I.H. Maumenee

520 total citations
5 papers, 400 citations indexed

About

I.H. Maumenee is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, I.H. Maumenee has authored 5 papers receiving a total of 400 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 1 paper in Pathology and Forensic Medicine and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in I.H. Maumenee's work include Retinal Development and Disorders (2 papers), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Photoreceptor and optogenetics research (1 paper). I.H. Maumenee is often cited by papers focused on Retinal Development and Disorders (2 papers), Hearing, Cochlea, Tinnitus, Genetics (1 paper) and Photoreceptor and optogenetics research (1 paper). I.H. Maumenee collaborates with scholars based in United States, Netherlands and Switzerland. I.H. Maumenee's co-authors include John R. Heckenlively, Gerald A. Fishman, R Nowakowski, Ching‐Hwa Sung, Carol Davenport, Samuel G. Jacobson, Peter Gouras, Jeremy Nathans, Susan V. Booker and Elias I. Traboulsi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Gut and Investigative Ophthalmology & Visual Science.

In The Last Decade

I.H. Maumenee

5 papers receiving 387 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I.H. Maumenee United States 3 351 217 73 68 31 5 400
Mai Al-Maghtheh United Kingdom 10 597 1.7× 138 0.6× 131 1.8× 86 1.3× 73 2.4× 11 623
Clayton P. Santiago United States 8 467 1.3× 84 0.4× 72 1.0× 67 1.0× 30 1.0× 22 548
S O'Gorman United States 6 432 1.2× 104 0.5× 102 1.4× 44 0.6× 71 2.3× 7 518
Kun Do Rhee United States 9 292 0.8× 110 0.5× 108 1.5× 38 0.6× 35 1.1× 9 373
Fred Zwas United States 8 284 0.8× 89 0.4× 161 2.2× 56 0.8× 34 1.1× 10 416
H. Pawar United States 5 281 0.8× 88 0.4× 75 1.0× 50 0.7× 27 0.9× 5 326
Pietro Farinelli Sweden 9 461 1.3× 107 0.5× 171 2.3× 68 1.0× 96 3.1× 13 508
Stefan Kustermann Germany 5 339 1.0× 118 0.5× 131 1.8× 32 0.5× 21 0.7× 6 378
Xi-Qin Ding United States 13 412 1.2× 239 1.1× 123 1.7× 72 1.1× 10 0.3× 25 470
Rafal Goraczniak United States 16 628 1.8× 245 1.1× 73 1.0× 40 0.6× 16 0.5× 22 722

Countries citing papers authored by I.H. Maumenee

Since Specialization
Citations

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

Fields of papers citing papers by I.H. Maumenee

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I.H. Maumenee. 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 I.H. Maumenee. The network helps show where I.H. Maumenee may publish in the future.

Co-authorship network of co-authors of I.H. Maumenee

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

All Works

5 of 5 papers shown
1.
Kerrison, John, Donald J. Zack, & I.H. Maumenee. (2004). Candidate Gene Analysis in X–linked Congenital Nystagmus (NYS1). Investigative Ophthalmology & Visual Science. 45(13). 4742–4742. 1 indexed citations
2.
Allikmets, Rando, Jana Zernant, Isabelle Perrault, et al.. (2004). MULTIALLELIC INHERITANCE AND/OR MODIFIER ALLELES IN LEBER CONGENITAL AMAUROSIS: ANALYSIS WITH THE LCA DISEASE CHIP. Investigative Ophthalmology & Visual Science. 45(13). 2444–2444. 2 indexed citations
3.
Abouzeid, Hana, et al.. (2004). Monogenic inheritance of Leber congenital amaurosis: causation by a novel mutation in CRB1.. Investigative Ophthalmology & Visual Science. 45(13). 4730–4730. 1 indexed citations
4.
Giardiello, Francis M., G. J. A. Offerhaus, Elias I. Traboulsi, et al.. (1991). Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.. Gut. 32(10). 1170–1174. 34 indexed citations
5.
Sung, Ching‐Hwa, Carol Davenport, I.H. Maumenee, et al.. (1991). Rhodopsin mutations in autosomal dominant retinitis pigmentosa.. Proceedings of the National Academy of Sciences. 88(15). 6481–6485. 362 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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