Kathrin N. Karle

2.2k total citations · 1 hit paper
24 papers, 1.4k citations indexed

About

Kathrin N. Karle is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Kathrin N. Karle has authored 24 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Kathrin N. Karle's work include Hereditary Neurological Disorders (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Neurological diseases and metabolism (6 papers). Kathrin N. Karle is often cited by papers focused on Hereditary Neurological Disorders (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Neurological diseases and metabolism (6 papers). Kathrin N. Karle collaborates with scholars based in Germany, United States and United Kingdom. Kathrin N. Karle's co-authors include Sibylle Jablonka, Michael Sendtner, Catia Andreassi, Wilfried Rossoll, Umrao R. Monani, Lüdger Schöls, Rebecca Schüle, Benjamin Bender, Peter Bauer and Saskia Biskup and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Cell Biology and Brain.

In The Last Decade

Kathrin N. Karle

24 papers receiving 1.4k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons

2003 523 citations Wilfried Rossoll, Sibylle Jablonka et al. The Journal of Cell Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kathrin N. Karle Germany	18	893	630	467	258	203	24	1.4k
Maria Luisa Mostacciuolo Italy	22	764 0.9×	184 0.3×	521 1.1×	140 0.5×	225 1.1×	48	1.2k
Chien‐Ping Ko United States	23	950 1.1×	598 0.9×	579 1.2×	96 0.4×	231 1.1×	38	1.4k
Angela Rosenbohm Germany	24	596 0.7×	621 1.0×	407 0.9×	227 0.9×	1.2k 5.9×	61	1.7k
P. F. Chance United States	21	373 0.4×	127 0.2×	608 1.3×	258 1.0×	315 1.6×	28	1.1k
Inge A. Meijer Canada	14	369 0.4×	119 0.2×	362 0.8×	169 0.7×	129 0.6×	22	811
Emilia Bellone Italy	24	681 0.8×	109 0.2×	1.0k 2.2×	405 1.6×	787 3.9×	100	1.8k
Kunihiko Ikeguchi Japan	18	816 0.9×	188 0.3×	794 1.7×	95 0.4×	502 2.5×	39	1.6k
Carly E. Siskind United States	17	396 0.4×	100 0.2×	953 2.0×	319 1.2×	473 2.3×	33	1.3k
Frank Zimmermann Germany	11	868 1.0×	77 0.1×	862 1.8×	342 1.3×	259 1.3×	18	1.7k
Chiara Pisciotta Italy	21	283 0.3×	83 0.1×	719 1.5×	259 1.0×	486 2.4×	51	1.1k

Countries citing papers authored by Kathrin N. Karle

Since Specialization

Citations

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

Fields of papers citing papers by Kathrin N. Karle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kathrin N. Karle

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Islam, Sumaiya A., Julia L. MacIsaac, Alexander M. Morin, et al.. (2017). DNA methylation signatures of chronic alcohol dependence in purified CD3+ T-cells of patients undergoing alcohol treatment. Scientific Reports. 7(1). 6605–6605. 14 indexed citations

Büchner, Boriana, Aleksandra Nadaj‐Pakleza, Jochen Schäfer, et al.. (2016). Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registry. Journal of Neurology. 263(5). 961–972. 59 indexed citations

Santo, Adriana Di, et al.. (2016). Validation of differential GDAP1 DNA methylation in alcohol dependence and its potential function as a biomarker for disease severity and therapy outcome. Epigenetics. 11(6). 456–463. 23 indexed citations

Lindig, Tobias, Benjamin Bender, Till‐Karsten Hauser, et al.. (2015). Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations. Journal of Neurology. 262(8). 1961–1971. 28 indexed citations

Bender, Benjamin, Uwe Klose, Tobias Lindig, et al.. (2014). Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS). Journal of Neurology. 261(12). 2351–2359. 30 indexed citations

Beetz, Christian, Nicole Koch, Mukhran Khundadze, et al.. (2014). A spastic paraplegia mouse model reveals REEP1-dependent ER shaping. Journal of Clinical Investigation. 124(6). 2809–2809. 2 indexed citations

Lutz, Ulrich, et al.. (2014). Clozapine serum concentrations in dopamimetic psychosis in Parkinson’s disease and related disorders. European Journal of Clinical Pharmacology. 70(12). 1471–1476. 17 indexed citations

Karle, Kathrin N., Felix Tonagel, Christian Wilhelm, et al.. (2014). Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier. Brain. 137(8). 2164–2177. 54 indexed citations

Karle, Kathrin N., Rebecca Schüle, Stephan Klebe, et al.. (2013). Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP). Orphanet Journal of Rare Diseases. 8(1). 158–158. 26 indexed citations

10.

Synofzik, Matthis, Anne S. Soehn, Janina Gburek‐Augustat, et al.. (2013). Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum. Orphanet Journal of Rare Diseases. 8(1). 41–41. 125 indexed citations

11.

Karle, Kathrin N., Saskia Biskup, Rebecca Schüle, et al.. (2013). De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS). Neurology. 81(23). 2039–2044. 57 indexed citations

12.

Khundadze, Mukhran, Katrin Kollmann, Nicole Koch, et al.. (2013). A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal System. PLoS Genetics. 9(12). e1003988–e1003988. 75 indexed citations

13.

Füger, Petra, Vrinda Sreekumar, Rebecca Schüle, et al.. (2012). Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model. PLoS Genetics. 8(11). e1003066–e1003066. 44 indexed citations

14.

Karle, Kathrin N., Diana Möckel, Evan Reid, & Lüdger Schöls. (2012). Axonal transport deficit in a KIF5A –/– mouse model. Neurogenetics. 13(2). 169–179. 61 indexed citations

15.

Klimpe, Sven, Rebecca Schüle, Jan Kassubek, et al.. (2011). Disease severity affects quality of life of hereditary spastic paraplegia patients. European Journal of Neurology. 19(1). 168–171. 30 indexed citations

16.

Schlipf, Nina, Christian Beetz, Rebecca Schüle, et al.. (2010). A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42). European Journal of Human Genetics. 18(9). 1065–1067. 16 indexed citations

17.

Bauer, Peter, Beate Winner, Rebecca Schüle, et al.. (2008). Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization. Neurogenetics. 10(1). 43–48. 20 indexed citations

18.

Schüle, Rebecca, Kathrin N. Karle, Stephan Klebe, et al.. (2008). Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia. Neurogenetics. 10(2). 97–104. 35 indexed citations

19.

Jablonka, Sibylle, Kathrin N. Karle, Beatrice Sandner, et al.. (2006). Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy. Human Molecular Genetics. 15(3). 511–518. 72 indexed citations

20.

Rossoll, Wilfried, Sibylle Jablonka, Catia Andreassi, et al.. (2003). Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneurons. The Journal of Cell Biology. 163(4). 801–812. 523 indexed citations breakdown →

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.

Explore authors with similar magnitude of impact