Hamad Al‐Mojalli

493 total citations
8 papers, 125 citations indexed

About

Hamad Al‐Mojalli is a scholar working on Nephrology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Hamad Al‐Mojalli has authored 8 papers receiving a total of 125 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Nephrology, 4 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Hamad Al‐Mojalli's work include Renal Diseases and Glomerulopathies (5 papers), Amino Acid Enzymes and Metabolism (2 papers) and Ion Transport and Channel Regulation (2 papers). Hamad Al‐Mojalli is often cited by papers focused on Renal Diseases and Glomerulopathies (5 papers), Amino Acid Enzymes and Metabolism (2 papers) and Ion Transport and Channel Regulation (2 papers). Hamad Al‐Mojalli collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Hamad Al‐Mojalli's co-authors include Brian F. Meyer, Mohamed H. Al‐Hamed, Arif O. Khan, Mohammed A. Aldahmesh, Fowzan S. Alkuraya, John A. Sayer, Pamela M. Carroll, Essam Al‐Sabban, Noel Edwards and Khalid Alhasan and has published in prestigious journals such as American Journal of Kidney Diseases, Human Mutation and Genetics in Medicine.

In The Last Decade

Hamad Al‐Mojalli

7 papers receiving 123 citations

Peers

Hamad Al‐Mojalli
Holly Mabillard United Kingdom
Mick Henderson United Kingdom
Katie B. Williams United States
Jennifer Arroyo United States
Kristin D׳Aco United States
Hamad Al‐Mojalli
Citations per year, relative to Hamad Al‐Mojalli Hamad Al‐Mojalli (= 1×) peers Marguerite Hureaux

Countries citing papers authored by Hamad Al‐Mojalli

Since Specialization
Citations

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

Fields of papers citing papers by Hamad Al‐Mojalli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hamad Al‐Mojalli

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

All Works

8 of 8 papers shown
2.
Al‐Hamed, Mohamed H., Maged H. Hussein, Hamad Al‐Mojalli, et al.. (2022). Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients. Human Mutation. 43(12). e24–e37. 8 indexed citations
3.
Alhasan, Khalid, et al.. (2019). Successful Treatment of Recurrent Focal Segmental Glomerulosclerosis After Transplantation in Children: A Single-Center Experience. Transplantation Proceedings. 51(2). 517–521. 2 indexed citations
4.
Al‐Hamed, Mohamed H., Essam Al‐Sabban, Hamad Al‐Mojalli, et al.. (2013). A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families. Journal of Human Genetics. 58(7). 480–489. 35 indexed citations
5.
Al‐Romaih, Khaldoun, Giulio Genovese, Hamad Al‐Mojalli, et al.. (2011). Genetic Diagnosis in Consanguineous Families With Kidney Disease by Homozygosity Mapping Coupled With Whole-Exome Sequencing. American Journal of Kidney Diseases. 58(2). 186–195. 14 indexed citations
6.
Al‐Owain, Mohammed, Namik Kaya, Hamad Alzaidan, et al.. (2010). Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy. Journal of Immunology Research. 2010(1). 586342–586342. 12 indexed citations
7.
Aldahmesh, Mohammed A., et al.. (2009). Characterization ofCTNSmutations in Arab patients with Cystinosis. Ophthalmic Genetics. 30(4). 185–189. 31 indexed citations
8.
Carroll, Pamela M., et al.. (2006). Novel mutations underlying nephrogenic diabetes insipidus in Arab families. Genetics in Medicine. 8(7). 443–447. 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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