T. Sander

1.5k total citations
10 papers, 660 citations indexed

About

T. Sander is a scholar working on Genetics, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, T. Sander has authored 10 papers receiving a total of 660 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Psychiatry and Mental health and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in T. Sander's work include Genetics and Neurodevelopmental Disorders (5 papers), Epilepsy research and treatment (4 papers) and Genomics and Rare Diseases (3 papers). T. Sander is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Epilepsy research and treatment (4 papers) and Genomics and Rare Diseases (3 papers). T. Sander collaborates with scholars based in Germany, United States and Australia. T. Sander's co-authors include Diéter Janz, G. Beck‐Mannagetta, M. Durner, Keith Johnson, David A. Greenberg, John P. Dahl, Jürgen Gallinat, Juergen Gallinat, Thomas N. Ferraro and Falk W. Lohoff and has published in prestigious journals such as Neurology, Human Molecular Genetics and Neuropsychopharmacology.

In The Last Decade

T. Sander

10 papers receiving 646 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
T. Sander Germany	10	343	287	193	182	126	10	660
J Schumacher Germany	7	497 1.4×	339 1.2×	149 0.8×	366 2.0×	100 0.8×	8	944
Johannes Schumacher Germany	13	273 0.8×	178 0.6×	352 1.8×	249 1.4×	249 2.0×	26	846
Michael John Owen United Kingdom	8	182 0.5×	125 0.4×	173 0.9×	216 1.2×	54 0.4×	27	485
В. Г. Каледа Russia	12	114 0.3×	179 0.6×	119 0.6×	193 1.1×	111 0.9×	109	549
D. Samolyk France	11	166 0.5×	108 0.4×	301 1.6×	251 1.4×	26 0.2×	14	579
Ling Morgan United States	10	148 0.4×	115 0.4×	98 0.5×	359 2.0×	49 0.4×	11	660
René Breuer Germany	14	235 0.7×	186 0.6×	89 0.5×	213 1.2×	82 0.7×	16	614
N. Craddock United Kingdom	8	207 0.6×	255 0.9×	109 0.6×	170 0.9×	100 0.8×	15	605
Jesús Machado‐Salas Mexico	11	145 0.4×	223 0.8×	188 1.0×	137 0.8×	86 0.7×	15	547
Brandi L. Galke United States	9	337 1.0×	158 0.6×	224 1.2×	356 2.0×	272 2.2×	9	983

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

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10 of 10 papers shown

Striano, Pasquale, Yvonne Weber, Mohammad R. Toliat, et al.. (2012). GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy. Neurology. 78(8). 557–562. 65 indexed citations

Kovel, Carolien G. F. de, Dalila Pinto, Ulrike Tauer, et al.. (2010). Whole-genome linkage scan for epilepsy-related photosensitivity: A mega-analysis. Epilepsy Research. 89(2-3). 286–294. 33 indexed citations

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

Neuhaus, Andres H., Carolin Opgen‐Rhein, Carsten Urbanek, et al.. (2009). COMT Val¹⁵⁸Met Polymorphism is Associated with Cognitive Flexibility in a Signal Discrimination Task in Schizophrenia. Pharmacopsychiatry. 42(4). 141–144. 12 indexed citations

Lang, Undine E., et al.. (2007). Gender-Dependent Association of the Functional Catechol-O-Methyltransferase Val158Met Genotype with Sensation Seeking Personality Trait. Neuropsychopharmacology. 32(9). 1950–1955. 66 indexed citations

Lohoff, Falk W., T. Sander, Thomas N. Ferraro, et al.. (2005). Confirmation of association between the Val66Met polymorphism in the brain‐derived neurotrophic factor (BDNF) gene and bipolar I disorder. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 139B(1). 51–53. 101 indexed citations

Sander, T., et al.. (2001). Genetic variation of the human glycine receptor subunit genes GLRA3 and GLRB and susceptibility to idiopathic generalized epilepsies. American Journal of Medical Genetics. 105(6). 534–538. 9 indexed citations

Sander, T., et al.. (1999). Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsy. Epilepsy Research. 33(2-3). 227–233. 13 indexed citations

Sander, T.. (1996). The genetics of idiopathic generalized epilepsy: implications for the understanding of its aetiology. Molecular Medicine Today. 2(4). 173–179. 38 indexed citations

10.

Durner, M., T. Sander, David A. Greenberg, et al.. (1991). Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients. Neurology. 41(10). 1651–1651. 155 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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