Kathrin N. Karle

2.2k citations

24 papers · 1.4k indexed · 1 hit paper · h-index 18

Molecular Biology top 10%
Genetics top 1%
Cellular and Molecular Neuroscience top 5%
Neurology top 5%
Neurology top 5%

Co-authors: Catia Andreassi Sibylle Jablonka Michael Sendtner Wilfried Rossoll Umrao R. Monani Lüdger Schöls Rebecca Schüle Benjamin Bender
Topics: Hereditary Neurological Disorders (11 papers)Neurogenetic and Muscular Disorders Research (8 papers)Neurological diseases and metabolism (6 papers)
Cited by: Genetics Neurology Cellular and Molecular Neuroscience
Journals: Journal of Clinical Investigation The Journal of Cell Biology Brain
Partner nations: Germany United States United Kingdom

In The Last Decade

Kathrin N. Karle

24 papers receiving 1.4k citations

Hit Papers

align trajectories

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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	DNA methylation signatures of chronic alcohol dependence in purified CD3+ T-cells of patients undergoing alcohol treatment 2017 ·Scientific Reports ·(unknown),Sumaiya A. Islam,Julia L. MacIsaac,Alexander M. Morin,Kathrin N. Karle,Adriana Di Santo,(unknown),(unknown),Anil Batra,Michael S. Kobor,Vanessa Nieratschker	14
2	Expanded phenotypic spectrum of the m.8344A>G “MERRF” mutation: data from the German mitoNET registry 2016 ·Journal of Neurology ·(unknown),Boriana Büchner,Aleksandra Nadaj‐Pakleza,Jochen Schäfer,Sandra L. Jackson,Diana Lehmann,Marcus Deschauer,Robert Kopajtich,(unknown),Klaus A. Kuhn,Kathrin N. Karle,Lüdger Schöls,Jörg B. Schulz,Joachim Weis,Holger Prokisch,Cornelia Kornblum,Kristl G. Claeys,Thomas Klopstock	59
3	Validation of differential GDAP1 DNA methylation in alcohol dependence and its potential function as a biomarker for disease severity and therapy outcome 2016 ·Epigenetics ·(unknown),Adriana Di Santo,Kathrin N. Karle,Anil Batra,Vanessa Nieratschker	23
4	Gray and white matter alterations in hereditary spastic paraplegia type SPG4 and clinical correlations 2015 ·Journal of Neurology ·Tobias Lindig,Benjamin Bender,Till‐Karsten Hauser,(unknown),(unknown),Uwe Klose,Kathrin N. Karle,Rebecca Schüle,Lüdger Schöls,Tim W. Rattay	28
5	Imaging features in conventional MRI, spectroscopy and diffusion weighted images of hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) 2014 ·Journal of Neurology ·Benjamin Bender,Uwe Klose,Tobias Lindig,Saskia Biskup,Thomas Nägele,Lüdger Schöls,Kathrin N. Karle	30
6	Clozapine serum concentrations in dopamimetic psychosis in Parkinson’s disease and related disorders 2014 ·European Journal of Clinical Pharmacology ·Ulrich Lutz,(unknown),(unknown),(unknown),(unknown),Thomas Gasser,Kathrin N. Karle,Anil Batra	17
7	Pure and syndromic optic atrophy explained by deep intronic OPA1 mutations and an intralocus modifier 2014 ·Brain ·(unknown),Kathrin N. Karle,Felix Tonagel,(unknown),Christian Wilhelm,(unknown),(unknown),Torsten Kluba,York Kamenisch,Valério Carelli,Julia Wolf,(unknown),Fiorella Speziani,Rebecca Schüle,Stephan Züchner,Lüdger Schöls,Bernd Wissinger,Matthis Synofzik	54
8	A spastic paraplegia mouse model reveals REEP1-dependent ER shaping 2014 ·Journal of Clinical Investigation ·Christian Beetz,Nicole Koch,Mukhran Khundadze,Geraldine Zimmer‐Bensch,Sándor Nietzsche,Nicole Hertel,(unknown),(unknown),Michaela Schweizer,Elisabeth Dirren,Kathrin N. Karle,Andrey Irintchev,Victoria Álvarez,Christoph Redies,Martin Westermann,Ingo Kurth,Thomas Deufel,Michael M. Kessels,Britta Qualmann,Christian A. Hübner	2
9	Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum 2013 ·Orphanet Journal of Rare Diseases ·Matthis Synofzik,Anne S. Soehn,Janina Gburek‐Augustat,Julia Schicks,Kathrin N. Karle,Rebecca Schüle,Tobias B. Haack,M. Schöning,Saskia Biskup,Sabine Rudnik‐Schöneborn,Jan Senderek,Karl‐Titus Hoffmann,Patrick MacLeod,Johannes Schwarz,Benjamin Bender,Stefan Krüger,Friedmar R. Kreuz,Peter Bauer,Lüdger Schöls	125
10	Electrophysiological characterisation of motor and sensory tracts in patients with hereditary spastic paraplegia (HSP) 2013 ·Orphanet Journal of Rare Diseases ·Kathrin N. Karle,Rebecca Schüle,Stephan Klebe,Susanne Otto,(unknown),Inga Liepelt‐Scarfone,Lüdger Schöls	26
11	A Hereditary Spastic Paraplegia Mouse Model Supports a Role of ZFYVE26/SPASTIZIN for the Endolysosomal System 2013 ·PLoS Genetics ·Mukhran Khundadze,Katrin Kollmann,Nicole Koch,Christoph Biskup,Sándor Nietzsche,Geraldine Zimmer‐Bensch,J. Christopher Hennings,Antje K. Huebner,Judit Symmank,Amir Jahić,Elena I. Ilina,Kathrin N. Karle,Lüdger Schöls,Michael M. Kessels,Thomas Braulke,Britta Qualmann,Ingo Kurth,Christian Beetz,Christian A. Hübner	75
12	De novo mutations in hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS) 2013 ·Neurology ·Kathrin N. Karle,Saskia Biskup,Rebecca Schüle,Katherine J. Schweitzer,Rejko Krüger,Peter Bauer,Benjamin Bender,Thomas Nägele,Lüdger Schöls	57
13	Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model 2012 ·PLoS Genetics ·Petra Füger,Vrinda Sreekumar,Rebecca Schüle,Jeannine V. Kern,(unknown),(unknown),Kathrin N. Karle,(unknown),(unknown),Matthias Flötenmeyer,Heinz Schwarz,Lüdger Schöls,Tobias M. Rasse	44
14	Axonal transport deficit in a KIF5A –/– mouse model 2012 ·Neurogenetics ·Kathrin N. Karle,Diana Möckel,Evan Reid,Lüdger Schöls	61
15	Disease severity affects quality of life of hereditary spastic paraplegia patients 2011 ·European Journal of Neurology ·Sven Klimpe,Rebecca Schüle,Jan Kassubek,Otto W. Witte,Zacharias Kohl,Stephan Klebe,Thomas Klopstock,(unknown),Kathrin N. Karle,Lüdger Schöls	30
16	A total of 220 patients with autosomal dominant spastic paraplegia do not display mutations in the SLC33A1 gene (SPG42) 2010 ·European Journal of Human Genetics ·Nina Schlipf,Christian Beetz,Rebecca Schüle,Giovanni Stévanin,Anne Kjersti Erichsen,Sylvie Forlani,Cécile Zaros,Kathrin N. Karle,Stephan Klebe,Sven Klimpe,Alexandra Dürr,Susanne Otto,Chantal Tallaksen,Olaf Rieß,Alexis Brice,Peter Bauer,Lüdger Schöls	16
17	Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridization 2008 ·Neurogenetics ·Peter Bauer,Beate Winner,Rebecca Schüle,Claudia Bauer,(unknown),Ute Hehr,Michael Bonin,Michael Walter,Kathrin N. Karle,Thomas Ringer,Olaf Rieß,Jürgen Winkler,Lüdger Schöls	20
18	Analysis of CYP7B1 in non-consanguineous cases of hereditary spastic paraplegia 2008 ·Neurogenetics ·Rebecca Schüle,(unknown),Kathrin N. Karle,(unknown),Stephan Klebe,Sven Klimpe,Michaela Auer‐Grumbach,Andrew H. Crosby,Christian A. Hübner,Lüdger Schöls,Thomas Deufel,Christian Beetz	35
19	Distinct and overlapping alterations in motor and sensory neurons in a mouse model of spinal muscular atrophy 2006 ·Human Molecular Genetics ·Sibylle Jablonka,Kathrin N. Karle,Beatrice Sandner,Catia Andreassi,Katja von Au,Michael Sendtner	72
20	Smn, the spinal muscular atrophy–determining gene product, modulates axon growth and localization of β-actin mRNA in growth cones of motoneuronsbreakdown → 2003 ·The Journal of Cell Biology ·Wilfried Rossoll,Sibylle Jablonka,Catia Andreassi,(unknown),Kathrin N. Karle,Umrao R. Monani,Michael Sendtner	523

About Kathrin N. Karle

Kathrin N. Karle is a scholar working on Neurology, Genetics and Cellular and Molecular Neuroscience, having authored 24 papers that have together received 1.4k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Neurological diseases and metabolism (6 papers). The work is most often cited by research in Genetics (630 citations), Neurology (258 citations) and Cellular and Molecular Neuroscience (467 citations). Kathrin N. Karle has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Catia Andreassi, Sibylle Jablonka, Michael Sendtner, Wilfried Rossoll, Umrao R. Monani, Lüdger Schöls, Rebecca Schüle, Benjamin Bender, Saskia Biskup and Peter Bauer. Their work appears in journals such as Journal of Clinical Investigation, The Journal of Cell Biology and Brain.

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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