Stephan Neudecker

479 total citations
14 papers, 333 citations indexed

About

Stephan Neudecker is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Stephan Neudecker has authored 14 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Cardiology and Cardiovascular Medicine and 3 papers in Genetics. Recurrent topics in Stephan Neudecker's work include Mitochondrial Function and Pathology (5 papers), Muscle Physiology and Disorders (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Stephan Neudecker is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Muscle Physiology and Disorders (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Stephan Neudecker collaborates with scholars based in Germany, Italy and Hungary. Stephan Neudecker's co-authors include Michael Krasnianski, Stephan Zierz, Marcus Deschauer, Tobias Müller, Frank N. Gellerich, Ying Chen, Sibylle Jakubiczka, Karsten Stock, Anna Krasnianski and Benedikt Schoser and has published in prestigious journals such as Brain, Obstetrics and Gynecology and Acta Neuropathologica.

In The Last Decade

Stephan Neudecker

14 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephan Neudecker Germany	10	170	106	59	43	38	14	333
Koji Abe Japan	10	121 0.7×	114 1.1×	54 0.9×	28 0.7×	27 0.7×	24	321
Osamu Yahara Japan	10	160 0.9×	132 1.2×	70 1.2×	81 1.9×	22 0.6×	24	354
Ziad Rifai United States	8	232 1.4×	55 0.5×	62 1.1×	66 1.5×	48 1.3×	9	361
K. Eger Germany	9	156 0.9×	127 1.2×	69 1.2×	84 2.0×	61 1.6×	19	464
Gong‐Lu Liu China	11	111 0.7×	70 0.7×	36 0.6×	95 2.2×	17 0.4×	20	309
Jordan T. Gladman United States	10	210 1.2×	51 0.5×	48 0.8×	76 1.8×	24 0.6×	13	406
Laura Adobbati Italy	9	140 0.8×	70 0.7×	20 0.3×	39 0.9×	39 1.0×	13	253
M A McShane United Kingdom	7	78 0.5×	106 1.0×	16 0.3×	79 1.8×	31 0.8×	12	347
Meghan C. Towne United States	15	234 1.4×	34 0.3×	22 0.4×	65 1.5×	24 0.6×	34	553
Louise Bier United States	9	90 0.5×	161 1.5×	21 0.4×	44 1.0×	27 0.7×	16	485

Countries citing papers authored by Stephan Neudecker

Since Specialization

Citations

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

Fields of papers citing papers by Stephan Neudecker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephan Neudecker

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

All Works

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14 of 14 papers shown

Kappes‐Horn, Karin, et al.. (2021). Diagnosis and Clinical Development of Sporadic Inclusion Body Myositis and Polymyositis With Mitochondrial Pathology: A Single-Center Retrospective Analysis. Journal of Neuropathology & Experimental Neurology. 80(11). 1060–1067. 9 indexed citations

Neudecker, Stephan, Karsten Stock, & Michael Krasnianski. (2006). Call-Fleming Postpartum Angiopathy in the Puerperium. Obstetrics and Gynecology. 107(Supplement). 446–449. 26 indexed citations

Krasnianski, Michael, et al.. (2006). Isolated bilateral blindness as the sole manifestation of transient ischaemic attacks. Acta Ophthalmologica Scandinavica. 84(3). 415–418. 8 indexed citations

Krasnianski, Anna, Marcus Deschauer, Stephan Neudecker, et al.. (2005). Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies. Brain. 128(8). 1870–1876. 68 indexed citations

Müller, Tobias, Marcus Deschauer, Stephan Neudecker, & Stephan Zierz. (2005). Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNASer (UCN) gene. Acta Neuropathologica. 110(4). 426–430. 5 indexed citations

Neudecker, Stephan, Michael Krasnianski, Erik Bahn, & Stephan Zierz. (2004). Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature. Acta Neuropathologica. 108(3). 257–9. 10 indexed citations

Krasnianski, Michael, Uwe Ehrt, Stephan Neudecker, & Stephan Zierz. (2004). Alfred Hauptmann, Siegfried Thannhauser, and an Endangered Muscular Disorder. Archives of Neurology. 61(7). 1139–41. 3 indexed citations

Krasnianski, Michael, et al.. (2004). Magnetic resonance angiography in a patient with Crohn’s disease associated cerebral vasculitis. Clinical Neurology and Neurosurgery. 106(2). 110–113. 16 indexed citations

Krasnianski, Michael, et al.. (2003). Yawning despite trismus in a patient with locked-in syndrome caused by a thrombosed megadolichobasilar artery. Clinical Neurology and Neurosurgery. 106(1). 44–46. 18 indexed citations

10.

Krasnianski, Michael, K. Eger, Stephan Neudecker, Sibylle Jakubiczka, & Stephan Zierz. (2003). Atypical Phenotypes in Patients With Facioscapulohumeral Muscular Dystrophy 4q35 Deletion. Archives of Neurology. 60(10). 1421–1421. 40 indexed citations

11.

Krasnianski, Michael, Stephan Neudecker, A Schlüter, & S. Zierz. (2003). Babinski-Nageotte’s syndrome andHemimedullary (Reinhold’s) syndromeare clinically and morphologicallydistinct conditions. Journal of Neurology. 250(8). 938–942. 13 indexed citations

12.

Krasnianski, Michael, Stephan Neudecker, K. Eger, Sibylle Jakubiczka, & Stephan Zierz. (2003). Typical facioscapulohumeraldystrophy phenotype in patients without FSHD 4q35deletion. Journal of Neurology. 250(9). 1084–1087. 4 indexed citations

13.

Vytopil, Michal, Enzo Ricci, Antonio Dello Russo, et al.. (2002). Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy. Neuromuscular Disorders. 12(10). 958–963. 42 indexed citations

14.

Gellerich, Frank N., Marcus Deschauer, Ying Chen, et al.. (2002). Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1556(1). 41–52. 71 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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