Bernd Wilken

2.0k total citations
36 papers, 1.0k citations indexed

About

Bernd Wilken is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bernd Wilken has authored 36 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bernd Wilken's work include Metabolism and Genetic Disorders (5 papers), Hereditary Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Bernd Wilken is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Hereditary Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Bernd Wilken collaborates with scholars based in Germany, United States and Austria. Bernd Wilken's co-authors include F. Hanefeld, Knut Brockmann, Jens Frahm, Diethelm W. Richter, Bernd Kruse, Evgeni Ponimaskin, Till Manzke, Markus Wick, Petra J. W. Pouwels and Jochen Herms and has published in prestigious journals such as PEDIATRICS, International Journal of Cancer and Epilepsia.

In The Last Decade

Bernd Wilken

34 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernd Wilken Germany 15 345 199 159 147 129 36 1.0k
Hironaka Igarashi Japan 21 429 1.2× 365 1.8× 61 0.4× 48 0.3× 412 3.2× 95 1.5k
James Provenzale United States 18 240 0.7× 259 1.3× 35 0.2× 303 2.1× 257 2.0× 31 1.4k
Yohan van de Looij Switzerland 20 345 1.0× 260 1.3× 67 0.4× 74 0.5× 72 0.6× 48 1.6k
Thomas Reithmeier Germany 19 268 0.8× 218 1.1× 33 0.2× 158 1.1× 239 1.9× 36 1.4k
Steffi Dreha‐Kulaczewski Germany 14 259 0.8× 189 0.9× 83 0.5× 52 0.4× 533 4.1× 33 1.1k
Ivan Voříšek Czechia 16 322 0.9× 416 2.1× 31 0.2× 70 0.5× 501 3.9× 24 1.2k
Kurt H. Bockhorst United States 21 157 0.5× 796 4.0× 42 0.3× 137 0.9× 94 0.7× 48 1.4k
Jonathan Murnick United States 19 240 0.7× 154 0.8× 63 0.4× 64 0.4× 321 2.5× 64 1.1k
Takashi Mito Japan 20 439 1.3× 102 0.5× 149 0.9× 86 0.6× 237 1.8× 53 1.4k
Josette Mancini France 19 484 1.4× 27 0.1× 137 0.9× 224 1.5× 90 0.7× 29 1.2k

Countries citing papers authored by Bernd Wilken

Since Specialization
Citations

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

Fields of papers citing papers by Bernd Wilken

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernd Wilken

This figure shows the co-authorship network connecting the top 25 collaborators of Bernd Wilken. A scholar is included among the top collaborators of Bernd Wilken 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 Bernd Wilken. Bernd Wilken 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.
Marschik, Peter B., Bernd Wilken, Christian P. Schaaf, et al.. (2025). Shared Environment – Different Genes: Speech-Language Development in a Pair of Dizygotic Twins with and Without MECP2 Mutation. The Journal of Genetic Psychology. 186(6). 452–467.
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Jost, Wolfgang H., Tobias Bäumer, Andrea Bevot, et al.. (2023). Botulinum neurotoxin type A in the interdisciplinary treatment of sialorrhea in adults and children—update and practice recommendations. Frontiers in Neurology. 14. 1275807–1275807. 5 indexed citations
4.
Zhang, Dajie, Bernd Wilken, Christa Einspieler, et al.. (2023). Learning about neurodiversity from parents – Auditory gestalt perception of prelinguistic vocalisations. Research in Developmental Disabilities. 138. 104515–104515. 1 indexed citations
5.
Schmidt, Julia, Steffi Dreha‐Kulaczewski, Maria-Patapia Zafeiriou, et al.. (2022). Somatic mosaicism in STAG2-associated cohesinopathies: Expansion of the genotypic and phenotypic spectrum. Frontiers in Cell and Developmental Biology. 10. 1025332–1025332. 6 indexed citations
6.
Feucht, Martha, Alfons Macaya, Bernd Wilken, et al.. (2022). Real-World Evidence Study on the Long-Term Safety of Everolimus in Patients With Tuberous Sclerosis Complex: Final Analysis Results. Frontiers in Pharmacology. 13. 802334–802334. 9 indexed citations
7.
Wilken, Bernd, et al.. (2022). A new model for fatty acid hydroxylase-associated neurodegeneration reveals mitochondrial and autophagy abnormalities. Frontiers in Cell and Developmental Biology. 10. 1000553–1000553. 7 indexed citations
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Kirkham, Fenella J., Federico Vigevano, Miquel Raspall‐Chaure, et al.. (2019). Health-related quality of life and the burden of prolonged seizures in noninstitutionalized children with epilepsy. Epilepsy & Behavior. 102. 106340–106340. 8 indexed citations
10.
Vigevano, Federico, Fenella J. Kirkham, Bernd Wilken, et al.. (2017). Effect of rescue medication on seizure duration in non-institutionalized children with epilepsy. European Journal of Paediatric Neurology. 22(1). 56–63. 16 indexed citations
11.
Dreha‐Kulaczewski, Steffi, Knut Brockmann, Marco Henneke, et al.. (2012). Assessment of myelination in hypomyelinating disorders by quantitative MRI. Journal of Magnetic Resonance Imaging. 36(6). 2 indexed citations
12.
Dreha‐Kulaczewski, Steffi, Knut Brockmann, Marco Henneke, et al.. (2012). Assessment of myelination in hypomyelinating disorders by quantitative MRI. Journal of Magnetic Resonance Imaging. 36(6). 1329–1338. 19 indexed citations
13.
Bien, Christian G., Henning Tiemeier, Robert Sassen, et al.. (2012). Rasmussen encephalitis: Incidence and course under randomized therapy with tacrolimus or intravenous immunoglobulins. Epilepsia. 54(3). 543–550. 106 indexed citations
14.
Sauter, Simone M., Detlef Böhm, Iris Bartels, et al.. (2007). Partial trisomy of distal 19q detected by quantitative real‐time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay. American Journal of Medical Genetics Part A. 143A(10). 1091–1099. 9 indexed citations
15.
Diepold, Katharina, Kevin Rostásy, Bernd Wilken, et al.. (2005). Levodopa‐responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections. Movement Disorders. 20(6). 764–767. 18 indexed citations
16.
Richter, Diethelm W., Till Manzke, Bernd Wilken, & Evgeni Ponimaskin. (2003). Serotonin receptors: guardians of stable breathing. Trends in Molecular Medicine. 9(12). 542–548. 153 indexed citations
17.
Rostásy, Kevin, Katharina Diepold, Johannes Buckard, et al.. (2003). Progressive muscle weakness after high-dose steroids in two children with CIDP. Pediatric Neurology. 29(3). 236–238. 11 indexed citations
18.
Huppke, Peter, et al.. (2002). Eosinophilic fasciitis leading to painless contractures. European Journal of Pediatrics. 161(10). 528–530. 22 indexed citations
19.
Wilken, Bernd, Peter Dechent, Jochen Herms, et al.. (2000). Quantitative proton magnetic resonance spectroscopy of focal brain lesions. Pediatric Neurology. 23(1). 22–31. 49 indexed citations
20.
Pouwels, Petra J. W., Knut Brockmann, Bernd Kruse, et al.. (1999). Regional Age Dependence of Human Brain Metabolites from Infancy to Adulthood as Detected by Quantitative Localized Proton MRS. Pediatric Research. 46(4). 474–474. 246 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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