Ahmed Alsuliman

658 total citations
22 papers, 451 citations indexed

About

Ahmed Alsuliman is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ahmed Alsuliman has authored 22 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 17 papers in Hematology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ahmed Alsuliman's work include Hemoglobinopathies and Related Disorders (16 papers), Iron Metabolism and Disorders (15 papers) and Prenatal Screening and Diagnostics (8 papers). Ahmed Alsuliman is often cited by papers focused on Hemoglobinopathies and Related Disorders (16 papers), Iron Metabolism and Disorders (15 papers) and Prenatal Screening and Diagnostics (8 papers). Ahmed Alsuliman collaborates with scholars based in Saudi Arabia, United States and India. Ahmed Alsuliman's co-authors include Amein K. Al‐Ali, Abdulrahman Alsultan, Martin H. Steinberg, David H.K. Chui, Anushruti Sarvaria, Takuya Sekine, Robert Sargeant, David Marin, Kate Stringaris and Hugues de Lavallade and has published in prestigious journals such as Blood, British Journal of Haematology and Haematologica.

In The Last Decade

Ahmed Alsuliman

20 papers receiving 446 citations

Peers

Countries citing papers authored by Ahmed Alsuliman

Since Specialization

Citations

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

Fields of papers citing papers by Ahmed Alsuliman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ahmed Alsuliman

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Primary myelofibrosis with concurrent paroxysmal nocturnal haemoglobinuria presenting with erectile dysfunction 2022 ·Oxford Medical Case Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ahmed Alsuliman	0
2	A case study on Green Buildings and its applicability in Bahrain 2021 ·(unknown), (unknown), Ahmed Alsuliman, (unknown), (unknown)	1
3	Co-inheritance of alpha globin gene deletion lowering serum iron level in female beta thalassemia patients 2019 ·Molecular Biology Reports ·Sayed AbdulAzeez, Noor B. Almandil, Zaki A. Naserullah, (unknown), Ahmed Alsuliman, (unknown), J. Francis Borgio	5
4	Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease 2018 ·Genetic Testing and Molecular Biomarkers ·Abdulrahman Alsultan, Ahmed Alsuliman, Aamer Aleem, Farjah Algahtani, Majid Alfadhel	11
5	<b><i>ANTXR1</i></b> Intronic Variants Are Associated with Fetal Hemoglobin in the Arab-Indian Haplotype of Sickle Cell Disease 2018 ·Acta Haematologica ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Ahmed Alsuliman, Chittibabu Vatte	5
6	KLF1 gene and borderline hemoglobin A2 in Saudi population 2018 ·Archives of Medical Science ·J. Francis Borgio, Sayed AbdulAzeez, (unknown), Zaki A. Naserullah, (unknown), Ahmed Alsuliman, (unknown), Amein K. Al‐Ali	17
7	The prevalence of abnormal leukocyte count, and its predisposing factors, in patients with sickle cell disease in Saudi Arabia 2017 ·Journal of Blood Medicine ·Anwar Ahmed, Yosra Z. Ali, Ahmed Alsuliman, (unknown), (unknown), (unknown), (unknown), Rayan A. Ahmed, Donna K. McClish, Hamdan Al‐Jahdali	20
8	The ‑α3.7 deletion in α‑globin genes increases the concentration of fetal hemoglobin and hemoglobin A2 in a Saudi Arabian population 2017 ·Molecular Medicine Reports ·J. Francis Borgio, Sayed AbdulAzeez, Noor B. Almandil, Zaki A. Naserullah, (unknown), Ahmed Alsuliman, (unknown), (unknown), (unknown), Mohammed Alkhalifah, Mohammed Akhtar, Hatem Qutub, Amein K. Al‐Ali	8
9	Demands and challenges for patients with sickle‐cell disease requiring hematopoietic stem cell transplantation in Saudi Arabia 2016 ·Pediatric Transplantation ·Abdulrahman Alsultan, Wasil Jastaniah, (unknown), (unknown), (unknown), Ahmed Alsuliman, (unknown)	12
10	Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia 2016 ·Blood Cells Molecules and Diseases ·Elmutaz Shaikho Elhaj Mohammed, (unknown), Abdulrahman Alsultan, Abdullah M. Al‐Rubaish, Fahad Al‐Muhanna, Zaki A. Naserullah, Ahmed Alsuliman, Hatem Qutub, Pradeep Kumar Patra, Paola Sebastiani, Kristin Baltrusaitis, John J. Farrell, Zhihua Jiang, Hongyuan Luo, David H.K. Chui, Amein K. Al‐Ali, Martin H. Steinberg	11
11	Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients 2015 ·Blood Cells Molecules and Diseases ·(unknown), J. Francis Borgio, Sayed AbdulAzeez, Ahmed Alsuliman, (unknown), Zaki A. Naserullah, (unknown), (unknown), (unknown), (unknown), Fahad Al‐Muhanna, Martin H. Steinberg, Amein K. Al‐Ali	14
12	BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia 2015 ·Blood Cells Molecules and Diseases ·Paola Sebastiani, John J. Farrell, (unknown), (unknown), (unknown), Heather M. Shappell, Harold Bae, Jacqueline N. Milton, Clinton T. Baldwin, Abdullah M. Al‐Rubaish, Zaki A. Naserullah, Fahd A Al-Muhanna, Ahmed Alsuliman, (unknown), Lindsay A. Farrer, Duyen Ngo, Vinod Vathipadiekal, David H.K. Chui, Amein K. Al‐Ali, Martin H. Steinberg	32
13	Polymorphisms Associated with the Arab-Indian Haplotype of Sickle Cell Anemia Are Candidate Fetal Hemoglobin Gene Modulators 2015 ·Blood ·Vinod Vathipadiekal, Abdulrahman Alsultan, John Farrell, Abdullah M. Al‐Rubaish, Fahad Al‐Muhanna, Zaki A. Naserullah, Ahmed Alsuliman, Pradeep Kumar Patra, Jacqueline N. Milton, Lindsay A. Farrer, David H.K. Chui, Amein K. Al‐Ali, Paola Sebastiani, Martin H. Steinberg	1
14	Leukemia-induced phenotypic and functional defects in natural killer cells predict failure to achieve remission in acute myeloid leukemia 2014 ·Haematologica ·Kate Stringaris, Takuya Sekine, (unknown), Ahmed Alsuliman, (unknown), Robert Sargeant, Jiří Pavlů, (unknown), Hugues de Lavallade, Anushruti Sarvaria, David Marin, Stephan Mielke, Jane F. Apperley, Elizabeth J. Shpall, John Barrett, Katy Rezvani	158
15	Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype 2013 ·Blood Cells Molecules and Diseases ·Duyen Ngo, Harold Bae, Martin H. Steinberg, Paola Sebastiani, Nadia Solovieff, Clinton T. Baldwin, Efthymia Melista, Surinder Safaya, Lindsay A. Farrer, Ahmed Alsuliman, Waleed H. Albuali, (unknown), Zaki A. Naserullah, Idowu Akinsheye, Patrick G. Gallagher, Hongyuan Luo, David H.K. Chui, John Farrell, Amein K. Al‐Ali, Abdulrahman Alsultan	42
16	Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign 2013 ·British Journal of Haematology ·Abdulrahman Alsultan, (unknown), Paula J. Griffin, Ahmed Alsuliman, Hazem A. Ghabbour, Paola Sebastiani, Waleed H. Albuali, Amein K. Al‐Ali, David H.K. Chui, Martin H. Steinberg	60
17	The Evolutionary Impact Of Malaria On The Saudi Arabian Genome 2013 ·Blood ·John J. Farrell, (unknown), Amein K. Al‐Ali, Abdullah M. Al‐Rubaish, Zaki A. Naserullah, Ahmed Alsuliman, Martin H. Steinberg, Clinton T. Baldwin	1
18	A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype 2012 ·American Journal of Hematology ·Abdulrahman Alsultan, Duyen Ngo, John J. Farrell, Idowu Akinsheye, Nadia Solovieff, Hazem A. Ghabbour, Amein K. Al‐Ali, Ahmed Alsuliman, (unknown), Waleed H. Albuali, (unknown), Clinton T. Baldwin, Lindsay A. Farrer, Hong Luo, Efthymia Melista, Surinder Safaya, (unknown), David H.K. Chui, Martin H. Steinberg	11
19	Co-Inheritance of Delta Thalassemia Might Contribute to the High Fetal Hemoglobin in Sickle Cell Anemia Patients with the Saudi-Indian Haplotype 2011 ·Blood ·Abdulrahman Alsultan, Duyen Ngo, John Farrell, Hazem A. Ghabbour, Idowu Akinsheye, Amein K. Al‐Ali, Ahmed Alsuliman, (unknown), Waleed H. Albuali, (unknown), Paola Sebastiani, Clinton T. Baldwin, David H.K. Chui, Martin H. Steinberg	1
20	A 15-year-old girl with pancytopenia and congenital defects 2009 ·Annals of Saudi Medicine ·Ahmed Alsuliman, (unknown)	0

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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