B. Müller
Impact in
- Neurology top 5%
- Neurological disorders and treatments
- Parkinson's Disease Mechanisms and Treatments
-
- Genetic Neurodegenerative Diseases
Papers in
-
- Muscle Physiology and Disorders 6
-
- Genetic Neurodegenerative Diseases 5
- Co-authors
- T. Grimm (6 shared papers)Gerhard Meng (5 shared papers)C R Müller (2 shared papers)T. Bettecken (2 shared papers)E. Schwinger (4 shared papers)Joanne Leung (2 shared papers)Sabina Liechti‐Gallati (2 shared papers)S. Kammerer (3 shared papers)
- Journals
- Human Genetics (4 papers)Journal of Medical Genetics (4 papers)Neurology (3 papers)Journal of Forensic Sciences (2 papers)Biochemical and Biophysical Research Communications (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
B. Müller
23 papers receiving 730 citations
Peers
Comparison fields: 5 of 63
- Neurology 303
- Cellular and Molecular Neuroscience 238
- Genetics 126
- Rheumatology 95
- Neurology 43
Countries citing papers authored by B. Müller
This map shows the geographic impact of B. 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 B. Müller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. Müller more than expected).
Fields of papers citing papers by B. Müller
This network shows the impact of papers produced by B. 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 B. Müller. The network helps show where B. Müller may publish in the future.
Co-authors
The 25 scholars most cited alongside B. Müller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 104 | |
| 2 | 2002 | 101 | |
| 3 | 1994 | 84 | |
| 4 | 2002 | 71 | |
| 5 | 1992 | 51 | |
| 6 | The autosomal dominant familial exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S533. | 1992 | 51 |
| 7 | 1995 | 49 | |
| 8 | Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene. | 1989 | 32 |
| 9 | 1990 | 27 | |
| 10 | 2003 | 23 | |
| 11 | 1996 | 22 | |
| 12 | 2001 | 22 | |
| 13 | 1996 | 19 | |
| 14 | Proximal spinal muscular atrophy (SMA) types II and III in the same sibship are not caused by different alleles at the SMA locus on 5q. | 1992 | 19 |
| 15 | 1989 | 17 | |
| 16 | 1994 | 10 | |
| 17 | 1996 | 10 | |
| 18 | 1992 | 9 | |
| 19 | 1995 | 9 | |
| 20 | 1996 | 6 |
About B. Müller
B. Müller is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Genetics and Neurology, having authored 23 papers that have together received 749 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (6 papers), Genetic Neurodegenerative Diseases (5 papers), Neurological disorders and treatments (5 papers), Coagulation, Bradykinin, Polyphosphates, and Angioedema (4 papers), Blood Coagulation and Thrombosis Mechanisms (4 papers), Neurogenetic and Muscular Disorders Research (3 papers), Parkinson's Disease Mechanisms and Treatments (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). The work is most often cited by research in Neurology (303 citations), Cellular and Molecular Neuroscience (238 citations), Genetics (126 citations), Rheumatology (95 citations) and Neurology (43 citations). B. Müller has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include T. Grimm, Gerhard Meng, C R Müller, T. Bettecken, E. Schwinger, Joanne Leung, Sabina Liechti‐Gallati, S. Kammerer, Andreas Braun and Christine Klein. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Neurology, Journal of Forensic Sciences and Biochemical and Biophysical Research Communications.
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.