Ralf Herrmann

3.4k citations
48 papers · 2.0k indexed · 1 hit paper · h-index 23

Ralf Herrmann

45 papers receiving 2.0k citations

Hit Papers

Muscular Dystrophy and Neuronal Migration Disorder Caused...5362001202620092017100200300400500

Peers

Ralf Herrmann
Comparison fields: 5 of 93
  • Molecular Biology 1.6k
  • Cell Biology 333
  • Developmental Neuroscience 84
  • Cardiology and Cardiovascular Medicine 435
  • Immunology and Allergy 107
Replace Marko Uutela with:
Marko Uutela Finland
Derek P. DiRocco United States
Ian Evans United Kingdom
Hideyuki Beppu United States
Yi Wei China
Marja Nissinen Finland
Judy U. Earley United States
Yoshio Katayama Japan
Paola Cattaneo Italy
M. Sarfarazi United Kingdom
Ralf Herrmann relative to Marko Uutela Finland Marko Uutela's profile →
Citations per field
00.5×4.9×
Marko Uutela · 1×
Citations per year

Countries citing papers authored by Ralf Herrmann

Since Specialization
Citations

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

Fields of papers citing papers by Ralf Herrmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Ralf Herrmann, 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 Ralf Herrmann Line = papers co-authored together Ralf Herrmann links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20216
2 201913
3 201569
4 201343
5 201381
6 201221
7 201051
8 20078
9 2007101
10
Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)
20061
11 200422
12 2003172
13
Muscular Dystrophy and Neuronal Migration Disorder Caused by Mutations in a Glycosyltransferase, POMGnT1breakdown →
2001536
14
Dose-intensification does not improve outcome in aggressive non-Hodgkin's lymphoma (NHL). Report of a randomized trial by the Australasian Leukemia and Lymphoma Group (ALLG).
20002
15 200041
16 199724
17 199729
18 199652
19 199534
20
Phase III study of 5-FU and carmustine versus 5-FU, carmustine, and doxorubicin in advanced gastric cancer.
198619

About Ralf Herrmann

Ralf Herrmann is a scholar working on Immunology and Allergy, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 48 papers that have together received 2.0k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (20 papers), Cardiomyopathy and Myosin Studies (6 papers), Nuclear Structure and Function (4 papers), Neonatal and fetal brain pathology (4 papers), Neonatal Respiratory Health Research (4 papers), Cell Adhesion Molecules Research (4 papers), Tissue Engineering and Regenerative Medicine (3 papers) and Ubiquitin and proteasome pathways (3 papers). The work is most often cited by research in Molecular Biology (1.6k citations), Cell Biology (333 citations) and Developmental Neuroscience (84 citations). Ralf Herrmann has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Thomas Voit, Volker Straub, Beril Talim, Tatsushi Toda, Haluk Topaloğlu, Hiroshi Manya, Kazuhiro Kobayashi, Hiroki Kano, Tamao Endo and Aruto Yoshida. Their work appears in journals such as Neuromuscular Disorders, PLoS ONE, The Journal of Clinical Endocrinology & Metabolism, European Journal of Human Genetics and Human Molecular 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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