Urs Meyer
Impact in
- Biological Psychiatry top 0.01%
- Tryptophan and brain disorders
- Pharmacology top 0.01%
- Pharmacogenetics and Drug Metabolism
Papers in
- Pharmacology 191
- Pharmacogenetics and Drug Metabolism 188
-
- Tryptophan and brain disorders 75
- Co-authors
- Joram Feldon (45 shared papers)Frank J. Gonzalez (22 shared papers)Benjamin K. Yee (15 shared papers)Ulrich M. Zanger (18 shared papers)Markus Hermann Heim (11 shared papers)Christoph Handschin (19 shared papers)Thomas Kronbach (13 shared papers)Manfred Schedlowski (9 shared papers)
- Journals
- Brain Behavior and Immunity (20 papers)Journal of Biological Chemistry (17 papers)Molecular Pharmacology (13 papers)Molecular Psychiatry (12 papers)Clinical Pharmacology & Therapeutics (12 papers)
- Partner nations
- SwitzerlandUnited StatesGermany
In The Last Decade
Urs Meyer
396 papers receiving 33.5k citations
Urs Meyer's Hit Papers
Peers
Comparison fields: 5 of 170
- Biological Psychiatry 5.1k
- Pharmacology 14.9k
- Behavioral Neuroscience 889
- Neurology 2.3k
- Psychiatry and Mental health 3.4k
Countries citing papers authored by Urs Meyer
This map shows the geographic impact of Urs 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 Urs Meyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Urs Meyer more than expected).
Fields of papers citing papers by Urs Meyer
This network shows the impact of papers produced by Urs 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 Urs Meyer. The network helps show where Urs Meyer may publish in the future.
Co-authors
The 25 scholars most cited alongside Urs Meyer, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 406 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. Hit paper breakdown → | 1994 | 852 |
| 2 | The Time of Prenatal Immune Challenge Determines the Specificity of Inflammation-Mediated Brain and Behavioral Pathology Hit paper breakdown → | 2006 | 686 |
| 3 | Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Hit paper breakdown → | 1994 | 676 |
| 4 | Characterization of the common genetic defect in humans deficient in debrisoquine metabolism Hit paper breakdown → | 1988 | 586 |
| 5 | Advances in Drug Research Hit paper breakdown → | 1964 | 557 |
| 6 | 2013 | 530 | |
| 7 | Oxidation of midazolam and triazolam by human liver cytochrome P450IIIA4. Hit paper breakdown → | 1989 | 495 |
| 8 | Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugs Hit paper breakdown → | 1988 | 487 |
| 9 | 2000 | 449 | |
| 10 | Cytochrome P-450 hPCN3, a Novel Cytochrome P-450 IIIA Gene Product That Is Differentially Expressed in Adult Human Liver Hit paper breakdown → | 1989 | 447 |
| 11 | MOLECULAR MECHANISMS OF GENETIC POLYMORPHISMS OF DRUG METABOLISM Hit paper breakdown → | 1997 | 440 |
| 12 | 2005 | 418 | |
| 13 | 2007 | 402 | |
| 14 | 2013 | 402 | |
| 15 | Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification Hit paper breakdown → | 1990 | 401 |
| 16 | 1973 | 389 | |
| 17 | Human Arylamine N -Acetyltransferase Genes: Isolation, Chromosomal Localization, and Functional Expression Hit paper breakdown → | 1990 | 384 |
| 18 | 2003 | 380 | |
| 19 | 1996 | 340 | |
| 20 | The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene. Hit paper breakdown → | 1989 | 336 |
About Urs Meyer
Urs Meyer is a scholar working on Pharmacology, Biological Psychiatry, Psychiatry and Mental health, Neurology and Cellular and Molecular Neuroscience, having authored 406 papers that have together received 35.5k indexed citations. Recurring topics across this work include Pharmacogenetics and Drug Metabolism (188 papers), Tryptophan and brain disorders (75 papers), Schizophrenia research and treatment (37 papers), Porphyrin Metabolism and Disorders (29 papers), Neuroinflammation and Neurodegeneration Mechanisms (21 papers), Drug Transport and Resistance Mechanisms (17 papers), Neurotransmitter Receptor Influence on Behavior (13 papers) and Maternal Mental Health During Pregnancy and Postpartum (12 papers). The work is most often cited by research in Biological Psychiatry (5.1k citations), Pharmacology (14.9k citations), Behavioral Neuroscience (889 citations), Neurology (2.3k citations) and Psychiatry and Mental health (3.4k citations). Urs Meyer has collaborated with scholars based in Switzerland, United States and Germany. Frequent co-authors include Joram Feldon, Frank J. Gonzalez, Benjamin K. Yee, Ulrich M. Zanger, Markus Hermann Heim, Christoph Handschin, Thomas Kronbach, Manfred Schedlowski, Juliet Richetto and Denis M. Grant. Their work appears in journals such as Brain Behavior and Immunity, Journal of Biological Chemistry, Molecular Pharmacology, Molecular Psychiatry and Clinical Pharmacology & Therapeutics.
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.