Bernhard Weschke

4.1k total citations
23 papers, 985 citations indexed

About

Bernhard Weschke is a scholar working on Molecular Biology, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Bernhard Weschke has authored 23 papers receiving a total of 985 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Psychiatry and Mental health and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Bernhard Weschke's work include Epilepsy research and treatment (3 papers), Pharmacological Effects and Toxicity Studies (3 papers) and Genomics and Rare Diseases (2 papers). Bernhard Weschke is often cited by papers focused on Epilepsy research and treatment (3 papers), Pharmacological Effects and Toxicity Studies (3 papers) and Genomics and Rare Diseases (2 papers). Bernhard Weschke collaborates with scholars based in Germany, United States and Netherlands. Bernhard Weschke's co-authors include Birgit Uhlenberg, Barbara Plecko, Heymut Omran, Uta Tacke, Cornelis Jakobs, Matthias R. Baumgartner, Michèl A.A.P. Willemsen, Philippa B. Mills, Peter Baxter and Peter T. Clayton and has published in prestigious journals such as Nature Medicine, PLoS ONE and Neurology.

In The Last Decade

Bernhard Weschke

22 papers receiving 969 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bernhard Weschke Germany 13 547 298 164 152 133 23 985
Birgit Uhlenberg Germany 10 529 1.0× 273 0.9× 81 0.5× 175 1.2× 160 1.2× 16 981
Ángeles García‐Cazorla Spain 16 550 1.0× 616 2.1× 129 0.8× 204 1.3× 132 1.0× 37 1.1k
Mizue Iai Japan 17 431 0.8× 117 0.4× 77 0.5× 191 1.3× 174 1.3× 48 856
Daria Diodato Italy 18 868 1.6× 535 1.8× 88 0.5× 89 0.6× 56 0.4× 44 1.2k
Denise Cassandrini Italy 23 735 1.3× 228 0.8× 252 1.5× 176 1.2× 57 0.4× 62 1.3k
Saadet Mercimek‐Andrews Canada 13 276 0.5× 189 0.6× 71 0.4× 226 1.5× 95 0.7× 52 623
Kaja Kristine Selmer Norway 22 342 0.6× 236 0.8× 337 2.1× 277 1.8× 189 1.4× 65 1.1k
Saadet Mercimek‐Mahmutoglu Canada 22 720 1.3× 777 2.6× 227 1.4× 377 2.5× 232 1.7× 51 1.7k
Hendrik Rosewich Germany 18 567 1.0× 137 0.5× 105 0.6× 120 0.8× 35 0.3× 34 857
Luc Régal Belgium 15 336 0.6× 84 0.3× 195 1.2× 117 0.8× 43 0.3× 33 689

Countries citing papers authored by Bernhard Weschke

Since Specialization
Citations

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

Fields of papers citing papers by Bernhard Weschke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bernhard Weschke

This figure shows the co-authorship network connecting the top 25 collaborators of Bernhard Weschke. A scholar is included among the top collaborators of Bernhard Weschke 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 Bernhard Weschke. Bernhard Weschke 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.
Schmid, Oliver, et al.. (2023). Successful Prenatal Treatment of Cardiac Rhabdomyoma in a Fetus with Tuberous Sclerosis. Pediatric Reports. 15(1). 245–253. 18 indexed citations
2.
Becker, Lena‐Luise, Hormos Salimi Dafsari, Jens Schallner, et al.. (2020). The clinical-phenotype continuum in DYNC1H1-related disorders—genomic profiling and proposal for a novel classification. Journal of Human Genetics. 65(11). 1003–1017. 31 indexed citations
3.
Rafay, Mubeen F., Kevin A. Shapiro, Gabrielle deVeber, et al.. (2020). Spectrum of cerebral arteriopathies in children with arterial ischemic stroke. Neurology. 94(23). e2479–e2490. 24 indexed citations
4.
Jaite, Charlotte, Viola Kappel, Gerd Diederichs, et al.. (2019). A comparison study of anxiety in children undergoing brain MRI vs adults undergoing brain MRI vs children undergoing an electroencephalogram. PLoS ONE. 14(3). e0211552–e0211552. 9 indexed citations
5.
Weschke, Bernhard, Christoph Hertzberg, Katarzyna Kotulska, et al.. (2019). First Results of the EPISTOP Study. Neuropediatrics. 1 indexed citations
6.
Weschke, Bernhard, et al.. (2017). Lacosamide Lowers Valproate and Levetiracetam Levels. Neuropediatrics. 48(3). 188–189. 5 indexed citations
7.
Weschke, Bernhard, et al.. (2017). Lacosamide Lowers Valproate and Levetiracetam Levels. Neuropediatrics. 48(S 01). S1–S45.
8.
Horn, Denise, Bernhard Weschke, Ellen Knierim, et al.. (2016). BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood. American Journal of Medical Genetics Part A. 170(9). 2274–2281. 21 indexed citations
9.
Krause, Patricia, Axel Lipp, Andreas Horn, et al.. (2016). Long-term results of deep brain stimulation in a cohort of eight children with isolated dystonia. Journal of Neurology. 263(11). 2319–2326. 26 indexed citations
10.
Thumfart, Julia, et al.. (2016). Acute renal failure unmasking Lesch-Nyhan disease in a patient with tuberous sclerosis complex. European Journal of Paediatric Neurology. 20(4). 649–651. 6 indexed citations
11.
Groeschel, Samuel, Jörn‐Sven Kühl, Annette Bley, et al.. (2016). Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients. JAMA Neurology. 73(9). 1133–1133. 90 indexed citations
12.
Obermeier, Patrick, Christian Hoppe, Lea Seeber, et al.. (2015). Acute Disseminated Encephalomyelitis After Human Parechovirus Infection. The Pediatric Infectious Disease Journal. 35(1). 35–38. 10 indexed citations
13.
Noort, Betteke Maria van, Bernhard Weschke, Christian Bachmann, et al.. (2015). Anti-NMDA receptor encephalitis presenting as atypical anorexia nervosa: an adolescent case report. European Child & Adolescent Psychiatry. 24(11). 1321–1324. 12 indexed citations
14.
Jaite, Charlotte, Christian Bachmann, Marc Dewey, et al.. (2013). Magnetresonanztomographie (MRT) bei Kindern und Jugendlichen. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie. 41(6). 447–451. 1 indexed citations
15.
Knierim, Ellen, Lilia Leisle, C. N. J. Wagner, et al.. (2010). Recurrent Stroke Due to a Novel Voltage Sensor Mutation in Ca v 2.1 Responds to Verapamil. Stroke. 42(2). e14–7. 36 indexed citations
16.
Mills, Philippa B., Eduard A. Struys, Cornelis Jakobs, et al.. (2006). Mutations in antiquitin in individuals with pyridoxine-dependent seizures. Nature Medicine. 12(3). 307–309. 392 indexed citations
17.
Ruf, Nico, et al.. (2006). Oligodendroglial transcription factor (OLIG1 and OLIG2) mutations are not associated with Pelizaeus–Merzbacher‐like leukodystrophy. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(3). 365–366. 1 indexed citations
18.
Uhlenberg, Birgit, Markus Schuelke, Franz Rüschendorf, et al.. (2004). Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease. The American Journal of Human Genetics. 75(2). 251–260. 217 indexed citations
19.
Siemes, H., Ulrich Brandl, H. L. Spohr, Sheri Volger, & Bernhard Weschke. (1998). Long-term follow-up study of vigabatrin in pretreated children with west syndrome. Seizure. 7(4). 293–297. 13 indexed citations
20.
Bartsch, Oliver, Bernhard Weschke, & Bruno Weber. (1988). Oestrogen treatment of constitutionally tall girls with 0.1 mg/day ethinyl oestradiol. European Journal of Pediatrics. 147(1). 59–63. 22 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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