Rainer König

2.3k total citations
36 papers, 992 citations indexed

About

Rainer König is a scholar working on Molecular Biology, Epidemiology and Genetics. According to data from OpenAlex, Rainer König has authored 36 papers receiving a total of 992 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Epidemiology and 5 papers in Genetics. Recurrent topics in Rainer König's work include Computational Drug Discovery Methods (3 papers), Genetic Syndromes and Imprinting (2 papers) and Gene expression and cancer classification (2 papers). Rainer König is often cited by papers focused on Computational Drug Discovery Methods (3 papers), Genetic Syndromes and Imprinting (2 papers) and Gene expression and cancer classification (2 papers). Rainer König collaborates with scholars based in Germany, United Kingdom and Nigeria. Rainer König's co-authors include Marcus Oswald, Christine Heym, Roland Eils, Gunnar Schramm, Denise Horn, Stefan Mundlos, Sigrid Fuchs, Judith G. Hall, Eva Klopocki and Claus‐Eric Ott and has published in prestigious journals such as Cancer Research, Oncogene and The American Journal of Human Genetics.

In The Last Decade

Rainer König

35 papers receiving 973 citations

Peers

Rainer König

GENET

SURGE

EPIDE

IMMUN

Hindi Al‐Hindi Saudi Arabia

Penny J. Norsworthy United Kingdom

Chela James United Kingdom

María Eugenia Sáez Spain

Mohammed Al Balwi Saudi Arabia

Zhigang Fan China

Christian Benner Finland

Tetsuya Nishimura Japan

Long Guo China

Miguel G. Toscano Spain

Hindi Al‐Hindi Saudi Arabia

Rainer König

449 ×1.0

207 ×0.7

GENET

165 ×1.2

SURGE

130 ×1.3

EPIDE

51 ×0.5

IMMUN

Citations per year, relative to Rainer König Rainer König (= 1×) peers Hindi Al‐Hindi

Countries citing papers authored by Rainer König

Since Specialization

Citations

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

Fields of papers citing papers by Rainer König

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rainer König

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

All Works

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20 of 20 papers shown

Grünewald, Benedikt, Jonathan Wickel, Nina Hahn, et al.. (2024). Targeted rescue of synaptic plasticity improves cognitive decline in sepsis-associated encephalopathy. Molecular Therapy. 32(7). 2113–2129. 11 indexed citations

Mahajan, Ujjwal Mukund, Johanna Erber, Florian Voit, et al.. (2023). Validation of the SACOV-19 score for identifying patients at risk of complicated or more severe COVID-19: a prospective study. Infection. 51(6). 1669–1678. 1 indexed citations

Chung, Ha‐Yeun, Jonathan Wickel, Marcus Oswald, et al.. (2022). Neurofilament light chain levels predict encephalopathy and outcome in community‐acquired pneumonia. Annals of Clinical and Translational Neurology. 10(2). 204–212. 6 indexed citations

König, Rainer, et al.. (2018). NBAS Gene Mutation Causes Insulin-Dependent Diabetes Mellitus in a Patient with a Multisystem Disorder Consisting Immunodeficiency and Extremely Short Stature.

Joos, Andreas, et al.. (2017). Differenzialdiagnose dissoziativer Anfälle. Der Nervenarzt. 88(10). 1147–1152. 1 indexed citations

Ebbinghaus, Matthias, Zhong‐Wei Zhou, Manuela Pacyna-Gengelbach, et al.. (2016). Tumor suppression in mice lacking GABARAP, an Atg8/LC3 family member implicated in autophagy, is associated with alterations in cytokine secretion and cell death. Cell Death and Disease. 7(4). e2205–e2205. 45 indexed citations

Speck, Tobias, Tillmann Michels, Antonio Sorrentino, et al.. (2015). A high‐throughput RNA i screen for detection of immune‐checkpoint molecules that mediate tumor resistance to cytotoxic T lymphocytes. EMBO Molecular Medicine. 7(4). 450–463. 29 indexed citations

Winnay, Jonathon N., Stefan Johansson, Tor Claudi, et al.. (2013). SHORT Syndrome with Partial Lipodystrophy Due to Impaired Phosphatidylinositol 3 Kinase Signaling. The American Journal of Human Genetics. 93(1). 150–157. 110 indexed citations

Kauferstein, Silke, Marnie Kopp, Rainer König, et al.. (2013). Genetic analysis of sudden unexplained death: A multidisciplinary approach. Forensic Science International. 229(1-3). 122–127. 30 indexed citations

10.

Plaimas, Kitiporn, Yulin Wang, Solomon O. Rotimi, et al.. (2013). Computational and experimental analysis identified 6-diazo-5-oxonorleucine as a potential agent for treating infection by Plasmodium falciparum. Infection Genetics and Evolution. 20. 389–395. 10 indexed citations

11.

Henrich, Kai‐Oliver, Tobias Bauer, Johannes H. Schulte, et al.. (2011). CAMTA1 , a 1p36 Tumor Suppressor Candidate, Inhibits Growth and Activates Differentiation Programs in Neuroblastoma Cells. Cancer Research. 71(8). 3142–3151. 64 indexed citations

12.

Schramm, Gunnar, et al.. (2010). Analyzing the regulation of metabolic pathways in human breast cancer. BMC Medical Genomics. 3(1). 39–39. 43 indexed citations

13.

Klopocki, Eva, Harald Schulze, Gabriele Strauß, et al.. (2007). Complex Inheritance Pattern Resembling Autosomal Recessive Inheritance Involving a Microdeletion in Thrombocytopenia–Absent Radius Syndrome. The American Journal of Human Genetics. 80(2). 232–240. 201 indexed citations

14.

Arnemann, Joachim, et al.. (2003). Alport syndrome with diffuse leiomyomatosis. American Journal of Medical Genetics Part A. 119A(3). 381–385. 31 indexed citations

15.

Driever, Pablo Hernáiz, et al.. (1996). Congenital microgastria, growth hormone deficiency and diabetes insipidus. European Journal of Pediatrics. 156(1). 37–40. 7 indexed citations

16.

Schrander‐Stumpel, C. T. R. M., Peter Meinecke, Golder N. Wilson, et al.. (1994). The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients. European Journal of Pediatrics. 153(6). 438–445. 88 indexed citations

17.

König, Rainer, et al.. (1991). Simpson‐Golabi‐Behmel syndrome with severe cardiac arrhythmias. American Journal of Medical Genetics. 38(2-3). 244–247. 23 indexed citations

18.

Sieg, Andreas, Rainer König, D. Ullrich, & Johan Fevery. (1990). Subfractionation of serum bilirubins by alkaline methanolysis and thin-layer chromatography. Journal of Hepatology. 11(2). 159–164. 31 indexed citations

19.

König, Rainer, Ulrike Schick, & Sigrun Fuchs. (1990). Townes-Brocks syndrome. European Journal of Pediatrics. 150(2). 100–103. 13 indexed citations

20.

König, Rainer & Christine Heym. (1978). Immunofluorescent localization of dopamine-β-hydroxylase in small intensely fluorescent cells of the rat superior cervical ganglion. Neuroscience Letters. 10(1-2). 187–191. 32 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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