Khalda Amr

2.4k total citations
106 papers, 1.5k citations indexed

About

Khalda Amr is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Khalda Amr has authored 106 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 20 papers in Genetics and 18 papers in Cancer Research. Recurrent topics in Khalda Amr's work include MicroRNA in disease regulation (14 papers), Cancer-related molecular mechanisms research (10 papers) and Connective tissue disorders research (8 papers). Khalda Amr is often cited by papers focused on MicroRNA in disease regulation (14 papers), Cancer-related molecular mechanisms research (10 papers) and Connective tissue disorders research (8 papers). Khalda Amr collaborates with scholars based in Egypt, United States and Spain. Khalda Amr's co-authors include Mohamed S. Abdel‐Hamid, Wafaa M. Ezzat, Mona El Gammal, Inas Mazen, Mona Aglan, Samia A. Temtamy, Víctor L. Ruiz‐Pérez, Pablo Lapunzina, Eulalia Valencia and Moushira Zaki and has published in prestigious journals such as The American Journal of Human Genetics, Gene and Stem Cells.

In The Last Decade

Khalda Amr

99 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
Khalda Amr Egypt 19 589 424 313 233 225 106 1.5k
Kalliopi I. Pappa Greece 26 777 1.3× 96 0.2× 348 1.1× 154 0.7× 196 0.9× 70 2.1k
Martin Jansen Austria 22 722 1.2× 410 1.0× 181 0.6× 106 0.5× 91 0.4× 39 1.9k
Ana María Pino Chile 15 564 1.0× 137 0.3× 120 0.4× 86 0.4× 177 0.8× 49 1.4k
Marjolein van Driel Netherlands 22 602 1.0× 112 0.3× 96 0.3× 151 0.6× 90 0.4× 32 1.5k
Lisheng Zhuo Japan 21 885 1.5× 149 0.4× 200 0.6× 129 0.6× 92 0.4× 42 1.9k
Akihiro Yoneda Japan 28 746 1.3× 156 0.4× 194 0.6× 59 0.3× 276 1.2× 99 2.2k
David Warburton United States 27 1.2k 2.0× 151 0.4× 228 0.7× 48 0.2× 79 0.4× 50 2.1k
Helene Solberg Denmark 18 1.0k 1.8× 196 0.5× 930 3.0× 127 0.5× 127 0.6× 24 2.4k
David B. Frank United States 22 1.1k 1.9× 123 0.3× 145 0.5× 51 0.2× 186 0.8× 57 2.6k
Vickram Srinivas United States 21 1.2k 2.1× 300 0.7× 1.1k 3.5× 313 1.3× 340 1.5× 25 2.1k

Countries citing papers authored by Khalda Amr

Since Specialization
Citations

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

Fields of papers citing papers by Khalda Amr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Khalda Amr

This figure shows the co-authorship network connecting the top 25 collaborators of Khalda Amr. A scholar is included among the top collaborators of Khalda Amr 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 Khalda Amr. Khalda Amr 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
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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
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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
5.
Mohamed, Mohamed R., et al.. (2021). Nanomaterial-induced mesenchymal stem cell differentiation into osteoblast for counteracting bone resorption in the osteoporotic rats. Tissue and Cell. 73. 101645–101645. 6 indexed citations
6.
Amr, Khalda, et al.. (2021). Correlation of methylation status in MTHFR promoter region with recurrent pregnancy loss. Journal of Genetic Engineering and Biotechnology. 19(1). 44–44. 10 indexed citations
7.
Amr, Khalda, et al.. (2020). A descriptive study of NPHS1 and NPHS2 mutations in children with congenital nephrotic syndrome. Gene Reports. 20. 100722–100722. 2 indexed citations
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Hassan, Akmal S., et al.. (2018). Transforming growth factor-β1 gene polymorphism in psoriasis vulgaris. Clinical Cosmetic and Investigational Dermatology. Volume 11. 415–419. 10 indexed citations
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Ezzat, Wafaa M., et al.. (2016). Relationship Between Serum microRNA155 and Telomerase Expression in Hepatocellular Carcinoma. Archives of Medical Research. 47(5). 349–355. 10 indexed citations
12.
Raslan, Hala M., et al.. (2016). Association of PTPN22 1858C→T polymorphism, HLA-DRB1 shared epitope and autoantibodies with rheumatoid arthritis. Rheumatology International. 36(8). 1167–1175. 11 indexed citations
13.
Amr, Khalda, et al.. (2016). The role of microRNA-31 and microRNA-21 as regulatory biomarkers in the activation of T lymphocytes of Egyptian lupus patients. Rheumatology International. 36(11). 1617–1625. 28 indexed citations
14.
Abdel-Maksoud, Sahar M., et al.. (2014). C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population. Molecular Biology Reports. 41(4). 2281–2286. 12 indexed citations
15.
Caparrós‐Martín, José A., Eulalia Valencia, Verónica Pulido, et al.. (2013). Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. American Journal of Medical Genetics Part A. 161(6). 1354–1369. 46 indexed citations
16.
Raslan, Hala M., et al.. (2011). Possible role of angiotensin-converting enzyme polymorphism on progression of hepatic fibrosis in chronic hepatitis C virus infection. Transactions of the Royal Society of Tropical Medicine and Hygiene. 105(7). 396–400. 3 indexed citations
17.
Lapunzina, Pablo, Mona Aglan, Samia A. Temtamy, et al.. (2010). Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta. The American Journal of Human Genetics. 87(1). 110–114. 205 indexed citations
18.
Amr, Khalda, et al.. (2009). Mutational Analysis of the α-L-Iduronidase Gene in Three Egyptian Families: Identification of Three Novel Mutations and Five Novel Polymorphisms. Genetic Testing and Molecular Biomarkers. 13(6). 761–764. 3 indexed citations
19.
Essawi, Mona L., H. E. Nasr, Inas Mazen, et al.. (2008). Low Incidence of Androgen Receptor Mutation Among Egyptian Children with Androgen Resistance. Egyptian Journal of Medical Human Genetics. 9(1). 111–120. 1 indexed citations
20.
Awady, Mostafa K. El, et al.. (1999). Assay for hepatitis C virus in peripheral blood mononuclear cells enhances sensitivity of diagnosis and monitoring of HCV-associated hepatitis. Clinica Chimica Acta. 283(1-2). 1–14. 32 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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