Katrin Adlkofer

1.2k total citations
9 papers, 967 citations indexed

About

Katrin Adlkofer is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Katrin Adlkofer has authored 9 papers receiving a total of 967 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Cellular and Molecular Neuroscience, 4 papers in Neurology and 3 papers in Molecular Biology. Recurrent topics in Katrin Adlkofer's work include Hereditary Neurological Disorders (5 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Katrin Adlkofer is often cited by papers focused on Hereditary Neurological Disorders (5 papers), Neurological diseases and metabolism (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Katrin Adlkofer collaborates with scholars based in Switzerland, Germany and United States. Katrin Adlkofer's co-authors include Ueli Suter, Jürgen Zielasek, Cary Lai, Rudolf Martini, Klaus V. Toyka, Adriano Aguzzi, Roland Naef, K. V. Toyka, Josef P. Magyar and Zlatko Dembić and has published in prestigious journals such as Nature Genetics, Journal of Neuroscience and Gene.

In The Last Decade

Katrin Adlkofer

9 papers receiving 942 citations

Peers

Katrin Adlkofer

CMN

MB

NEURO

CB

Laura E. Warner United States

C. Stewart Gillespie United Kingdom

Erich E. Sirkowski United States

Federica Taioli Italy

Irene Sargiannidou Cyprus

H. W. Müller Germany

James Powell United States

Daniel E. Syroid United States

Igor Kobsar Germany

Joanna M. Solowska United States

Laura E. Warner United States

Katrin Adlkofer

1.1k ×1.4

CMN

488 ×1.6

MB

364 ×1.3

NEURO

332 ×1.4

NEURO

243 ×1.2

CB

Citations per year, relative to Katrin Adlkofer Katrin Adlkofer (= 1×) peers Laura E. Warner

Countries citing papers authored by Katrin Adlkofer

Since Specialization

Citations

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

Fields of papers citing papers by Katrin Adlkofer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrin Adlkofer

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

All Works

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9 of 9 papers shown

1.

Trenkle, Thomas, Michael McClelland, Katrin Adlkofer, & John Welsh. (2000). Major transcript variants of VAV3, a new member of the VAV family of guanine nucleotide exchange factors. Gene. 245(1). 139–149. 35 indexed citations

2.

Adlkofer, Katrin & Cary Lai. (2000). Role of neuregulins in glial cell development. Glia. 29(2). 104–111. 141 indexed citations

3.

Naef, Roland, et al.. (1997). Aberrant Protein Trafficking inTremblerSuggests a Disease Mechanism for Hereditary Human Peripheral Neuropathies. Molecular and Cellular Neuroscience. 9(1). 13–25. 96 indexed citations

4.

Adlkofer, Katrin, Roland Naef, & Ulrich W. Suter. (1997). Analysis of compound heterozygous mice reveals that theTrembler mutation can behave as a gain-of-function allele. Journal of Neuroscience Research. 49(6). 671–680. 46 indexed citations

5.

Adlkofer, Katrin, et al.. (1997). Heterozygous Peripheral Myelin Protein 22-Deficient Mice Are Affected by a Progressive Demyelinating Tomaculous Neuropathy. Journal of Neuroscience. 17(12). 4662–4671. 127 indexed citations

6.

Adlkofer, Katrin, Roland Naef, & Ueli Suter. (1997). Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain‐of‐function allele. Journal of Neuroscience Research. 49(6). 671–680. 3 indexed citations

7.

Hagmann, Michael, Katrin Adlkofer, Petra Pfeiffer, et al.. (1996). Dramatic Changes in the Ratio of Homologous Recombination to Nonhomologous DNA-End Joining in Oocytes and Early Embryos ofXenopus laevis. Biological Chemistry Hoppe-Seyler. 377(4). 239–250. 33 indexed citations

8.

Magyar, Josef P., Rudolf Martini, Adriano Aguzzi, et al.. (1996). Impaired Differentiation of Schwann Cells in Transgenic Mice with IncreasedPMP22Gene Dosage. Journal of Neuroscience. 16(17). 5351–5360. 188 indexed citations

9.

Adlkofer, Katrin, Rudolf Martini, Adriano Aguzzi, et al.. (1995). Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nature Genetics. 11(3). 274–280. 298 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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