Olaf Rieß

466 total citations
17 papers, 283 citations indexed

About

Olaf Rieß is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Olaf Rieß has authored 17 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 11 papers in Molecular Biology and 7 papers in Neurology. Recurrent topics in Olaf Rieß's work include Genetic Neurodegenerative Diseases (14 papers), Neurological disorders and treatments (7 papers) and Mitochondrial Function and Pathology (5 papers). Olaf Rieß is often cited by papers focused on Genetic Neurodegenerative Diseases (14 papers), Neurological disorders and treatments (7 papers) and Mitochondrial Function and Pathology (5 papers). Olaf Rieß collaborates with scholars based in Germany, United States and Austria. Olaf Rieß's co-authors include Jörg T. Epplen, Stephan von Hörsten, Huu Phuc Nguyen, Carsten Holzmann, Andreas Bauer, Karl Zilles, Michael A. Johnson, Stephen C. Fowler, Andreas Matusch and Ina Schmitt and has published in prestigious journals such as PLoS ONE, Brain Research and Journal of Neurochemistry.

In The Last Decade

Olaf Rieß

17 papers receiving 277 citations

Peers

Olaf Rieß

CMN

NEURO

GENET

Zinah Wassouf Germany

José Luis Etcheverry Argentina

S. Chamberlain United Kingdom

Pilar Mazzetti Peru

Luis E. Almaguer-Mederos Cuba

Marie‐Lorraine Monin France

Kärt Mätlik Finland

Anna Castaldo Italy

Alicia Brocht United States

Kemal Kabakci Germany

Zinah Wassouf Germany

Olaf Rieß

117 ×0.5

CMN

125 ×0.8

144 ×1.2

NEURO

37 ×1.3

GENET

44 ×2.1

Citations per year, relative to Olaf Rieß Olaf Rieß (= 1×) peers Zinah Wassouf

Countries citing papers authored by Olaf Rieß

Since Specialization

Citations

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

Fields of papers citing papers by Olaf Rieß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olaf Rieß

This figure shows the co-authorship network connecting the top 25 collaborators of Olaf Rieß. A scholar is included among the top collaborators of Olaf Rieß 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 Olaf Rieß. Olaf Rieß is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

Novati, Arianna, et al.. (2018). The BACHD rat model of Huntington disease shows slowed learning in a Go/No-Go-like test of visual discrimination. Behavioural Brain Research. 359. 116–126. 2 indexed citations

Canneva, Fabio, Kerstin Raber, Maja Puchades, et al.. (2018). Early Alterations in Operant Performance and Prominent Huntingtin Aggregation in a Congenic F344 Rat Line of the Classical CAGn51trunc Model of Huntington Disease. Frontiers in Neuroscience. 12. 11–11. 10 indexed citations

Massioui, Nicole El, Charlotte Lamirault, Olaf Rieß, et al.. (2018). The Alteration of Emotion Regulation Precedes the Deficits in Interval Timing in the BACHD Rat Model for Huntington Disease. Frontiers in Integrative Neuroscience. 12. 14–14. 8 indexed citations

Rieß, Olaf, et al.. (2017). Further investigation of phenotypes and confounding factors of progressive ratio performance and feeding behavior in the BACHD rat model of Huntington disease. PLoS ONE. 12(3). e0173232–e0173232. 10 indexed citations

Rieß, Olaf, et al.. (2017). The BACHD Rat Model of Huntington Disease Shows Signs of Fronto-Striatal Dysfunction in Two Operant Conditioning Tests of Short-Term Memory. PLoS ONE. 12(1). e0169051–e0169051. 15 indexed citations

Clemens, Laura E., et al.. (2014). Reduced Motivation in the BACHD Rat Model of Huntington Disease Is Dependent on the Choice of Food Deprivation Strategy. PLoS ONE. 9(8). e105662–e105662. 16 indexed citations

Osterhaus, Gregory L., Kelli Lauderdale, Stephen C. Fowler, et al.. (2012). Motor function and dopamine release measurements in transgenic Huntington's disease model rats. Brain Research. 1450. 148–156. 27 indexed citations

Casteels, Cindy, Caroline Vandeputte, Tom Dresselaers, et al.. (2009). Metabolic and type 1 cannabinoid receptor mapping in the early phase of a transgenic rat model of Huntington’s disease. 2 indexed citations

Miller, Benjamin, Adam G. Walker, Stephen C. Fowler, et al.. (2009). Dysregulation of coordinated neuronal firing patterns in striatum of freely behaving transgenic rats that model Huntington's disease. Neurobiology of Disease. 37(1). 106–113. 28 indexed citations

10.

Bauer, Andreas, Karl Zilles, Andreas Matusch, et al.. (2005). Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation. Journal of Neurochemistry. 94(3). 639–650. 41 indexed citations

11.

Sander, Thomas, Rebekka Kretz, Herbert Schulz, et al.. (1998). Replication Analysis of a Putative Susceptibility Locus (EGI) for Idiopathic Generalized Epilepsy on Chromosome 8q24. Epilepsia. 39(7). 715–720. 13 indexed citations

12.

Rieß, Olaf & Gert‐Jan B. van Ommen. (1996). Report of the Fourth International Workshop on Human Chromosome 4 Mapping 1996. Cytogenetic and Genome Research. 74(1-2). 57–69. 5 indexed citations

13.

Schmitt, Ina, Jörg T. Epplen, & Olaf Rieß. (1995). Predominant neuronal expression of the gene responsible for dentatorubral-pallidoluysian atrophy (DRPLA) in rat. Human Molecular Genetics. 4(9). 1619–1624. 17 indexed citations

14.

Epplen, Jörg T., Johannes Buitkamp, Cornelia Epplen, Winfried Mäueler, & Olaf Rieß. (1995). Indirect DNA/gene diagnoses via electrophoresis – an obsolete principle?. Electrophoresis. 16(1). 683–690. 8 indexed citations

15.

Rieß, Olaf, et al.. (1994). Toward the complete genomic map and molecular pathology of human chromosome 4. Human Genetics. 94(1). 1–18. 9 indexed citations

16.

Rieß, Olaf, et al.. (1993). Improved PCR conditions for the stretch of (CAG)_n repeats causing Huntington's disease. Human Molecular Genetics. 2(6). 637–637. 67 indexed citations

17.

Epplen, Cornelia, et al.. (1993). Simple repetitive (GAA)_n loci in the human genome. Electrophoresis. 14(1). 973–977. 5 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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