T. Sander

1.6k total citations
31 papers, 1.3k citations indexed

About

T. Sander is a scholar working on Psychiatry and Mental health, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, T. Sander has authored 31 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Psychiatry and Mental health, 13 papers in Cellular and Molecular Neuroscience and 9 papers in Molecular Biology. Recurrent topics in T. Sander's work include Epilepsy research and treatment (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Neuroscience and Neuropharmacology Research (7 papers). T. Sander is often cited by papers focused on Epilepsy research and treatment (11 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Neuroscience and Neuropharmacology Research (7 papers). T. Sander collaborates with scholars based in Germany, Austria and United States. T. Sander's co-authors include Laura Schmidt, H. Rommelspacher, Jerzy Samochowiec, Michael N. Smolka, Simone Kühn, Helmut Harms, Klaus‐Peter Lesch, Lutz G. Schmidt, Diéter Janz and G. Beck‐Mannagetta and has published in prestigious journals such as Physical review. B, Condensed matter, Journal of Applied Physics and Neurology.

In The Last Decade

T. Sander

30 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Sander Germany 18 659 449 363 297 109 31 1.3k
Zbigniew Jankowski Poland 14 264 0.4× 316 0.7× 141 0.4× 200 0.7× 77 0.7× 79 1.2k
Yana V. Syagailo Germany 18 648 1.0× 653 1.5× 332 0.9× 287 1.0× 285 2.6× 29 1.8k
Michel Simonneau France 26 623 0.9× 998 2.2× 141 0.4× 451 1.5× 34 0.3× 77 2.5k
W.M.A. Verhoeven Netherlands 21 490 0.7× 446 1.0× 384 1.1× 174 0.6× 227 2.1× 90 1.3k
Susan M. Ferguson United States 22 1.3k 1.9× 736 1.6× 98 0.3× 156 0.5× 101 0.9× 55 2.1k
Ivanka Savić Sweden 25 618 0.9× 168 0.4× 1.0k 2.8× 198 0.7× 76 0.7× 42 1.9k
Toshiaki Hashimoto Japan 27 297 0.5× 568 1.3× 531 1.5× 639 2.2× 187 1.7× 152 2.5k
D. S. Jessop United Kingdom 28 477 0.7× 259 0.6× 97 0.3× 79 0.3× 69 0.6× 56 2.8k
Masahito Miyazaki Japan 22 252 0.4× 315 0.7× 383 1.1× 486 1.6× 84 0.8× 81 2.0k
R.D. Todd United States 27 942 1.4× 1.2k 2.6× 301 0.8× 197 0.7× 108 1.0× 44 2.1k

Countries citing papers authored by T. Sander

Since Specialization
Citations

This map shows the geographic impact of T. Sander'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 T. Sander with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Sander more than expected).

Fields of papers citing papers by T. Sander

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of T. Sander

This figure shows the co-authorship network connecting the top 25 collaborators of T. Sander. A scholar is included among the top collaborators of T. Sander 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 T. Sander. T. Sander 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
2.
Schubert, F., Tomislav Majić, Undine E. Lang, et al.. (2012). DTNBP1 (Dysbindin) Gene Variants: In Vivo Evidence for Effects on Hippocampal Glutamate Status. Current Pharmaceutical Biotechnology. 13(8). 1513–1521. 8 indexed citations
3.
Lang, Undine E., Rainer Hellweg, Malek Bajbouj, et al.. (2008). Gender-dependent Association of a Functional NGF Polymorphism with Anxiety-related Personality Traits. Pharmacopsychiatry. 41(5). 196–199. 24 indexed citations
4.
Lenzen, Kirsten P., Armin Heils, Susanne Lorenz, et al.. (2005). Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy. Epilepsy Research. 63(2-3). 113–118. 49 indexed citations
5.
Windemuth, Christine, Herbert Schulz, Kathrin Saar, et al.. (2002). No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures. Epilepsy Research. 51(1-2). 23–29. 5 indexed citations
6.
Sander, T., et al.. (2001). Allelic and genotypic variation of 13 European beech (Fagus sylvatica L.) - populations in Hesse, Germany. 8(1). 13–24. 4 indexed citations
7.
Ziehe, Martin, et al.. (2000). Genetic variation of beech (Fagus sylvatica L.) in Germany: joint evaluation of genetic inventories from several Federal States.. 55(13). 403–408. 6 indexed citations
8.
Schmidt, Laura & T. Sander. (2000). Genetics of alcohol withdrawal. European Psychiatry. 15(2). 135–139. 31 indexed citations
9.
Schmidt, Laura, T. Sander, Simone Kühn, et al.. (2000). Different allele distribution of a regulatory MAOA gene promoter polymorphism in antisocial and anxious-depressive alcoholics. Journal of Neural Transmission. 107(6). 681–689. 79 indexed citations
10.
Sander, T.. (2000). Genome search for susceptibility loci of common idiopathic generalised epilepsies. Human Molecular Genetics. 9(10). 1465–1472. 124 indexed citations
11.
Kremerskothen, Joachim, Kerstin Hallmann, T. Sander, et al.. (2000). Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy. Molecular and Cellular Probes. 14(4). 255–260. 11 indexed citations
12.
Sander, T., et al.. (2000). Genetic variation of European beech (Fagus sylvatica L.) along an altitudinal transect at mount Vogelsberg in Hesse, Germany. Molecular Ecology. 9(9). 1349–1361. 22 indexed citations
13.
Sander, T., Christian Peters, Jerzy Samochowiec, et al.. (1999). Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy. American Journal of Medical Genetics. 88(4). 305–310. 34 indexed citations
14.
Sander, T., Christian Peters, Diéter Janz, et al.. (1998). The gene encoding the α1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy. Epilepsy Research. 29(2). 115–122. 16 indexed citations
15.
Sander, T., Helmut Harms, P. Dufeu, et al.. (1997). Dopamine D4 receptor exon III alleles and variation of novelty seeking in alcoholics. American Journal of Medical Genetics. 74(5). 483–487. 106 indexed citations
16.
Sander, T., S. N. Holmes, J. J. Harris, D. K. Maude, & J.C. Portal. (1996). Magnetoresistance oscillations due to intersubband scattering in a two-dimensional electron system. Surface Science. 361-362. 564–568. 7 indexed citations
17.
Sander, T., Helmut Harms, Jan Podschus, et al.. (1995). Dopamine D1, D2 and D3 receptor genes in alcohol dependence. Psychiatric Genetics. 5(4). 171–176. 82 indexed citations
18.
Sander, T., Thomas Hildmann, Diéter Janz, et al.. (1995). The phenotypic spectrum related to the human epilepsy susceptibility gene “EJM1”. Annals of Neurology. 38(2). 210–217. 34 indexed citations
19.
Sander, T., Diéter Janz, Christian Ramel, et al.. (1995). Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies. Neurology. 45(9). 1713–1720. 17 indexed citations
20.
Janz, Diéter, G. Beck‐Mannagetta, & T. Sander. (1992). Do idiopathic generalized epilepsies share a common susceptibility gene?. PubMed. 42(4 Suppl 5). 48–55. 54 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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