Bandar Al‐Saud

1.7k total citations
37 papers, 493 citations indexed

About

Bandar Al‐Saud is a scholar working on Immunology, Genetics and Epidemiology. According to data from OpenAlex, Bandar Al‐Saud has authored 37 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Immunology, 10 papers in Genetics and 8 papers in Epidemiology. Recurrent topics in Bandar Al‐Saud's work include Immunodeficiency and Autoimmune Disorders (22 papers), Blood disorders and treatments (6 papers) and Immune Cell Function and Interaction (6 papers). Bandar Al‐Saud is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (22 papers), Blood disorders and treatments (6 papers) and Immune Cell Function and Interaction (6 papers). Bandar Al‐Saud collaborates with scholars based in Saudi Arabia, Canada and United States. Bandar Al‐Saud's co-authors include Hamoud Al‐Mousa, Rand Arnaout, Hasan Al‐Dhekri, Saleh Al‐Muhsen, Abdulaziz Al‐Ghonaium, Sigurveig Sigurdardottir, Osama Alsmadi, Abbas Hawwari, Zobaida Alsum and Anas M. Alazami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Allergy and Clinical Immunology and Frontiers in Immunology.

In The Last Decade

Bandar Al‐Saud

32 papers receiving 485 citations

Peers

Bandar Al‐Saud
Rand Arnaout Saudi Arabia
Nesrin Gülez Türkiye
Hasan Al‐Dhekri Saudi Arabia
Caner Aytekin Türkiye
Adina Kay Knight United States
Ottavia M. Delmonte United States
Rand Arnaout Saudi Arabia
Bandar Al‐Saud
Citations per year, relative to Bandar Al‐Saud Bandar Al‐Saud (= 1×) peers Rand Arnaout

Countries citing papers authored by Bandar Al‐Saud

Since Specialization
Citations

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

Fields of papers citing papers by Bandar Al‐Saud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bandar Al‐Saud

This figure shows the co-authorship network connecting the top 25 collaborators of Bandar Al‐Saud. A scholar is included among the top collaborators of Bandar Al‐Saud 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 Bandar Al‐Saud. Bandar Al‐Saud 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
2.
Al‐Saud, Bandar, et al.. (2024). A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report. Frontiers in Immunology. 15. 1329610–1329610. 2 indexed citations
3.
Al‐Saud, Bandar, Reem Mohammed, Hasan Al‐Dhekri, et al.. (2023). Quality of Life Evaluation in Saudi Arabian Pediatric Patients with Primary Immunodeficiency Diseases Receiving 20% Subcutaneous IgG Infusions at Home. Journal of Clinical Immunology. 43(6). 1360–1366. 1 indexed citations
4.
Sheikh, Farrukh, Hasan Al‐Dhekri, Bandar Al‐Saud, et al.. (2022). Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia. Journal of Clinical Immunology. 43(2). 479–484.
5.
Janssen, Erin, Anas M. Alazami, Abdullah Alsuliman, et al.. (2022). A homozygous truncating mutation of FGL2 is associated with immune dysregulation. Journal of Allergy and Clinical Immunology. 151(2). 572–578.e1. 2 indexed citations
6.
Ayas, Mouhab, Amal Al-Seraihy, Khawar Siddiqui, et al.. (2020). Hematopoietic stem cell transplantation in children with Griscelli syndrome type 2: a single-center report on 35 patients. Bone Marrow Transplantation. 55(10). 2026–2034. 14 indexed citations
7.
Al‐Saud, Bandar, et al.. (2020). A Case with Purine Nucleoside Phosphorylase Deficiency Suffering from Late-Onset Systemic Lupus Erythematosus and Lymphoma. Journal of Clinical Immunology. 40(6). 833–839. 19 indexed citations
8.
Jacob, Minnie, Xian Luo, Hamoud Al‐Mousa, et al.. (2019). Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker Discovery. Metabolites. 9(11). 274–274. 19 indexed citations
10.
Al‐Saud, Bandar & Sigurveig Sigurdardottir. (2018). Early Introduction of Egg and the Development of Egg Allergy in Children: A Systematic Review and Meta-Analysis. International Archives of Allergy and Immunology. 177(4). 350–359. 26 indexed citations
11.
Alazami, Anas M., Bandar Al‐Saud, Dorota Monies, et al.. (2018). Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency. Frontiers in Immunology. 9. 203–203. 48 indexed citations
12.
Al‐Saud, Bandar, Hamoud Al‐Mousa, Abdulaziz Al‐Ghonaium, et al.. (2015). Primary Immunodeficiency Diseases in Saudi Arabia: a Tertiary Care Hospital Experience over a Period of Three Years (2010–2013). Journal of Clinical Immunology. 35(7). 651–660. 34 indexed citations
13.
Alsum, Zobaida, Abbas Hawwari, Hanif Khalak, et al.. (2012). Clinical and Molecular Characterization of Autosomal Recessive Hyper IgE Syndrome in Saudi Arabia. Journal of Allergy and Clinical Immunology. 129(2). AB83–AB83. 1 indexed citations
14.
Alsum, Zobaida, Abbas Hawwari, Osama Alsmadi, et al.. (2012). Clinical, Immunological and Molecular Characterization of DOCK8 and DOCK8-like Deficient Patients: Single Center Experience of Twenty Five Patients. Journal of Clinical Immunology. 33(1). 55–67. 57 indexed citations
15.
Al‐Dhekri, Hasan, Hamoud Al‐Mousa, Mouhab Ayas, et al.. (2011). Allogeneic Hematopoietic Stem Cell Transplantation in Leukocyte Adhesion Deficiency Type 1: A Single Center Experience. Biology of Blood and Marrow Transplantation. 17(8). 1245–1249. 10 indexed citations
16.
Alsum, Zobaida, Bandar Al‐Saud, Abdulaziz Al‐Ghonaium, et al.. (2011). Disseminated Cryptococcal Infection in Patient With Novel JAK3 Mutation Severe Combined Immunodeficiency, With Resolution After Stem Cell Transplantation. The Pediatric Infectious Disease Journal. 31(2). 204–206. 8 indexed citations
17.
Kaya, Namik, Saleh Al‐Muhsen, Bandar Al‐Saud, et al.. (2010). ICF Syndrome in Saudi Arabia: Immunological, Cytogenetic and Molecular Analysis. Journal of Clinical Immunology. 31(2). 245–252. 10 indexed citations
18.
Al‐Saud, Bandar, Osama Alsmadi, Saleh Al‐Muhsen, et al.. (2009). A novel mutation in purine nucleoside phosphorylase in a child with normal uric acid levels. Clinical Biochemistry. 42(16-17). 1725–1727. 15 indexed citations
19.
Ayas, Mouhab, Abdullah Al‐Jefri, Ali Alahmari, et al.. (2009). Unrelated cord blood transplantation in pediatric patients: a report from Saudi Arabia. Bone Marrow Transplantation. 45(8). 1281–1286. 9 indexed citations
20.
Ackerley, Cameron, et al.. (2006). Nuclear and mitochondrial localization of the putative RNA helicase DHX32. Experimental and Molecular Pathology. 81(3). 245–248. 13 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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