Claudia Mischung

957 total citations
6 papers, 565 citations indexed

About

Claudia Mischung is a scholar working on Molecular Biology, Neurology and Cell Biology. According to data from OpenAlex, Claudia Mischung has authored 6 papers receiving a total of 565 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Neurology and 2 papers in Cell Biology. Recurrent topics in Claudia Mischung's work include Neurofibromatosis and Schwannoma Cases (2 papers), Neuroblastoma Research and Treatments (1 paper) and Protein Kinase Regulation and GTPase Signaling (1 paper). Claudia Mischung is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (2 papers), Neuroblastoma Research and Treatments (1 paper) and Protein Kinase Regulation and GTPase Signaling (1 paper). Claudia Mischung collaborates with scholars based in Germany, Australia and United Kingdom. Claudia Mischung's co-authors include Stefan Mundlos, Sigrid Tinschert, Peter Nürnberg, Hartmut Peters, Raimund Fahsold, Annegret Buske, Christoph Gille, Andreas Gewies, Dieter Kaufmann and Sven Hoffmeyer and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Claudia Mischung

6 papers receiving 554 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Claudia Mischung Germany	6	234	205	133	119	82	6	565
Peter Jun United States	15	301 1.3×	207 1.0×	28 0.2×	81 0.7×	69 0.8×	20	741
Nobuo Ito Japan	11	229 1.0×	174 0.8×	103 0.8×	43 0.4×	97 1.2×	30	555
Allen M. Spiegel United States	12	314 1.3×	44 0.2×	184 1.4×	78 0.7×	114 1.4×	12	704
Emilia Ballarè Italy	13	347 1.5×	70 0.3×	61 0.5×	213 1.8×	29 0.4×	14	757
Chalurmpon Srichomthong Thailand	16	342 1.5×	49 0.2×	116 0.9×	356 3.0×	31 0.4×	49	676
Stephen G. Romansky United States	11	133 0.6×	73 0.4×	81 0.6×	44 0.4×	103 1.3×	23	420
Florian Wernig United Kingdom	11	226 1.0×	62 0.3×	50 0.4×	40 0.3×	39 0.5×	38	655
P Bouloux United Kingdom	6	159 0.7×	87 0.4×	20 0.2×	146 1.2×	27 0.3×	7	466
J Asai Japan	10	189 0.8×	101 0.5×	21 0.2×	42 0.4×	63 0.8×	16	456
Elizabeth Salisbury United States	18	489 2.1×	26 0.1×	356 2.7×	193 1.6×	82 1.0×	24	951

Countries citing papers authored by Claudia Mischung

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Mischung

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Mischung

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

All Works

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6 of 6 papers shown

1.

Bertram, Lars, Johannes Helmuth, Claudia Mischung, et al.. (2020). Mutation spectrum and polygenic score in German patients with familial hypercholesterolemia. Clinical Genetics. 98(5). 457–467. 11 indexed citations

2.

Türkmen, Seval, Gao Guo, Masoud Garshasbi, et al.. (2009). CA8 Mutations Cause a Novel Syndrome Characterized by Ataxia and Mild Mental Retardation with Predisposition to Quadrupedal Gait. PLoS Genetics. 5(5). e1000487–e1000487. 109 indexed citations

3.

Mischung, Claudia, et al.. (2007). Detection of novel NF1 mutations and rapid mutation prescreening with Pyrosequencing. Electrophoresis. 28(23). 4295–4301. 12 indexed citations

4.

Thiele, Hölger, Wolfgang Höhne, Michael L. Cunningham, et al.. (2001). Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nature Genetics. 28(1). 37–41. 182 indexed citations

5.

Nürnberg, Peter, Hölger Thiele, David Chandler, et al.. (2001). Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia. Nature Genetics. 28(1). 37–41. 20 indexed citations

6.

Fahsold, Raimund, Sven Hoffmeyer, Claudia Mischung, et al.. (2000). Minor Lesion Mutational Spectrum of the Entire NF1 Gene Does Not Explain Its High Mutability but Points to a Functional Domain Upstream of the GAP-Related Domain. The American Journal of Human Genetics. 66(3). 790–818. 231 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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