Hamoud Al‐Mousa

4.6k total citations
56 papers, 896 citations indexed

About

Hamoud Al‐Mousa is a scholar working on Immunology, Genetics and Hematology. According to data from OpenAlex, Hamoud Al‐Mousa has authored 56 papers receiving a total of 896 indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Immunology, 18 papers in Genetics and 14 papers in Hematology. Recurrent topics in Hamoud Al‐Mousa's work include Immunodeficiency and Autoimmune Disorders (38 papers), Immune Cell Function and Interaction (14 papers) and Blood disorders and treatments (10 papers). Hamoud Al‐Mousa is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (38 papers), Immune Cell Function and Interaction (14 papers) and Blood disorders and treatments (10 papers). Hamoud Al‐Mousa collaborates with scholars based in Saudi Arabia, France and United States. Hamoud Al‐Mousa's co-authors include Bandar Al‐Saud, Rand Arnaout, Hasan Al‐Dhekri, Saleh Al‐Muhsen, Abdulaziz Al‐Ghonaium, Abbas Hawwari, Anas M. Alazami, Waleed Al–Herz, Osama Alsmadi and Capucine Pïcard and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Journal of Allergy and Clinical Immunology.

In The Last Decade

Hamoud Al‐Mousa

52 papers receiving 881 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hamoud Al‐Mousa Saudi Arabia 17 662 253 152 150 121 56 896
D Barge United Kingdom 18 510 0.8× 146 0.6× 197 1.3× 171 1.1× 126 1.0× 28 822
Toshinao Kawai Japan 16 483 0.7× 126 0.5× 164 1.1× 106 0.7× 63 0.5× 50 930
María R. López-Álvarez Spain 20 793 1.2× 139 0.5× 132 0.9× 169 1.1× 40 0.3× 77 1.3k
Francesca Mazzetta Italy 17 480 0.7× 133 0.5× 160 1.1× 210 1.4× 123 1.0× 21 863
Beate Fischer Germany 8 793 1.2× 295 1.2× 78 0.5× 69 0.5× 161 1.3× 10 911
Alain Fischer France 10 483 0.7× 110 0.4× 212 1.4× 166 1.1× 61 0.5× 15 751
Fabien Touzot France 21 458 0.7× 261 1.0× 490 3.2× 161 1.1× 56 0.5× 45 1.2k
Sho Hokibara Japan 13 688 1.0× 94 0.4× 119 0.8× 73 0.5× 109 0.9× 18 974
Emily S.J. Edwards Australia 15 628 0.9× 132 0.5× 185 1.2× 132 0.9× 48 0.4× 37 993
Emanuele Marchi United Kingdom 15 350 0.5× 77 0.3× 242 1.6× 146 1.0× 56 0.5× 28 887

Countries citing papers authored by Hamoud Al‐Mousa

Since Specialization
Citations

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

Fields of papers citing papers by Hamoud Al‐Mousa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hamoud Al‐Mousa

This figure shows the co-authorship network connecting the top 25 collaborators of Hamoud Al‐Mousa. A scholar is included among the top collaborators of Hamoud Al‐Mousa 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 Hamoud Al‐Mousa. Hamoud Al‐Mousa 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.
Nademi, Zohreh, Alexandra Laberko, Dmitry Balashov, et al.. (2025). Outcomes of Hematopoietic Stem Cell Transplantation in 5 Patients with Autosomal Recessive RIPK1-Deficiency. Journal of Clinical Immunology. 45(1). 65–65. 3 indexed citations
2.
Al‐Mazrou, Amer, Ali Almehaidib, Khalid A. Alsaleem, et al.. (2025). Homozygous Loss of Function PIK3CD Mutation in Multiple Siblings Leading To B Cell Dysregulation and Autoimmunity. Journal of Clinical Immunology. 45(1). 139–139.
3.
Al‐Mousa, Hamoud & Mohamed‐Ridha Barbouche. (2023). Genetics of Inborn Errors of Immunity in highly consanguineous Middle Eastern and North African populations. Seminars in Immunology. 67. 101763–101763. 8 indexed citations
4.
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
5.
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.
6.
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
7.
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
8.
Alsum, Zobaida, Mofareh AlZahrani, Hamoud Al‐Mousa, et al.. (2020). Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB. Frontiers in Pediatrics. 8. 9–9. 4 indexed citations
9.
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.
11.
Al‐Mousa, Hamoud, Mohamed Abouelhoda, Dorota Monies, et al.. (2018). High Incidence of Severe Combined Immunodeficiency Disease in Saudi Arabia Detected Through Combined T Cell Receptor Excision Circle and Next Generation Sequencing of Newborn Dried Blood Spots. Frontiers in Immunology. 9. 782–782. 54 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.
Al–Herz, Waleed & Hamoud Al‐Mousa. (2013). Combined immunodeficiency: The Middle East experience. Journal of Allergy and Clinical Immunology. 131(3). 658–660. 25 indexed citations
14.
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
15.
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
16.
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
17.
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
18.
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
19.
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
20.
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

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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