Jobst Meyer

8.6k total citations
41 papers, 1.8k citations indexed

About

Jobst Meyer is a scholar working on Psychiatry and Mental health, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Jobst Meyer has authored 41 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Psychiatry and Mental health, 19 papers in Molecular Biology and 14 papers in Cognitive Neuroscience. Recurrent topics in Jobst Meyer's work include Autism Spectrum Disorder Research (12 papers), Attention Deficit Hyperactivity Disorder (10 papers) and Bipolar Disorder and Treatment (10 papers). Jobst Meyer is often cited by papers focused on Autism Spectrum Disorder Research (12 papers), Attention Deficit Hyperactivity Disorder (10 papers) and Bipolar Disorder and Treatment (10 papers). Jobst Meyer collaborates with scholars based in Germany, United States and United Kingdom. Jobst Meyer's co-authors include Klaus‐Peter Lesch, Christine M. Freitag, Haukur Pálmason, Christiane Seitz, Susanne Jatzke, H. Beckmann, Rainald Mößner, Susann Hänig, Gerald Stöber and Peter Riederer and has published in prestigious journals such as Biological Psychiatry, The American Journal of Human Genetics and Neuropsychopharmacology.

In The Last Decade

Jobst Meyer

41 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jobst Meyer Germany 24 590 573 508 446 387 41 1.8k
Ursula M. D’Souza United Kingdom 20 506 0.9× 527 0.9× 331 0.7× 301 0.7× 697 1.8× 34 1.7k
Paul McBride United States 19 712 1.2× 588 1.0× 673 1.3× 249 0.6× 415 1.1× 43 2.2k
Keeley J. Brookes United Kingdom 26 759 1.3× 453 0.8× 488 1.0× 321 0.7× 269 0.7× 57 1.9k
Stella G. Giakoumaki Greece 24 620 1.1× 378 0.7× 518 1.0× 247 0.6× 431 1.1× 60 1.6k
Raffaella Romano Italy 21 532 0.9× 481 0.8× 770 1.5× 296 0.7× 476 1.2× 43 1.8k
Maria Skibińska Poland 26 835 1.4× 383 0.7× 472 0.9× 426 1.0× 585 1.5× 107 2.1k
Yana V. Syagailo Germany 18 332 0.6× 653 1.1× 208 0.4× 287 0.6× 648 1.7× 29 1.8k
Shiro Suda Japan 22 320 0.5× 450 0.8× 739 1.5× 501 1.1× 458 1.2× 29 1.9k
Sibylle G. Schwab Germany 31 473 0.8× 1.0k 1.8× 400 0.8× 1.2k 2.8× 641 1.7× 62 2.7k
Virginia L. Willour United States 24 608 1.0× 665 1.2× 209 0.4× 788 1.8× 408 1.1× 45 2.3k

Countries citing papers authored by Jobst Meyer

Since Specialization
Citations

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

Fields of papers citing papers by Jobst Meyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jobst Meyer

This figure shows the co-authorship network connecting the top 25 collaborators of Jobst Meyer. A scholar is included among the top collaborators of Jobst Meyer 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 Jobst Meyer. Jobst Meyer 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
1.
Waltes, Regina, Christine M. Freitag, Thomas Lempp, et al.. (2019). Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study. Journal of Neural Transmission. 126(12). 1679–1693. 4 indexed citations
2.
Schote, Andrea B., Martina Bonenberger, Haukur Pálmason, et al.. (2016). Glucocorticoid receptor variants in childhood attention-deficit/hyperactivity disorder and comorbid psychiatric disorders. Psychiatry Research. 246. 275–283. 13 indexed citations
3.
Chiocchetti, Andreas G., Marnie Kopp, Regina Waltes, et al.. (2014). Variants of the CNTNAP2 5′ promoter as risk factors for autism spectrum disorders: a genetic and functional approach. Molecular Psychiatry. 20(7). 839–849. 37 indexed citations
4.
Ribasès, Marta, Josep Antoni Ramos‐Quiroga, Amaia Hervás, et al.. (2012). Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association withDRD1. The World Journal of Biological Psychiatry. 13(4). 281–292. 30 indexed citations
5.
Hänig, Susann, et al.. (2011). Risk factors of autistic symptoms in children with ADHD. European Child & Adolescent Psychiatry. 20(11-12). 561–570. 32 indexed citations
6.
Freitag, Christine M., Susann Hänig, Anna Schneider, et al.. (2011). Biological and psychosocial environmental risk factors influence symptom severity and psychiatric comorbidity in children with ADHD. Journal of Neural Transmission. 119(1). 81–94. 46 indexed citations
7.
Freitag, Christine M., Konstantin Agelopoulos, Matthias Rothermundt, et al.. (2009). Adenosine A2A receptor gene (ADORA2A) variants may increase autistic symptoms and anxiety in autism spectrum disorder. European Child & Adolescent Psychiatry. 19(1). 67–74. 58 indexed citations
8.
Pálmason, Haukur, Dirk Moser, Christian Vogler, et al.. (2009). Attention-deficit/hyperactivity disorder phenotype is influenced by a functional catechol-O-methyltransferase variant. Journal of Neural Transmission. 117(2). 259–267. 27 indexed citations
9.
Lesch, Klaus‐Peter, Nina Timmesfeld, Tobias Renner, et al.. (2008). Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. Journal of Neural Transmission. 115(11). 1573–1585. 268 indexed citations
10.
Schimmelmann, Benno G., Susann Friedel, Astrid Dempfle, et al.. (2007). No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD. Journal of Neural Transmission. 114(4). 523–526. 25 indexed citations
11.
Wendland, Jens R., Michael Hampe, Timothy K. Newman, et al.. (2005). Structural variation of the monoamine oxidase A gene promoter repeat polymorphism in nonhuman primates. Genes Brain & Behavior. 5(1). 40–45. 29 indexed citations
12.
Hohoff, Christa, Katharina Domschke, Philipp Sand, et al.. (2004). Norepinephrine transporter (NET) promoter and 5′-UTR polymorphisms: association analysis in panic disorder. Neuroscience Letters. 377(1). 40–43. 32 indexed citations
13.
14.
Steinke, Verena, Jobst Meyer, Yana V. Syagailo, et al.. (2003). The genomic organization of the murine Mlc1 ( Wkl1 , KIAA0027 ) gene. Journal of Neural Transmission. 110(4). 333–343. 5 indexed citations
15.
Syagailo, Yana V., Olga Okladnova, Rainald Mößner, et al.. (2002). Structural and functional characterization of the human PAX7 5′-flanking regulatory region. Gene. 294(1-2). 259–268. 15 indexed citations
16.
Meyer, Jobst, Rainald Mößner, Thomas Tatschner, et al.. (2002). Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene ( HTR2C ) are not associated with bipolar disorder in females. Journal of Neural Transmission. 109(5-6). 939–946. 13 indexed citations
17.
Meyer, Jobst, Guillermo J. Ortega, Yana V. Syagailo, et al.. (2001). A missense mutation in a novel gene encoding a putative cation channel is associated with catatonic schizophrenia in a large pedigree. Molecular Psychiatry. 6(3). 302–306. 73 indexed citations
18.
Lesch, Klaus‐Peter, Susanne Jatzke, Jobst Meyer, et al.. (1999). Mosaicism for a serotonin transporter gene promoter-associated deletion: decreased recombination in depression. Journal of Neural Transmission. 106(11-12). 1223–1230. 29 indexed citations
19.
Stöber, Gerald, Susanne Jatzke, Jobst Meyer, et al.. (1998). Short CAG repeats within the hSKCa3 gene associated with schizophrenia. Neuroreport. 9(16). 3595–3599. 31 indexed citations
20.
Meyer, Jobst, Philipp Wiedemann, Olga Okladnova, et al.. (1998). Cloning and functional characterization of the human norepinephrine transporter gene promoter. Journal of Neural Transmission. 105(10-12). 1341–1350. 57 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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