Robert P. Igo

2.5k total citations
21 papers, 749 citations indexed

About

Robert P. Igo is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Robert P. Igo has authored 21 papers receiving a total of 749 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Ophthalmology. Recurrent topics in Robert P. Igo's work include Genetic Associations and Epidemiology (8 papers), Retinal Diseases and Treatments (4 papers) and Glaucoma and retinal disorders (4 papers). Robert P. Igo is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Retinal Diseases and Treatments (4 papers) and Glaucoma and retinal disorders (4 papers). Robert P. Igo collaborates with scholars based in United States, Canada and Germany. Robert P. Igo's co-authors include Sudha K. Iyengar, Ellen M. Wijsman, Wendy H. Raskind, Barbara Truitt, Ted Holzman, Virginia W. Berninger, Zoran Brkanac, Jonathan H. Lass, Jeremy Fondran and Jennifer B. Thomson and has published in prestigious journals such as PLoS ONE, Journal of Nutrition and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Robert P. Igo

20 papers receiving 738 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert P. Igo United States 14 237 215 181 152 142 21 749
J. M. Teikari Finland 15 451 1.9× 347 1.6× 136 0.8× 30 0.2× 2 0.0× 23 719
Nan Wei China 18 299 1.3× 333 1.5× 322 1.8× 66 0.4× 2 0.0× 47 994
Zakariya Jarrar United Kingdom 6 569 2.4× 413 1.9× 154 0.9× 11 0.1× 2 0.0× 12 688
Ruzhi Deng China 16 191 0.8× 306 1.4× 212 1.2× 15 0.1× 43 860
Peter Dimitrov Australia 20 828 3.5× 552 2.6× 312 1.7× 18 0.1× 1 0.0× 40 1.1k
Stefan Löfgren Sweden 15 129 0.5× 99 0.5× 517 2.9× 77 0.5× 46 771
Norimitsu Ban Japan 16 323 1.4× 132 0.6× 316 1.7× 14 0.1× 31 880
Jimmy D. Bartlett United States 15 432 1.8× 262 1.2× 56 0.3× 10 0.1× 4 0.0× 31 817
Zhenyang Zhao United States 12 305 1.3× 90 0.4× 304 1.7× 6 0.0× 22 627
Ai Ogawa Japan 8 47 0.2× 53 0.2× 170 0.9× 74 0.5× 14 527

Countries citing papers authored by Robert P. Igo

Since Specialization
Citations

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

Fields of papers citing papers by Robert P. Igo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert P. Igo. 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 Robert P. Igo. The network helps show where Robert P. Igo may publish in the future.

Co-authorship network of co-authors of Robert P. Igo

This figure shows the co-authorship network connecting the top 25 collaborators of Robert P. Igo. A scholar is included among the top collaborators of Robert P. Igo 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 Robert P. Igo. Robert P. Igo 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.
Halladay, Christopher, Tamer Hadi, Paul B. Greenberg, et al.. (2019). Genetically-guided algorithm development and sample size optimization for age-related macular degeneration cases and controls in electronic health records from the VA Million Veteran Program.. PubMed. 2019. 153–162. 3 indexed citations
2.
Hall, Noémi B., Robert P. Igo, Barbara Truitt, et al.. (2014). Polymorphisms in TICAM2 and IL1B are associated with TB. Genes and Immunity. 16(2). 127–133. 43 indexed citations
3.
Li, Yi‐Ju, Mollie Minear, Xuejun Qin, et al.. (2014). Mitochondrial Polymorphism A10398G and Haplogroup I Are Associated With Fuchs' Endothelial Corneal Dystrophy. Investigative Ophthalmology & Visual Science. 55(7). 4577–4577. 16 indexed citations
4.
Zhang, Xiaolin, Robert P. Igo, Jeremy Fondran, et al.. (2013). Association of Smoking and Other Risk Factors With Fuchs' Endothelial Corneal Dystrophy Severity and Corneal Thickness. Investigative Ophthalmology & Visual Science. 54(8). 5829–5829. 51 indexed citations
5.
Meyers, Kristin J., Elizabeth J. Johnson, Paul S. Bernstein, et al.. (2013). Genetic Determinants of Macular Pigments in Women of the Carotenoids in Age-Related Eye Disease Study. Investigative Ophthalmology & Visual Science. 54(3). 2333–2333. 75 indexed citations
6.
Meyers, Kristin J., Julie A. Mares, Robert P. Igo, et al.. (2013). Genetic Evidence for Role of Carotenoids in Age-Related Macular Degeneration in the Carotenoids in Age-Related Eye Disease Study (CAREDS). Investigative Ophthalmology & Visual Science. 55(1). 587–587. 102 indexed citations
7.
Engelman, Corinne D., Kristin J. Meyers, Sudha K. Iyengar, et al.. (2012). Vitamin D Intake and Season Modify the Effects of the GC and CYP2R1 Genes on 25-Hydroxyvitamin D Concentrations. Journal of Nutrition. 143(1). 17–26. 59 indexed citations
8.
Igo, Robert P., Laura J. Kopplin, Peronne Joseph, et al.. (2012). Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy. PLoS ONE. 7(10). e46742–e46742. 36 indexed citations
9.
Igo, Robert P. & Audrey H. Schnell. (2011). Comparison of Requirements and Capabilities of Major Multipurpose Software Packages. Methods in molecular biology. 850. 539–558.
10.
Kopplin, Laura J., Robert P. Igo, Jeremy Fondran, et al.. (2011). A Multicenter Study to Map Genes for Fuchs Endothelial Corneal Dystrophy: Baseline Characteristics and Heritability. Cornea. 31(1). 26–35. 83 indexed citations
11.
Schnell, Amanda, Xiangqing Sun, Robert P. Igo, & Robert C. Elston. (2011). Some Capabilities for Model-Based and Model-Free Linkage Analysis using the Program Package S.A.G.E. (Statistical Analysis for Genetic Epidemiology). Human Heredity. 72(4). 237–246. 4 indexed citations
12.
Kopplin, Laura J., Robert P. Igo, Ying Wang, et al.. (2010). Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. Genes and Immunity. 11(8). 609–621. 44 indexed citations
13.
Wijsman, Ellen M., Joseph H. Rothstein, Robert P. Igo, et al.. (2010). Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families. Human Genetics. 127(6). 705–719. 13 indexed citations
14.
Sinha, Ritwik, et al.. (2009). Bayesian intervals for linkage locations. Genetic Epidemiology. 33(7). 604–616. 3 indexed citations
15.
Igo, Robert P., Jing Li, & Katrina A.B. Goddard. (2008). Association mapping by generalized linear regression with density‐based haplotype clustering. Genetic Epidemiology. 33(1). 16–26. 4 indexed citations
16.
Bickeböller, Heike, Katrina A.B. Goddard, Robert P. Igo, et al.. (2007). Issues in association mapping with high-density SNP data and diverse family structures. Genetic Epidemiology. 31(S1). S22–S33. 3 indexed citations
17.
Raskind, Wendy H., Robert P. Igo, N.H. Chapman, et al.. (2005). A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency. Molecular Psychiatry. 10(7). 699–711. 58 indexed citations
18.
Igo, Robert P., Nicola H. Chapman, Virginia W. Berninger, et al.. (2005). Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(1). 15–27. 39 indexed citations
19.
Chapman, Nicola H., Robert P. Igo, Jennifer B. Thomson, et al.. (2004). Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 131B(1). 67–75. 73 indexed citations
20.
Igo, Robert P. & John F. Ash. (1998). The Na+-dependent glutamate and aspartate transporter supports glutathione maintenance and survival of CHO-K1 cells.. Somatic Cell and Molecular Genetics. 24(6). 341–352. 9 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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