Solaf M. Elsayed

1.9k total citations
63 papers, 1.1k citations indexed

About

Solaf M. Elsayed is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Solaf M. Elsayed has authored 63 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Hematology. Recurrent topics in Solaf M. Elsayed's work include Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (5 papers) and Connective tissue disorders research (4 papers). Solaf M. Elsayed is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Lysosomal Storage Disorders Research (5 papers) and Connective tissue disorders research (4 papers). Solaf M. Elsayed collaborates with scholars based in Egypt, Germany and United Kingdom. Solaf M. Elsayed's co-authors include Rabah M. Shawky, Ezzat Elsobky, Moushira Zaki, Ghada M. El‐Sayed, David M. Yousem, Bart Loeys, Hal Dietz, Shawna M. Pyott, Melanie Pepin and Emily H. Turner and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Solaf M. Elsayed

57 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Solaf M. Elsayed Egypt 15 548 471 146 109 100 63 1.1k
Anju Shukla India 18 610 1.1× 496 1.1× 134 0.9× 100 0.9× 63 0.6× 112 1.2k
Tony Roscioli Australia 24 877 1.6× 769 1.6× 81 0.6× 109 1.0× 54 0.5× 85 1.7k
Virginia K. Proud United States 17 549 1.0× 320 0.7× 83 0.6× 122 1.1× 59 0.6× 32 1.1k
Manfred Stuhrmann Germany 24 527 1.0× 384 0.8× 62 0.4× 87 0.8× 97 1.0× 94 1.9k
Christina Fagerberg Denmark 17 312 0.6× 285 0.6× 114 0.8× 111 1.0× 79 0.8× 46 877
Nadia Sakati Saudi Arabia 22 819 1.5× 546 1.2× 123 0.8× 160 1.5× 33 0.3× 78 1.7k
Chitra Prasad Canada 23 687 1.3× 409 0.9× 204 1.4× 223 2.0× 49 0.5× 72 1.7k
Séverine Drunat France 21 581 1.1× 443 0.9× 93 0.6× 144 1.3× 72 0.7× 57 1.1k
L.I. Al-Gazali United Arab Emirates 22 691 1.3× 553 1.2× 231 1.6× 207 1.9× 59 0.6× 60 1.5k
Mary Ann Mitnick United States 18 1.3k 2.3× 472 1.0× 157 1.1× 88 0.8× 52 0.5× 26 2.1k

Countries citing papers authored by Solaf M. Elsayed

Since Specialization
Citations

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

Fields of papers citing papers by Solaf M. Elsayed

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Solaf M. Elsayed. 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 Solaf M. Elsayed. The network helps show where Solaf M. Elsayed may publish in the future.

Co-authorship network of co-authors of Solaf M. Elsayed

This figure shows the co-authorship network connecting the top 25 collaborators of Solaf M. Elsayed. A scholar is included among the top collaborators of Solaf M. Elsayed 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 Solaf M. Elsayed. Solaf M. Elsayed 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.
Elsayed, Solaf M., et al.. (2025). Clinical and molecular characteristics of fructose 1, 6 bisphosphatase deficiency in 6 Egyptian patients and two common variants. Orphanet Journal of Rare Diseases. 20(1). 595–595.
2.
3.
Emam, Manal A., et al.. (2024). Bone Health Assessment in Patients with Methylmalonic Acidemia. QJM. 117(Supplement_2). 1 indexed citations
4.
El‐Beshlawy, Amal, et al.. (2024). Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion. SHILAP Revista de lepidopterología. 25(1).
5.
Elsayed, Solaf M., et al.. (2023). Extra-hepatic portal vein thrombosis in children: single center experience. Clinical and Experimental Hepatology. 9(1). 37–45. 1 indexed citations
6.
Elsayed, Solaf M., et al.. (2022). A novel ABHD5 mutation in two Chanarin Dorfman siblings with severe and heterogeneous clinical phenotype. Genes & Diseases. 10(3). 690–693. 2 indexed citations
7.
Elsayed, Solaf M., et al.. (2018). Frequency of inborn errors of metabolism screening for children with unexplained acute encephalopathy at an emergency department. Neuropsychiatric Disease and Treatment. Volume 14. 1715–1720. 5 indexed citations
8.
Auclair, Martine, Faraj Terro, Mona Nemani, et al.. (2016). Maladaptative Autophagy Impairs Adipose Function in Congenital Generalized Lipodystrophy due to Cavin-1 Deficiency. The Journal of Clinical Endocrinology & Metabolism. 101(7). 2892–2904. 13 indexed citations
9.
Elsayed, Solaf M. & Beat Thöny. (2015). BH4 deficiency with unusual presentations: Challenges and lessons. SHILAP Revista de lepidopterología. 17(3). 241–242. 1 indexed citations
10.
El-Sobky, Tamer A., et al.. (2015). Orthopaedic manifestations of Proteus syndrome in a child with literature update. Bone Reports. 3. 104–108. 11 indexed citations
11.
Pyott, Shawna M., Thao Tran, Dru F. Leistritz, et al.. (2013). WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 92(4). 590–597. 170 indexed citations
12.
Eğin, Yonca, Solaf M. Elsayed, Mohamed Sakr, & Nejat Akar. (2012). TNF-α-308 G/A Polymorphism in Egyptian Budd-Chiari Syndrome Patients. SHILAP Revista de lepidopterología. 29(4). 420–421. 2 indexed citations
13.
Elsayed, Solaf M., et al.. (2011). Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients. SHILAP Revista de lepidopterología. 2011(4). 299–305. 7 indexed citations
14.
Elsayed, Solaf M., et al.. (2011). Phenotypic and Genetic Characterization of a Cohort of Pediatric Wilson Disease Patients. BMC Pediatrics. 11(1). 56–56. 43 indexed citations
15.
Coleman, Rosalind, Laura Moro, Catherine Dacou‐Voutetakis, et al.. (2010). Clinical and genetic characterization of chanarin-dorfman syndrome patients: first report of large deletions in the ABHD5 gene. Orphanet Journal of Rare Diseases. 5(1). 33–33. 40 indexed citations
16.
Shawky, Rabah M., Solaf M. Elsayed, & Heba Elsedfy. (2009). Triple A syndrome presenting with myopathy: An Egyptian patient. Egyptian Journal of Medical Human Genetics. 10(1). 1 indexed citations
17.
Elsayed, Solaf M. & Ghada M. El‐Sayed. (2009). Phenotype of apoptotic lymphocytes in children with Down syndrome. Immunity & Ageing. 6(1). 2–2. 23 indexed citations
18.
Elsayed, Solaf M., et al.. (2008). Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations. Journal of Human Genetics. 53(8). 681–687. 33 indexed citations
19.
Ebermann, Inga, Solaf M. Elsayed, Gudrun Nürnberg, et al.. (2008). DOUBLE HOMOZYGOSITY FOR MUTATIONS OF AGL AND SCN9A MIMICKING NEUROHEPATOPATHY SYNDROME. Neurology. 70(24). 2343–2344. 7 indexed citations
20.
Shawky, Rabah M., et al.. (2007). MURCS Association: a Case Report. Egyptian Journal of Medical Human Genetics. 8(2). 219–224. 1 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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