Kathrin Müller

5.2k total citations
39 papers, 1.2k citations indexed

About

Kathrin Müller is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Kathrin Müller has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Neurology, 16 papers in Genetics and 15 papers in Molecular Biology. Recurrent topics in Kathrin Müller's work include Amyotrophic Lateral Sclerosis Research (17 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Kathrin Müller is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (17 papers), Neurogenetic and Muscular Disorders Research (15 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). Kathrin Müller collaborates with scholars based in Germany, Sweden and United States. Kathrin Müller's co-authors include Jochen H. Weishaupt, Albert C. Ludolph, Axel Freischmidt, Peter M. Andersen, Markus Otto, Patrick Weydt, Alexander E. Volk, Peter Wiegand, Karin M. Danzer and Michael N. Smolka and has published in prestigious journals such as PLoS ONE, Brain and Annals of Neurology.

In The Last Decade

Kathrin Müller

39 papers receiving 1.2k citations

Peers

Kathrin Müller

NEURO

GENET

PHYSI

NEURO

Ione Woollacott United Kingdom

Satoshi Kaneko Japan

Anne Sieben Belgium

Wouter van Rheenen Netherlands

Marsel Mesulam United States

B. Ford United States

M. Muglia Italy

Anne Noreau Canada

Sampath Arepalli United States

Lis Hasholt Denmark

Ione Woollacott United Kingdom

Kathrin Müller

816 ×1.4

NEURO

462 ×1.0

314 ×0.9

GENET

465 ×2.8

PHYSI

278 ×1.7

NEURO

Citations per year, relative to Kathrin Müller Kathrin Müller (= 1×) peers Ione Woollacott

Countries citing papers authored by Kathrin Müller

Since Specialization

Citations

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

Fields of papers citing papers by Kathrin Müller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathrin Müller

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

All Works

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20 of 20 papers shown

Müller, Kathrin, Peter M. Andersen, Stefan L. Marklund, et al.. (2022). A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity. Journal of Neurology. 270(3). 1770–1773. 7 indexed citations

Osmanovic, Alma, Helge Martens, Kathrin Müller, et al.. (2021). Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients. Genes. 13(1). 84–84. 7 indexed citations

Müller, Kathrin, Ki‐Wook Oh, Angelica Nordin, et al.. (2021). De novo mutations in SOD1 are a cause of ALS. Journal of Neurology Neurosurgery & Psychiatry. 93(2). 201–206. 31 indexed citations

Brenner, Dávid, Kathrin Müller, Serena Lattante, et al.. (2021). FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees. Neurogenetics. 23(1). 59–65. 3 indexed citations

Bauer, Margit, D.J. Reinert, Sylwia Huber, et al.. (2020). Biophysical and structural investigation of the regulation of human GTP cyclohydrolase I by its regulatory protein GFRP. Journal of Structural Biology. 213(1). 107691–107691. 3 indexed citations

Brenner, Dávid, Kathrin Müller, Regina Gastl, et al.. (2018). Analysis of CACNA1A CAG repeat lengths in patients with familial ALS. Neurobiology of Aging. 74. 235.e5–235.e8. 4 indexed citations

Türk, Matthias, Rolf Schröder, Andreas Hofmann, et al.. (2017). Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients. Neurobiology of Aging. 56. 213.e1–213.e5. 5 indexed citations

Müller, Kathrin, Philipp Soergel, Peter Hillemanns, & Matthias Jentschke. (2016). Accuracy of Colposcopically Guided Diagnostic Methods for the Detection of Cervical Intraepithelial Neoplasia. Geburtshilfe und Frauenheilkunde. 76(2). 182–187. 15 indexed citations

Endo, Satoshi, Ryo Honda, Kathrin Müller, et al.. (2016). Instability of C154Y variant of aldo-keto reductase 1C3. Chemico-Biological Interactions. 276. 194–202. 9 indexed citations

10.

Maier, André, Nikolaus Deigendesch, Kathrin Müller, et al.. (2015). Interleukin-1 Antagonist Anakinra in Amyotrophic Lateral Sclerosis—A Pilot Study. PLoS ONE. 10(10). e0139684–e0139684. 53 indexed citations

11.

Mennigen, Eva, Sarah Rodehacke, Kathrin Müller, et al.. (2014). Exploring adolescent cognitive control in a combined interference switching task. Neuropsychologia. 61. 175–189. 7 indexed citations

12.

Ripke, Stephan, Thomas Hübner, Eva Mennigen, et al.. (2014). Common Neural Correlates of Intertemporal Choices and Intelligence in Adolescents. Journal of Cognitive Neuroscience. 27(2). 387–399. 15 indexed citations

13.

Haß, Johanna, Esther Walton, Holger Kirsten, et al.. (2013). A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. PLoS ONE. 8(6). e64872–e64872. 20 indexed citations

14.

Müller, Kathrin. (2013). Altered Reward Processing in Adolescents With Prenatal Exposure to Maternal Cigarette Smoking. JAMA Psychiatry. 70(8). 847–847. 42 indexed citations

15.

Ripke, Stephan, Thomas Hübner, Eva Mennigen, et al.. (2012). Reward processing and intertemporal decision making in adults and adolescents: The role of impulsivity and decision consistency. Brain Research. 1478. 36–47. 50 indexed citations

16.

Prehn‐Kristensen, Alexander, Ina Molzow, Manuel Munz, et al.. (2011). Sleep restores daytime deficits in procedural memory in children with attention-deficit/hyperactivity disorder. Research in Developmental Disabilities. 32(6). 2480–2488. 48 indexed citations

17.

Zeckey, Christian, Frank Hildebrand, Kathrin Müller, et al.. (2010). Activity of Lymphocyte Subpopulations in Polymicrobial Sepsis and DHEA Treatment in IL-6 Knockout Mice. Journal of Innate Immunity. 2(5). 469–477. 10 indexed citations

18.

Müller, Kathrin, Rachel Herndon Klein, E. Miltner, & Peter Wiegand. (2007). Improved STR typing of telogen hair root and hair shaft DNA. Electrophoresis. 28(16). 2835–2842. 27 indexed citations

19.

Müller, Kathrin, Rachel Herndon Klein, E. Miltner, & Peter Wiegand. (2007). Q8—A short amplicon multiplex including the German DNA database systems. Forensic Science International Genetics. 1(2). 205–207. 9 indexed citations

20.

Schreiner, Dietmar, Kathrin Müller, & H.W. Hofer. (2006). The intracellular domain of the human protocadherin hFat1 interacts with Homer signalling scaffolding proteins. FEBS Letters. 580(22). 5295–5300. 24 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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