Eike Wegener

509 total citations
7 papers, 210 citations indexed

About

Eike Wegener is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Eike Wegener has authored 7 papers receiving a total of 210 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Eike Wegener's work include Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers) and RNA modifications and cancer (2 papers). Eike Wegener is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers) and RNA modifications and cancer (2 papers). Eike Wegener collaborates with scholars based in Germany, Israel and Canada. Eike Wegener's co-authors include Peter Huppke, Jutta Gärtner, Cornelia Brendel, Hauke Werner, Igor Nudelman, Valery Belakhov, Timor Baasov, Jutta Gärtner, Hanno J. Bolz and André Fischer and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Experimental Neurology.

In The Last Decade

Eike Wegener

7 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eike Wegener Germany	6	116	104	57	30	20	7	210
Marianna De Franceschi Italy	6	201 1.7×	265 2.5×	46 0.8×	28 0.9×	3 0.1×	6	380
Nisha Broodie United States	3	193 1.7×	61 0.6×	7 0.1×	16 0.5×	10 0.5×	3	268
Shujie Yu China	8	113 1.0×	106 1.0×	22 0.4×	21 0.7×	2 0.1×	14	202
Nicholas Rajan Belgium	8	213 1.8×	98 0.9×	39 0.7×	31 1.0×		12	256
Vamsee Pillalamarri United States	9	204 1.8×	222 2.1×	22 0.4×	12 0.4×	4 0.2×	10	388
Sonia Amabile Italy	6	148 1.3×	156 1.5×	33 0.6×	20 0.7×	1 0.1×	12	242
Vichithra R. B. Liyanage Canada	8	326 2.8×	283 2.7×	118 2.1×	11 0.4×	2 0.1×	8	452
Emmanuelle Lagrue France	8	110 0.9×	79 0.8×	41 0.7×	9 0.3×		20	229
Davide Aprile Italy	10	94 0.8×	61 0.6×	8 0.1×	47 1.6×	2 0.1×	17	213
Kirill Shkura United Kingdom	5	127 1.1×	58 0.6×	9 0.2×	5 0.2×	4 0.2×	5	212

Countries citing papers authored by Eike Wegener

Since Specialization

Citations

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

Fields of papers citing papers by Eike Wegener

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eike Wegener

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

All Works

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7 of 7 papers shown

1.

Wong, Keit Men, Eike Wegener, Alireza Baradaran‐Heravi, et al.. (2023). Evaluation of Novel Enhancer Compounds in Gentamicin-Mediated Readthrough of Nonsense Mutations in Rett Syndrome. International Journal of Molecular Sciences. 24(14). 11665–11665. 2 indexed citations

2.

Huppke, Peter, Eike Wegener, Jonathan Gilley, et al.. (2019). Homozygous NMNAT2 mutation in sisters with polyneuropathy and erythromelalgia. Experimental Neurology. 320. 112958–112958. 46 indexed citations

3.

Kettwig, Matthias, Orly Elpeleg, Eike Wegener, et al.. (2016). Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review. BMC Neurology. 16(1). 74–74. 17 indexed citations

4.

Huppke, Peter, Eike Wegener, Hanno J. Bolz, et al.. (2014). Tectonic gene mutations in patients with Joubert syndrome. European Journal of Human Genetics. 23(5). 616–620. 28 indexed citations

5.

Wegener, Eike, Cornelia Brendel, André Fischer, et al.. (2014). Characterization of the MeCP2R168X Knockin Mouse Model for Rett Syndrome. PLoS ONE. 9(12). e115444–e115444. 26 indexed citations

6.

Kolanczyk, Mateusz, Victor Mautner, Nadine Kossler, et al.. (2011). MIA is a potential biomarker for tumour load in neurofibromatosis type 1. BMC Medicine. 9(1). 82–82. 12 indexed citations

7.

Brendel, Cornelia, Valery Belakhov, Hauke Werner, et al.. (2010). Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model. Journal of Molecular Medicine. 89(4). 389–398. 79 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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