Mona Aglan

4.3k citations
91 papers · 3.5k · h-index 31

Impact in

    • Congenital limb and hand anomalies
  • Genetics top 1%
    • Connective tissue disorders research
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology

Papers in

    • Connective tissue disorders research 32
    • Genomics and Rare Diseases 23
    • Genomic variations and chromosomal abnormalities 6
    • Craniofacial Disorders and Treatments 5
    • Congenital limb and hand anomalies 18

Mona Aglan

89 papers receiving 3.4k citations

Peers

Mona Aglan
Comparison fields: 5 of 107
  • Developmental Biology 233
  • Genetics 1.6k
  • Orthopedics and Sports Medicine 175
  • Clinical Biochemistry 64
  • Immunology 243
Replace Samia Ali Temtamy with:
Samia Ali Temtamy Egypt
Víctor L. Ruiz‐Pérez Spain
Riyana Babul‐Hirji Canada
Carole McKeown United Kingdom
Carmel Toomes United Kingdom
Maja Di Rocco Italy
Peter Meinecke Germany
F.F.B. Elder United States
Trine Prescott Norway
Charles J Shaw-Smith United Kingdom
Mona Aglan relative to Samia Ali Temtamy Egypt Samia Ali Temtamy's profile →
Citations per field
00.5×1.5×
Samia Ali Temtamy · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Mona Aglan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mona Aglan Line = papers co-authored together Mona Aglan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 91 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2013371
2 2011268
3 2010245
4 2013243
5 2011182
6 2010147
7 2015108
8 2008101
9 2013101
10 201891
11 201286
12 200985
13 201084
14 201473
15 201462
16 201861
17 201861
18 201956
19 200953
20 201252

About Mona Aglan

Mona Aglan is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Molecular Biology and Orthopedics and Sports Medicine, having authored 91 papers that have together received 3.5k indexed citations. Recurring topics across this work include Connective tissue disorders research (32 papers), Genomics and Rare Diseases (23 papers), Congenital limb and hand anomalies (18 papers), Fetal and Pediatric Neurological Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Craniofacial Disorders and Treatments (5 papers), Lysosomal Storage Disorders Research (4 papers) and Bone Metabolism and Diseases (4 papers). The work is most often cited by research in Developmental Biology (233 citations), Genetics (1.6k citations), Orthopedics and Sports Medicine (175 citations), Clinical Biochemistry (64 citations) and Immunology (243 citations). Mona Aglan has collaborated with scholars based in Egypt, Spain and Italy. Frequent co-authors include Samia Ali Temtamy, Víctor L. Ruiz‐Pérez, Pablo Daniel Lapunzina, Jose Antonio Caparros-Martin, Víctor Martínez‐Glez, Ghada Ahmed Otaify, Khalda Said Amr, Adel Mohamed Ashour, Maha Saad Zaki and Verónica Pulido. Their work appears in journals such as The American Journal of Human Genetics, Human Mutation, Genetics in Medicine, Osteoporosis International and Journal of Medical Genetics.

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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