Moeen Al-Sayed

643 total citations
11 papers, 106 citations indexed

About

Moeen Al-Sayed is a scholar working on Physiology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Moeen Al-Sayed has authored 11 papers receiving a total of 106 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Physiology, 5 papers in Clinical Biochemistry and 3 papers in Rheumatology. Recurrent topics in Moeen Al-Sayed's work include Metabolism and Genetic Disorders (5 papers), Diet and metabolism studies (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Moeen Al-Sayed is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Diet and metabolism studies (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Moeen Al-Sayed collaborates with scholars based in Saudi Arabia, United States and Egypt. Moeen Al-Sayed's co-authors include Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, Zuhair Rahbeeni, Hamad Alzaidan, Nawal Makhseed, Majid Alfadhel, Johannes Häberle, Tawfeg Ben‐Omran, Khalid Al‐Thihli and Fatma Al Jasmi and has published in prestigious journals such as Molecular Genetics and Metabolism, Clinical Genetics and The American Journal of Emergency Medicine.

In The Last Decade

Moeen Al-Sayed

11 papers receiving 105 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Moeen Al-Sayed Saudi Arabia	6	70	52	23	20	19	11	106
Detlef Knoll New Zealand	7	80 1.1×	66 1.3×	29 1.3×	21 1.1×	27 1.4×	11	119
Anil Jalan India	6	80 1.1×	58 1.1×	24 1.0×	23 1.1×	23 1.2×	17	137
Mick Henderson United Kingdom	6	114 1.6×	100 1.9×	35 1.5×	52 2.6×	21 1.1×	6	175
CA Graham United Kingdom	4	53 0.8×	40 0.8×	6 0.3×	6 0.3×	26 1.4×	6	90
Cynthia A. Cameron United States	6	101 1.4×	68 1.3×	20 0.9×	40 2.0×	20 1.1×	7	145
Archibald E. Garrod United Kingdom	3	82 1.2×	79 1.5×	19 0.8×	21 1.1×	3 0.2×	4	156
Femke Molema Netherlands	7	136 1.9×	65 1.3×	38 1.7×	24 1.2×	55 2.9×	7	156
Cynthia LeMons United States	5	71 1.0×	43 0.8×	33 1.4×	23 1.1×	15 0.8×	5	117
Ruth Day United Kingdom	4	47 0.7×	34 0.7×	32 1.4×	17 0.8×	4 0.2×	6	89
Jennifer Seminara United States	4	159 2.3×	82 1.6×	58 2.5×	31 1.6×	32 1.7×	5	211

Countries citing papers authored by Moeen Al-Sayed

Since Specialization

Citations

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

Fields of papers citing papers by Moeen Al-Sayed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Moeen Al-Sayed. 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 Moeen Al-Sayed. The network helps show where Moeen Al-Sayed may publish in the future.

Co-authorship network of co-authors of Moeen Al-Sayed

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Aldhalaan, Hesham, Albandary AlBakheet, Moeen Al-Sayed, et al.. (2023). Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature. Frontiers in Pediatrics. 10. 1051534–1051534. 2 indexed citations

Sulaiman, Raashda A., et al.. (2022). Emergency management of critically ill adult patients with inherited metabolic disorders. The American Journal of Emergency Medicine. 55. 138–142. 1 indexed citations

Al‐Owain, Mohammed, Ola Khalifa, Maged H. Hussein, et al.. (2019). Optic neuropathy in classical methylmalonic acidemia. Ophthalmic Genetics. 40(4). 313–322. 2 indexed citations

Al‐Hassnan, Zuhair N., Ola Khalifa, Dalal Bubshait, et al.. (2018). The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients. Molecular Genetics and Metabolism Reports. 15. 50–54. 6 indexed citations

Al-Sayed, Moeen, et al.. (2018). Human subjects in clinical trials: Ethical considerations and concerns. Journal of Translational Science. 4(6). 3 indexed citations

Bakshi, Nasir, Said Mohamed, Zuhair Rahbeeni, et al.. (2018). Spectrum of bone marrow pathology and hematological abnormalities in methylmalonic acidemia. American Journal of Medical Genetics Part A. 176(3). 687–691. 6 indexed citations

Alfadhel, Majid, Fuad Al Mutairi, Nawal Makhseed, et al.. (2016). Guidelines for acute management of hyperammonemia in the Middle East region. Therapeutics and Clinical Risk Management. 12. 479–479. 29 indexed citations

Hendriksz, Christian J., Barbara K. Burton, Moeen Al-Sayed, et al.. (2016). Impact of long-term elosulfase alfa treatment on pulmonary function in patients with Morquio syndrome type A. Molecular Genetics and Metabolism. 117(2). S56–S56. 1 indexed citations

Imtiaz, Faiqa, Mohamed S. Rashed, Bashayer Al‐Mubarak, et al.. (2011). Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin. Molecular Genetics and Metabolism. 104(4). 688–690. 16 indexed citations

10.

Shaheen, Ranad, Mohammed Al‐Owain, Mustafa A. Salih, et al.. (2010). Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs. Clinical Genetics. 79(1). 60–70. 14 indexed citations

11.

Faiyaz‐Ul‐Haque, Muhammad, Mohammed Al‐Owain, Fouad Al‐Dayel, et al.. (2009). Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency. European Journal of Pediatrics. 168(12). 1467–1471. 26 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.

Explore authors with similar magnitude of impact