Associated Papers
Integration of metabolomic and genetic data reveals novel variants underpinning the human metabolome: the Coronary Artery Risk Development in Young Adults (CARDIA) study.
Krishnan M et al.
Medrxiv : the Preprint Server for Health Sciences, 2026
The impact of single nucleotide polymorphisms on the absorption, distribution, metabolism, and excretion of dietary (poly)phenols: a critical systematic review.
Tosi N et al.
Food & Function, 2025
Integrated multiplexed assays of variant effect reveal determinants of catechol-O-methyltransferase gene expression.
Hoskins I et al.
Molecular Systems Biology, 2024
Integrated multiplexed assays of variant effect reveal cis-regulatory determinants of catechol-O-methyltransferase gene expression.
Hoskins I et al.
Biorxiv : the Preprint Server for Biology, 2023
In silico methods for predicting functional synonymous variants.
Lin BC et al.
Genome Biology, 2023
Brain radiotoxicity-related 15CAcBRT gene expression signature predicts survival prognosis of glioblastoma patients.
Reyes-González J et al.
Neuro-oncology, 2023
Pharmacogenomic profile of actionable molecular variants related to drugs commonly used in anesthesia: WES analysis reveals new mutations.
Parada-Márquez JF et al.
Frontiers in Pharmacology, 2023
Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population.
Gaither JBS et al.
Gigascience, 2021
Interaction Between Environmental Risk Factors and Catechol-O-Methyltransferase (COMT) and X-Ray Repair Cross-Complementing Protein 1 (XRCC1) Gene Polymorphisms in Risk of Lung Cancer Among Non-Smoking Chinese Women: A Case-Control Study.
Pan JL et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2018
Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.
Baronas K et al.
Acta Medica Lituanic, 2018
Development of an AmpliSeqTM Panel for Next-Generation Sequencing of a Set of Genetic Predictors of Persisting Pain.
Kringel D et al.
Frontiers in Pharmacology, 2018
Sufentanil and midazolam dosing and pharmacogenetic factors in pediatric analgosedation and withdrawal syndrome.
Hronová K et al.
Physiological Research, 2016
Linking unfounded beliefs to genetic dopamine availability.
Schmack K et al.
Frontiers in Human Neuroscience, 2015
Genetic variation and response to morphine in cancer patients: catechol-O-methyltransferase and multidrug resistance-1 gene polymorphisms are associated with central side effects.
Ross JR et al.
Cancer, 2008
Association of genetic polymorphisms of ACADSB and COMT with human hypertension.
Kamide K et al.
Journal of Hypertension, 2007
Rarity of Somatic Mutation and Frequency of Normal Sequence Variation Detected in Sporadic Colon Adenocarcinoma Using High-Throughput cDNA Sequencing.
Kan T et al.
Bioinformatics and Biology Insights, 2007
Genetic susceptibility to tardive dyskinesia among schizophrenia subjects: IV. Role of dopaminergic pathway gene polymorphisms.
Srivastava V et al.
Pharmacogenetics and Genomics, 2006
Evidence for a susceptibility locus for panic disorder near the catechol-O-methyltransferase gene on chromosome 22.
Hamilton SP et al.
Biological Psychiatry, 2002
Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11.
Li T et al.
Molecular Psychiatry, 2000
Systematic mutation analysis of the catechol O-methyltransferase gene as a candidate gene for schizophrenia.
Chen CH et al.
The American Journal of Psychiatry, 1999
Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis.
van Esch AA et al.
The Netherlands Journal of Medicine, 0
Insights into S-adenosyl-l-methionine (SAM)-dependent methyltransferase related diseases and genetic polymorphisms.
Li J et al.
Mutation Research. Reviews in Mutation Research, 0