J. M. Schröder

6.2k total citations
118 papers, 2.7k citations indexed

About

J. M. Schröder is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, J. M. Schröder has authored 118 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Cellular and Molecular Neuroscience, 35 papers in Molecular Biology and 31 papers in Neurology. Recurrent topics in J. M. Schröder's work include Hereditary Neurological Disorders (33 papers), Genetic Neurodegenerative Diseases (18 papers) and Inflammatory Myopathies and Dermatomyositis (11 papers). J. M. Schröder is often cited by papers focused on Hereditary Neurological Disorders (33 papers), Genetic Neurodegenerative Diseases (18 papers) and Inflammatory Myopathies and Dermatomyositis (11 papers). J. M. Schröder collaborates with scholars based in Germany, Belgium and United States. J. M. Schröder's co-authors include Joachim Weis, Jan De Bleecker, Boél De Paepe, Mária Judit Molnár, Stefan Quasthoff, Jan Senderek, Jean‐Jacques Martin, Matthias Vorgerd, Gábor Rácz and Stephan Züchner and has published in prestigious journals such as Journal of Clinical Investigation, Nature Neuroscience and Brain.

In The Last Decade

J. M. Schröder

113 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. M. Schröder Germany 32 1.0k 1.0k 815 411 366 118 2.7k
Saeed Bohlega Saudi Arabia 34 1.3k 1.2× 876 0.9× 1.2k 1.4× 322 0.8× 192 0.5× 130 3.8k
Minoru Tomita Japan 32 1.1k 1.0× 448 0.4× 636 0.8× 819 2.0× 151 0.4× 188 4.2k
Juan J. Vílchez Spain 32 1.5k 1.4× 1.5k 1.5× 894 1.1× 209 0.5× 351 1.0× 130 3.0k
G. Saïd France 26 587 0.6× 620 0.6× 984 1.2× 281 0.7× 260 0.7× 77 2.2k
Gérard Saïd France 31 1.5k 1.4× 812 0.8× 1.5k 1.8× 414 1.0× 517 1.4× 84 4.2k
Naoki Hattori Japan 30 596 0.6× 616 0.6× 767 0.9× 262 0.6× 189 0.5× 115 3.3k
Hannu Somer Finland 37 3.2k 3.1× 917 0.9× 448 0.5× 379 0.9× 619 1.7× 108 4.7k
K Tashiro Japan 30 705 0.7× 605 0.6× 740 0.9× 182 0.4× 113 0.3× 143 2.4k
Satoshi Ueno Japan 29 896 0.9× 506 0.5× 526 0.6× 226 0.5× 124 0.3× 143 2.4k
John T. Sladky United States 31 1.5k 1.4× 856 0.8× 908 1.1× 159 0.4× 192 0.5× 59 3.0k

Countries citing papers authored by J. M. Schröder

Since Specialization
Citations

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

Fields of papers citing papers by J. M. Schröder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. M. Schröder. 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 J. M. Schröder. The network helps show where J. M. Schröder may publish in the future.

Co-authorship network of co-authors of J. M. Schröder

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

All Works

20 of 20 papers shown
1.
Karsai, Gergely, Florian Kraft, Natja Haag, et al.. (2019). DEGS1-associated aberrant sphingolipid metabolism impairs nervous system function in humans. Journal of Clinical Investigation. 129(3). 1229–1239. 71 indexed citations
2.
Laššuthová, Petra, Katharina Vill, Sevim Erdem‐Özdamar, et al.. (2018). Novel SBF2 mutations and clinical spectrum of Charcot‐Marie‐Tooth neuropathy type 4B2. Clinical Genetics. 94(5). 467–472. 7 indexed citations
3.
Nolte, Kay, Andreas Janecke, Matthias Vorgerd, Joachim Weis, & J. M. Schröder. (2008). Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene. Acta Neuropathologica. 116(5). 491–506. 28 indexed citations
4.
Schoser, Benedikt, J. M. Schröder, T. Grimm, Damien Sternberg, & Wolfram Kreß. (2007). A large german kindred with cold‐aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene. Muscle & Nerve. 35(5). 599–606. 15 indexed citations
5.
Haubrich, C., Timo Krings, Jan Senderek, et al.. (2002). Hypertrophic nerve roots in a case of Roussy-Lévy syndrome. Neuroradiology. 44(11). 933–937. 5 indexed citations
6.
Senderek, Jan, et al.. (2001). Phenotypic variation of a novel nonsense mutation in the P0 intracellular domain. Journal of the Neurological Sciences. 192(1-2). 49–51. 12 indexed citations
7.
Soulimane, Tewfik, et al.. (2000). Multiple Deletions of mtDNA Remove the Light Strand Origin of Replication. Biochemical and Biophysical Research Communications. 279(2). 595–601. 11 indexed citations
8.
Senderek, Jan, Benita Hermanns, Ute Lehmann, et al.. (2000). Charcot‐Marie‐Tooth Neuropathy Type 2 and P0 Point Mutations: Two Novel Amino Acid Substitutions (Asp61Gly; Tyr119Cys) and a Possible “Hotspot” on Thr124Met. Brain Pathology. 10(2). 235–248. 55 indexed citations
9.
Schröder, J. M.. (1999). Pathologie peripherer Nerven. RWTH Publications (RWTH Aachen). 10 indexed citations
10.
Stögbauer, Florian, Peter R. Young, Gregor Kuhlenbäumer, et al.. (1999). Autosomal dominant burning feet syndrome. Journal of Neurology Neurosurgery & Psychiatry. 67(1). 78–81. 17 indexed citations
11.
Schröder, J. M.. (1998). On sub-, pseudo- and quasimaximal spaces. Commentationes Mathematicae Universitatis Carolinae. 39(1). 197–206. 3 indexed citations
12.
Schröder, J. M., Martina Dören, Birgitt Schneider, & M. Öettel. (1996). Are the antioxidative effects of 17β-estradiol modified by concomitant administration of a progestin?. Maturitas. 25(2). 133–139. 18 indexed citations
13.
Molnár, Mária Judit, et al.. (1996). A large-scale deletion of mitochondrial DNA in a case with pure mitochondrial myopathy and neuropathy. Acta Neuropathologica. 91(6). 654–658. 12 indexed citations
14.
Schröder, J. M.. (1996). Developmental and pathological changes at the node and paranode in human sural nerves. Microscopy Research and Technique. 34(5). 422–435. 15 indexed citations
15.
Quasthoff, Stefan, et al.. (1995). Calcium potentials and tetrodotoxin-resistant sodium potentials in unmyelinated C fibres of biopsied human sural nerve. Neuroscience. 69(3). 955–965. 104 indexed citations
16.
Weis, Joachim, et al.. (1993). Renaut Bodies Contain Elastic Fiber Components. Journal of Neuropathology & Experimental Neurology. 52(5). 444–451. 24 indexed citations
17.
18.
Dieler, R. & J. M. Schröder. (1990). Increase of elastic fibres in muscle spindles of rats following single or repeated denervation with or without reinnervation. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 417(3). 213–221. 4 indexed citations
19.
Schröder, J. M. & W. Wechsler. (1965). Ödem und Nekrose in der grauen und weißen Substanz beim experimentellen Hirntrauma: Licht- und elektronenmikroskopische Untersuchungen. Acta Neuropathologica. 5(1). 82–111. 8 indexed citations
20.
Schröder, J. M., et al.. (1956). [Blood supply of the cheek after food intake].. PubMed. 45(23-24). 943–7.

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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