Jobst Meyer

3.0k total citations · 1 hit paper
48 papers, 2.3k citations indexed

About

Jobst Meyer is a scholar working on Molecular Biology, Behavioral Neuroscience and Genetics. According to data from OpenAlex, Jobst Meyer has authored 48 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 12 papers in Behavioral Neuroscience and 12 papers in Genetics. Recurrent topics in Jobst Meyer's work include Stress Responses and Cortisol (12 papers), Hormonal Regulation and Hypertension (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Jobst Meyer is often cited by papers focused on Stress Responses and Cortisol (12 papers), Hormonal Regulation and Hypertension (7 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Jobst Meyer collaborates with scholars based in Germany, Luxembourg and United Kingdom. Jobst Meyer's co-authors include Jutta Wirth, W. Schempp, Gerd Scherer, Thomas Wagner, U. Wolf, Juan J. Pasantes, F. Dagna Bricarelli, Niels Tommerup, Bernhard Zabel and Elisabeth Hustert and has published in prestigious journals such as Cell, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Jobst Meyer

47 papers receiving 2.3k citations

Hit Papers

Autosomal sex reversal and campomelic dysplasia are cause... 1994 2026 2004 2015 1994 400 800 1.2k

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 19 1.3k 1.2k 256 214 169 48 2.3k
Marcel Nelen Netherlands 26 1.1k 0.8× 1.6k 1.3× 74 0.3× 283 1.3× 188 1.1× 56 3.5k
William Davies United Kingdom 26 1.2k 0.9× 1.0k 0.8× 156 0.6× 56 0.3× 263 1.6× 70 2.2k
Yuichiro Itoh United States 28 1.3k 1.0× 761 0.6× 178 0.7× 99 0.5× 30 0.2× 53 2.5k
David Schlessinger United States 31 2.2k 1.7× 2.4k 1.9× 119 0.5× 86 0.4× 69 0.4× 61 3.8k
Françoise Muscatelli France 31 2.2k 1.7× 2.7k 2.2× 327 1.3× 213 1.0× 36 0.2× 65 4.4k
Tiziano Pramparo United States 27 1.2k 0.9× 1.7k 1.4× 48 0.2× 136 0.6× 84 0.5× 50 2.7k
Nicole A. Datson Netherlands 35 822 0.6× 1.9k 1.6× 56 0.2× 210 1.0× 144 0.9× 72 4.1k
Pablo V. Gejman United States 28 980 0.8× 1.5k 1.2× 109 0.4× 148 0.7× 288 1.7× 58 3.4k
Chengji J. Zhou United States 35 795 0.6× 1.8k 1.5× 91 0.4× 183 0.9× 53 0.3× 77 3.1k
Katrin Anlag Germany 9 1.5k 1.2× 2.1k 1.7× 474 1.9× 201 0.9× 22 0.1× 9 3.7k

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.
Schote, Andrea B., et al.. (2022). Real sweating in a virtual stress environment: Investigation of the stress reactivity in people with primary focal hyperhidrosis. PLoS ONE. 17(8). e0272247–e0272247. 5 indexed citations
2.
Schote, Andrea B., Nicole Frank, Ernesto Tarragón, et al.. (2020). Genome-wide linkage analysis of families with primary hyperhidrosis. PLoS ONE. 15(12). e0244565–e0244565. 8 indexed citations
3.
Kluwe‐Schiavon, Bruno, Andrea B. Schote, Matthias Vonmoos, et al.. (2019). Psychiatric symptoms and expression of glucocorticoid receptor gene in cocaine users: A longitudinal study. Journal of Psychiatric Research. 121. 126–134. 5 indexed citations
4.
Schote, Andrea B., et al.. (2018). Sex, ADHD symptoms, and CHRNA5 genotype influence reaction time but not response inhibition. Journal of Neuroscience Research. 97(2). 215–224. 1 indexed citations
5.
Schote, Andrea B., Matthias Vonmoos, Lea M. Hulka, et al.. (2018). Glucocorticoid receptor gene variants and lower expression of NR3C1 are associated with cocaine use. Addiction Biology. 24(4). 730–742. 22 indexed citations
6.
Streit, Fabian, Jerome C. Foo, Robert Kumsta, et al.. (2018). Temporal dynamics of cortisol-associated changes in mRNA expression of glucocorticoid responsive genes FKBP5, GILZ, SDPR, PER1, PER2 and PER3 in healthy humans. Psychoneuroendocrinology. 102. 63–67. 21 indexed citations
7.
Tarragón, Ernesto, et al.. (2017). Psychometric Properties of the German Translated Version and Adaptation of the Food Craving Inventory. Frontiers in Psychology. 8. 736–736. 8 indexed citations
8.
Brückl, Tanja, et al.. (2015). Association of ABCB1 gene variants, plasma antidepressant concentration, and treatment response: Results from a randomized clinical study. Journal of Psychiatric Research. 73. 86–95. 44 indexed citations
9.
Frings, Christian, et al.. (2015). The role of the glucocorticoid receptor gene ( NR3C1 ) for the processing of aversive stimuli. Neuroscience Research. 107. 8–13. 2 indexed citations
10.
Schote, Andrea B., et al.. (2014). Elevated Social Stress Levels and Depressive Symptoms in Primary Hyperhidrosis. PLoS ONE. 9(3). e92412–e92412. 46 indexed citations
11.
Zilles‐Wegner, David, Jobst Meyer, Neil Thomas, et al.. (2012). Genetic polymorphisms of 5-HTT and DAT but not COMT differentially affect verbal and visuospatial working memory functioning. European Archives of Psychiatry and Clinical Neuroscience. 262(8). 667–676. 38 indexed citations
12.
Cao-Lei, Lei, Robert Kumsta, Stefan Wüst, et al.. (2011). Transcriptional control of the human glucocorticoid receptor: identification and analysis of alternative promoter regions. Human Genetics. 129(5). 533–543. 50 indexed citations
13.
Kumsta, Robert, Dirk Moser, Fabian Streit, et al.. (2008). Characterization of a glucocorticoid receptor gene (GR, NR3C1) promoter polymorphism reveals functionality and extends a haplotype with putative clinical relevance. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(4). 476–482. 45 indexed citations
14.
Hesse, Judith, et al.. (2007). Haploinsufficiency of the SERPINA6 gene is associated with severe muscle fatigue: A de novo mutation in corticosteroid-binding globulin deficiency. Journal of Neural Transmission. 114(5). 563–569. 11 indexed citations
15.
Moser, Dirk, Anne Molitor, Robert Kumsta, et al.. (2007). The glucocorticoid receptor gene exon 1-F promoter is not methylated at the NGFI-A binding site in human hippocampus. The World Journal of Biological Psychiatry. 8(4). 262–268. 46 indexed citations
17.
Rubie, Claudia, Florian I. Schmidt, Michael Knapp, et al.. (2001). The human dopamine transporter gene: the 5′-flanking region reveals five diallelic polymorphic sites in a Caucasian population sample. Neuroscience Letters. 297(2). 125–128. 37 indexed citations
18.
Meyer, Jobst. (1997). Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations. Human Molecular Genetics. 6(1). 91–98. 141 indexed citations
19.
Meyer, Jobst, et al.. (1996). SOX20, a new member of the SOX gene family, is located on chromosome 17p13. Cytogenetic and Genome Research. 72(2-3). 246–249. 19 indexed citations
20.
Wagner, Thomas, Jutta Wirth, Jobst Meyer, et al.. (1994). Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9. Cell. 79(6). 1111–1120. 1236 indexed citations breakdown →

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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