Birgit Uhlenberg

1.3k total citations
16 papers, 981 citations indexed

About

Birgit Uhlenberg is a scholar working on Molecular Biology, Cancer Research and Genetics. According to data from OpenAlex, Birgit Uhlenberg has authored 16 papers receiving a total of 981 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cancer Research and 2 papers in Genetics. Recurrent topics in Birgit Uhlenberg's work include RNA modifications and cancer (3 papers), Cancer-related molecular mechanisms research (3 papers) and RNA Research and Splicing (3 papers). Birgit Uhlenberg is often cited by papers focused on RNA modifications and cancer (3 papers), Cancer-related molecular mechanisms research (3 papers) and RNA Research and Splicing (3 papers). Birgit Uhlenberg collaborates with scholars based in Germany, United States and United Kingdom. Birgit Uhlenberg's co-authors include Bernhard Weschke, Nico Ruf, Peter Nürnberg, Heymut Omran, Michèl A.A.P. Willemsen, Uta Tacke, Philippa B. Mills, Cornelis Jakobs, Barbara Plecko and Matthias R. Baumgartner and has published in prestigious journals such as Nature Medicine, Neurology and PEDIATRICS.

In The Last Decade

Birgit Uhlenberg

16 papers receiving 971 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Birgit Uhlenberg Germany 10 529 273 175 160 114 16 981
Bernhard Weschke Germany 13 547 1.0× 298 1.1× 152 0.9× 133 0.8× 114 1.0× 23 985
Christine Barnérias France 20 704 1.3× 236 0.9× 283 1.6× 140 0.9× 104 0.9× 73 1.4k
Ángeles García‐Cazorla Spain 16 550 1.0× 616 2.3× 204 1.2× 132 0.8× 153 1.3× 37 1.1k
Caterina Garone Italy 21 1.3k 2.5× 641 2.3× 182 1.0× 138 0.9× 67 0.6× 45 1.7k
Mizue Iai Japan 17 431 0.8× 117 0.4× 191 1.1× 174 1.1× 32 0.3× 48 856
Valentina Emmanuele United States 16 895 1.7× 361 1.3× 99 0.6× 104 0.7× 105 0.9× 39 1.1k
Karine Lascelles United Kingdom 16 295 0.6× 102 0.4× 183 1.0× 137 0.9× 27 0.2× 25 858
Denise Cassandrini Italy 23 735 1.4× 228 0.8× 176 1.0× 57 0.4× 134 1.2× 62 1.3k
Anne-Sophie Lèbre France 18 769 1.5× 316 1.2× 218 1.2× 81 0.5× 27 0.2× 38 1.1k
Mercédes Pineda Spain 18 499 0.9× 161 0.6× 278 1.6× 41 0.3× 39 0.3× 29 1.0k

Countries citing papers authored by Birgit Uhlenberg

Since Specialization
Citations

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

Fields of papers citing papers by Birgit Uhlenberg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Birgit Uhlenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Birgit Uhlenberg. A scholar is included among the top collaborators of Birgit Uhlenberg 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 Birgit Uhlenberg. Birgit Uhlenberg 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.
Sobreira, Nara, Lisa G. Riley, Wendy Gold, et al.. (2017). Mutations in RARS cause a hypomyelination disorder akin to Pelizaeus–Merzbacher disease. European Journal of Human Genetics. 25(10). 1134–1141. 33 indexed citations
2.
Müller‐Myhsok, Bertram, Denise Horn, Alexander Diers, et al.. (2012). Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects. European Journal of Human Genetics. 21(4). 367–372. 3 indexed citations
3.
Uhlenberg, Birgit, et al.. (2010). Epithelioid Hemangioendothelioma of the Lung Presenting With Pneumonia and Heart Rhythm Disturbances in a Teenage Girl. Journal of Pediatric Hematology/Oncology. 32(4). 274–276. 6 indexed citations
4.
Weber, Sven C., Birgit Uhlenberg, Klemens Raile, Uwe Querfeld, & Dominik N. Müller. (2010). Polyoma virus‐associated progressive multifocal leukoencephalopathy after renal transplantation: Regression following withdrawal of mycophenolate mofetil. Pediatric Transplantation. 15(2). E19–24. 18 indexed citations
5.
Ruf, Nico & Birgit Uhlenberg. (2008). Analysis of human alternative first exons and copy number variation of the GJA12 gene in patients with Pelizaeus–Merzbacher‐like disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(2). 226–232. 10 indexed citations
6.
Everts, Regula, Franz Kaufmann, Birgit Uhlenberg, et al.. (2008). Cognitive Functioning, Behavior, and Quality of Life After Stroke in Childhood. Child Neuropsychology. 14(4). 323–338. 117 indexed citations
7.
König, Kai, Brigitte G. Dorner, Alexander Diers, et al.. (2007). Atypical Tetanus in a Completely Immunized 14-Year-Old Boy. PEDIATRICS. 120(5). e1355–e1358. 11 indexed citations
8.
Mills, Philippa B., Eduard A. Struys, Cornelis Jakobs, et al.. (2006). Mutations in antiquitin in individuals with pyridoxine-dependent seizures. Nature Medicine. 12(3). 307–309. 392 indexed citations
9.
Ruf, Nico, et al.. (2006). Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus–Merzbacher‐like leukodystrophy. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(3). 365–366. 1 indexed citations
10.
Uhlenberg, Birgit, Verena Varnholt, Frank K.H. van Landeghem, et al.. (2005). Atypical manifestation of childhood primary cerebral lymphoma restricted to the leptomeninges. European Journal of Pediatrics. 164(10). 653–654. 3 indexed citations
11.
Ketelsen, U.‐P., et al.. (2005). Congenital Myopathy with Arrest of Myogenesis Prior to Formation of Myotubes. Neuropediatrics. 36(4). 246–251. 4 indexed citations
12.
Everts, Regula, Jelena Pavlović, Birgit Uhlenberg, et al.. (2005). Cognitive functioning after stroke in childhood – a clinical study. Neuropediatrics. 36(2). 1 indexed citations
13.
Wolf, Nicole I., Inga Harting, Eugen Boltshauser, et al.. (2005). Leukoencephalopathy with ataxia, hypodontia, and hypomyelination. Neurology. 64(8). 1461–1464. 53 indexed citations
14.
Ruf, Nico, Birgit Uhlenberg, Robert Terkeltaub, Peter Nürnberg, & Frank Rutsch. (2004). The mutational spectrum ofENPP1as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI). Human Mutation. 25(1). 98–98. 95 indexed citations
15.
Uhlenberg, Birgit, Markus Schuelke, Franz Rüschendorf, et al.. (2004). Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease. The American Journal of Human Genetics. 75(2). 251–260. 217 indexed citations
16.
Sifringer, Marco, Birgit Uhlenberg, R. Hanke, et al.. (2003). Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy. Human Genetics. 114(2). 149–156. 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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