O. Riess

714 total citations
9 papers, 510 citations indexed

About

O. Riess is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, O. Riess has authored 9 papers receiving a total of 510 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 4 papers in Neurology. Recurrent topics in O. Riess's work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Neurological disorders and treatments (2 papers). O. Riess is often cited by papers focused on Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (4 papers) and Neurological disorders and treatments (2 papers). O. Riess collaborates with scholars based in Germany, Poland and Austria. O. Riess's co-authors include Lüdger Schöls, H. Przuntek, G. Amoiridis, Rejko Krüger, Jörg T. Epplen, J. Haan, Liang Tong, Yun Freudenberg‐Hua, Rong Jiang and Jürgen Tomiuk and has published in prestigious journals such as Brain, Neurology and Human Molecular Genetics.

In The Last Decade

O. Riess

9 papers receiving 504 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
O. Riess Germany	8	356	325	250	69	54	9	510
Rébecca Gaudet Canada	10	255 0.7×	325 1.0×	81 0.3×	63 0.9×	29 0.5×	13	478
Sandra Martins Portugal	15	329 0.9×	351 1.1×	171 0.7×	13 0.2×	21 0.4×	39	503
Khanh-Nhat Tran-Viet United States	13	216 0.6×	186 0.6×	72 0.3×	188 2.7×	84 1.6×	16	735
Sascha Hering Austria	7	304 0.9×	226 0.7×	245 1.0×	18 0.3×	13 0.2×	9	411
Lorenzo Nanetti Italy	15	491 1.4×	400 1.2×	270 1.1×	23 0.3×	20 0.4×	51	721
Carl T. Fulp United States	7	196 0.6×	208 0.6×	118 0.5×	66 1.0×	40 0.7×	8	533
Ralph Oehlmann United States	8	237 0.7×	215 0.7×	311 1.2×	19 0.3×	40 0.7×	10	583
Pascale Ribaı̈ France	13	498 1.4×	361 1.1×	281 1.1×	18 0.3×	11 0.2×	18	638
Elisabetta Indelicato Austria	12	221 0.6×	202 0.6×	161 0.6×	12 0.2×	17 0.3×	40	397
K. Verhoeven Belgium	8	319 0.9×	265 0.8×	87 0.3×	14 0.2×	46 0.9×	13	582

Countries citing papers authored by O. Riess

Since Specialization

Citations

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

Fields of papers citing papers by O. Riess

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of O. Riess

This figure shows the co-authorship network connecting the top 25 collaborators of O. Riess. A scholar is included among the top collaborators of O. 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 O. Riess. O. 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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9 of 9 papers shown

1.

Gomes, Marina de Nadai Bonin, et al.. (2013). PIK3R1 mutations in SHORT syndrome. Clinical Genetics. 86(3). 292–294. 31 indexed citations

2.

Jiang, Rong, Huu Phuc Nguyen, Jürgen Tomiuk, et al.. (2008). Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease. Human Molecular Genetics. 17(8). 1137–1146. 69 indexed citations

3.

Sotlar, Karl, et al.. (2006). Progression-specific Genes Identified by Expression Profiling of Matched Ductal Carcinomas in situ and Invasive Breast Tumors, Combining Laser Capture Microdissection and Oligonucleotide Microarray Analysis. Geburtshilfe und Frauenheilkunde. 66(S 01). 18 indexed citations

4.

Kobayashi, Hirokazu, Rejko Krüger, Katerina Markopoulou, et al.. (2002). Haploinsufficiency at the -synuclein gene underlies phenotypic severity in familial Parkinson's disease. Brain. 126(1). 32–42. 36 indexed citations

5.

Laccone, Franco, Ulrike Engel, Elke Holinski‐Feder, et al.. (1999). DNA analysis of Huntington's disease: five year experience in Germany, Austria and Switzerland (1993-1997). University of Regensburg Publication Server (University of Regensburg). 1 indexed citations

6.

Dichgans, Martin, Lüdger Schöls, Josef Herzog, et al.. (1999). Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families. Neurology. 52(4). 849–849. 25 indexed citations

7.

Schöls, Lüdger, Rejko Krüger, G. Amoiridis, et al.. (1998). Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds. Journal of Neurology Neurosurgery & Psychiatry. 64(1). 67–73. 140 indexed citations

8.

Schöls, Lüdger, J. Haan, O. Riess, G. Amoiridis, & H. Przuntek. (1998). Sleep disturbance in spinocerebellar ataxias. Neurology. 51(6). 1603–1607. 102 indexed citations

9.

Riess, O.. (1997). SCA6 is caused by moderate CAG expansion in the alpha1A-voltage- dependent calcium channel gene. Human Molecular Genetics. 6(8). 1289–1293. 88 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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