Magda Barsoum‐Homsy

1.1k total citations
19 papers, 812 citations indexed

About

Magda Barsoum‐Homsy is a scholar working on Ophthalmology, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Magda Barsoum‐Homsy has authored 19 papers receiving a total of 812 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Ophthalmology, 6 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Magda Barsoum‐Homsy's work include Glaucoma and retinal disorders (5 papers), Ophthalmology and Eye Disorders (5 papers) and Retinopathy of Prematurity Studies (3 papers). Magda Barsoum‐Homsy is often cited by papers focused on Glaucoma and retinal disorders (5 papers), Ophthalmology and Eye Disorders (5 papers) and Retinopathy of Prematurity Studies (3 papers). Magda Barsoum‐Homsy collaborates with scholars based in Canada, United States and Türkiye. Magda Barsoum‐Homsy's co-authors include Line Chevrette, Nurten Akarsu, Mansoor Sarfarazi, Glen Brice, Altaf Hossain, Ivaylo Stoilov, M. Erol Turaçlı, Richard A. Lewis, Miguel Coca‐Prados and Nusret Özdemir and has published in prestigious journals such as Ophthalmology, The American Journal of Human Genetics and Genomics.

In The Last Decade

Magda Barsoum‐Homsy

19 papers receiving 784 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Magda Barsoum‐Homsy Canada 11 485 308 263 114 101 19 812
Line Chevrette Canada 9 532 1.1× 282 0.9× 267 1.0× 82 0.7× 104 1.0× 12 769
S. Merin Israel 21 386 0.8× 387 1.3× 198 0.8× 135 1.2× 19 0.2× 52 1.1k
Victor H. K. Yong Singapore 13 508 1.0× 351 1.1× 480 1.8× 91 0.8× 12 0.1× 19 920
Aimee M. Juan United States 15 299 0.6× 467 1.5× 178 0.7× 50 0.4× 7 0.1× 19 807
Francisco J. López United States 16 283 0.6× 236 0.8× 164 0.6× 95 0.8× 6 0.1× 24 633
Marin L. Gantner United States 11 258 0.5× 377 1.2× 109 0.4× 89 0.8× 5 0.0× 18 671
Edward A. Felinski United States 7 251 0.5× 337 1.1× 140 0.5× 34 0.3× 6 0.1× 7 732
Mikiro Mori Japan 15 226 0.5× 452 1.5× 134 0.5× 68 0.6× 6 0.1× 35 836
Shuo Huang United States 14 152 0.3× 305 1.0× 90 0.3× 32 0.3× 7 0.1× 20 530

Countries citing papers authored by Magda Barsoum‐Homsy

Since Specialization
Citations

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

Fields of papers citing papers by Magda Barsoum‐Homsy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Magda Barsoum‐Homsy. 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 Magda Barsoum‐Homsy. The network helps show where Magda Barsoum‐Homsy may publish in the future.

Co-authorship network of co-authors of Magda Barsoum‐Homsy

This figure shows the co-authorship network connecting the top 25 collaborators of Magda Barsoum‐Homsy. A scholar is included among the top collaborators of Magda Barsoum‐Homsy 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 Magda Barsoum‐Homsy. Magda Barsoum‐Homsy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Kaloustian, Vazken M. Der, et al.. (2005). Congenital microcephaly, juvenile retinal dystrophy and normal mentation in a mildly dysmorphic child. Canadian Journal of Ophthalmology. 40(2). 195–199. 4 indexed citations
2.
Barr, Cathy L., et al.. (2003). Linkage study between congenital cataracts and five crystallin loci. American Journal of Medical Genetics Part A. 121A(1). 15–19. 1 indexed citations
3.
Stoilov, Ivaylo, Nurten Akarsu, Magda Barsoum‐Homsy, et al.. (1998). Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1. The American Journal of Human Genetics. 62(3). 573–584. 288 indexed citations
4.
Child, Anne H., Glen Brice, Trushna Desai, et al.. (1998). Novel TIGR/MYOC mutations in families with juvenile onset primary open angle glaucoma.. Journal of Medical Genetics. 35(12). 989–992. 58 indexed citations
5.
Roy, Marie‐Sylvie, et al.. (1997). Pattern Electroretinogram and Spatial Contrast Sensitivity in Primary Congenital Glaucoma. Ophthalmology. 104(12). 2136–2142. 5 indexed citations
6.
Milot, Jean, et al.. (1997). Recombinant interferon alfa-2b in the treatment of vision-threatening capillary hemangiomas in childhood. Journal of American Association for Pediatric Ophthalmology and Strabismus. 1(4). 226–230. 28 indexed citations
7.
Roy, Marie‐Sylvie, et al.. (1996). On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness. Documenta Ophthalmologica. 92(3). 159–165. 30 indexed citations
8.
Sarfarazi, Mansoor, et al.. (1995). Assignment of a Locus (GLC3A) for Primary Congenital Glaucoma (Buphthalmos) to 2p21 and Evidence for Genetic Heterogeneity. Genomics. 30(2). 171–177. 184 indexed citations
9.
Barsoum‐Homsy, Magda, et al.. (1995). Clinical Evaluation of Aminocaproic, Acid for Managing Traumatic Hyphema in Children. Ophthalmology. 102(11). 1646–1653. 14 indexed citations
10.
Roy, Marie‐Sylvie, et al.. (1995). Maturation of Binocular Pattern Visual Evoked Potentials in Normal Full-Term and Preterm Infants from 1 to 6 Months of Age. Pediatric Research. 37(2). 140–144. 41 indexed citations
11.
Héon, Elise, et al.. (1992). The Spectrum of Associated Ocular and Systemic Malformations. Ophthalmic Paediatrics and Genetics. 13(2). 137–143. 39 indexed citations
12.
Roy, Monique, et al.. (1992). Ocular findings and visual evoked potential response in the Prader-Willi syndrome.. PubMed. 27(6). 307–12. 11 indexed citations
13.
Lemieux, Nicole, Jean Milot, Magda Barsoum‐Homsy, et al.. (1989). First cytogenetic evidence of homozygosity for the retinoblastoma deletion in chromosome 13. Cancer Genetics and Cytogenetics. 43(1). 73–78. 7 indexed citations
14.
Barsoum‐Homsy, Magda, et al.. (1989). Bimedial rectus recession measured from the limbus for congenital esotropia.. PubMed. 24(7). 304–7. 4 indexed citations
15.
Brownstein, Seymour, et al.. (1988). Inferior oblique myositis presenting as superior oblique muscle palsy.. PubMed. 23(3). 124–7. 9 indexed citations
16.
Barsoum‐Homsy, Magda & Line Chevrette. (1986). Incidence and Prognosis of Childhood Glaucoma. Ophthalmology. 93(10). 1323–1327. 53 indexed citations
17.
Brownstein, Seymour, et al.. (1984). Nonteratoicl Medulloepiothelioma of the Ciliary Body. Ophthalmology. 91(9). 1118–1122. 10 indexed citations
18.
Barsoum‐Homsy, Magda. (1983). Congenital Double Elevator Palsy. Journal of Pediatric Ophthalmology & Strabismus. 20(5). 185–191. 18 indexed citations
19.
Barsoum‐Homsy, Magda. (1981). Medial rectus insertion site in congenital esotropia.. PubMed. 16(4). 181–6. 8 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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