Ines F. Scheller

474 total citations
6 papers, 180 citations indexed

About

Ines F. Scheller is a scholar working on Molecular Biology, Genetics and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Ines F. Scheller has authored 6 papers receiving a total of 180 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Genetics and 1 paper in Endocrinology, Diabetes and Metabolism. Recurrent topics in Ines F. Scheller's work include RNA and protein synthesis mechanisms (3 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Ines F. Scheller is often cited by papers focused on RNA and protein synthesis mechanisms (3 papers), RNA Research and Splicing (3 papers) and RNA modifications and cancer (2 papers). Ines F. Scheller collaborates with scholars based in Germany, United States and Australia. Ines F. Scheller's co-authors include Vicente A. Yépez, Julien Gagneur, Christian Mertes, Mirjana Gušić, Holger Prokisch, Muhammed Hasan Çelik, Laura S. Kremer, Michaela Müller, Laure Frésard and Leonhard Wachutka and has published in prestigious journals such as Nature Communications, Nature Protocols and The American Journal of Human Genetics.

In The Last Decade

Ines F. Scheller

6 papers receiving 178 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ines F. Scheller Germany	4	120	75	18	12	10	6	180
Newell Belnap United States	7	84 0.7×	49 0.7×	13 0.7×	8 0.7×	6 0.6×	12	126
Leonhard Wachutka Germany	5	181 1.5×	45 0.6×	27 1.5×	13 1.1×	6 0.6×	7	232
Christel Thauvin France	6	81 0.7×	37 0.5×	14 0.8×	16 1.3×	6 0.6×	11	146
Neethukrishna Kausthubham India	7	112 0.9×	68 0.9×	6 0.3×	14 1.2×	11 1.1×	13	194
G. C. Chan United Kingdom	2	87 0.7×	129 1.7×	35 1.9×	5 0.4×	18 1.8×	3	193
Mona Mohammad Almramhi United Kingdom	8	117 1.0×	58 0.8×	6 0.3×	15 1.3×	9 0.9×	13	189
William L. Macken United Kingdom	6	106 0.9×	40 0.5×	12 0.7×	16 1.3×	5 0.5×	11	146
Charu Kaiwar United States	6	56 0.5×	61 0.8×	7 0.4×	11 0.9×	7 0.7×	10	103
Muhammed Hasan Çelik Germany	7	265 2.2×	99 1.3×	29 1.6×	5 0.4×	10 1.0×	11	330

Countries citing papers authored by Ines F. Scheller

Since Specialization

Citations

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

Fields of papers citing papers by Ines F. Scheller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ines F. Scheller. 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 Ines F. Scheller. The network helps show where Ines F. Scheller may publish in the future.

Co-authorship network of co-authors of Ines F. Scheller

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

All Works

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6 of 6 papers shown

1.

Pang, Cheng‐Yoong, Ines F. Scheller, Cheuk‐Wing Fung, et al.. (2025). An outlier approach: advancing diagnosis of neurological diseases through integrating proteomics into multi-omics guided exome reanalysis. npj Genomic Medicine. 10(1). 36–36. 1 indexed citations

2.

Huber, Sandra, Franziska R. Traube, Marc Seifert, et al.. (2024). Analysis of 3760 hematologic malignancies reveals rare transcriptomic aberrations of driver genes. Genome Medicine. 16(1). 70–70. 1 indexed citations

3.

Scheller, Ines F., et al.. (2023). Improved detection of aberrant splicing with FRASER 2.0 and the intron Jaccard index. The American Journal of Human Genetics. 110(12). 2056–2067. 12 indexed citations

4.

Mertes, Christian, Ines F. Scheller, Vicente A. Yépez, et al.. (2021). Detection of aberrant splicing events in RNA-seq data using FRASER. Nature Communications. 12(1). 529–529. 84 indexed citations

5.

Yépez, Vicente A., Christian Mertes, Michaela Müller, et al.. (2021). Detection of aberrant gene expression events in RNA sequencing data. Nature Protocols. 16(2). 1276–1296. 65 indexed citations

6.

Veihelmann, A., T. Brill, Manfred Blobner, et al.. (1997). Inhibition of nitric oxide synthesis improves detoxication in inflammatory liver dysfunction in vivo. American Journal of Physiology-Gastrointestinal and Liver Physiology. 273(2). G530–G536. 17 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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