Ulrike Grieben

780 total citations
14 papers, 348 citations indexed

About

Ulrike Grieben is a scholar working on Molecular Biology, Surgery and Cellular and Molecular Neuroscience. According to data from OpenAlex, Ulrike Grieben has authored 14 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 3 papers in Surgery and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Ulrike Grieben's work include Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Ulrike Grieben is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Genetic Neurodegenerative Diseases (3 papers) and Glycosylation and Glycoproteins Research (2 papers). Ulrike Grieben collaborates with scholars based in Germany, United States and Switzerland. Ulrike Grieben's co-authors include Julia B. Hennermann, Johan L.K. Van Hove, Gunter Scharer, Simone Spuler, Jeanette Schulz‐Menger, Martin Hasilik, Peter Kellman, Christian Thiel, Ludwig Lehle and Edyta Błaszczyk and has published in prestigious journals such as Scientific Reports, Biochemical Journal and The Lancet Neurology.

In The Last Decade

Ulrike Grieben

14 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ulrike Grieben Germany 10 239 65 57 56 54 14 348
Jaume Colomer Spain 11 356 1.5× 102 1.6× 35 0.6× 37 0.7× 62 1.1× 19 422
Michela Ripolone Italy 13 349 1.5× 121 1.9× 63 1.1× 67 1.2× 34 0.6× 40 526
Tomoko Lee Japan 14 317 1.3× 42 0.6× 51 0.9× 61 1.1× 74 1.4× 43 400
Sabine Grønborg Denmark 11 207 0.9× 41 0.6× 69 1.2× 74 1.3× 36 0.7× 25 330
Heiko Brennenstuhl Germany 11 180 0.8× 47 0.7× 74 1.3× 99 1.8× 10 0.2× 25 315
Anna Marcé‐Grau Spain 10 139 0.6× 63 1.0× 48 0.8× 52 0.9× 26 0.5× 19 284
Hideaki Ohtsubo Japan 10 192 0.8× 41 0.6× 20 0.4× 40 0.7× 11 0.2× 14 305
Ohad Wormser Israel 11 173 0.7× 20 0.3× 65 1.1× 31 0.6× 26 0.5× 28 275
Tim M. Strom Germany 4 173 0.7× 51 0.8× 76 1.3× 50 0.9× 5 0.1× 4 336

Countries citing papers authored by Ulrike Grieben

Since Specialization
Citations

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

Fields of papers citing papers by Ulrike Grieben

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrike Grieben

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

All Works

14 of 14 papers shown
1.
Grieben, Ulrike, et al.. (2022). Statins Aggravate the Risk of Insulin Resistance in Human Muscle. International Journal of Molecular Sciences. 23(4). 2398–2398. 8 indexed citations
2.
Popp, Oliver, Ulrike Grieben, Kathrin Saar, et al.. (2020). Statin-induced myopathic changes in primary human muscle cells and reversal by a prostaglandin F2 alpha analogue. Scientific Reports. 10(1). 2158–2158. 18 indexed citations
3.
Błaszczyk, Edyta, Ulrike Grieben, Florian von Knobelsdorff‐Brenkenhoff, et al.. (2019). Subclinical myocardial injury in patients with Facioscapulohumeral muscular dystrophy 1 and preserved ejection fraction – assessment by cardiovascular magnetic resonance. Journal of Cardiovascular Magnetic Resonance. 21(1). 25–25. 16 indexed citations
4.
Moshourab, Rabih, et al.. (2016). A Molecular Signature of Myalgia in Myotonic Dystrophy 2. EBioMedicine. 7. 205–211. 16 indexed citations
5.
Grieben, Ulrike, Wolfgang Utz, Matthias A. Dieringer, et al.. (2016). Cardiac Involvement in Myotonic Dystrophy Type 2 Patients With Preserved Ejection Fraction. Circulation Cardiovascular Imaging. 9(7). 36 indexed citations
6.
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
7.
Hennermann, Julia B., et al.. (2011). Prediction of long‐term outcome in glycine encephalopathy: a clinical survey. Journal of Inherited Metabolic Disease. 35(2). 253–261. 63 indexed citations
8.
Valadares, Eugênia Ribeiro, et al.. (2011). Juvenile neuronal ceroid-lipofuscinosis: clinical and molecular investigation in a large family in Brazil. Arquivos de Neuro-Psiquiatria. 69(1). 13–18. 8 indexed citations
9.
Hagen, Maja von der, Ana Ferreiro, Ulrike Grieben, et al.. (2010). Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM). Neuropediatrics. 41(2). 1 indexed citations
10.
Kirschner, Janbernd, Joachim Schessl, Ulrike Schara, et al.. (2010). Treatment of Duchenne muscular dystrophy with ciclosporin A: a randomised, double-blind, placebo-controlled multicentre trial. The Lancet Neurology. 9(11). 1053–1059. 46 indexed citations
11.
Klopocki, Eva, Luitgard Graul‐Neumann, Ulrike Grieben, et al.. (2007). A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH. European Journal of Pediatrics. 167(8). 903–908. 43 indexed citations
12.
Hagen, Maja von der, Angela M. Kaindl, Katrin Koehler, et al.. (2005). Facing the genetic heterogeneity in neuromuscular disorders: Linkage analysis as an economic diagnostic approach towards the molecular diagnosis. Neuromuscular Disorders. 16(1). 4–13. 16 indexed citations
13.
Thiel, Christian, Markus Schwarz, Martin Hasilik, et al.. (2002). Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig. Biochemical Journal. 367(1). 195–201. 46 indexed citations
14.
Grieben, Ulrike, et al.. (1992). [Bromoderma tuberosum caused by anticonvulsive treatment with potassium bromide].. PubMed. 43(12). 792–4. 7 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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