Holger Trucks

1.4k total citations
5 papers, 279 citations indexed

About

Holger Trucks is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Holger Trucks has authored 5 papers receiving a total of 279 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Holger Trucks's work include Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Holger Trucks is often cited by papers focused on Genomics and Rare Diseases (1 paper), Ion channel regulation and function (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). Holger Trucks collaborates with scholars based in Germany, Australia and Italy. Holger Trucks's co-authors include Susannah T. Bellows, Michael Wittig, Heather C. Mefford, Leanne M. Dibbens, Costin Leu, Thomas Sander, Samuel F. Berkovic, Ingrid E. Scheffer, Zühal Yapıcı and T. Sander and has published in prestigious journals such as Human Molecular Genetics, Epilepsia and Neurobiology of Disease.

In The Last Decade

Holger Trucks

5 papers receiving 273 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Holger Trucks Germany	5	176	119	52	49	30	5	279
Adeline Ngoh United Kingdom	8	175 1.0×	136 1.1×	136 2.6×	69 1.4×	35 1.2×	15	367
Shujie Yu China	8	106 0.6×	113 0.9×	41 0.8×	26 0.5×	9 0.3×	14	202
Victoria‐Elisabeth Gruber Austria	7	50 0.3×	118 1.0×	34 0.7×	56 1.1×	19 0.6×	9	244
Mafalda Barbosa Portugal	7	221 1.3×	166 1.4×	13 0.3×	68 1.4×	33 1.1×	8	330
Claudia Di Berardino Italy	4	113 0.6×	189 1.6×	74 1.4×	85 1.7×	16 0.5×	7	280
Elizabeth Butler United States	7	299 1.7×	208 1.7×	146 2.8×	59 1.2×	30 1.0×	13	468
Caroline F. Bruinsma Netherlands	5	225 1.3×	223 1.9×	13 0.3×	30 0.6×	36 1.2×	5	318
Elżbieta Szczepanik Poland	9	48 0.3×	113 0.9×	41 0.8×	28 0.6×	24 0.8×	32	208
Stavroula Psoni Greece	8	313 1.8×	212 1.8×	37 0.7×	20 0.4×	17 0.6×	11	393
Paul Thiry Belgium	7	186 1.1×	141 1.2×	165 3.2×	84 1.7×	72 2.4×	8	333

Countries citing papers authored by Holger Trucks

Since Specialization

Citations

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

Fields of papers citing papers by Holger Trucks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Holger Trucks

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

All Works

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5 of 5 papers shown

1.

Menzler, Katja, Anke Hermsen, Sebastian Bauer, et al.. (2014). A common SCN1A splice‐site polymorphism modifies the effect of carbamazepine on cortical excitability—A pharmacogenetic transcranial magnetic stimulation study. Epilepsia. 55(2). 362–369. 23 indexed citations

2.

Dejanovic, Borislav, Dennis Lal, Claudia B. Catarino, et al.. (2014). Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy. Neurobiology of Disease. 67. 88–96. 43 indexed citations

3.

Biancheri, Roberta, Denise Cassandrini, Rosanna Trovato, et al.. (2013). EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. Journal of Neurology. 260(7). 1866–1870. 19 indexed citations

4.

Steinlein, Ortrud K., et al.. (2011). Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta. BMC Medical Genetics. 12(1). 152–152. 26 indexed citations

5.

Dibbens, Leanne M., Saul A. Mullen, Katherine L. Helbig, et al.. (2009). Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Human Molecular Genetics. 18(19). 3626–3631. 168 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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