia, et al.. (2021). The rate of secondary genomic findings in the Saudi population. American Journal of Medical Genetics Part A. 188(1). 83–88. 7 indexed citations
6.
Alswaid, Abdulrahman, et al.. (2020). Incidental discovery of an interstitial emphysematous cystitis with liver abscess: A report of hematogenous spread of infection. Urology Case Reports. 31. 101134–101134. 1 indexed citations
7.
8.
Alrifai, Muhammad Talal, et al.. (2018). Epilepsy in Propionic Acidemia: Case Series of 14 Saudi Patients. Journal of Child Neurology. 33(11). 713–717. 5 indexed citations
9.
Balwi, Mohammed Al, et al.. (2018). Tetrasomy 18p: case report and review of literature. The Application of Clinical Genetics. Volume 11. 9–14. 11 indexed citations
10.
Almontashiri, Naif A. M., Abdulrahman Alswaid, Andrea M. Oza, et al.. (2017). Recurrent variants in OTOF are significant contributors to prelingual nonsydromic hearing loss in Saudi patients. Genetics in Medicine. 20(5). 536–544. 19 indexed citations
11.
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
12.
Alswaid, Abdulrahman, et al.. (2014). Blepharo‐cheilo‐dontic (BCD) syndrome: Expanding the phenotype, case report and review of literature. American Journal of Medical Genetics Part A. 164(6). 1525–1529. 5 indexed citations
13.
Alswaid, Abdulrahman, et al.. (2013). Hereditary deletion of the entire FAM20C gene in a patient with Raine syndrome. American Journal of Medical Genetics Part A. 161(12). 3155–3160. 33 indexed citations
14.
Aldahmesh, Mohammed A., Arif O. Khan, Jawahir Y. Mohamed, et al.. (2012). Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes. Genetics in Medicine. 14(12). 955–962. 47 indexed citations
15.
Suzuki, Shigeru, Ok‐Hwa Kim, Yoshio Makita, et al.. (2011). Axial spondylometaphyseal dysplasia: Additional reports. American Journal of Medical Genetics Part A. 155(10). 2521–2528. 8 indexed citations
16.
Christiansen, Helena E., Ulrike Schwarze, Shawna M. Pyott, et al.. (2010). Homozygosity for a Missense Mutation in SERPINH1, which Encodes the Collagen Chaperone Protein HSP47, Results in Severe Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 86(3). 389–398. 228 indexed citations
17.
Faiyaz‐Ul‐Haque, Muhammad, Syed Hassan Ejaz Zaidi, Abdulrahman Alswaid, et al.. (2008). A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome. Atherosclerosis. 203(2). 466–471. 23 indexed citations
18.
Abu‐Amero, Khaled K., et al.. (2007). LC‐MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice‐acceptor site mutation in the SLC7A9 gene. Journal of Inherited Metabolic Disease. 30(4). 611–611. 10 indexed citations
19.
Dagoneau, Nathalie, Catherine Benoist-Lasselin, Céline Huber, et al.. (2004). ADAMTS10 Mutations in Autosomal Recessive Weill-Marchesani Syndrome. The American Journal of Human Genetics. 75(5). 801–806. 207 indexed citations
20.
Bond, Jacquelyn, Daniel J. Hampshire, Kelly Springell, et al.. (2003). Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size. The American Journal of Human Genetics. 73(5). 1170–1177. 133 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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