B. Müller

1.2k total citations
23 papers, 744 citations indexed

About

B. Müller is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, B. Müller has authored 23 papers receiving a total of 744 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in B. Müller's work include Muscle Physiology and Disorders (6 papers), Neurological disorders and treatments (5 papers) and Genetic Neurodegenerative Diseases (5 papers). B. Müller is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Neurological disorders and treatments (5 papers) and Genetic Neurodegenerative Diseases (5 papers). B. Müller collaborates with scholars based in Germany, United States and United Kingdom. B. Müller's co-authors include T. Grimm, Gerhard Meng, C R Müller, T. Bettecken, E. Schwinger, Joanne Leung, S. Kammerer, Sabina Liechti‐Gallati, Andreas Braun and Christine Klein and has published in prestigious journals such as Neurology, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

B. Müller

23 papers receiving 724 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Müller Germany 15 334 272 269 158 132 23 744
Carmen Serrano Spain 14 270 0.8× 501 1.8× 267 1.0× 82 0.5× 68 0.5× 31 844
John Wolff United States 18 154 0.5× 481 1.8× 411 1.5× 137 0.9× 80 0.6× 23 844
Hideji Hashida Japan 19 434 1.3× 672 2.5× 520 1.9× 81 0.5× 43 0.3× 49 1.2k
James F. Gusella United States 10 498 1.5× 670 2.5× 606 2.3× 113 0.7× 47 0.4× 16 1.0k
Fabrice Lisovoski France 13 234 0.7× 234 0.9× 301 1.1× 80 0.5× 47 0.4× 21 722
H G Harley United Kingdom 18 298 0.9× 778 2.9× 790 2.9× 215 1.4× 46 0.3× 35 1.0k
Alice B. Schindler United States 15 202 0.6× 607 2.2× 396 1.5× 104 0.7× 201 1.5× 37 1.0k
V. Volpini Spain 17 167 0.5× 571 2.1× 369 1.4× 222 1.4× 21 0.2× 33 996
H. Smeets Netherlands 11 247 0.7× 785 2.9× 571 2.1× 360 2.3× 47 0.4× 21 1.1k
Friedmar R. Kreuz Germany 17 129 0.4× 498 1.8× 441 1.6× 197 1.2× 105 0.8× 30 923

Countries citing papers authored by B. Müller

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of B. Müller

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

All Works

20 of 20 papers shown
1.
Foncke, E.M.J., Christine Klein, J.H.T.M. Koelman, et al.. (2003). Hereditary myoclonus–dystonia associated with epilepsy. Neurology. 60(12). 1988–1990. 22 indexed citations
2.
Müller, B., Katja Hedrich, Norman Kock, et al.. (2002). Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia. The American Journal of Human Genetics. 71(6). 1303–1311. 102 indexed citations
3.
Klein, Christine, Liu Liu, Dana Doheny, et al.. (2002). ε‐sarcoglycan mutations found in combination with other dystonia gene mutations. Annals of Neurology. 52(5). 675–679. 69 indexed citations
4.
Agrawal, S., et al.. (2002). Allele Frequencies of Microsatellite Repeat Loci in Bhargavas, Chaturvedis, and Brahmins of North India. Journal of Forensic Sciences. 47(3). 678–681. 4 indexed citations
5.
Agrawal, S., et al.. (2002). Distribution of Allele Frequencies of Six STR Markers in North Indians. Journal of Forensic Sciences. 47(3). 682–685. 6 indexed citations
6.
Augood, S.J., Zane Hollingsworth, David S. Albers, et al.. (2002). Dopamine transmission in DYT1 dystonia: A biochemical and autoradiographical study. Neurology. 59(3). 445–448. 101 indexed citations
7.
Czesnik, Dirk, et al.. (2001). Noradrenergic modulation of calcium currents and synaptic transmission in the olfactory bulb of Xenopus laevis tadpoles. European Journal of Neuroscience. 13(6). 1093–1100. 22 indexed citations
8.
9.
Braun, Annika, et al.. (1996). A novel sequence polymorphism in the promoter region of the human B2-bradykinin receptor gene. Human Genetics. 97(5). 688–689. 22 indexed citations
10.
Gasser, Thomas, et al.. (1996). Linkage studies in alcohol‐responsive myoclonic dystonia. Movement Disorders. 11(4). 363–370. 19 indexed citations
11.
Braun, Andreas, et al.. (1995). Identification of Polymorphic Sites of the Human Bradykinin B2 Receptor Gene. Biochemical and Biophysical Research Communications. 211(1). 234–240. 49 indexed citations
12.
Müller, B., et al.. (1995). Autosomal dominant exudative vitreoretinopathy: linkage analysis and its clinical application.. PubMed. 4(1). 43–6. 3 indexed citations
13.
14.
Grimm, T., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1994). On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis.. Journal of Medical Genetics. 31(3). 183–186. 84 indexed citations
15.
Zonana, J., Melanie A. Jones, Angus Clarke, et al.. (1994). Detection of de novo mutations and analysis of their origin in families with X linked hypohidrotic ectodermal dysplasia.. Journal of Medical Genetics. 31(4). 287–292. 10 indexed citations
16.
Müller, B., Gerhard Meng, Sabina Liechti‐Gallati, et al.. (1992). Estimation of the male and female mutation rates in Duchenne muscular dystrophy (DMD). Human Genetics. 89(2). 204–206. 9 indexed citations
17.
Vieregge, P., et al.. (1992). Parkinson's disease in twins. Neurology. 42(8). 1453–1453. 51 indexed citations
18.
Grimm, T., B. Müller, C R Müller, & M. Janka. (1990). Theoretical considerations on germline mosaicism in Duchenne muscular dystrophy.. Journal of Medical Genetics. 27(11). 683–687. 27 indexed citations
19.
Hejtmancik, J. Fielding, G. Romeo, Mikael Lindlöf, et al.. (1989). A genetic linkage map of five marker loci in and around the Duchenne muscular dystrophy locus. Genomics. 4(1). 105–109. 17 indexed citations
20.
Grimm, T., et al.. (1989). Hot spot of recombination within DXS164 in the Duchenne muscular dystrophy gene.. PubMed. 45(3). 368–72. 31 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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