Mark Borchert

5.3k total citations
126 papers, 3.6k citations indexed

About

Mark Borchert is a scholar working on Ophthalmology, Radiology, Nuclear Medicine and Imaging and Epidemiology. According to data from OpenAlex, Mark Borchert has authored 126 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Ophthalmology, 48 papers in Radiology, Nuclear Medicine and Imaging and 42 papers in Epidemiology. Recurrent topics in Mark Borchert's work include Ophthalmology and Visual Impairment Studies (37 papers), Glaucoma and retinal disorders (24 papers) and Retinopathy of Prematurity Studies (22 papers). Mark Borchert is often cited by papers focused on Ophthalmology and Visual Impairment Studies (37 papers), Glaucoma and retinal disorders (24 papers) and Retinopathy of Prematurity Studies (22 papers). Mark Borchert collaborates with scholars based in United States, United Kingdom and Canada. Mark Borchert's co-authors include Susan A. Cotter, Kristina Tarczy‐Hornoch, Rohit Varma, Ge Wen, Pamela Garcia‐Filion, Roberta McKean‐Cowdin, Stanley P. Azen, Jesse Lin, Cassandra Fink and Sean P. Donahue and has published in prestigious journals such as Blood, PEDIATRICS and Ophthalmology.

In The Last Decade

Mark Borchert

119 papers receiving 3.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Mark Borchert 1.6k 1.2k 1.1k 624 562 126 3.6k
David G. Hunter 925 0.6× 743 0.6× 626 0.6× 354 0.6× 524 0.9× 227 3.3k
David A. Leske 1.5k 1.0× 1.4k 1.1× 931 0.8× 669 1.1× 216 0.4× 154 3.7k
Jeong‐Min Hwang 2.2k 1.4× 672 0.6× 1.2k 1.1× 915 1.5× 544 1.0× 332 4.3k
David R. Stager 2.3k 1.5× 2.4k 2.0× 818 0.7× 417 0.7× 394 0.7× 135 4.3k
Terry A. Cox 2.1k 1.4× 464 0.4× 1.2k 1.1× 500 0.8× 307 0.5× 89 3.4k
Glen A. Gole 1.2k 0.8× 759 0.6× 1.7k 1.5× 118 0.2× 420 0.7× 101 3.5k
Terri L. Young 2.7k 1.7× 2.3k 1.9× 2.7k 2.4× 126 0.2× 604 1.1× 122 4.5k
Arthur L. Rosenbaum 1.0k 0.7× 596 0.5× 581 0.5× 1.1k 1.8× 201 0.4× 138 4.1k
William Tasman 2.6k 1.6× 624 0.5× 2.4k 2.2× 286 0.5× 1.0k 1.8× 124 5.1k
Byron L. Lam 3.3k 2.1× 879 0.7× 1.6k 1.4× 931 1.5× 3.0k 5.3× 271 6.7k

Countries citing papers authored by Mark Borchert

Since Specialization
Citations

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

Fields of papers citing papers by Mark Borchert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Borchert

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Borchert. A scholar is included among the top collaborators of Mark Borchert 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 Mark Borchert. Mark Borchert 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.
Reid, Mark W., Eric D. Gaier, Gena Heidary, et al.. (2025). Agreement and Accuracy of Papilledema and Pseudopapilledema Classification Among Pediatric Neuro-Ophthalmologists Using Optic Disc Photographs. Journal of Neuro-Ophthalmology. 45(4). 433–439.
2.
Nallasamy, Sudha, et al.. (2024). Disparities in Amblyopia Treatment Outcomes. Ophthalmology. 132(3). 335–342.
3.
Štingl, Katarína, Krunoslav Stingl, Mark W. Reid, et al.. (2023). Full-field Scotopic Threshold Improvement after Voretigene Neparvovec-rzyl Treatment Correlates with Chorioretinal Atrophy. Ophthalmology. 130(7). 764–770. 29 indexed citations
4.
Chang, Melinda Y. & Mark Borchert. (2020). Quantitative visual assessment in children with cortical/cerebral visual impairment (CVI) using eye tracking. Investigative Ophthalmology & Visual Science. 61(7). 2150–2150. 2 indexed citations
5.
Chang, Melinda Y. & Mark Borchert. (2019). Papilledema Treated by Cranial Expansion in a 5-Year-Old Boy with Camurati-Engelmann Syndrome. Ophthalmology. 126(11). 1579–1579. 1 indexed citations
6.
Borchert, Mark, Grant T. Liu, Stacy L. Pineles, & Amy Waldman. (2017). Pediatric Optic Neuritis: What Is New. Journal of Neuro-Ophthalmology. 37(1). S14–S22. 22 indexed citations
7.
Garcia‐Filion, Pamela, et al.. (2014). Absence of age-related optic disk changes in young children with optic nerve hypoplasia. Eye. 28(5). 562–566. 1 indexed citations
8.
Williams, Marian E., et al.. (2013). Autism assessment in children with optic nerve hypoplasia and other vision impairments. Developmental Medicine & Child Neurology. 56(1). 66–72. 29 indexed citations
9.
Tarczy‐Hornoch, Kristina, Susan A. Cotter, Mark Borchert, et al.. (2013). Prevalence and Causes of Visual Impairment in Asian and Non-Hispanic White Preschool Children. Ophthalmology. 120(6). 1220–1226. 45 indexed citations
10.
Garcia‐Filion, Pamela, et al.. (2012). Serum Prolactin Concentrations in Relation to Hypopituitarism and Obesity in Children with Optic Nerve Hypoplasia. Hormone Research in Paediatrics. 77(5). 277–280. 11 indexed citations
11.
Prasov, Lev, Tehmina Masud, Shagufta Khaliq, et al.. (2012). ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Human Molecular Genetics. 21(16). 3681–3694. 51 indexed citations
12.
Kim, Jeniffer S., Ge Wen, Kristina Tarczy‐Hornoch, et al.. (2011). Racial/Ethnic Differences in Axial Length in Preschool Children: Multi-Ethnic Pediatric Eye Disease Study (MEPEDS). Investigative Ophthalmology & Visual Science. 52(14). 6329–6329. 2 indexed citations
13.
Fink, Cassandra, et al.. (2010). Evolving Central Hypothyroidism in Children with Optic Nerve Hypoplasia. Journal of Pediatric Endocrinology and Metabolism. 23(1-2). 53–8. 14 indexed citations
14.
Tarczy‐Hornoch, Kristina, et al.. (2008). Prevalence of Hyperopia in African-American and Hispanic Preschool Children: The Multi-Ethnic Pediatric Eye Disease Study. Investigative Ophthalmology & Visual Science. 49(13). 3130–3130. 2 indexed citations
15.
Choudhury, Farzana, Kristina Tarczy‐Hornoch, Mark Borchert, et al.. (2008). Effect of Cyclopentolate versus Atropine on Cycloplegic Refraction: The Multi-Ethnic Pediatric Eye Disease Study. Investigative Ophthalmology & Visual Science. 49(13). 1454–1454. 4 indexed citations
16.
Cotter, Susan A., et al.. (2007). Relationship of Fixation Preference to Amblyopia in Preschool Children: The Multi-Ethnic Pediatric Eye Disease Study. Investigative Ophthalmology & Visual Science. 48(13). 2380–2380. 1 indexed citations
17.
Cotter, Susan A., et al.. (2007). Age-, Gender- and Ethnicity-Related Differences in Axial Length in Preschool Children: The Multi-Ethnic Pediatric Eye Disease Study. Investigative Ophthalmology & Visual Science. 48(13). 4831–4831. 1 indexed citations
18.
Varma, Rohit, Susan A. Cotter, J. Deneen, et al.. (2007). Prevalence of Amblyopia and Strabismus in a Population-Based Sample of Preschool African-American and Hispanic Children: The Multi-Ethnic Pediatric Eye Disease Study. Investigative Ophthalmology & Visual Science. 48(13). 2379–2379. 35 indexed citations
19.
Borchert, Mark. (2006). Early detection of optic nerve hypoplasia may improve outcomes. AAP News. 27(5). 18–19.
20.
Appukuttan, Binoy, Elizabeth M. Gillanders, Suh-Hang Hank Juo, et al.. (1999). Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31. The American Journal of Human Genetics. 65(6). 1639–1646. 77 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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