Ghada El‐Kamah

659 total citations
46 papers, 364 citations indexed

About

Ghada El‐Kamah is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Ghada El‐Kamah has authored 46 papers receiving a total of 364 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 12 papers in Genetics and 11 papers in Genetics. Recurrent topics in Ghada El‐Kamah's work include Hemoglobinopathies and Related Disorders (8 papers), Iron Metabolism and Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Ghada El‐Kamah is often cited by papers focused on Hemoglobinopathies and Related Disorders (8 papers), Iron Metabolism and Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Ghada El‐Kamah collaborates with scholars based in Egypt, United States and United Kingdom. Ghada El‐Kamah's co-authors include Sonia Abdelhak, Khalda Amr, Hala T. El‐Bassyouni, Hanan H. Afifi, Khaled R. Gaber, Yosr Hamdi, Abdelhamid Barakat, Lilia Romdhane, Soheir Adam and Ghada M. H. Abdel‐Salam and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Molecular Biology of the Cell.

In The Last Decade

Ghada El‐Kamah

40 papers receiving 356 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ghada El‐Kamah Egypt 10 142 82 77 54 49 46 364
Jeffery R. Sawyer United States 9 256 1.8× 85 1.0× 44 0.6× 28 0.5× 37 0.8× 24 478
Mai Sato Japan 16 130 0.9× 54 0.7× 68 0.9× 89 1.6× 130 2.7× 81 686
Hyunnam Ryu South Korea 9 77 0.5× 78 1.0× 27 0.4× 46 0.9× 97 2.0× 29 374
Hee Jo Baek South Korea 13 211 1.5× 39 0.5× 21 0.3× 53 1.0× 52 1.1× 67 565
Gordana Sušić Serbia 8 135 1.0× 24 0.3× 51 0.7× 40 0.7× 13 0.3× 17 353
Ana Fernández‐Teijeiro Spain 11 102 0.7× 25 0.3× 15 0.2× 52 1.0× 89 1.8× 31 360
Sita Bhella Canada 6 151 1.1× 78 1.0× 136 1.8× 27 0.5× 23 0.5× 44 442
Grażyna Sobol Poland 13 70 0.5× 12 0.1× 57 0.7× 77 1.4× 56 1.1× 42 377
Nobuyuki Hyakuna Japan 11 90 0.6× 22 0.3× 38 0.5× 36 0.7× 39 0.8× 33 364
Takeshi Rikiishi Japan 11 94 0.7× 41 0.5× 18 0.2× 47 0.9× 32 0.7× 27 273

Countries citing papers authored by Ghada El‐Kamah

Since Specialization
Citations

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

Fields of papers citing papers by Ghada El‐Kamah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ghada El‐Kamah

This figure shows the co-authorship network connecting the top 25 collaborators of Ghada El‐Kamah. A scholar is included among the top collaborators of Ghada El‐Kamah 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 Ghada El‐Kamah. Ghada El‐Kamah 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.
El‐Bassyouni, Hala T., et al.. (2025). Insight into Apert Syndrome: Reporting on Six Patients and Increasing Awareness. Molecular Neurobiology. 62(9). 11089–11098.
2.
Amr, Khalda, et al.. (2024). Genomic insights into Duchene muscular dystrophy: Analysis of 1250 patients reveals 30% novel genetic patterns and 6 novel variants. Journal of Genetic Engineering and Biotechnology. 22(4). 100436–100436. 1 indexed citations
3.
Bento, Celeste, Carsten W. Lederer, Petros Kountouris, et al.. (2024). Global Globin Network and adopting genomic variant database requirements for thalassemia. Database. 2024. 1 indexed citations
4.
Hamdy, Mona, et al.. (2023). Studying the pathogenicity of 26 variants characterized in the first molecular analyses of Egyptian aplastic anemia patients. Journal of Genetic Engineering and Biotechnology. 21(1). 149–149. 1 indexed citations
5.
6.
Abdel‐Salam, Ghada M. H., Hanan H. Afifi, Mohamed S. Abdel‐Hamid, et al.. (2023). Expanding the phenotypic spectrum and clinical severity associated with WLS gene. Journal of Human Genetics. 68(9). 607–613. 1 indexed citations
7.
Ashaat, Engy A., et al.. (2022). Correlating SFTPC gene variants to interstitial lung disease in Egyptian children. Journal of Genetic Engineering and Biotechnology. 20(1). 117–117. 3 indexed citations
8.
Amr, Khalda, et al.. (2021). Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease. Genes. 12(10). 1552–1552. 5 indexed citations
9.
El‐Kamah, Ghada, et al.. (2021). Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1. Molecular Genetics & Genomic Medicine. 9(12). e1631–e1631. 10 indexed citations
10.
El‐Kamah, Ghada, Yehia Z. Gad, Sonia Abdelhak, et al.. (2020). Developing a Road Map to Spread Genomic Knowledge in Africa: 10th Conference of the African Society of Human Genetics, Cairo, Egypt. American Journal of Tropical Medicine and Hygiene. 102(4). 719–723. 7 indexed citations
11.
El‐Kamah, Ghada, et al.. (2020). Use of echocardiography and glutathione S-transferase to detect heart complications in β-thalassemic patients. Egyptian Pharmaceutical Journal. 19(3). 244–244. 1 indexed citations
12.
El‐Kamah, Ghada, et al.. (2020). Comparison of two vital pulp therapies in β-Thalassemic children. SHILAP Revista de lepidopterología. 1(1). 33–41.
13.
Afifi, Hanan H., et al.. (2019). Lenz–Majewski syndrome in a patient from Egypt. American Journal of Medical Genetics Part A. 179(10). 2039–2042. 4 indexed citations
14.
Amr, Khalda, Patrycja Pawlikowska, Saïd Aoufouchi, Filippo Rosselli, & Ghada El‐Kamah. (2019). Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family. Molecular Genetics & Genomic Medicine. 7(7). e00777–e00777. 7 indexed citations
15.
Amr, Khalda, Hala T. El‐Bassyouni, Samira Ismail, et al.. (2019). Genetic assessment of ten Egyptian patients with Sjögren–Larsson syndrome: expanding the clinical spectrum and reporting a novel ALDH3A2 mutation. Archives of Dermatological Research. 311(9). 721–730. 8 indexed citations
16.
Amr, Khalda, et al.. (2013). Mutational spectrum of Xeroderma pigmentosum group A in Egyptian patients. Gene. 533(1). 52–56. 12 indexed citations
17.
Abdel‐Salam, Ghada M. H., Noriko Miyake, Maha M. Eid, et al.. (2011). A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder. American Journal of Medical Genetics Part A. 155(11). 2885–2896. 21 indexed citations
18.
Abdel‐Salam, Ghada M. H., Ghada El‐Kamah, Gillian Rice, et al.. (2010). Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome. Neuropediatrics. 41(1). 18–23. 26 indexed citations
19.
El‐Kamah, Ghada, et al.. (2009). Ligneous Conjunctivitis with Oral Mucous Membrane Involvement and Decreased Plasminogen Level. Pediatric Dermatology. 26(4). 448–451. 5 indexed citations
20.
El‐Kamah, Ghada, et al.. (2009). Heterogeneity and atypical presentation in infantile systemic hyalinosis with severe labio-gingival. Dermatology Online Journal. 15(5). 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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