Maren Runte

832 total citations
10 papers, 534 citations indexed

About

Maren Runte is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Maren Runte has authored 10 papers receiving a total of 534 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Maren Runte's work include Genetic Syndromes and Imprinting (4 papers), RNA modifications and cancer (2 papers) and Retinal Development and Disorders (2 papers). Maren Runte is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), RNA modifications and cancer (2 papers) and Retinal Development and Disorders (2 papers). Maren Runte collaborates with scholars based in Germany, Australia and United States. Maren Runte's co-authors include Jörg T. Epplen, Karin Buiting, Bernhard Horsthemke, Denise Horn, Raymonda Varon, Gabriele Dekomien, Joseph Wagstaff, Monika Cohen, Gabriele Gillessen‐Kaesbach and Peter M. Kroisel and has published in prestigious journals such as Human Molecular Genetics, Electrophoresis and Human Genetics.

In The Last Decade

Maren Runte

9 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maren Runte Germany 7 445 380 105 85 26 10 534
Jack S. Hsiao United States 5 374 0.8× 217 0.6× 47 0.4× 38 0.4× 20 0.8× 7 475
Naiara Akizu United States 11 380 0.9× 229 0.6× 50 0.5× 32 0.4× 15 0.6× 19 484
Ryan N. Traylor United States 7 279 0.6× 376 1.0× 115 1.1× 55 0.6× 16 0.6× 7 494
Kelly E. Jackson United States 8 204 0.5× 211 0.6× 50 0.5× 11 0.1× 24 0.9× 15 375
Silvina Epsztejn‐Litman Israel 9 482 1.1× 169 0.4× 36 0.3× 17 0.2× 18 0.7× 16 540
Marina Murdolo Italy 13 383 0.9× 491 1.3× 146 1.4× 61 0.7× 32 1.2× 20 663
Anouck Schneider France 12 134 0.3× 199 0.5× 62 0.6× 18 0.2× 11 0.4× 21 355
Malgorzata Schmidt Australia 12 394 0.9× 519 1.4× 67 0.6× 20 0.2× 20 0.8× 19 638
Tomasz M. Kuliński Poland 14 648 1.5× 213 0.6× 83 0.8× 132 1.6× 19 0.7× 17 707
Christoph Dotter Austria 6 312 0.7× 166 0.4× 35 0.3× 138 1.6× 14 0.5× 7 377

Countries citing papers authored by Maren Runte

Since Specialization
Citations

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

Fields of papers citing papers by Maren Runte

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maren Runte

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

All Works

10 of 10 papers shown
2.
Runte, Maren, et al.. (2010). Semantik der Sinne : die lexikografische Erfassung von Geschmacksadjektiven. ZHAW Digital Collection. 26. 109–128. 1 indexed citations
3.
Runte, Maren, Raymonda Varon, Denise Horn, Bernhard Horsthemke, & Karin Buiting. (2004). Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader?Willi syndrome. Human Genetics. 116(3). 228–230. 78 indexed citations
4.
Varon, Raymonda, Denise Horn, Monika Cohen, et al.. (2004). SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome. Human Genetics. 114(6). 553–561. 41 indexed citations
5.
Runte, Maren, Christina Lich, Michael Zeschnigk, et al.. (2001). Comprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15. European Journal of Human Genetics. 9(7). 519–526. 9 indexed citations
6.
Runte, Maren. (2001). The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A. Human Molecular Genetics. 10(23). 2687–2700. 300 indexed citations
7.
Dekomien, Gabriele, et al.. (2000). Generalized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene. Cytogenetic and Genome Research. 90(3-4). 261–267. 56 indexed citations
8.
Runte, Maren, Gabriele Dekomien, & Jörg T. Epplen. (2000). Evaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance. Animal Genetics. 31(3). 223–227. 12 indexed citations
9.
Klein, Wolfram, A Tromm, Thomas Griga, et al.. (2000). TheIL-10 gene is not involved in the predisposition to inflammatory bowel disease. Electrophoresis. 21(17). 3578–3582. 33 indexed citations
10.
Klein, Wolfram, A Tromm, Thomas Griga, et al.. (2000). The IL-10 gene is not involved in the predisposition to inflammatory bowel disease. Electrophoresis. 21(17). 3578–3582. 4 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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