What is he best known for?
The fields of study he is best known for:
Bryan L. Roth mainly focuses on Receptor, Neuroscience, Pharmacology, G protein-coupled receptor and 5-HT receptor.
His Receptor study is focused on Biochemistry in general.
Bryan L. Roth combines subjects such as Schizophrenia and Serotonin with his study of Neuroscience.
His Pharmacology study combines topics in areas such as Antidepressant, Mechanism of action, Atypical antipsychotic and Partial agonist.
His work focuses on many connections between G protein-coupled receptor and other disciplines, such as Rhodopsin-like receptors, that overlap with his field of interest in Protein engineering.
His 5-HT receptor research integrates issues from Endocrinology, Serotonergic and Anxiety.
His most cited work include:
- A SARS-CoV-2 protein interaction map reveals targets for drug repurposing. (1317 citations)
- Morphometric evidence for neuronal and glial prefrontal cell pathology in major depression (1234 citations)
- Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand (1212 citations)
What are the main themes of his work throughout his whole career to date?
Bryan L. Roth spends much of his time researching Receptor, Pharmacology, Stereochemistry, G protein-coupled receptor and Agonist.
His Receptor research incorporates elements of Signal transduction and Neuroscience.
His Pharmacology research is multidisciplinary, incorporating elements of Clozapine, Atypical antipsychotic, Dopamine receptor D2, Opioid and In vivo.
His Stereochemistry research is multidisciplinary, relying on both Salvinorin A, Structure–activity relationship, Chemical synthesis and Binding site.
He interconnects Computational biology and G protein in the investigation of issues within G protein-coupled receptor.
His work carried out in the field of 5-HT receptor brings together such families of science as Endocrinology, Antagonist and Serotonergic.
He most often published in these fields:
- Receptor (49.30%)
- Pharmacology (29.20%)
- Stereochemistry (20.10%)
What were the highlights of his more recent work (between 2015-2021)?
- Receptor (49.30%)
- Pharmacology (29.20%)
- G protein-coupled receptor (18.53%)
In recent papers he was focusing on the following fields of study:
The scientist’s investigation covers issues in Receptor, Pharmacology, G protein-coupled receptor, Neuroscience and Agonist.
His Receptor study combines topics from a wide range of disciplines, such as Stereochemistry and Cell biology.
His Pharmacology study incorporates themes from Antagonist, 5-HT receptor, Opioid, Prepulse inhibition and In vivo.
His work deals with themes such as Computational biology, Allosteric regulation and Ligand, which intersect with G protein-coupled receptor.
His study in the field of Dopamine, Dopamine receptor and Chemogenetics also crosses realms of Structure and function.
As a part of the same scientific study, Bryan L. Roth usually deals with the Agonist, concentrating on Muscarinic acetylcholine receptor and frequently concerns with Low dose and Cell signaling.
Between 2015 and 2021, his most popular works were:
- A SARS-CoV-2 protein interaction map reveals targets for drug repurposing. (1317 citations)
- DREADDs for Neuroscientists. (641 citations)
- Structure-based discovery of opioid analgesics with reduced side effects (460 citations)
In his most recent research, the most cited papers focused on:
- Gene
- Enzyme
- Internal medicine
His main research concerns Receptor, G protein-coupled receptor, Neuroscience, Pharmacology and Computational biology.
The Receptor study combines topics in areas such as Melatonin and Cell biology.
His work in G protein-coupled receptor addresses subjects such as Hallucinogen, which are connected to disciplines such as Structural biology.
His Neuroscience research includes elements of κ-opioid receptor and Function.
His studies in Pharmacology integrate themes in fields like Dopaminergic, Endogenous agonist and In vivo.
His biological study spans a wide range of topics, including Human genome, Human physiology, Comparative genomics, Druggability and Drug discovery.
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