Wolfgang Nachbauer

3.4k total citations
45 papers, 1.1k citations indexed

About

Wolfgang Nachbauer is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Wolfgang Nachbauer has authored 45 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Cellular and Molecular Neuroscience, 26 papers in Neurology and 25 papers in Molecular Biology. Recurrent topics in Wolfgang Nachbauer's work include Genetic Neurodegenerative Diseases (39 papers), Mitochondrial Function and Pathology (23 papers) and Neurological disorders and treatments (14 papers). Wolfgang Nachbauer is often cited by papers focused on Genetic Neurodegenerative Diseases (39 papers), Mitochondrial Function and Pathology (23 papers) and Neurological disorders and treatments (14 papers). Wolfgang Nachbauer collaborates with scholars based in Austria, Germany and Italy. Wolfgang Nachbauer's co-authors include Sylvia Boesch, Caterina Mariotti, Paola Giunti, Andreas Eigentler, Michael Parkinson, Werner Poewe, Elisabetta Indelicato, Julia Wanschitz, Theresa A. Zesiewicz and David R. Lynch and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Wolfgang Nachbauer

44 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wolfgang Nachbauer Austria 18 813 784 396 120 89 45 1.1k
Giovanna De Michele Italy 22 897 1.1× 664 0.8× 593 1.5× 76 0.6× 174 2.0× 57 1.2k
Jonas Alex Morales Saute Brazil 24 832 1.0× 724 0.9× 498 1.3× 53 0.4× 187 2.1× 78 1.3k
Akito Kume Japan 12 733 0.9× 694 0.9× 350 0.9× 88 0.7× 63 0.7× 29 1.1k
George Wilmot United States 23 1.4k 1.7× 1.3k 1.7× 765 1.9× 173 1.4× 116 1.3× 49 1.8k
Antonio Petrucci Italy 20 537 0.7× 509 0.6× 492 1.2× 48 0.4× 91 1.0× 44 1.1k
Kimberly L. Ferrante United States 11 625 0.8× 754 1.0× 469 1.2× 83 0.7× 53 0.6× 24 1.2k
Myriam Rai Belgium 16 618 0.8× 788 1.0× 143 0.4× 125 1.0× 43 0.5× 32 1.1k
Katrin S. Lindenberg Germany 14 817 1.0× 942 1.2× 295 0.7× 107 0.9× 40 0.4× 32 1.2k
Hiroyuki Morino Japan 20 564 0.7× 685 0.9× 494 1.2× 72 0.6× 216 2.4× 78 1.2k
Claire‐Marie Dhaenens France 23 262 0.3× 792 1.0× 166 0.4× 102 0.8× 86 1.0× 64 1.1k

Countries citing papers authored by Wolfgang Nachbauer

Since Specialization
Citations

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

Fields of papers citing papers by Wolfgang Nachbauer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfgang Nachbauer

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfgang Nachbauer. A scholar is included among the top collaborators of Wolfgang Nachbauer 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 Wolfgang Nachbauer. Wolfgang Nachbauer 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.
Indelicato, Elisabetta, David Pellerin, Wolfgang Nachbauer, et al.. (2025). GAA ‐ FGF14 Expansions and CACNA1A Variants: Phenotypic Overlap and Diagnostic Implications. Movement Disorders. 40(10). 2262–2268.
2.
Haschka, David, Elisabetta Indelicato, Christian Kremser, et al.. (2024). Genetic Determined Iron Starvation Signature in Friedreich's Ataxia. Movement Disorders. 39(7). 1088–1098. 4 indexed citations
3.
Lynch, David R., Angie Goldsberry, Christian Rummey, et al.. (2023). Propensity matched comparison of omaveloxolone treatment to Friedreich ataxia natural history data. Annals of Clinical and Translational Neurology. 11(1). 4–16. 24 indexed citations
4.
Eschlboeck, Sabine, Hans H. Goebel, Alessandra Fanciulli, et al.. (2023). Development and Validation of a Prognostic Model to Predict Overall Survival in Multiple System Atrophy. Movement Disorders Clinical Practice. 10(9). 1368–1376. 4 indexed citations
5.
Indelicato, Elisabetta, Klaus Faserl, Matthias Amprosi, et al.. (2023). Skeletal muscle proteome analysis underpins multifaceted mitochondrial dysfunction in Friedreich’s ataxia. Frontiers in Neuroscience. 17. 1289027–1289027. 13 indexed citations
6.
Indelicato, Elisabetta, Alexander Kirchmair, Matthias Amprosi, et al.. (2023). Skeletal muscle transcriptomics dissects the pathogenesis of Friedreich’s ataxia. Human Molecular Genetics. 32(13). 2241–2250. 5 indexed citations
7.
Amprosi, Matthias, Elisabetta Indelicato, Andreas Eigentler, et al.. (2023). Toward the Definition of Patient-Reported Outcome Measurements in Hereditary Spastic Paraplegia. Neurology Genetics. 9(1). e200052–e200052. 4 indexed citations
8.
Lynch, David R., Melanie Chin, Sylvia Boesch, et al.. (2022). Efficacy of Omaveloxolone in Friedreich's Ataxia: Delayed‐Start Analysis of the MOXIe Extension. Movement Disorders. 38(2). 313–320. 55 indexed citations
9.
Lynch, David R., Melanie Chin, Martin B. Delatycki, et al.. (2020). Safety and Efficacy of Omaveloxolone in Friedreich Ataxia (MOXIe Study). Annals of Neurology. 89(2). 212–225. 177 indexed citations
10.
Amprosi, Matthias, Michael Zech, Ruth Steiger, et al.. (2020). Familial writer’s cramp: a clinical clue for inherited coenzyme Q10 deficiency. Neurogenetics. 22(1). 81–86. 5 indexed citations
11.
Indelicato, Elisabetta, Alessandra Fanciulli, Wolfgang Nachbauer, et al.. (2019). Cardiovascular autonomic testing in the work-up of cerebellar ataxia: insight from an observational single center study. Journal of Neurology. 267(4). 1097–1102. 4 indexed citations
12.
Indelicato, Elisabetta, Wolfgang Nachbauer, Christine Fauth, et al.. (2018). SYNE1-ataxia: Novel genotypic and phenotypic findings. Parkinsonism & Related Disorders. 62. 210–214. 17 indexed citations
13.
Indelicato, Elisabetta, Alessandra Fanciulli, Wolfgang Nachbauer, et al.. (2018). Autonomic function testing in spinocerebellar ataxia type 2. Clinical Autonomic Research. 28(3). 341–346. 11 indexed citations
14.
Indelicato, Elisabetta, Wolfgang Nachbauer, Andreas Eigentler, et al.. (2017). Ten years of follow-up in a large family with familial hemiplegic migraine type 1: Clinical course and implications for treatment. Cephalalgia. 38(6). 1167–1176. 13 indexed citations
15.
Ilg, Winfried, Amy J. Bastian, Sylvia Boesch, et al.. (2013). Consensus Paper: Management of Degenerative Cerebellar Disorders. The Cerebellum. 13(2). 248–268. 125 indexed citations
16.
Egger, Karl, Christian Clemm von Hohenberg, Michael Schocke, et al.. (2013). White Matter Changes in Patients with Friedreich Ataxia after Treatment with Erythropoietin. Journal of Neuroimaging. 24(5). 504–508. 17 indexed citations
17.
Hohenberg, Christian Clemm von, Michael Schocke, Wolfgang Nachbauer, et al.. (2013). Radial diffusivity in the cerebellar peduncles correlates with clinical severity in Friedreich ataxia. Neurological Sciences. 34(8). 1459–1462. 25 indexed citations
18.
Nachbauer, Wolfgang, Sylvia Boesch, Rainer Schneider, et al.. (2013). Bioenergetics of the Calf Muscle in Friedreich Ataxia Patients Measured by 31P-MRS Before and After Treatment with Recombinant Human Erythropoietin. PLoS ONE. 8(7). e69229–e69229. 25 indexed citations
19.
Ehling, Rainer, Lenka Nosková, Viktor Stránecký, et al.. (2013). Cerebellar dysfunction in a family harboring the PSEN1 mutation co-segregating with a Cathepsin D variant p.A58V. Journal of the Neurological Sciences. 326(1-2). 75–82. 17 indexed citations
20.
Eigentler, Andreas, et al.. (2011). The scale for the assessment and rating of ataxia correlates with dysarthria assessment in Friedreich's ataxia. Journal of Neurology. 259(3). 420–426. 15 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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