Markus M. N�then

772 total citations
14 papers, 621 citations indexed

About

Markus M. N�then is a scholar working on Genetics, Cellular and Molecular Neuroscience and Clinical Psychology. According to data from OpenAlex, Markus M. N�then has authored 14 papers receiving a total of 621 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Cellular and Molecular Neuroscience and 5 papers in Clinical Psychology. Recurrent topics in Markus M. N�then's work include Bipolar Disorder and Treatment (4 papers), Genetic Associations and Epidemiology (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Markus M. N�then is often cited by papers focused on Bipolar Disorder and Treatment (4 papers), Genetic Associations and Epidemiology (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Markus M. N�then collaborates with scholars based in Germany, United States and Sweden. Markus M. N�then's co-authors include Peter Propping, Helge Neidt, Marcella Rietschel, Andreas Papassotiropoulos, Wolfgang Maier, Sven Cichon, Wolfgang Maier, Michael Knapp, Petra Franke and Thomas G. Schulze and has published in prestigious journals such as Human Genetics, American Journal of Medical Genetics and Der Hautarzt.

In The Last Decade

Markus M. N�then

14 papers receiving 602 citations

Peers

Markus M. N�then

CMN

PMH

GENET

Helge Neidt Germany

U. Balling Germany

Tokutaro Komiyama Japan

Richard D. Todd United States

Christo Minov Germany

Stephen Morris United States

Anne Tammimäki Finland

Raymond Crowe United States

B P Riley United Kingdom

Katsumasa Miyasato Japan

Helge Neidt Germany

Markus M. N�then

564 ×1.9

CMN

265 ×1.6

217 ×1.5

PMH

160 ×1.1

GENET

174 ×1.4

Citations per year, relative to Markus M. N�then Markus M. N�then (= 1×) peers Helge Neidt

Countries citing papers authored by Markus M. N�then

Since Specialization

Citations

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

Fields of papers citing papers by Markus M. N�then

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Markus M. N�then. 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 Markus M. N�then. The network helps show where Markus M. N�then may publish in the future.

Co-authorship network of co-authors of Markus M. N�then

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

All Works

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14 of 14 papers shown

Schumacher, Johannes, A Otte, Tim Becker, et al.. (2003). No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach. Human Genetics. 114(1). 115–117. 13 indexed citations

Franke, Petra, Tao Wang, Markus M. N�then, et al.. (2001). Nonreplication of association between ?-opioid-receptor gene (OPRM1) A118G polymorphism and substance dependence. American Journal of Medical Genetics. 105(1). 114–119. 81 indexed citations

Rietschel, Marcella, Margot Albus, Ernst Franzek, et al.. (2000). Association study of the tryptophan hydroxylase gene and bipolar affective disorder using family-based internal controls. American Journal of Medical Genetics. 96(3). 310–311. 11 indexed citations

Cichon, Sven, Markus M. N�then, Marcella Rietschel, & Peter Propping. (2000). Pharmacogenetics of schizophrenia. American Journal of Medical Genetics. 97(1). 98–106. 39 indexed citations

Vogt, Ina R., Daphne Shimron‐Abarbanell, Helge Neidt, et al.. (2000). Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia. American Journal of Medical Genetics. 96(2). 217–221. 54 indexed citations

Schulze, Thomas G., Harald Krauß, Harald Scherk, et al.. (2000). Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder. American Journal of Medical Genetics. 96(6). 801–803. 138 indexed citations

Franke, Petra, Markus M. N�then, Helge Neidt, et al.. (1999). Human ?-opioid receptor gene and susceptibility to heroin and alcohol dependence. American Journal of Medical Genetics. 88(5). 462–464. 51 indexed citations

Hebebrand, Johannes, Sven Cichon, Gerd Lehmkuhl, et al.. (1999). Tourette syndrome and the norepinephrine transporter gene: Results of a systematic mutation screening. American Journal of Medical Genetics. 88(2). 158–163. 34 indexed citations

Gustavsson, Petter, Markus M. N�then, Helge Neidt, et al.. (1999). No association between serotonin transporter gene polymorphisms and personality traits. American Journal of Medical Genetics. 88(4). 430–436. 60 indexed citations

10.

Meyer, Klaus, et al.. (1999). Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors: Replication tests. American Journal of Medical Genetics. 88(2). 168–172. 75 indexed citations

11.

N�then, Markus M., Margot Albus, Ernst Franzek, et al.. (1998). Adenosine A1 receptor and bipolar affective disorder: systematic screening of the gene and association studies. American Journal of Medical Genetics. 81(1). 18–23. 13 indexed citations

12.

Grigoroiu‐Serbânescu, Maria, et al.. (1998). Patterns of parental transmission and familial aggregation models in bipolar affective disorder. American Journal of Medical Genetics. 81(5). 397–404. 21 indexed citations

13.

Rietschel, Marcella, et al.. (1994). Pemphigus chronicus benignus familiaris (Morbus Hailey-Hailey) und bipolare affektive Erkrankung bei drei Mitgliedern einer Familie. Der Hautarzt. 45(5). 313–317. 6 indexed citations

14.

N�then, Markus M., Thomas Eggermann, Jeanette Erdmann, et al.. (1993). Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome). Human Genetics. 92(4). 347–349. 25 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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