Wolfgang Mueller‐Felber

1.1k total citations
19 papers, 302 citations indexed

About

Wolfgang Mueller‐Felber is a scholar working on Molecular Biology, Neurology and Surgery. According to data from OpenAlex, Wolfgang Mueller‐Felber has authored 19 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Neurology and 4 papers in Surgery. Recurrent topics in Wolfgang Mueller‐Felber's work include Neurogenetic and Muscular Disorders Research (4 papers), Metabolism and Genetic Disorders (3 papers) and RNA modifications and cancer (3 papers). Wolfgang Mueller‐Felber is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Metabolism and Genetic Disorders (3 papers) and RNA modifications and cancer (3 papers). Wolfgang Mueller‐Felber collaborates with scholars based in Germany, United States and Austria. Wolfgang Mueller‐Felber's co-authors include C. Anthuber, Bernhard Schuessler, Th. Dimpfl, Skadi Beblo, Berthold Koletzko, A. Roscher, Ania C. Muntau, D. Pongratz, Benedikt Schoser and Eduardo F. Tizzano and has published in prestigious journals such as Neurology, American Journal of Roentgenology and Multiple Sclerosis Journal.

In The Last Decade

Wolfgang Mueller‐Felber

19 papers receiving 291 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wolfgang Mueller‐Felber Germany 8 120 106 105 68 55 19 302
Mariateresa Falco Italy 9 46 0.4× 94 0.9× 36 0.3× 20 0.3× 10 0.2× 22 334
Anna Venerando Italy 8 92 0.8× 87 0.8× 28 0.3× 56 0.8× 14 0.3× 11 325
Marina Macchiaiolo Italy 10 117 1.0× 114 1.1× 13 0.1× 34 0.5× 12 0.2× 45 328
Daniel Dahlberg Norway 13 103 0.9× 47 0.4× 24 0.2× 42 0.6× 17 0.3× 28 367
Chantal Gendrot France 11 68 0.6× 82 0.8× 12 0.1× 26 0.4× 10 0.2× 15 301
Maja Djordjevic Serbia 11 20 0.2× 118 1.1× 68 0.6× 6 0.1× 94 1.7× 40 360
M�ximo Poza Spain 11 145 1.2× 37 0.3× 40 0.4× 7 0.1× 22 0.4× 15 316
Nagahide Goya Japan 7 29 0.2× 47 0.4× 14 0.1× 96 1.4× 17 0.3× 22 337
Moshe Levin Israel 9 21 0.2× 86 0.8× 9 0.1× 38 0.6× 38 0.7× 17 306
Christian Wentzel Sweden 7 64 0.5× 196 1.8× 18 0.2× 11 0.2× 10 0.2× 8 373

Countries citing papers authored by Wolfgang Mueller‐Felber

Since Specialization
Citations

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

Fields of papers citing papers by Wolfgang Mueller‐Felber

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wolfgang Mueller‐Felber. 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 Wolfgang Mueller‐Felber. The network helps show where Wolfgang Mueller‐Felber may publish in the future.

Co-authorship network of co-authors of Wolfgang Mueller‐Felber

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

All Works

19 of 19 papers shown
1.
Bader, Ingrid, Michael Freilinger, Franz Landauer, et al.. (2022). A recurrent single-amino acid deletion (p.Glu500del) in the head domain of ß-cardiac myosin in two unrelated boys presenting with polyhydramnios, congenital axial stiffness and skeletal myopathy. Orphanet Journal of Rare Diseases. 17(1). 279–279. 2 indexed citations
2.
Dangouloff, Tamara, Arthur H.M. Burghes, Eduardo F. Tizzano, et al.. (2019). 244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10–12, 2019, Hoofdorp, The Netherlands. Neuromuscular Disorders. 30(1). 93–103. 50 indexed citations
3.
Shieh, Perry B., Gyula Acsádi, Wolfgang Mueller‐Felber, et al.. (2018). Safety and Efficacy of Nusinersen in Infants/Children with Spinal Muscular Atrophy (SMA): Part 1 of the Phase 2 EMBRACE Study (P2.324). Neurology. 90(15_supplement). 2 indexed citations
4.
Baumann, Matthias, Wolfgang Mueller‐Felber, Benedikt Schoser, et al.. (2018). Pattern of myogenesis and vascular repair in early and advanced lesions of juvenile dermatomyositis. Neuromuscular Disorders. 28(12). 973–985. 12 indexed citations
5.
Acsádi, Gyula, Wolfgang Mueller‐Felber, T. B. B. Crawford, et al.. (2018). B.06 Safety and efficacy of nusinersen in infants/children with spinal muscular atrophy (SMA): part 1 of the phase 2 EMBRACE study. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 45(s2). S13–S13. 6 indexed citations
6.
Mueller‐Felber, Wolfgang, et al.. (2017). Unilateral Tongue Fasciculation Associated with Genetic Paraganglioma Syndrome. Neuropediatrics. 49(1). 78–79. 2 indexed citations
7.
Acsádi, Gyula, Thomas O. Crawford, Randal Richardson, et al.. (2017). Safety and efficacy of nusinersen in infants/children with spinal muscular atrophy (SMA): part 1 of the phase 2 EMBRACE study. Neuromuscular Disorders. 27. S210–S211. 2 indexed citations
8.
Iuso, Arcangela, Tomasz Kmieć, Elżbieta Jurkiewicz, et al.. (2011). Identification of a second major locus for neurodegeneration with brain iron accumulation. Neuropediatrics. 42(S 01). 3 indexed citations
9.
Blaschek, Astrid, P Lohse, Ingo Borggraefe, et al.. (2010). Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis. Multiple Sclerosis Journal. 16(12). 1517–1520. 3 indexed citations
10.
Borggraefe, Ingo, Kai Boetzel, John Boehmer, et al.. (2008). Return to Participation – Significant Improvement after Bilateral Pallidal Stimulation in Rapidly ProgressiveDYT-1Dystonia. Neuropediatrics. 39(4). 239–242. 11 indexed citations
11.
Byrne, Barry J., Laura E. Case, Luciano Merlini, et al.. (2008). The Pompe Registry: tracking Pompe disease symptoms in a broad patient population. Pediatric Rheumatology. 6(S1). 2 indexed citations
12.
Heidenreich, Jens O., Thomas Klopstock, Timo Schirmer, et al.. (2006). Chronic Progressive External Ophthalmoplegia: MR Spectroscopy and MR Diffusion Studies in the Brain. American Journal of Roentgenology. 187(3). 820–824. 15 indexed citations
13.
Mueller‐Felber, Wolfgang, et al.. (2006). Serum Levels of Matrix Metalloproteinases-2 and -9 and Their Tissue Inhibitors in Inflammatory Neuromuscular Disorders. European Neurology. 55(4). 204–208. 18 indexed citations
14.
Broekaert, Ilse, et al.. (2004). O0068 VISUAL EVOKED POTENTIALS IN INFANTS AFTER DIETARY SUPPLY OF DOCOSAHEXAENOIC ACID AND 5-METHYL-TETRAHYDROFOLATE DURING PREGNANCY. Journal of Pediatric Gastroenterology and Nutrition. 39(Supplement 1). S33–S34. 3 indexed citations
15.
Beblo, Skadi, et al.. (2001). Fish oil supplementation improves visual evoked potentials in children with phenylketonuria. Neurology. 57(8). 1488–1491. 52 indexed citations
16.
Goebels, Norbert, et al.. (2000). Inflammatory myopathy in POEMS syndrome. Neurology. 55(9). 1413–1414. 7 indexed citations
17.
Dimpfl, Th., et al.. (1998). Myogenic changes of the levator ani muscle in premenopausal women: The impact of vaginal delivery and age. Neurourology and Urodynamics. 17(3). 197–205. 5 indexed citations
18.
Dimpfl, Th., et al.. (1998). Myogenic changes of the levator ani muscle in premenopausal women: The impact of vaginal delivery and age. Neurourology and Urodynamics. 17(3). 197–205. 90 indexed citations
19.
Zafeiriou, Dimitrios, et al.. (1995). Deficiency in complex IV (cytochrome c oxidase) of the respiratory chain, presenting as a leukodystrophy in two siblings with Leigh syndrome. Brain and Development. 17(2). 117–121. 17 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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