Erik Riesch

1.3k total citations
2 papers, 64 citations indexed

About

Erik Riesch is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Erik Riesch has authored 2 papers receiving a total of 64 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Genetics, 1 paper in Surgery and 1 paper in Molecular Biology. Recurrent topics in Erik Riesch's work include Glycogen Storage Diseases and Myoclonus (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Pancreatic function and diabetes (1 paper). Erik Riesch is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Pancreatic function and diabetes (1 paper). Erik Riesch collaborates with scholars based in Switzerland, Germany and Finland. Erik Riesch's co-authors include Johannes R. Lemke, Hannu Kalimo, Maria Kousi, Sarenur Gökben, Liisa Myllykangas, Aarno Palotie, Füsun Alehan, Stella Calafato, Anna‐Elina Lehesjoki and Meral Topçu and has published in prestigious journals such as Journal of Medical Genetics and American Journal of Medical Genetics Part A.

In The Last Decade

Erik Riesch

2 papers receiving 62 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erik Riesch Switzerland	2	32	31	19	16	12	2	64
Catrinel Iliescu Romania	6	37 1.2×	55 1.8×	12 0.6×	10 0.6×	10 0.8×	14	95
Julija Pavaine United Kingdom	5	59 1.8×	15 0.5×	22 1.2×	17 1.1×	7 0.6×	7	98
Amy Kritzer United States	7	45 1.4×	41 1.3×	36 1.9×	17 1.1×	7 0.6×	16	122
Kamer Tezcan United States	5	35 1.1×	33 1.1×	5 0.3×	36 2.3×	5 0.4×	5	126
Nora Aljawini Saudi Arabia	4	54 1.7×	11 0.4×	30 1.6×	5 0.3×	12 1.0×	6	120
G. Pitelet France	3	33 1.0×	21 0.7×	17 0.9×	17 1.1×	54 4.5×	4	93
Scott A. Melville United States	2	39 1.2×	29 0.9×	34 1.8×	7 0.4×	4 0.3×	2	86
Katie Golden‐Grant United States	5	31 1.0×	37 1.2×	10 0.5×	4 0.3×	17 1.4×	5	72
Marie‐Aude Spitz France	7	99 3.1×	53 1.7×	9 0.5×	7 0.4×	6 0.5×	11	136
Chontelle King New Zealand	6	48 1.5×	51 1.6×	5 0.3×	9 0.6×	12 1.0×	6	109

Countries citing papers authored by Erik Riesch

Since Specialization

Citations

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

Fields of papers citing papers by Erik Riesch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erik Riesch

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

All Works

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2 of 2 papers shown

1.

Courage, Carolina, Christopher B. Jackson, Marta Owczarek‐Lipska, et al.. (2019). Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome. American Journal of Medical Genetics Part A. 179(12). 2447–2453. 9 indexed citations

2.

Kousi, Maria, Verneri Anttila, Angela Schulz, et al.. (2012). Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. Journal of Medical Genetics. 49(6). 391–399. 55 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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