Karsten Haug

1.6k total citations
12 papers, 680 citations indexed

About

Karsten Haug is a scholar working on Molecular Biology, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Karsten Haug has authored 12 papers receiving a total of 680 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Psychiatry and Mental health and 5 papers in Genetics. Recurrent topics in Karsten Haug's work include Epilepsy research and treatment (6 papers), Ion channel regulation and function (4 papers) and Neuroscience and Neuropharmacology Research (4 papers). Karsten Haug is often cited by papers focused on Epilepsy research and treatment (6 papers), Ion channel regulation and function (4 papers) and Neuroscience and Neuropharmacology Research (4 papers). Karsten Haug collaborates with scholars based in Germany, Switzerland and United States. Karsten Haug's co-authors include Armin Heils, Bryan T. MacDonald, Andrew Escayg, Thomas Sander, Miriam H. Meisler, Kerstin Hallmann, Johannes Rebstock, Thomas Sander, Ortrud K. Steinlein and Uwe Runge and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Neuroreport.

In The Last Decade

Karsten Haug

12 papers receiving 663 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karsten Haug Germany 9 405 332 287 213 106 12 680
Katrien Smets Belgium 11 232 0.6× 264 0.8× 239 0.8× 126 0.6× 74 0.7× 13 567
Sawa Yasumoto Japan 17 344 0.8× 569 1.7× 253 0.9× 345 1.6× 190 1.8× 44 947
Marilena Vecchi Italy 15 255 0.6× 285 0.9× 99 0.3× 367 1.7× 164 1.5× 32 735
Hisashi Kawawaki Japan 12 173 0.4× 177 0.5× 96 0.3× 116 0.5× 78 0.7× 63 541
Nienke E. Verbeek Netherlands 18 308 0.8× 351 1.1× 152 0.5× 392 1.8× 136 1.3× 23 777
Noriyuki Akasaka Japan 14 175 0.4× 214 0.6× 122 0.4× 245 1.2× 122 1.2× 27 566
R. Gaggero Italy 16 162 0.4× 396 1.2× 153 0.5× 227 1.1× 199 1.9× 33 715
Husheng Wu China 12 336 0.8× 231 0.7× 302 1.1× 155 0.7× 40 0.4× 34 597
Shuji Wakai Japan 13 148 0.4× 84 0.3× 79 0.3× 62 0.3× 57 0.5× 35 376
Takeshi Okinaga Japan 14 160 0.4× 99 0.3× 58 0.2× 74 0.3× 79 0.7× 27 411

Countries citing papers authored by Karsten Haug

Since Specialization
Citations

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

Fields of papers citing papers by Karsten Haug

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karsten Haug

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

All Works

12 of 12 papers shown
1.
Stümm, Markus, Michael Entezami, Karsten Haug, et al.. (2013). Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe. Prenatal Diagnosis. 34(2). 185–191. 32 indexed citations
2.
Zechner, Ulrich, Nicolai Kohlschmidt, Karsten Haug, et al.. (2009). Familial Sotos syndrome caused by a novel missense mutation, C2175S, in NSD1 and associated with normal intelligence, insulin dependent diabetes, bronchial asthma, and lipedema. European Journal of Medical Genetics. 52(5). 306–310. 15 indexed citations
3.
Brichta, Lars, Irmgard Hölker, Karsten Haug, Thomas Klockgether, & Brunhilde Wirth. (2006). In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate. Annals of Neurology. 59(6). 970–975. 116 indexed citations
4.
Haug, Karsten, Thomas Sander, Uwe Runge, et al.. (2002). A Splice-Site Mutation in GABRG2 Associated With Childhood Absence Epilepsy and Febrile Convulsions. Archives of Neurology. 59(7). 1137–1137. 215 indexed citations
5.
Haug, Karsten, Kerstin Hallmann, Johannes Rebstock, et al.. (2001). The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy. Epilepsy Research. 47(3). 243–246. 29 indexed citations
6.
Haug, Karsten, et al.. (2001). Familial fatal fetal cardiomyopathy with isolated myocardial calcifications: A new syndrome?. American Journal of Medical Genetics. 101(3). 255–258. 5 indexed citations
7.
Escayg, Andrew, Armin Heils, Bryan T. MacDonald, et al.. (2001). A Novel SCN1A Mutation Associated with Generalized Epilepsy with Febrile Seizures Plus—and Prevalence of Variants in Patients with Epilepsy. The American Journal of Human Genetics. 68(4). 866–873. 220 indexed citations
8.
Haug, Karsten, Kerstin Hallmann, Steve Horvath, et al.. (2000). No evidence for association between the KCNQ3 gene and susceptibility to idiopathic generalized epilepsy. Epilepsy Research. 42(1). 57–62. 8 indexed citations
9.
Haug, Karsten, Thomas Sander, Kerstin Hallmann, et al.. (2000). The voltage-gated sodium channel β2-subunit gene and idiopathic generalized epilepsy. Neuroreport. 11(12). 2687–2689. 15 indexed citations
10.
Heils, Armin, Karsten Haug, Wolfram S. Kunz, et al.. (2000). Interleukin‐1β gene polymorphism and susceptibility to temporal lobe epilepsy with hippocampal sclerosis. Annals of Neurology. 48(6). 948–949. 1 indexed citations
11.
Haug, Karsten, et al.. (2000). OFD II, OFD VI, and Joubert syndrome manifestations in 2 sibs. American Journal of Medical Genetics. 91(2). 135–137. 19 indexed citations
12.
Haug, Karsten, Thomas Sander, Kerstin Hallmann, et al.. (2000). Association analysis between a regulatory-promoter polymorphism of the human monoamine oxidase A gene and idiopathic generalized epilepsy. Epilepsy Research. 39(2). 127–132. 5 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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