Abdulrahman Alsultan

2.6k total citations
70 papers, 1.5k citations indexed

About

Abdulrahman Alsultan is a scholar working on Hematology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Abdulrahman Alsultan has authored 70 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Hematology, 29 papers in Genetics and 18 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Abdulrahman Alsultan's work include Hemoglobinopathies and Related Disorders (23 papers), Iron Metabolism and Disorders (18 papers) and Acute Lymphoblastic Leukemia research (15 papers). Abdulrahman Alsultan is often cited by papers focused on Hemoglobinopathies and Related Disorders (23 papers), Iron Metabolism and Disorders (18 papers) and Acute Lymphoblastic Leukemia research (15 papers). Abdulrahman Alsultan collaborates with scholars based in Saudi Arabia, United States and India. Abdulrahman Alsultan's co-authors include David H.K. Chui, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Clinton T. Baldwin, Duyen Ngo, Idowu Akinsheye, George J. Dover, Abdullah Alangari and Raif S. Geha and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Abdulrahman Alsultan

64 papers receiving 1.5k 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 Alsultan Saudi Arabia 18 801 720 380 305 285 70 1.5k
Shalini Shenoy United States 23 929 1.2× 851 1.2× 154 0.4× 588 1.9× 206 0.7× 87 1.6k
Deborah Hurst United States 17 788 1.0× 1.0k 1.5× 232 0.6× 330 1.1× 373 1.3× 32 1.8k
Isabel Badell Spain 24 279 0.3× 806 1.1× 265 0.7× 264 0.9× 234 0.8× 108 1.6k
Courtney D. Fitzhugh United States 22 1.7k 2.1× 1.3k 1.8× 155 0.4× 822 2.7× 390 1.4× 85 2.2k
Mouhab Ayas Saudi Arabia 21 251 0.3× 756 1.1× 196 0.5× 200 0.7× 316 1.1× 92 1.3k
N Philippe France 18 266 0.3× 456 0.6× 327 0.9× 235 0.8× 255 0.9× 59 1.4k
Maurizio Miano Italy 19 146 0.2× 620 0.9× 262 0.7× 174 0.6× 158 0.6× 68 1.1k
Michael L. Graham United States 15 531 0.7× 781 1.1× 281 0.7× 201 0.7× 200 0.7× 32 1.3k
G. M. Bartelds Netherlands 13 323 0.4× 334 0.5× 1.0k 2.6× 106 0.3× 178 0.6× 15 1.9k
Dipika Mohanty India 22 664 0.8× 885 1.2× 95 0.3× 328 1.1× 117 0.4× 90 1.4k

Countries citing papers authored by Abdulrahman Alsultan

Since Specialization
Citations

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

Fields of papers citing papers by Abdulrahman Alsultan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Abdulrahman Alsultan

This figure shows the co-authorship network connecting the top 25 collaborators of Abdulrahman Alsultan. A scholar is included among the top collaborators of Abdulrahman Alsultan 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 Alsultan. Abdulrahman Alsultan 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.
Brock, Matthew E., et al.. (2024). Utilizing video prompting with people with severe disabilities: A systematic literature review. Children and Youth Services Review. 161. 107652–107652.
2.
Alotaibi, Ghazi, et al.. (2024). Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program”. Journal of Epidemiology and Global Health. 14(3). 1242–1248. 3 indexed citations
3.
Alsultan, Abdulrahman, et al.. (2023). Antithrombin Deficiency Is Associated with a Novel Homozygous Detrimental Mutation in SERPINC1 Gene in a Saudi Female. SHILAP Revista de lepidopterología. 2023. 1–4. 1 indexed citations
4.
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6.
Jastaniah, Wasil, et al.. (2020). Incidence trends of childhood acute lymphoblastic leukemia in Saudi Arabia: Increasing incidence or competing risks?. Cancer Epidemiology. 67. 101764–101764. 17 indexed citations
7.
Alsultan, Abdulrahman, et al.. (2020). Travel burden and geographic access to health care among children with cancer in Saudi Arabia. Eastern Mediterranean Health Journal. 26(11). 1355–1361. 3 indexed citations
8.
Alsultan, Abdulrahman, Ahmed Alsuliman, Aamer Aleem, Farjah Algahtani, & Majid Alfadhel. (2018). Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease. Genetic Testing and Molecular Biomarkers. 22(9). 561–567. 11 indexed citations
9.
Jastaniah, Wasil, et al.. (2018). Prevalence of hereditary cancer susceptibility syndromes in children with cancer in a highly consanguineous population. Cancer Epidemiology. 55. 88–95. 13 indexed citations
10.
11.
Jastaniah, Wasil, et al.. (2017). Treatment results in children with myeloid leukemia of Down syndrome in Saudi Arabia: A multicenter SAPHOS leukemia group study. Leukemia Research. 58. 48–54. 2 indexed citations
12.
Shamseldin, Hanan E., et al.. (2016). A lethal phenotype associated with tissue plasminogen deficiency in humans. Human Genetics. 135(10). 1209–1211. 1 indexed citations
13.
Balwi, Mohammed Al, et al.. (2016). Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients. Cancer Genetics. 209(4). 171–176. 11 indexed citations
14.
Alsultan, Abdulrahman, et al.. (2016). Activation-resistant homozygous protein C R229W mutation causing familial perinatal intracranial hemorrhage and delayed onset of thrombosis. Thrombosis Research. 143. 17–21. 3 indexed citations
15.
16.
Ngo, Duyen, Harold Bae, Martin H. Steinberg, et al.. (2013). Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype. Blood Cells Molecules and Diseases. 51(1). 22–26. 42 indexed citations
17.
Alangari, Abdullah, Abdulrahman Alsultan, Nouran Adly, et al.. (2012). LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency. Journal of Allergy and Clinical Immunology. 130(2). 481–488.e2. 163 indexed citations
18.
Alsultan, Abdulrahman, et al.. (2012). Spontaneous Remission of Juvenile Myelomonocytic Leukemia withNRASMutation. Pediatric Hematology and Oncology. 29(7). 624–626.
19.
Alsultan, Abdulrahman, et al.. (2010). SARCOIDOSIS PRESENTING WITH MASSIVE SPLENOMEGALY IN A CHILD WITH A HISTORY OF IRIDOCYCLITIS AND SENSORINEURAL DEAFNESS. Pediatric Hematology and Oncology. 27(6). 490–495. 4 indexed citations
20.
Alsultan, Abdulrahman, et al.. (2009). Tacrolimus as an alternative to cyclosporine in the maintenance phase of immunosuppressive therapy for severe aplastic anemia in children. Pediatric Blood & Cancer. 52(5). 626–630. 20 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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