Everson Nogoceke

3.8k total citations
33 papers, 1.7k citations indexed

About

Everson Nogoceke is a scholar working on Molecular Biology, Ophthalmology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Everson Nogoceke has authored 33 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 12 papers in Ophthalmology and 12 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Everson Nogoceke's work include Retinal Diseases and Treatments (12 papers), Research on Leishmaniasis Studies (10 papers) and Trypanosoma species research and implications (9 papers). Everson Nogoceke is often cited by papers focused on Retinal Diseases and Treatments (12 papers), Research on Leishmaniasis Studies (10 papers) and Trypanosoma species research and implications (9 papers). Everson Nogoceke collaborates with scholars based in Germany, Switzerland and United States. Everson Nogoceke's co-authors include Henryk M. Kalisz, Leopold Flohé, Michael Kieß, Daniel U. Gommel, Marisa Montemartini, Peter M. Steinert, Sascha Fauser, Mahavir Singh, Piotr Szczęsny and Jayashree Sahni and has published in prestigious journals such as Journal of Biological Chemistry, The EMBO Journal and Scientific Reports.

In The Last Decade

Everson Nogoceke

33 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Everson Nogoceke Germany 19 774 598 450 446 412 33 1.7k
Aslam A. Khan United States 15 297 0.4× 209 0.3× 301 0.7× 82 0.2× 100 0.2× 29 1.2k
Pei Zhang China 23 1.2k 1.5× 16 0.0× 73 0.2× 25 0.1× 123 0.3× 109 2.1k
Kojiro Matsumoto Japan 27 1.3k 1.6× 24 0.0× 116 0.3× 23 0.1× 448 1.1× 81 2.1k
Jing Shao China 13 1.9k 2.4× 25 0.0× 35 0.1× 67 0.2× 442 1.1× 22 2.6k
Ying Zheng China 21 556 0.7× 16 0.0× 95 0.2× 35 0.1× 85 0.2× 43 1.1k
Attila Zalatnai Hungary 19 389 0.5× 16 0.0× 51 0.1× 44 0.1× 272 0.7× 80 1.2k
Hideki Kimura Japan 20 754 1.0× 41 0.1× 56 0.1× 38 0.1× 86 0.2× 60 1.3k
Denis Sviridov United States 21 601 0.8× 12 0.0× 53 0.1× 32 0.1× 116 0.3× 40 1.4k
Roger Drew Australia 18 1.0k 1.4× 5 0.0× 251 0.6× 47 0.1× 129 0.3× 47 2.1k

Countries citing papers authored by Everson Nogoceke

Since Specialization
Citations

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

Fields of papers citing papers by Everson Nogoceke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Everson Nogoceke

This figure shows the co-authorship network connecting the top 25 collaborators of Everson Nogoceke. A scholar is included among the top collaborators of Everson Nogoceke 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 Everson Nogoceke. Everson Nogoceke 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.
Acar, İlhan E., Tessel E. Galesloot, Ulrich F. O. Luhmann, et al.. (2023). Whole Genome Sequencing Identifies Novel Common and Low-Frequency Variants Associated With Age-Related Macular Degeneration. Investigative Ophthalmology & Visual Science. 64(14). 24–24. 4 indexed citations
2.
Lorés‐Motta, Laura, Anna E. van Beek, Esther Willems, et al.. (2021). Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. The American Journal of Human Genetics. 108(8). 1367–1384. 43 indexed citations
3.
Sahni, Jayashree, Sunil Patel, Pravin U. Dugel, et al.. (2019). Simultaneous Inhibition of Angiopoietin-2 and Vascular Endothelial Growth Factor-A with Faricimab in Diabetic Macular Edema. Ophthalmology. 126(8). 1155–1170. 179 indexed citations
4.
Göpfert, Jens, et al.. (2019). Development and Evaluation of an Ultrasensitive Free VEGF-A Immunoassay for Analysis of Human Aqueous Humor. Bioanalysis. 11(9). 875–886. 5 indexed citations
5.
Biarnés, Marc, Vassil Vassilev, Everson Nogoceke, et al.. (2018). Precision medicine for age-related macular degeneration: current developments and prospects. Expert Review of Precision Medicine and Drug Development. 3(4). 249–263. 2 indexed citations
6.
Emri, Eszter, B. Merle, Johanna M. Colijn, et al.. (2018). A new perspective on lipid research in age-related macular degeneration. Progress in Retinal and Eye Research. 67. 56–86. 167 indexed citations
7.
Ullmer, Christoph, Everson Nogoceke, Guido R. Hartmann, et al.. (2016). LYSOPHOSPHATIDIC ACIDS AND AUTOTAXIN IN RETINAL VEIN OCCLUSION. Retina. 36(12). 2311–2318. 11 indexed citations
8.
Looker, Helen C., Marco Colombo, Sibylle Hess, et al.. (2015). Biomarkers of rapid chronic kidney disease progression in type 2 diabetes. Kidney International. 88(4). 888–896. 124 indexed citations
9.
Looker, Helen C., Marco Colombo, Felix Agakov, et al.. (2015). Protein biomarkers for the prediction of cardiovascular disease in type 2 diabetes. Diabetologia. 58(6). 1363–1371. 53 indexed citations
10.
Castro, Caio César Silva de, et al.. (2010). Genetic Variants of the DDR1 Gene Are Associated with Vitiligo in Two Independent Brazilian Population Samples. Journal of Investigative Dermatology. 130(7). 1813–1818. 28 indexed citations
11.
Brandenburg, Jens, Bernd Schimanski, Everson Nogoceke, et al.. (2007). Multifunctional class I transcription in Trypanosoma brucei depends on a novel protein complex. The EMBO Journal. 26(23). 4856–4866. 53 indexed citations
12.
Hofmann, Birgit, Heike Budde, Karsten Bruns, et al.. (2001). Structures of Tryparedoxins Revealing Interaction with Trypanothione. Biological Chemistry. 382(3). 459–71. 50 indexed citations
13.
López, Jorge A., Wanderley de Souza, Leopold Flohé, et al.. (2000). Evidence for a trypanothione-dependent peroxidase system in Trypanosoma cruzi. Free Radical Biology and Medicine. 28(5). 767–772. 43 indexed citations
14.
Kalisz, Henryk M., et al.. (2000). Crystallisation of tryparedoxin I from Crithidia fasciculata. BioFactors. 11(1-2). 73–75. 7 indexed citations
15.
Steinert, Peter M., Kurt E.J. Dittmar, Henryk M. Kalisz, et al.. (1999). Cytoplasmic localization of the trypanothione peroxidase system in Crithidia fasciculata. Free Radical Biology and Medicine. 26(7-8). 844–849. 25 indexed citations
16.
Guerrero, Sergio A., Leopold Flohé, Henryk M. Kalisz, et al.. (1999). Sequence, heterologous expression and functional characterization of tryparedoxin1 from Crithidia fasciculata. European Journal of Biochemistry. 259(3). 789–794. 25 indexed citations
17.
Kalisz, Henryk M., Everson Nogoceke, Daniel U. Gommel, et al.. (1999). Crystallization and preliminary X-ray analysis of tryparedoxin I fromCrithidia fasciculata. Acta Crystallographica Section D Biological Crystallography. 55(3). 696–698. 9 indexed citations
18.
Montemartini, Marisa, Everson Nogoceke, Mahavir Singh, et al.. (1998). Sequence Analysis of the Tryparedoxin Peroxidase Gene fromCrithidia fasciculata and Its Functional Expression in Escherichia coli. Journal of Biological Chemistry. 273(9). 4864–4871. 61 indexed citations
19.
Gommel, Daniel U., Everson Nogoceke, Michael Morr, et al.. (1997). Catalytic Characteristics of Tryparedoxin. European Journal of Biochemistry. 248(3). 913–918. 92 indexed citations
20.
Nogoceke, Everson, Daniel U. Gommel, Michael Kieß, Henryk M. Kalisz, & Leopold Flohé. (1997). A Unique Cascade of Oxidoreductases Catalyses Trypanothione-Mediated Peroxide Metabolism in Crithidia fasciculata. Biological Chemistry. 378(8). 827–36. 242 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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