Gudrun Schottmann

789 total citations
10 papers, 199 citations indexed

About

Gudrun Schottmann is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Gudrun Schottmann has authored 10 papers receiving a total of 199 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 3 papers in Clinical Biochemistry. Recurrent topics in Gudrun Schottmann's work include Metabolism and Genetic Disorders (3 papers), Hereditary Neurological Disorders (3 papers) and RNA modifications and cancer (2 papers). Gudrun Schottmann is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Hereditary Neurological Disorders (3 papers) and RNA modifications and cancer (2 papers). Gudrun Schottmann collaborates with scholars based in Germany, Netherlands and Austria. Gudrun Schottmann's co-authors include Markus Schuelke, Esther Gill, Peter Meinecke, Denise Horn, Susanne Morales-Gonzalez, Alfried Kohlschütter, Ulrike Schara, Klaus Rüther, Werner Stenzel and Katja von Au and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Movement Disorders.

In The Last Decade

Gudrun Schottmann

9 papers receiving 194 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gudrun Schottmann Germany 9 123 55 41 39 39 10 199
Esther Gill Germany 10 151 1.2× 43 0.8× 32 0.8× 62 1.6× 42 1.1× 13 224
Malavika Hebbar India 9 207 1.7× 28 0.5× 39 1.0× 28 0.7× 67 1.7× 19 290
Elisa Rahikkala Finland 9 163 1.3× 24 0.4× 61 1.5× 37 0.9× 21 0.5× 38 269
Marie‐France Rioux Canada 6 140 1.1× 32 0.6× 37 0.9× 117 3.0× 24 0.6× 8 270
Hannah E. Steele United Kingdom 9 180 1.5× 27 0.5× 53 1.3× 77 2.0× 32 0.8× 14 275
Mathieu Lachance Canada 5 227 1.8× 58 1.1× 47 1.1× 78 2.0× 31 0.8× 8 321
Vedrana Milić Rašić Serbia 8 151 1.2× 32 0.6× 14 0.3× 70 1.8× 36 0.9× 12 211
Fabrizia Stregapede Italy 9 83 0.7× 38 0.7× 41 1.0× 90 2.3× 21 0.5× 17 205
Gautham Arunachal India 8 93 0.8× 15 0.3× 34 0.8× 28 0.7× 26 0.7× 51 171
Claire Guissart France 12 174 1.4× 40 0.7× 42 1.0× 76 1.9× 13 0.3× 22 301

Countries citing papers authored by Gudrun Schottmann

Since Specialization
Citations

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

Fields of papers citing papers by Gudrun Schottmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gudrun Schottmann

This figure shows the co-authorship network connecting the top 25 collaborators of Gudrun Schottmann. A scholar is included among the top collaborators of Gudrun Schottmann 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 Gudrun Schottmann. Gudrun Schottmann 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
1.
Schottmann, Gudrun, Jürgen Kohlhase, Nastassja Himmelreich, et al.. (2024). Impact of genetic test interpretation on a VPS13B missense variant in Cohen syndrome. Frontiers in Neuroscience. 18. 1488133–1488133.
2.
Gušić, Mirjana, Gudrun Schottmann, René G. Feichtinger, et al.. (2019). Bi-Allelic UQCRFS1 Variants Are Associated with Mitochondrial Complex III Deficiency, Cardiomyopathy, and Alopecia Totalis. The American Journal of Human Genetics. 106(1). 102–111. 31 indexed citations
3.
Dušek, Petr, Ralf Mekle, Marta Skowrońska, et al.. (2019). Brain Iron and Metabolic Abnormalities in C19orf12 Mutation Carriers: A 7.0 Tesla MRI Study in Mitochondrial Membrane Protein–Associated Neurodegeneration. Movement Disorders. 35(1). 142–150. 11 indexed citations
4.
Schottmann, Gudrun, Jana Marie Schwarz, Esther Gill, et al.. (2017). Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia. Mitochondrion. 37. 46–54. 15 indexed citations
5.
Schottmann, Gudrun, Carmen Lorenz, Natalie Weinhold, et al.. (2016). A movement disorder with dystonia and ataxia caused by a mutation in the HIBCH gene. Movement Disorders. 31(11). 1733–1739. 23 indexed citations
6.
Schottmann, Gudrun, Heinz Jungbluth, Ulrike Schara, et al.. (2015). Recessive truncating IGHMBP2 mutations presenting as axonal sensorimotor neuropathy. Neurology. 84(5). 523–531. 27 indexed citations
7.
Schottmann, Gudrun, Dominik Seelow, Franziska Seifert, et al.. (2015). Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy. Neurology Genetics. 1(4). e32–e32. 20 indexed citations
8.
Kirschner, Janbernd, David Schorling, Dieter Hauschke, et al.. (2013). Somatropin treatment of spinal muscular atrophy: A placebo-controlled, double-blind crossover pilot study. Neuromuscular Disorders. 24(2). 134–142. 24 indexed citations
9.
Horn, Denise, Gudrun Schottmann, & Peter Meinecke. (2010). Hyperphosphatasia with mental retardation, brachytelephalangy, and a distinct facial gestalt: Delineation of a recognizable syndrome. European Journal of Medical Genetics. 53(2). 85–88. 22 indexed citations
10.
Schottmann, Gudrun, Klaus Rüther, G. Stoltenburg, et al.. (2009). Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X). Clinical Genetics. 76(1). 38–45. 26 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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