Rainer Koenig

1.3k total citations
32 papers, 732 citations indexed

About

Rainer Koenig is a scholar working on Molecular Biology, Genetics and Computational Theory and Mathematics. According to data from OpenAlex, Rainer Koenig has authored 32 papers receiving a total of 732 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 13 papers in Genetics and 3 papers in Computational Theory and Mathematics. Recurrent topics in Rainer Koenig's work include Connective tissue disorders research (4 papers), RNA modifications and cancer (4 papers) and Craniofacial Disorders and Treatments (4 papers). Rainer Koenig is often cited by papers focused on Connective tissue disorders research (4 papers), RNA modifications and cancer (4 papers) and Craniofacial Disorders and Treatments (4 papers). Rainer Koenig collaborates with scholars based in Germany, Nigeria and United Kingdom. Rainer Koenig's co-authors include Martin Zenker, André Reis, Michael Hofbeck, H. U. Tietze, Ezekiel Adebiyi, Wolfram Kreß, Anita Rauch, Helmuth-Guenther Doerr, G. Buheitel and H. Singer and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Journal of Bone and Mineral Research.

In The Last Decade

Rainer Koenig

30 papers receiving 715 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rainer Koenig Germany 15 553 243 238 110 48 32 732
Enguerran Mouly France 11 519 0.9× 154 0.6× 286 1.2× 173 1.6× 30 0.6× 15 907
Sara R. Fagerlie United States 11 842 1.5× 221 0.9× 95 0.4× 70 0.6× 47 1.0× 16 960
Yuichi Wakabayashi Japan 14 592 1.1× 122 0.5× 244 1.0× 254 2.3× 49 1.0× 47 941
Reet Rein Estonia 11 280 0.5× 127 0.5× 191 0.8× 70 0.6× 47 1.0× 17 636
Charles F. Towne United States 11 446 0.8× 305 1.3× 168 0.7× 128 1.2× 96 2.0× 11 903
Huei San Leong Australia 9 390 0.7× 110 0.5× 108 0.5× 90 0.8× 29 0.6× 11 686
Steven J. Wu United States 6 1.2k 2.2× 141 0.6× 158 0.7× 86 0.8× 36 0.8× 7 1.5k
Bum-Kyu Lee United States 13 942 1.7× 243 1.0× 124 0.5× 79 0.7× 25 0.5× 15 1.1k
Ruth Williams United Kingdom 9 672 1.2× 160 0.7× 150 0.6× 42 0.4× 37 0.8× 23 865
Chenghao Xuan China 18 887 1.6× 152 0.6× 87 0.4× 177 1.6× 57 1.2× 35 1.1k

Countries citing papers authored by Rainer Koenig

Since Specialization
Citations

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

Fields of papers citing papers by Rainer Koenig

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rainer Koenig

This figure shows the co-authorship network connecting the top 25 collaborators of Rainer Koenig. A scholar is included among the top collaborators of Rainer Koenig 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 Rainer Koenig. Rainer Koenig 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
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Damiani, Claudia, Alessia Cappelli, Olubanke Olujoke Ogunlana, et al.. (2024). Combination of computational techniques and RNAi reveal targets in Anopheles gambiae for malaria vector control. PLoS ONE. 19(7). e0305207–e0305207.
3.
Oswald, Marcus, et al.. (2023). Machine learning on large scale perturbation screens for SARS-CoV-2 host factors identifies β-catenin/CBP inhibitor PRI-724 as a potent antiviral. Frontiers in Microbiology. 14. 1193320–1193320. 1 indexed citations
4.
Aromolaran, Olufemi, Itunuoluwa Isewon, Marcus Oswald, et al.. (2023). Heuristic-enabled active machine learning: A case study of predicting essential developmental stage and immune response genes in Drosophila melanogaster. PLoS ONE. 18(8). e0288023–e0288023. 3 indexed citations
5.
Ogunlana, Olubanke Olujoke, et al.. (2022). Anopheles gambiae Trehalase Inhibitors for Malaria Vector Control: A Molecular Docking and Molecular Dynamics Study. Insects. 13(11). 1070–1070. 10 indexed citations
6.
Aromolaran, Olufemi, et al.. (2021). Identifying essential genes across eukaryotes by machine learning. NAR Genomics and Bioinformatics. 3(4). lqab110–lqab110. 15 indexed citations
7.
8.
Aromolaran, Olufemi, et al.. (2021). Predicting host dependency factors of pathogens in Drosophila melanogaster using machine learning. Computational and Structural Biotechnology Journal. 19. 4581–4592. 3 indexed citations
9.
Ogunlana, Olubanke Olujoke, et al.. (2020). Anopheles metabolic proteins in malaria transmission, prevention and control: a review. Parasites & Vectors. 13(1). 465–465. 30 indexed citations
10.
Aromolaran, Olufemi, et al.. (2020). Essential gene prediction in Drosophila melanogaster using machine learning approaches based on sequence and functional features. Computational and Structural Biotechnology Journal. 18. 612–621. 28 indexed citations
11.
Fischer‐Zirnsak, Björn, Rainer Koenig, Nilay Güneş, et al.. (2019). SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy. Journal of Human Genetics. 64(7). 609–616. 9 indexed citations
12.
Donato, Nataliya Di, Andreas Rump, Rainer Koenig, et al.. (2013). Severe forms of Baraitser–Winter syndrome are caused by ACTB mutations rather than ACTG1 mutations. European Journal of Human Genetics. 22(2). 179–183. 59 indexed citations
13.
Perdu, Bram, Phillis Lakeman, Geert Mortier, et al.. (2010). Two novel WTX mutations underscore the unpredictability of male survival in osteopathia striata with cranial sclerosis. Clinical Genetics. 80(4). 383–388. 22 indexed citations
14.
Zenker, Martin, Katarina Lehmann, Heidi Barth, et al.. (2006). Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. Journal of Medical Genetics. 44(2). 131–135. 136 indexed citations
15.
Zenker, Martin, G. Buheitel, R. Rauch, et al.. (2004). Genotype-phenotype correlations in Noonan syndrome. The Journal of Pediatrics. 144(3). 368–374. 177 indexed citations
16.
Koenig, Rainer. (2003). Teebi hypertelorism syndrome. Clinical Dysmorphology. 12(3). 187–189. 5 indexed citations
17.
Koenig, Rainer, et al.. (2003). SHORT syndrome. Clinical Dysmorphology. 12(1). 45–49. 16 indexed citations
18.
Koenig, Rainer, et al.. (2002). Spectrum of the acrocallosal syndrome. American Journal of Medical Genetics. 108(1). 7–11. 20 indexed citations
19.
Raedle, Jochen, Waltraut Friedl, Hartmut Engels, et al.. (2001). A de novo deletion of chromosome 5q causing familial adenomatous polyposis, dysmorphic features, and mild mental retardation. The American Journal of Gastroenterology. 96(10). 3016–3020. 37 indexed citations
20.
Koenig, Rainer & J Spranger. (1986). Cryptophthalmos ‐ syndactyly syndrome without cryptophthalmos. Clinical Genetics. 29(5). 413–416. 21 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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