Mohammed El‐Khateeb

506 total citations
15 papers, 351 citations indexed

About

Mohammed El‐Khateeb is a scholar working on Molecular Biology, Immunology and Genetics. According to data from OpenAlex, Mohammed El‐Khateeb has authored 15 papers receiving a total of 351 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Immunology and 3 papers in Genetics. Recurrent topics in Mohammed El‐Khateeb's work include Inflammasome and immune disorders (3 papers), IL-33, ST2, and ILC Pathways (2 papers) and Gout, Hyperuricemia, Uric Acid (2 papers). Mohammed El‐Khateeb is often cited by papers focused on Inflammasome and immune disorders (3 papers), IL-33, ST2, and ILC Pathways (2 papers) and Gout, Hyperuricemia, Uric Acid (2 papers). Mohammed El‐Khateeb collaborates with scholars based in Jordan, United States and Cyprus. Mohammed El‐Khateeb's co-authors include Hasan A. Majeed, Hatem El‐Shanti, Kamel Ajlouni, Marwan K. Tayeh, Yacoub M. Irshaid, Nabiha Salem, André Mégarbané, Zainab Lafi, Dana Hyassat and Valérie Delague and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Annals of Neurology.

In The Last Decade

Mohammed El‐Khateeb

14 papers receiving 343 citations

Peers

Mohammed El‐Khateeb
Dan Chang China
Patricia L. Brazee United States
Yini Ke China
M. Forino Italy
Ken Saida Japan
Andrea Ottria Netherlands
Mohammed El‐Khateeb
Citations per year, relative to Mohammed El‐Khateeb Mohammed El‐Khateeb (= 1×) peers Christina V Jones

Countries citing papers authored by Mohammed El‐Khateeb

Since Specialization
Citations

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

Fields of papers citing papers by Mohammed El‐Khateeb

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammed El‐Khateeb. 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 Mohammed El‐Khateeb. The network helps show where Mohammed El‐Khateeb may publish in the future.

Co-authorship network of co-authors of Mohammed El‐Khateeb

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

All Works

15 of 15 papers shown
1.
Bdour, Muawyah Al, et al.. (2024). The association of endothelial nitric oxide synthase (eNOS) gene polymorphisms and diabetic retinopathy among patients with type 2 diabetes: A case-control study.. PubMed. 30. 390–398.
2.
Bdour, Muawyah Al, et al.. (2021). Lack of relationship between Alu repetitive elements in angiotensin converting enzyme and the severity of diabetic retinopathy. Journal of Medical Biochemistry. 40(3). 302–309. 7 indexed citations
3.
Bdour, Muawyah Al, et al.. (2021). The relationship between aldose reductase gene C106T polymorphism and the severity of retinopathy in Type 2 diabetic patients. Journal of Research in Medical Sciences. 26(1). 2–2. 8 indexed citations
4.
Irshaid, Yacoub M., et al.. (2020). SLCO1B1 Gene Polymorphisms (rs2306283 and rs4149056) and Statin-Induced Myopathy in Jordanian Diabetics. PubMed. 16(3). 281–288. 4 indexed citations
5.
El‐Khateeb, Mohammed, et al.. (2017). Association of genetic polymorphisms of MERTK with multiple sclerosis among Jordanians. Biomedical Research-tokyo. 28(1). 399–404. 3 indexed citations
6.
El‐Khateeb, Mohammed, et al.. (2016). Ex vivo differentiation of human bone marrow-derived stem cells into neuronal cell-like lineages. SHILAP Revista de lepidopterología. Volume 4. 35–44. 3 indexed citations
7.
Lafi, Zainab, Yacoub M. Irshaid, Mohammed El‐Khateeb, Kamel Ajlouni, & Dana Hyassat. (2015). Association of rs7041 and rs4588 Polymorphisms of the Vitamin D Binding Protein and the rs10741657 Polymorphism of CYP2R1 with Vitamin D Status Among Jordanian Patients. Genetic Testing and Molecular Biomarkers. 19(11). 629–636. 42 indexed citations
8.
Sughayer, Maher A., et al.. (2014). Epstein-Barr virus and Hodgkin lymphoma in Jordan. Hematology/Oncology and Stem Cell Therapy. 7(2). 85–89. 11 indexed citations
9.
Abujbara, Mousa, et al.. (2014). Permanent neonatal diabetes mellitus in Jordan. Journal of Pediatric Endocrinology and Metabolism. 27(9-10). 879–83. 8 indexed citations
10.
Shammas, Christos, Emmanuel Kanavakis, Mohammed El‐Khateeb, et al.. (2010). ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia. Clinical Chemistry and Laboratory Medicine (CCLM). 48(12). 1713–1718. 8 indexed citations
11.
El‐Shanti, Hatem, Hasan A. Majeed, & Mohammed El‐Khateeb. (2006). Familial Mediterranean fever in Arabs. The Lancet. 367(9515). 1016–1024. 99 indexed citations
12.
El‐Khateeb, Mohammed, et al.. (2006). Familial Mediterranean fever in the Syrian population: gene mutation frequencies, carrier rates and phenotype–genotype correlation. European Journal of Medical Genetics. 49(6). 481–486. 62 indexed citations
13.
Majeed, Hasan A., et al.. (2005). The Spectrum of Familial Mediterranean Fever Gene Mutations in Arabs: Report of a Large Series. Seminars in Arthritis and Rheumatism. 34(6). 813–818. 61 indexed citations
14.
Christodoulou, Kyproula, Amar Mubaidin, Mohammed El‐Khateeb, et al.. (2000). A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1–p12. Annals of Neurology. 48(6). 877–884. 33 indexed citations
15.
Alkan, Şefik Ş., et al.. (1976). Induction of T cell response to haptens coupled to mycobacteria. Journal of Immunological Methods. 10(2-3). 197–206. 2 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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