C R Müller
- Molecular Biology
- Clinical Biochemistry top 5%
- Genetics
- Biochemistry top 10%
- Genetics
- Co-authors
- T. GrimmB. MüllerGerhard MengT. BetteckenSabina Liechti‐GallatiWerner WolzJean‐Louis GuénetXavier Montagutelli
- Topics
- Muscle Physiology and Disorders (6 papers)Amino Acid Enzymes and Metabolism (4 papers)Metabolism and Genetic Disorders (4 papers)
- Partner nations
- GermanyUnited StatesSlovakia
In The Last Decade
C R Müller
17 papers receiving 360 citations
Peers
Comparison fields: 5 of 58
- Molecular Biology 262
- Clinical Biochemistry 132
- Genetics 70
- Biochemistry 56
- Genetics 55
Countries citing papers authored by C R Müller
This map shows the geographic impact of C R Müller'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 C R Müller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites C R Müller more than expected).
Fields of papers citing papers by C R Müller
This network shows the impact of papers produced by C R Müller. 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 C R Müller. The network helps show where C R Müller may publish in the future.
Co-authorship network of co-authors of C R Müller
This figure shows the co-authorship network connecting the top 25 collaborators of C R Müller. A scholar is included among the top collaborators of C R Müller 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 C R Müller. C R Müller is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 20 | |
| 2 | Phenotypic variability in siblings with calpainopathy (LGMD2A). | 12 |
| 3 | 1 | |
| 4 | 19 | |
| 5 | Long-term MRI and clinical follow-up of symptomatic and presymptomatic carriers of dysferlin gene mutations. | 16 |
| 6 | 13 | |
| 7 | 11 | |
| 8 | [Significance of mutation analysis in patients with haemophilia A]. | 4 |
| 9 | Alkaptonuria caused by compound heterozygote mutations. | 5 |
| 10 | 24 | |
| 11 | 39 | |
| 12 | 84 | |
| 13 | 81 | |
| 14 | 11 | |
| 15 | 27 | |
| 16 | 19 | |
| 17 | 1 |
About C R Müller
C R Müller is a scholar working on Clinical Biochemistry, Aging and Biochemistry, having authored 17 papers that have together received 387 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (6 papers), Amino Acid Enzymes and Metabolism (4 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Clinical Biochemistry (132 citations), Biochemistry (56 citations) and Genetics (55 citations). C R Müller has collaborated with scholars based in Germany, United States and Slovakia. Frequent co-authors include T. Grimm, B. Müller, Gerhard Meng, T. Bettecken, Sabina Liechti‐Gallati, Werner Wolz, Jean‐Louis Guénet, Xavier Montagutelli, M. Janka and Stefan Schmidt. Their work appears in journals such as Genomics, Journal of Medical Genetics and European Journal of 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.