Thomas Sander

4.1k total citations
52 papers, 2.2k citations indexed

About

Thomas Sander is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Genetics. According to data from OpenAlex, Thomas Sander has authored 52 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 24 papers in Molecular Biology and 14 papers in Genetics. Recurrent topics in Thomas Sander's work include Neurotransmitter Receptor Influence on Behavior (14 papers), Neuroscience and Neuropharmacology Research (14 papers) and Receptor Mechanisms and Signaling (9 papers). Thomas Sander is often cited by papers focused on Neurotransmitter Receptor Influence on Behavior (14 papers), Neuroscience and Neuropharmacology Research (14 papers) and Receptor Mechanisms and Signaling (9 papers). Thomas Sander collaborates with scholars based in Germany, United States and Poland. Thomas Sander's co-authors include Georg Winterer, Ulf R. Rapp, Karin Moelling, P. Beimling, B. Heimann, Bryan T. MacDonald, Karsten Haug, Andrew Escayg, Armin Heils and Miriam H. Meisler and has published in prestigious journals such as Nature, PLoS ONE and NeuroImage.

In The Last Decade

Thomas Sander

52 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Thomas Sander Germany	28	961	843	565	560	369	52	2.2k
Vibeke S. Catts Australia	23	862 0.9×	619 0.7×	315 0.6×	574 1.0×	279 0.8×	48	2.7k
Thomas Sander Germany	30	1.2k 1.2×	1.6k 2.0×	640 1.1×	1.0k 1.8×	306 0.8×	67	2.9k
Paul R. Buckland United Kingdom	35	1.6k 1.6×	1.1k 1.3×	1.0k 1.8×	422 0.8×	319 0.9×	82	3.3k
Tomoko Toyota Japan	31	1.5k 1.5×	818 1.0×	850 1.5×	344 0.6×	398 1.1×	87	2.8k
Gillian Spurlock United Kingdom	25	1.2k 1.3×	938 1.1×	913 1.6×	561 1.0×	269 0.7×	60	2.8k
Frances E. Jensen United States	23	852 0.9×	1.4k 1.6×	225 0.4×	665 1.2×	487 1.3×	31	2.9k
Hugh Gurling United Kingdom	26	834 0.9×	417 0.5×	1.0k 1.8×	573 1.0×	389 1.1×	58	2.1k
Yoko Kinoshita Japan	28	715 0.7×	616 0.7×	571 1.0×	395 0.7×	224 0.6×	73	2.1k
Rami Abou Jamra Germany	29	1.4k 1.4×	544 0.6×	1.1k 2.0×	407 0.7×	244 0.7×	99	2.8k
Maile R. Brown United States	16	1.0k 1.1×	511 0.6×	557 1.0×	227 0.4×	284 0.8×	18	1.6k

Countries citing papers authored by Thomas Sander

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Sander

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Sander

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

All Works

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20 of 20 papers shown

Reinthaler, Eva M., Dennis Lal, Wiktor Jurkowski, et al.. (2014). Analysis of ELP4, SRPX2, and interacting genes in typical and atypical rolandic epilepsy. Epilepsia. 55(8). e89–93. 40 indexed citations

Lal, Dennis, Eva M. Reinthaler, Mohammad R. Toliat, et al.. (2013). Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy. PLoS ONE. 8(10). 18 indexed citations

Stölting, Gabriel, Julian Schubert, Rima Nabbout, et al.. (2013). Regulation of ClC-2 gating by intracellular ATP. Pflügers Archiv - European Journal of Physiology. 465(10). 1423–1437. 27 indexed citations

Pernhorst, Katharina, Pitt Niehusmann, Karen M. J. van Loo, et al.. (2011). Promoter Variants Determine γ-Aminobutyric Acid Homeostasis-Related Gene Transcription in Human Epileptic Hippocampi. Journal of Neuropathology & Experimental Neurology. 70(12). 1080–1088. 16 indexed citations

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

Giegling, Ina, Antonio Drago, Martin Schäfer, et al.. (2010). Lack of association between 71 variations located in candidate genes and response to acute haloperidol treatment. Psychopharmacology. 214(3). 719–728. 2 indexed citations

Giegling, Ina, Antonio Drago, Vita Dolžan, et al.. (2010). Glutamatergic gene variants impact the clinical profile of efficacy and side effects of haloperidol. Pharmacogenetics and Genomics. 21(4). 206–216. 18 indexed citations

Gallinat, Jürgen, et al.. (2009). Met carriers of BDNF Val66Met genotype show increased N-acetylaspartate concentration in the anterior cingulate cortex. NeuroImage. 49(1). 767–771. 38 indexed citations

Preuschhof, Claudia, Hauke R. Heekeren, Shu Li, et al.. (2009). KIBRA and CLSTN2 polymorphisms exert interactive effects on human episodic memory. Neuropsychologia. 48(2). 402–408. 60 indexed citations

10.

Winterer, Georg, Francesco Musso, Andreas Konrad, et al.. (2007). Association of attentional network function with exon 5 variations of the CHRNA4 gene. Human Molecular Genetics. 16(18). 2165–2174. 54 indexed citations

11.

Lohoff, Falk W., John P. Dahl, Thomas N. Ferraro, et al.. (2006). Variations in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) are Associated with Bipolar I Disorder. Neuropsychopharmacology. 31(12). 2739–2747. 52 indexed citations

12.

Fehr, Christoph, Thomas Sander, André Tadić, et al.. (2006). Confirmation of association of the GABRA2 gene with alcohol dependence by subtype-specific analysis. Psychiatric Genetics. 16(1). 9–17. 142 indexed citations

13.

Gallinat, Jürgen, Malek Bajbouj, Thomas Sander, et al.. (2003). Association of the G1947A COMT (Val108/158Met) gene polymorphism with prefrontal P300 during information processing. Biological Psychiatry. 54(1). 40–48. 137 indexed citations

14.

Sander, Thomas, et al.. (2000). Genetic variation of the glutamate transporter EAAT2 gene and vulnerability to alcohol dependence. Psychiatric Genetics. 10(3). 103–107. 32 indexed citations

15.

Sander, Thomas, Jerzy Samochowiec, Michael N. Smolka, et al.. (1999). Association analysis of exonic variants of the gene encoding the GABAB receptor and alcohol dependence. Psychiatric Genetics. 9(2). 69–74. 19 indexed citations

16.

Sander, Thomas, Rebekka Kretz, Herbert Schulz, et al.. (1998). Replication Analysis of a Putative Susceptibility Locus (EGI) for Idiopathic Generalized Epilepsy on Chromosome 8q24. Epilepsia. 39(7). 715–720. 13 indexed citations

17.

Delbrück, Sebastian, Sophia Brismar Wendel, Ingrid Grunewald, et al.. (1997). A novel allelic variant of the human serotonin transporter gene regulatory polymorphism. Cytogenetic and Genome Research. 79(3-4). 214–220. 62 indexed citations

18.

Finckh, Ulrich, Mario Giraldo‐Velásquez, Jörg Pelz, et al.. (1996). Dopamine D2 receptor gene (DRD2) haplotypes in Caucasians. Gene. 179(2). 251–255. 20 indexed citations

19.

Sander, Thomas & Laura Schmidt. (1994). Molecular Biological Perspectives in Treating Neuropsychiatric Disorders with Dopaminergic Drugs. Pharmacopsychiatry. 27(S 1). 11–14. 5 indexed citations

20.

Mant, R., Philip Asherson, Andrew A. Hicks, et al.. (1991). Exclusion of close linkage between GABA a receptor subunit 1a gene and schizophrenia using a microsatellite repeat marker. ORCA Online Research @Cardiff (Cardiff University). 1 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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