K. Ricker

7.7k citations
112 papers · 5.5k · 2 hit papers · h-index 37

Impact in

Papers in

K. Ricker

107 papers receiving 5.3k citations

K. Ricker's Hit Papers

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9 2001 · 925 citations
9250+11+22Years since publication250500750

Peers

K. Ricker
Comparison fields: 5 of 99
  • Cellular and Molecular Neuroscience 3.4k
  • Neurology 1.2k
  • Cardiology and Cardiovascular Medicine 1.5k
  • Molecular Biology 4.0k
  • Cell Biology 388
Replace Matthias Vorgerd with:
Matthias Vorgerd Germany
Heinz Jungbluth United Kingdom
Mary E. Stevens United States
Emmanuel Fournier France
G. Salviati Italy
Evelyne Souil France
Teit E. Johansen Denmark
Romeo Betto Italy
David Beeson United Kingdom
Géraldine Cancel‐Tassin France
K. Ricker relative to Matthias Vorgerd Germany Matthias Vorgerd's profile →
Citations per field
00.5×2.6×
Matthias Vorgerd · 1×
Citations per year

Countries citing papers authored by K. Ricker

Since Specialization
Citations

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

Fields of papers citing papers by K. Ricker

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside K. Ricker, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with K. Ricker Line = papers co-authored together K. Ricker links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 112 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9
Hit paper breakdown →
2001925
2
The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia
Hit paper breakdown →
1992556
3 2003300
4 1994169
5 1987152
6 1984146
7 2001144
8
Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia.
1995133
9 1995108
10 1994107
11 198197
12 199390
13 198489
14 198784
15 199983
16 198383
17 198177
18 199374
19 200472
20 199370

About K. Ricker

K. Ricker is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Cardiology and Cardiovascular Medicine and Epidemiology, having authored 112 papers that have together received 5.5k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (48 papers), Ion channel regulation and function (38 papers), Cardiac electrophysiology and arrhythmias (14 papers), Mitochondrial Function and Pathology (13 papers), Neuroscience and Neural Engineering (11 papers), Myasthenia Gravis and Thymoma (10 papers), Muscle Physiology and Disorders (10 papers) and Cardiomyopathy and Myosin Studies (10 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (3.4k citations), Neurology (1.2k citations), Cardiology and Cardiovascular Medicine (1.5k citations), Molecular Biology (4.0k citations) and Cell Biology (388 citations). K. Ricker has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Frank Lehmann‐Horn, Reinhardt Rüdel, Manuela C. Koch, Laura P.W. Ranum, Christina L. Liquori, Wolfram Kreß, Melinda L. Moseley, Susan L. Naylor, Michaël Otto and Thomas J. Jentsch. Their work appears in journals such as Journal of Neurology, Neurology, Muscle & Nerve, Neuromuscular Disorders and Human Genetics.

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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