Markus Storbeck

693 total citations
16 papers, 384 citations indexed

About

Markus Storbeck is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Markus Storbeck has authored 16 papers receiving a total of 384 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Cancer Research and 5 papers in Genetics. Recurrent topics in Markus Storbeck's work include Cancer Genomics and Diagnostics (7 papers), RNA Research and Splicing (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Markus Storbeck is often cited by papers focused on Cancer Genomics and Diagnostics (7 papers), RNA Research and Splicing (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). Markus Storbeck collaborates with scholars based in Germany, Italy and United Kingdom. Markus Storbeck's co-authors include Brunhilde Wirth, Irmgard Hölker, Rainer Kimmig, Corinna Keup, Sabine Kasimir‐Bauer, Oliver Hoffmann, Raoul Heller, Siegfried Hauch, Markus Sprenger‐Haussels and Peter F. Hahn and has published in prestigious journals such as PLoS ONE, Neurology and Cancer Research.

In The Last Decade

Markus Storbeck

15 papers receiving 380 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Markus Storbeck Germany 12 276 108 97 60 60 16 384
Yi-Hong Zhou United States 12 276 1.0× 117 1.1× 52 0.5× 51 0.8× 25 0.4× 12 442
Yimin Huang China 10 224 0.8× 117 1.1× 41 0.4× 27 0.5× 49 0.8× 19 377
Ander Saenz‐Antoñanzas Spain 11 221 0.8× 96 0.9× 87 0.9× 38 0.6× 61 1.0× 17 377
Tamador Elsir Sweden 8 234 0.8× 102 0.9× 83 0.9× 106 1.8× 12 0.2× 9 353
Marie Strickland United Kingdom 5 191 0.7× 138 1.3× 107 1.1× 25 0.4× 40 0.7× 5 341
Rishi V. Puram United States 5 365 1.3× 46 0.4× 208 2.1× 58 1.0× 122 2.0× 6 630
Yasunari Yamanaka Japan 9 221 0.8× 93 0.9× 26 0.3× 33 0.6× 23 0.4× 14 320
Linda L. Grasfeder United States 4 402 1.5× 40 0.4× 55 0.6× 70 1.2× 39 0.7× 5 499
Kelsey C. Bertrand United States 10 215 0.8× 93 0.9× 86 0.9× 44 0.7× 14 0.2× 22 346
Xike Zhu China 11 170 0.6× 63 0.6× 27 0.3× 72 1.2× 35 0.6× 21 344

Countries citing papers authored by Markus Storbeck

Since Specialization
Citations

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

Fields of papers citing papers by Markus Storbeck

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Markus Storbeck

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

All Works

16 of 16 papers shown
1.
2.
Storbeck, Markus, et al.. (2023). Optimized Workflow for Whole Genome and Transcriptome Next‐Generation Sequencing of Single Cells or Limited Nucleic Acid Samples. Current Protocols. 3(5). e753–e753. 2 indexed citations
3.
Zanni, Ginevra, Matthias Eckenweiler, Markus Storbeck, et al.. (2022). CAPRIN1P512L causes aberrant protein aggregation and associates with early-onset ataxia. Cellular and Molecular Life Sciences. 79(10). 526–526. 9 indexed citations
4.
Keup, Corinna, Siegfried Hauch, Markus Storbeck, et al.. (2021). Integrative statistical analyses of multiple liquid biopsy analytes in metastatic breast cancer. Genome Medicine. 13(1). 85–85. 34 indexed citations
5.
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Gualandi, Francesca, Elisabetta Sette, F. Fortunato, et al.. (2019). Report of a novel ATP7A mutation causing distal motor neuropathy. Neuromuscular Disorders. 29(10). 776–785. 13 indexed citations
8.
Kasimir‐Bauer, Sabine, Oliver Hoffmann, Markus Sprenger‐Haussels, et al.. (2019). Abstract P4-01-10: The analysis of cell-free DNA and circulating tumor cells from one blood tube might empower treatment decisions in metastatic breast cancer patients. Cancer Research. 79(4_Supplement). P4–1. 1 indexed citations
9.
Keup, Corinna, Markus Storbeck, Siegfried Hauch, et al.. (2019). Cell-Free DNA Variant Sequencing Using CTC-Depleted Blood for Comprehensive Liquid Biopsy Testing in Metastatic Breast Cancer. Cancers. 11(2). 238–238. 21 indexed citations
10.
Gabriel, Elke, Irmgard Hölker, Aruljothi Mariappan, et al.. (2018). Novel insights into SMALED2: BICD2 mutations increase microtubule stability and cause defects in axonal and NMJ development. Human Molecular Genetics. 27(10). 1772–1784. 16 indexed citations
11.
Storbeck, Markus, Beate Horsberg Eriksen, Andreas Unger, et al.. (2017). Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features. European Journal of Human Genetics. 25(9). 1040–1048. 34 indexed citations
12.
Storbeck, Markus, Raoul Heller, Irmgard Hölker, et al.. (2016). Biallelic Loss of Proprioception-Related PIEZO2 Causes Muscular Atrophy with Perinatal Respiratory Distress, Arthrogryposis, and Scoliosis. The American Journal of Human Genetics. 99(5). 1206–1216. 72 indexed citations
13.
Unger, Andreas, Gabriele Dekomien, Rudolf A. Kley, et al.. (2016). Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement. Neurology. 87(21). 2235–2243. 25 indexed citations
14.
Heesen, Ludwig, Michael Peitz, Laura Torres‐Benito, et al.. (2015). Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals. Cellular and Molecular Life Sciences. 73(10). 2089–2104. 32 indexed citations
15.
Storbeck, Markus, et al.. (2014). Neuronal-Specific Deficiency of the Splicing Factor Tra2b Causes Apoptosis in Neurogenic Areas of the Developing Mouse Brain. PLoS ONE. 9(2). e89020–e89020. 18 indexed citations
16.
Grellscheid, Sushma Nagaraja, Caroline Dalgliesh, Markus Storbeck, et al.. (2011). Identification of Evolutionarily Conserved Exons as Regulated Targets for the Splicing Activator Tra2β in Development. PLoS Genetics. 7(12). e1002390–e1002390. 61 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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