Mona Aglan

4.2k total citations
70 papers, 1.6k citations indexed

About

Mona Aglan is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Mona Aglan has authored 70 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 33 papers in Molecular Biology and 13 papers in Rheumatology. Recurrent topics in Mona Aglan's work include Connective tissue disorders research (24 papers), Bone and Dental Protein Studies (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Mona Aglan is often cited by papers focused on Connective tissue disorders research (24 papers), Bone and Dental Protein Studies (10 papers) and Genomic variations and chromosomal abnormalities (10 papers). Mona Aglan collaborates with scholars based in Egypt, United States and Spain. Mona Aglan's co-authors include Samia A. Temtamy, Víctor L. Ruiz‐Pérez, Pablo Lapunzina, Eulalia Valencia, José A. Caparrós‐Martín, Víctor Martínez‐Glez, Ghada A. Otaify, Khalda Amr, Adel M. Ashour and Maha S. Zaki and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Gene.

In The Last Decade

Mona Aglan

66 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
Mona Aglan Egypt 22 992 802 354 188 155 70 1.6k
Giedré Grigelioniené Sweden 22 862 0.9× 651 0.8× 254 0.7× 114 0.6× 127 0.8× 57 1.3k
Víctor Martínez‐Glez Spain 22 813 0.8× 603 0.8× 309 0.9× 175 0.9× 231 1.5× 61 1.4k
Yasemin Alanay Türkiye 26 1.0k 1.0× 994 1.2× 321 0.9× 181 1.0× 98 0.6× 108 2.1k
Francis Rousseau France 13 736 0.7× 902 1.1× 121 0.3× 160 0.9× 117 0.8× 21 1.5k
Nursel Elçioğlu Türkiye 19 1.3k 1.3× 1.2k 1.5× 145 0.4× 137 0.7× 83 0.5× 70 2.0k
Cecilia Giunta Switzerland 28 1.5k 1.6× 805 1.0× 581 1.6× 320 1.7× 109 0.7× 69 2.4k
Jeroen Knijnenburg Netherlands 22 578 0.6× 473 0.6× 150 0.4× 153 0.8× 128 0.8× 47 1.4k
James O’Sullivan United Kingdom 22 510 0.5× 1.4k 1.7× 198 0.6× 99 0.5× 214 1.4× 40 2.0k
Abdelaziz Sefiani Morocco 21 526 0.5× 964 1.2× 141 0.4× 84 0.4× 85 0.5× 123 1.8k
Abdulrahman Alswaid Saudi Arabia 16 698 0.7× 509 0.6× 159 0.4× 74 0.4× 83 0.5× 29 1.1k

Countries citing papers authored by Mona Aglan

Since Specialization
Citations

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

Fields of papers citing papers by Mona Aglan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mona Aglan

This figure shows the co-authorship network connecting the top 25 collaborators of Mona Aglan. A scholar is included among the top collaborators of Mona Aglan 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 Mona Aglan. Mona Aglan 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.
Aglan, Mona, et al.. (2025). COL1-related overlap disorder: An emerging phenotype linked to mono- and bi-allelic COL1A1/2 variants. Archives of Oral Biology. 178. 106344–106344.
2.
Abdel‐Hamid, Mohamed S., et al.. (2022). Osteoporosis-pseudoglioma syndrome in four new patients: identification of two novel LRP5 variants and insights on patients’ management using bisphosphonates therapy. Osteoporosis International. 33(7). 1501–1510. 6 indexed citations
3.
Kague, Érika, Francesco Turci, Kate Robson Brown, et al.. (2021). 3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease. Bone Research. 9(1). 39–39. 39 indexed citations
4.
Horn, Denise, Julián Nevado, Nadja Ehmke, et al.. (2021). Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly. Genetics in Medicine. 23(4). 679–688. 5 indexed citations
5.
Ashaat, Engy A., Ghada A. Otaify, Samira Ismail, et al.. (2021). First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous <b><i>CANT1</i></b> Mutations. Molecular Syndromology. 12(5). 279–288. 5 indexed citations
6.
Besio, Roberta, Laura Leoni, Lina Cipolla, et al.. (2019). Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate. Disease Models & Mechanisms. 12(6). 52 indexed citations
7.
8.
Ismail, Somaia, et al.. (2018). ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.. PubMed. 27(3). 305–323. 4 indexed citations
9.
10.
Caparrós‐Martín, José A., Alessandro De Luca, François Cartault, et al.. (2015). Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium. Human Molecular Genetics. 24(14). 4126–4137. 42 indexed citations
11.
Valencia, Eulalia, José A. Caparrós‐Martín, Ma Salomé Sirerol-Piquer, et al.. (2014). Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects. American Journal of Medical Genetics Part A. 164(5). 1143–1150. 24 indexed citations
12.
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
13.
Abdel‐Salam, Ghada M. H., Mohamed S. Abdel‐Hamid, Mahmoud Y. Issa, et al.. (2013). Further delineation of the clinical spectrum in RNU4ATAC related microcephalic osteodysplastic primordial dwarfism type I. American Journal of Medical Genetics Part A. 161(8). 1875–1881. 14 indexed citations
14.
Shaheen, Ranad, Mona Aglan, Kim M. Keppler‐Noreuil, et al.. (2013). Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome. The American Journal of Human Genetics. 92(4). 598–604. 86 indexed citations
15.
Martínez‐Glez, Víctor, Eulalia Valencia, José A. Caparrós‐Martín, et al.. (2011). Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta. Human Mutation. 33(2). 343–350. 155 indexed citations
16.
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
17.
Hanson, Dan, Philip Murray, Amit Sud, et al.. (2009). The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1. The American Journal of Human Genetics. 84(6). 801–806. 81 indexed citations
18.
Temtamy, Samia A. & Mona Aglan. (2008). Brachydactyly. Orphanet Journal of Rare Diseases. 3(1). 15–15. 88 indexed citations
19.
Zaki, Moushira, et al.. (2005). Assessment of Pubertal Development in Egyptian Girls. Journal of Pediatric Endocrinology and Metabolism. 18(6). 577–84. 30 indexed citations
20.
Zaki, Maha S., et al.. (2004). Familial congenital brachial palsy: a report of two affected Egyptian families.. PubMed. 15(1). 27–36. 4 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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