Stefan Waibel

1.7k total citations
13 papers, 677 citations indexed

About

Stefan Waibel is a scholar working on Neurology, Genetics and Neurology. According to data from OpenAlex, Stefan Waibel has authored 13 papers receiving a total of 677 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 8 papers in Genetics and 3 papers in Neurology. Recurrent topics in Stefan Waibel's work include Amyotrophic Lateral Sclerosis Research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Stefan Waibel is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (11 papers), Neurogenetic and Muscular Disorders Research (8 papers) and Parkinson's Disease Mechanisms and Treatments (3 papers). Stefan Waibel collaborates with scholars based in Germany, Sweden and Switzerland. Stefan Waibel's co-authors include Albert C. Ludolph, Alexander Reuter, Thomas Meyer, Peter M. Andersen, S. Malessa, Eran Blaugrund, Hadas Schori, Orlando Guntinas‐Lichius, D. N. Angelov and Michal Schwartz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Annals of the New York Academy of Sciences.

In The Last Decade

Stefan Waibel

13 papers receiving 666 citations

Peers

Countries citing papers authored by Stefan Waibel

Since Specialization

Citations

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

Fields of papers citing papers by Stefan Waibel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefan Waibel

This figure shows the co-authorship network connecting the top 25 collaborators of Stefan Waibel. A scholar is included among the top collaborators of Stefan Waibel 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 Stefan Waibel. Stefan Waibel 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:

13 of 13 papers shown

#	Work	Indexed citations
1	Seasonal patterns and associations in the incidence of acute ischemic stroke requiring mechanical thrombectomy 2021 ·European Journal of Neurology ·Philipp Bücke, Hans Henkes, G. Arnold, Birgit Herting, Eric Jüttler, Christof Klötzsch, A. Lindner, (unknown), L. Niehaus, Matthias Reinhard, Stefan Waibel, Thomas Horvath, Hansjörg Bäzner, Marta Aguilar Pérez	3
2	A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany 2012 ·Neurobiology of Aging ·Jochen H. Weishaupt, Stefan Waibel, Anna Birve, Alexander E. Volk, Benjamin Mayer, Thomas Meyer, Albert C. Ludolph, Peter M. Andersen	42
3	NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis 2012 ·Human Molecular Genetics ·Hylke M. Blauw, Wouter van Rheenen, Max Koppers, Philip Van Damme, Stefan Waibel, Robin Lemmens, Paul W.J. van Vught, Thomas Meyer, Claudia Schulte, Thomas Gasser, Edwin Cuppen, R. Jeroen Pasterkamp, Wim Robberecht, Albert C. Ludolph, Jan H. Veldink, Leonard H. van den Berg	35
4	Truncating mutations in FUS/TLS give rise to a more aggressive ALS‐phenotype than missense mutations: a clinico‐genetic study in Germany 2012 ·European Journal of Neurology ·Stefan Waibel, Manuela Neumann, Angela Rosenbohm, A. Birve, Alexander E. Volk, Jochen H. Weishaupt, Thomas Meyer, Ulrich Müller, Peter M. Andersen, Albert C. Ludolph	48
5	The modulation of Amyotrophic Lateral Sclerosis risk by Ataxin-2 intermediate polyglutamine expansions is a specific effect 2011 ·Neurobiology of Disease ·Suzana Gispert, Alexander Kurz, Stefan Waibel, Peter Bauer, Inga Liepelt, Christof Geisen, Aaron D. Gitler, Tim Becker, Markus Weber, Daniela Berg, Peter M. Andersen, Rejko Krüger, Olaf Rieß, Albert C. Ludolph, Georg Auburger	64
6	Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic? 2010 ·Journal of Neurology Neurosurgery & Psychiatry ·Ansgar Felbecker, (unknown), Paul N. Valdmanis, (unknown), Stefan Waibel, Peter Steinbach, Guy A. Rouleau, Albert C. Ludolph, Peter M. Andersen	50
7	The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families 2010 ·Journal of Neurology ·(unknown), Ansgar Felbecker, Stefan Waibel, Peter Steinbach, Pia Winter, Albert C. Ludolph	18
8	Novel missense and truncating mutations in FUS/TLS in familial ALS 2010 ·Neurology ·Stefan Waibel, (unknown), (unknown), Thomas Meyer, (unknown)	61
9	Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization 2008 ·Amyotrophic Lateral Sclerosis ·Sarah A. Shoichet, Stefan Waibel, (unknown), Anne D. Sperfeld, (unknown), Ines Müller, Fikret Erdogan, Albert C. Ludolph, Hans‐Hilger Ropers, Reinhard Ullmann	15
10	Late-onset motoneuron disease caused by a functionally modified AMPA receptor subunit 2005 ·Proceedings of the National Academy of Sciences ·Rohini Kuner, Anthony Groom, I. Bresink, Hans‐Christian Kornau, Vanya Stefovska, Gerald Müller, (unknown), (unknown), Stefan Waibel, Albert C. Ludolph, Chrysanthy Ikonomidou, Peter H. Seeburg, Lechosław Turski	73
11	Mechanisms of Disease: Motoneuron Disease Aggravated by Transgenic Expression of a Functionally Modified AMPA Receptor Subunit 2005 ·Annals of the New York Academy of Sciences ·Rohini Kuner, Anthony Groom, Gerald Müller, Hans‐Christian Kornau, Vanya Stefovska, I. Bresink, (unknown), (unknown), Stefan Waibel, Albert C. Ludolph, Chrysanthy Ikonomidou, Peter H. Seeburg, Lechosław Turski	13
12	Rasagiline alone and in combination with riluzole prolongs survival in an ALS mouse model 2004 ·Journal of Neurology ·Stefan Waibel, Alexander Reuter, S. Malessa, Eran Blaugrund, (unknown)	97
13	Therapeutic vaccine for acute and chronic motor neuron diseases: Implications for amyotrophic lateral sclerosis 2003 ·Proceedings of the National Academy of Sciences ·D. N. Angelov, Stefan Waibel, Orlando Guntinas‐Lichius, (unknown), Wolfram F. Neiss, (unknown), Eti Yoles, Jonathan Kipnis, Hadas Schori, Alexander Reuter, Albert C. Ludolph, Michal Schwartz	158

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