Eve L. Bingham

1.2k total citations
30 papers, 980 citations indexed

About

Eve L. Bingham is a scholar working on Molecular Biology, Ophthalmology and Immunology. According to data from OpenAlex, Eve L. Bingham has authored 30 papers receiving a total of 980 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Ophthalmology and 8 papers in Immunology. Recurrent topics in Eve L. Bingham's work include Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (8 papers) and Genetic Syndromes and Imprinting (3 papers). Eve L. Bingham is often cited by papers focused on Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (8 papers) and Genetic Syndromes and Imprinting (3 papers). Eve L. Bingham collaborates with scholars based in United States, Poland and Sweden. Eve L. Bingham's co-authors include Paul A. Sieving, Julia E. Richards, David Ginsburg, Mark S. Roth, Kelaginamane Hiriyanna, Julie Richards, Kathleen M. Scott, F. Naarendorp, M. Alpern and Christina L. McHenry and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gastroenterology and Advanced Functional Materials.

In The Last Decade

Eve L. Bingham

30 papers receiving 956 citations

Peers

Eve L. Bingham
Briggs E. Cook United States
A. Tyl Hewitt United States
Eddy Anglade United States
Anastasios Georgiadis United Kingdom
Joseph Collin United Kingdom
Shweta Singhal United Kingdom
Eve L. Bingham
Citations per year, relative to Eve L. Bingham Eve L. Bingham (= 1×) peers Nobuhiko Matsuo

Countries citing papers authored by Eve L. Bingham

Since Specialization
Citations

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

Fields of papers citing papers by Eve L. Bingham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eve L. Bingham. 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 Eve L. Bingham. The network helps show where Eve L. Bingham may publish in the future.

Co-authorship network of co-authors of Eve L. Bingham

This figure shows the co-authorship network connecting the top 25 collaborators of Eve L. Bingham. A scholar is included among the top collaborators of Eve L. Bingham 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 Eve L. Bingham. Eve L. Bingham 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.
Urbanchek, Melanie G., Shiuhyang Kuo, Zhifa Wang, et al.. (2016). 904 Dynamic Functioning of Latissimus Dorsi Muscle NeoSphincters Compared to Native Anal Sphincters in the Rat. Gastroenterology. 150(4). S1194–S1194. 1 indexed citations
2.
Kato, Hiroko, et al.. (2015). Fabrication of Large Size Ex Vivo- Produced Oral Mucosal Equivalents for Clinical Application. Tissue Engineering Part C Methods. 21(9). 872–880. 20 indexed citations
3.
Ignatoski, Kathleen M. Woods, et al.. (2010). Differentiation of precursors into parathyroid-like cells for treatment of hypoparathyroidism. Surgery. 148(6). 1186–1190. 22 indexed citations
4.
Bingham, Eve L., Shih‐Ping Cheng, Kathleen M. Woods Ignatoski, & Gerard M. Doherty. (2008). Differentiation of Human Embryonic Stem Cells to a Parathyroid-Like Phenotype. Stem Cells and Development. 18(7). 1071–1080. 43 indexed citations
5.
Ayyagari, Radha, F. Yesim Demirci, Jiafan Liu, et al.. (2002). X-Linked Recessive Atrophic Macular Degeneration from RPGR Mutation. Genomics. 80(2). 166–171. 112 indexed citations
6.
Weinberg, David V., Paul A. Sieving, Eve L. Bingham, Lee M. Jampol, & M. B. Mets. (2001). Bietti Crystalline Retinopathy and Juvenile Retinoschisis in a Family With a Novel RS1 Mutation. Archives of Ophthalmology. 119(11). 1719–1719. 5 indexed citations
7.
Thompson, Debra A., P Gyürüs, Eve L. Bingham, et al.. (2000). Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.. PubMed. 41(13). 4293–9. 214 indexed citations
8.
Ayyagari, Radha, et al.. (2000). Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy. Human Genetics. 107(1). 75–82. 29 indexed citations
9.
Hiriyanna, Kelaginamane, Eve L. Bingham, Beverly M. Yashar, et al.. (1999). Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change. Human Mutation. 14(5). 423–427. 38 indexed citations
10.
Walpole, Susannah M., Eve L. Bingham, Jillian Durham, et al.. (1999). Identification and Characterization of the Human Homologue (RAI2) of a Mouse Retinoic Acid-Induced Gene in Xp22. Genomics. 55(3). 275–283. 18 indexed citations
11.
Sieving, Paul A., et al.. (1999). Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. American Journal of Ophthalmology. 128(2). 179–184. 59 indexed citations
12.
Mendoza‐Londono, Roberto, Kelaginamane Hiriyanna, Eve L. Bingham, et al.. (1999). A Colombian family with X-linked juvenile retinoschisis with three affected females: Finding of a frameshift mutation. Ophthalmic Genetics. 20(1). 37–43. 33 indexed citations
13.
Hou, Yu‐Chih, Julia E. Richards, Eve L. Bingham, et al.. (1996). Linkage Study of Best‘s Vitelliform Macular Dystrophy (VMD2) in a Large North American Family. Human Heredity. 46(4). 211–220. 13 indexed citations
14.
Pawar, Hemant, et al.. (1996). X-Linked Juvenile Retinoschisis: Localization between <i>(DXS1195, DXS418</i><i>)</i> and <i>AFM291wf</i><i>5</i> on a Single YAC. Human Heredity. 46(6). 329–335. 9 indexed citations
15.
Sieving, Paul A., et al.. (1996). Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation.. PubMed. 94. 275–94; discussion 295. 7 indexed citations
16.
Pawar, Hemant, Eve L. Bingham, Kathryn L. Lunetta, et al.. (1995). Refined Genetic Mapping of Juvenile X-Linked Retinoschisis. Human Heredity. 45(4). 206–210. 7 indexed citations
17.
Sieving, Paul A., Julie Richards, F. Naarendorp, et al.. (1995). Dark-light: model for nightblindness from the human rhodopsin Gly-90-->Asp mutation.. Proceedings of the National Academy of Sciences. 92(3). 880–884. 122 indexed citations
18.
Roth, Mark S., Joseph H. Antin, Eve L. Bingham, & David Ginsburg. (1990). USE OF POLYMERASE CHAIN REACTION-DETECTED SEQUENCE POLYMORPHISMS TO DOCUMENT ENGRAFTMENT FOLLOWING ALLOGENEIC BONE MARROW TRANSPLANTATION. Transplantation. 49(4). 714–719. 44 indexed citations
19.
Niederhuber, John E., Lawrence B. Schook, & Eve L. Bingham. (1982). Production of a hybridoma T suppressor cell and suppressor factor.. PubMed. 92(2). 146–52. 1 indexed citations
20.
Schook, Lawrence B., Eve L. Bingham, David H. Gutmann, & John E. Niederhuber. (1982). Characterization and expression of H‐2I region gene products on bone marrow‐derived macrophages. European Journal of Immunology. 12(12). 991–997. 13 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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