Bernd Ringelstein

1.1k total citations
20 papers, 586 citations indexed

About

Bernd Ringelstein is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Epidemiology. According to data from OpenAlex, Bernd Ringelstein has authored 20 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Epidemiology. Recurrent topics in Bernd Ringelstein's work include Hereditary Neurological Disorders (7 papers), Acute Ischemic Stroke Management (6 papers) and Neurological diseases and metabolism (3 papers). Bernd Ringelstein is often cited by papers focused on Hereditary Neurological Disorders (7 papers), Acute Ischemic Stroke Management (6 papers) and Neurological diseases and metabolism (3 papers). Bernd Ringelstein collaborates with scholars based in Germany, Belgium and United States. Bernd Ringelstein's co-authors include Peter Young, Didier Leys, Gudrun Boysen, Philip M. Bath, Ewa Lindenstrøm, Desmond O’Neill, Peter Paul De Deyn, Reijo J. Marttila, Pål Friis and Alexander GG Turpie and has published in prestigious journals such as The Lancet, Neurology and Pain.

In The Last Decade

Bernd Ringelstein

20 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernd Ringelstein Germany 11 244 163 151 129 111 20 586
Philipp Bücke Switzerland 11 210 0.9× 285 1.7× 24 0.2× 116 0.9× 89 0.8× 21 502
Bernard Infeld Australia 13 232 1.0× 184 1.1× 47 0.3× 45 0.3× 26 0.2× 18 469
Oliver Maier Germany 13 262 1.1× 110 0.7× 181 1.2× 51 0.4× 25 0.2× 61 862
A. Staal Netherlands 12 185 0.8× 235 1.4× 81 0.5× 205 1.6× 22 0.2× 27 705
John E. Brooks Canada 10 230 0.9× 135 0.8× 39 0.3× 36 0.3× 63 0.6× 11 455
T P Enevoldson United Kingdom 15 105 0.4× 349 2.1× 23 0.2× 171 1.3× 56 0.5× 27 673
N. Tanahashi Japan 14 129 0.5× 177 1.1× 67 0.4× 66 0.5× 15 0.1× 36 517
Rosaria Renna Italy 13 87 0.4× 116 0.7× 72 0.5× 101 0.8× 15 0.1× 38 539
Shingo Mitaki Japan 13 80 0.3× 91 0.6× 56 0.4× 48 0.4× 15 0.1× 45 461
N. Heye Germany 14 114 0.5× 305 1.9× 27 0.2× 90 0.7× 13 0.1× 33 619

Countries citing papers authored by Bernd Ringelstein

Since Specialization
Citations

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

Fields of papers citing papers by Bernd Ringelstein

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Ringelstein

This figure shows the co-authorship network connecting the top 25 collaborators of Bernd Ringelstein. A scholar is included among the top collaborators of Bernd Ringelstein 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 Bernd Ringelstein. Bernd Ringelstein 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.
Baracchini, Claudio, José M. Valdueza, Massimo Del Sette, et al.. (2012). CCSVI and MS: a statement from the European Society of neurosonology and cerebral hemodynamics. Journal of Neurology. 259(12). 2585–2589. 29 indexed citations
2.
Ritter, Martin, Peter U. Heuschmann, Rainer Dziewas, et al.. (2011). Heart rate monitoring on the stroke unit. What does heart beat tell about prognosis? An observational study. BMC Neurology. 11(1). 47–47. 26 indexed citations
3.
Ruscheweyh, Ruth, Michael Deppe, Hubertus Lohmann, et al.. (2011). Pain is associated with regional grey matter reduction in the general population. Pain. 152(4). 904–911. 64 indexed citations
4.
Diener, Hans‐Christoph, F. Aichner, Christoph Bode, et al.. (2010). Primary and secondary prevention of cerebral ischemia. Aktuelle Neurologie. 37(4). e2–e22. 1 indexed citations
5.
Kuhlenbäumer, Gregor, Frauke Friedrichs, Bernhard Kis, et al.. (2007). Association between Single Nucleotide Polymorphisms in the Lysyl Oxidase-Like 1 Gene and Spontaneous Cervical Artery Dissection. Cerebrovascular Diseases. 24(4). 343–348. 21 indexed citations
6.
Sprigg, Nikola, Laura J. Gray, Philip M. Bath, et al.. (2006). Relationship between outcome and baseline blood pressure and other haemodynamic measures in acute ischaemic stroke: data from the TAIST trial. Journal of Hypertension. 24(7). 1413–1417. 74 indexed citations
7.
Hacke, Werner, Walter Huber, Bernd Ringelstein, et al.. (2006). Obituary to Prof. Klaus Poeck, MD, FRSM, FRCP. Journal of Neurology. 253(10). 1379–1380. 1 indexed citations
8.
Timmerman, Vincent, et al.. (2005). Absence of mutations in the prion-protein gene in a large cohort of HMSN patients. Neuromuscular Disorders. 15(8). 549–551. 2 indexed citations
9.
Sprigg, Nikola, Laura J. Gray, Philip M. Bath, et al.. (2005). Compression Stockings and the Prevention of Symptomatic Venous Thromboembolism: Data From the Tinzaparin in Acute Ischemic Stroke Trial. Journal of Stroke and Cerebrovascular Diseases. 14(5). 203–209. 6 indexed citations
10.
Schirmacher, Anja, Bernd Ringelstein, Peter Young, et al.. (2004). Genomic organization and mutation analysis of three candidate genes for hereditary neuralgic amyotrophy. Muscle & Nerve. 29(4). 601–604. 1 indexed citations
11.
Kuhlenbäumer, Gregor, Peter Young, C. Oberwittler, et al.. (2002). Giant axonal neuropathy (GAN): Case report and two novel mutations in the gigaxonin gene. Neurology. 58(8). 1273–1276. 36 indexed citations
12.
Young, Peter, et al.. (2002). Clinical features and molecular genetics of hereditary peripheral neuropathies. Journal of Neurology. 249(12). 1629–1650. 42 indexed citations
13.
Bath, Philip M., Ewa Lindenstrøm, Gudrun Boysen, et al.. (2001). Tinzaparin in acute ischaemic stroke (TAIST): a randomised aspirin-controlled trial. The Lancet. 358(9283). 702–710. 177 indexed citations
14.
Kuhlenbäumer, Gregor, Anja Schirmacher, Jan Meuleman, et al.. (1999). A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes. Genomics. 62(2). 242–250. 14 indexed citations
15.
Nabavi, Darius G., Holger Reinecke, Gernot Schulte‐Altedorneburg, et al.. (1999). Absence of circulating microemboli in patients with lone atrial fibrillation. Neurological Research. 21(6). 566–568. 6 indexed citations
16.
Meuleman, Jan, Gregor Kuhlenbäumer, Anja Schirmacher, et al.. (1999). Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25. European Journal of Human Genetics. 7(8). 920–927. 23 indexed citations
17.
Young, Peter, Heiko Wiebusch, Florian Stögbauer, et al.. (1997). A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsies. Neurology. 48(2). 450–452. 52 indexed citations
18.
Young, Peter, Heiko Wiebusch, Florian Stögbauer, et al.. (1997). PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies. Neurology. 49(5). 1478–1479. 1 indexed citations
19.
Young, Peter, Heiko Wiebusch, Florian Stögbauer, et al.. (1996). Four frequently observed polymorphisms in the 3‘‐UTR of human peripheral myelin protein 22 (PMP22): identification of different haplotypes. Clinical Genetics. 49(6). 321–322. 1 indexed citations
20.
Weiller, Cornelius, et al.. (1991). Infarctions and non-invasive diagnosis in Moyamoya Disease: Two case report. Neurosurgical Review. 14(1). 75–77. 9 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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