Roland Spiegel

1.5k total citations
28 papers, 950 citations indexed

About

Roland Spiegel is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Roland Spiegel has authored 28 papers receiving a total of 950 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Cellular and Molecular Neuroscience. Recurrent topics in Roland Spiegel's work include Genetic Neurodegenerative Diseases (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Mitochondrial Function and Pathology (4 papers). Roland Spiegel is often cited by papers focused on Genetic Neurodegenerative Diseases (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Mitochondrial Function and Pathology (4 papers). Roland Spiegel collaborates with scholars based in Switzerland, United States and Germany. Roland Spiegel's co-authors include M Weigell-Weber, Kenneth H. Fischbeck, Albert R. La Spada, Anita E. Harding, Carolyn L. Warner, Woon-Chee Yee, I Hausmanowa-Pétrusewicz, Klaus L. Leenders, Peter Vontobel and A. Weindl and has published in prestigious journals such as Nature Genetics, Brain and Neurology.

In The Last Decade

Roland Spiegel

28 papers receiving 932 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roland Spiegel Switzerland 12 654 595 295 140 102 28 950
Nina Barišić Croatia 17 396 0.6× 261 0.4× 161 0.5× 106 0.8× 184 1.8× 61 860
Barbara Leube Germany 16 269 0.4× 504 0.8× 492 1.7× 204 1.5× 32 0.3× 27 989
J. Colomer Spain 17 479 0.7× 214 0.4× 213 0.7× 84 0.6× 260 2.5× 42 934
Robyn Labrum United Kingdom 14 488 0.7× 400 0.7× 175 0.6× 84 0.6× 44 0.4× 21 772
Fumi Urano Japan 12 653 1.0× 417 0.7× 121 0.4× 204 1.5× 54 0.5× 21 1.1k
Sandrine Tardieu France 17 330 0.5× 720 1.2× 300 1.0× 76 0.5× 83 0.8× 25 985
Nobuyoshi Fukuhara Japan 17 693 1.1× 205 0.3× 139 0.5× 63 0.5× 48 0.5× 35 1.1k
Anna Modoni Italy 21 767 1.2× 540 0.9× 333 1.1× 53 0.4× 63 0.6× 58 1.1k
E. Peter Bosch United States 16 327 0.5× 179 0.3× 187 0.6× 73 0.5× 45 0.4× 21 688
Michiya Ohta Japan 19 421 0.6× 305 0.5× 235 0.8× 46 0.3× 114 1.1× 36 990

Countries citing papers authored by Roland Spiegel

Since Specialization
Citations

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

Fields of papers citing papers by Roland Spiegel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roland Spiegel

This figure shows the co-authorship network connecting the top 25 collaborators of Roland Spiegel. A scholar is included among the top collaborators of Roland Spiegel 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 Roland Spiegel. Roland Spiegel 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.
Mihaylova, Violeta, Juliane Bremer, Roman Guggenberger, et al.. (2021). Collagen VI-Related Myopathy Caused by Compound Heterozygous Mutations of COL6A3 in a Consanguineous Kurdish Family. Journal of Clinical Neuromuscular Disease. 22(3). 173–179. 3 indexed citations
2.
Mihaylova, Violeta, et al.. (2020). Novel truncating mutations of MYO18B causing congenital myopathy in a Swiss patient. Neurology Genetics. 6(4). e458–e458. 4 indexed citations
3.
Matthews, Emma, Christoph Neuwirth, Fatima Jaffer, et al.. (2018). Atypical periodic paralysis and myalgia. Neurology. 90(5). e412–e418. 35 indexed citations
4.
DiMauro, S. & Roland Spiegel. (2011). Progress and problems in muscle glycogenoses.. PubMed. 30(2). 96–102. 32 indexed citations
5.
Huang, Dorothy Jane, Matthew R. Nelson, Bernhard Zimmermann, et al.. (2006). Reliable detection of Trisomy 21 using MALDI-TOF mass spectrometry. Genetics in Medicine. 8(11). 728–734. 15 indexed citations
6.
Pajic, Bojan, M Weigell-Weber, Isaak Schipper, et al.. (2006). A NOVEL COMPLEX MUTATION EVENT IN THE PERIPHERIN/RDS GENE IN A FAMILY WITH RETINAL PATTERN DYSTROPHY. Retina. 26(8). 947–953. 3 indexed citations
7.
Spiegel, Roland, Albert R. La Spada, Wolfram Kreß, Kenneth H. Fischbeck, & Werner Schmid. (1996). Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Human Mutation. 8(1). 32–37. 16 indexed citations
8.
Weigell-Weber, M, Werner Schmid, & Roland Spiegel. (1996). Psychiatric symptoms and CAG expansion in Huntington's disease. American Journal of Medical Genetics. 67(1). 53–57. 2 indexed citations
9.
Weigell-Weber, M, et al.. (1996). Genetic heterogeneity in autosomal dominant pattern dystrophy of the retina.. PubMed. 2(11). 6–6. 8 indexed citations
10.
Wildhaber, Johannes H., Walter Seelentag, Roland Spiegel, & Martin H. Schöni. (1996). Cystic fibrosis associated with neuronal intestinal dysplasia type B: A case report. Journal of Pediatric Surgery. 31(7). 951–954. 6 indexed citations
11.
Antonini, Angelo, Klaus L. Leenders, Roland Spiegel, et al.. (1996). Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease. Brain. 119(6). 2085–2095. 261 indexed citations
12.
Weigell-Weber, M, Werner Schmid, & Roland Spiegel. (1996). Psychiatric symptoms and CAG expansion in Huntington's disease. American Journal of Medical Genetics. 67(1). 53–57. 38 indexed citations
13.
Schmid, Werner, et al.. (1995). Rapid detection of sex chromosomal aneuploidies by PCR.. PubMed. 101. 111–4. 1 indexed citations
14.
Spiegel, Roland. (1995). [Huntington's chorea: clinical aspects, genetics and current diagnosis].. PubMed. 52(12). 814–20. 1 indexed citations
15.
16.
Robinson, Wendy P., et al.. (1993). Parental origin of the supernumerary chromosome in trisomy 18. Clinical Genetics. 44(2). 57–61. 29 indexed citations
17.
Spiegel, Roland, et al.. (1993). Two novel mutations: 5108delAG and 5816insG in the NF1 gene detected by SSCP analysis. Human Molecular Genetics. 2(9). 1491–1492. 8 indexed citations
18.
Melki, Judith, Sonia Abdelhak, P Burlet, et al.. (1992). Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.. Journal of Medical Genetics. 29(3). 171–174. 26 indexed citations
19.
Spada, Albert R. La, Anita E. Harding, Carolyn L. Warner, et al.. (1992). Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy. Nature Genetics. 2(4). 301–304. 280 indexed citations
20.
Spiegel, Roland, Albert Schinzel, Peggy Shelbourne, et al.. (1992). [Molecular genetics diagnosis of Steinert's myotonic dystrophy].. PubMed. 122(42). 1553–8. 1 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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