Peter Reilich

2.7k total citations
47 papers, 1.4k citations indexed

About

Peter Reilich is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Peter Reilich has authored 47 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 14 papers in Cell Biology. Recurrent topics in Peter Reilich's work include Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (12 papers) and Genetic Neurodegenerative Diseases (10 papers). Peter Reilich is often cited by papers focused on Muscle Physiology and Disorders (17 papers), Cardiomyopathy and Myosin Studies (12 papers) and Genetic Neurodegenerative Diseases (10 papers). Peter Reilich collaborates with scholars based in Germany, United Kingdom and United States. Peter Reilich's co-authors include Maggie C. Walter, Hanns Lochmüller, D. Pongratz, Wolfgang Müller‐Felber, Benedikt Schoser, Beate Schlotter, Simone Thiele, M. Toepfer, Nicolai Schramm and Wolfram Kreß and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Brain.

In The Last Decade

Peter Reilich

47 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Reilich Germany 21 746 274 257 256 251 47 1.4k
Angela Berardinelli Italy 22 1.2k 1.6× 333 1.2× 272 1.1× 163 0.6× 289 1.2× 70 1.8k
Kevin J. Felice United States 23 643 0.9× 350 1.3× 501 1.9× 100 0.4× 177 0.7× 65 1.7k
Robert T. Leshner United States 20 604 0.8× 164 0.6× 248 1.0× 151 0.6× 86 0.3× 49 1.6k
W. Mortier Germany 20 974 1.3× 298 1.1× 135 0.5× 511 2.0× 363 1.4× 54 1.5k
A. Laquérrière France 23 590 0.8× 336 1.2× 92 0.4× 134 0.5× 82 0.3× 77 1.5k
Francesca Magri Italy 23 1.3k 1.7× 320 1.2× 425 1.7× 74 0.3× 207 0.8× 74 1.7k
Marina Pedemonte Italy 21 1.0k 1.4× 163 0.6× 243 0.9× 214 0.8× 176 0.7× 57 1.3k
Olavo M. Vasconcelos United States 16 610 0.8× 288 1.1× 95 0.4× 255 1.0× 246 1.0× 25 1.1k
Velina Guergueltcheva Bulgaria 23 899 1.2× 561 2.0× 133 0.5× 308 1.2× 114 0.5× 52 1.6k
Susana Quijano-Roy France 18 961 1.3× 175 0.6× 406 1.6× 173 0.7× 458 1.8× 51 1.3k

Countries citing papers authored by Peter Reilich

Since Specialization
Citations

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

Fields of papers citing papers by Peter Reilich

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Reilich

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Reilich. A scholar is included among the top collaborators of Peter Reilich 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 Peter Reilich. Peter Reilich 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.
2.
Müller, Katharina, Sonja Schönecker, Katharina Kamm, et al.. (2024). Diagnostic accuracy and confounders of vagus nerve ultrasound in amyotrophic lateral sclerosis—a single-center case series and pooled individual patient data meta-analysis. Journal of Neurology. 271(9). 6255–6263. 1 indexed citations
3.
Walter, Maggie C., Peter Reilich, Sabine Krause, et al.. (2021). Congenital myopathy and epidermolysis bullosa due to PLEC variant. Neuromuscular Disorders. 31(11). 1212–1217. 3 indexed citations
4.
Hiebeler, Miriam, Angela Abicht, Peter Reilich, & Maggie C. Walter. (2021). Effect of Discontinuation of Nusinersen Treatment in Long-Standing SMA3. Journal of Neuromuscular Diseases. 8(4). 537–542. 3 indexed citations
5.
Reilich, Peter, et al.. (2019). Charcot-Marie-Tooth disease type 2CC due to a frameshift mutation of the neurofilament heavy polypeptide gene in an Austrian family. Neuromuscular Disorders. 29(5). 392–397. 8 indexed citations
6.
Schreiber‐Katz, Olivia, et al.. (2016). Disease burden of spinal muscular atrophy in Germany. Orphanet Journal of Rare Diseases. 11(1). 58–58. 87 indexed citations
7.
Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations
8.
Walter, Maggie C., Peter Reilich, Simone Thiele, et al.. (2013). Treatment of dysferlinopathy with deflazacort: a double-blind, placebo-controlled clinical trial. Orphanet Journal of Rare Diseases. 8(1). 26–26. 78 indexed citations
9.
Reilich, Peter, Rita Horváth, Sabine Krause, et al.. (2011). The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene. Journal of Neurology. 258(11). 1987–1997. 71 indexed citations
10.
Reilich, Peter, Benedikt Schoser, Nicolai Schramm, et al.. (2010). The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy. Neuromuscular Disorders. 20(4). 255–259. 67 indexed citations
11.
McNeill, Alisdair, Daniel Birchall, Volker Straub, et al.. (2009). Lower Limb Radiology of Distal Myopathy due to the S60F Myotilin Mutation. European Neurology. 62(3). 161–166. 11 indexed citations
12.
Strach, Katharina, Torsten Sommer, Carsten H. Meyer, et al.. (2008). Clinical, genetic, and cardiac magnetic resonance imaging findings in primary desminopathies. Neuromuscular Disorders. 18(6). 475–482. 31 indexed citations
13.
Krause, Sabine, Maggie C. Walter, Benedikt Schoser, et al.. (2007). Brain imaging and neuropsychology in late-onset dementia due to a novel mutation (R93C) of valosin-containing protein. Clinical Neuropathology. 26(9). 232–240. 18 indexed citations
14.
Walter, Maggie C., Peter Reilich, Angela Huebner, et al.. (2007). Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P. Brain. 130(6). 1485–1496. 59 indexed citations
15.
Reilich, Peter, et al.. (2007). An episode of geniospasm in sleep: Toward new insights into pathophysiology?. Movement Disorders. 23(2). 274–276. 7 indexed citations
16.
Müller, Juliane S., Henriett Pikó, Benedikt Schoser, et al.. (2006). Novel splice site mutation in the caveolin-3 gene leading to autosomal recessive limb girdle muscular dystrophy. Neuromuscular Disorders. 16(7). 432–436. 19 indexed citations
17.
Dekomien, Gabriele, Beate Schlotter‐Weigel, Peter Reilich, et al.. (2004). Respiratory insufficiency as a presenting symptom of LGMD2D in adulthood.. PubMed. 23(1). 1–5. 13 indexed citations
18.
Schoser, Benedikt, Christiane Schneider‐Gold, Wolfram Kreß, et al.. (2004). Muscle pathology in 57 patients with myotonic dystrophy type 2. Muscle & Nerve. 29(2). 275–281. 55 indexed citations
19.
Walter, Maggie C., Thomas N. Witt, Peter Reilich, et al.. (2004). Deletion of the LMNA initiator codon leading to a neurogenic variant of autosomal dominant Emery–Dreifuss muscular dystrophy. Neuromuscular Disorders. 15(1). 40–44. 28 indexed citations
20.
Walter, Maggie C., Hanns Lochmüller, M. Toepfer, et al.. (2000). High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study. Journal of Neurology. 247(1). 22–28. 164 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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