Associated Papers
Integrated multiplexed assays of variant effect reveal determinants of catechol-O-methyltransferase gene expression.
Hoskins I et al.
Molecular Systems Biology, 2024
38355921 (PubMed )
Supplement: 44320_2024_18_MOESM5_ESM.zip › MSB-2023-12096_DatasetEV4 › Dataset_EV4.xls › Sheet1
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
38014045 (PubMed )
Supplement: media-1.xlsx › Table_3
Neonatal opioid toxicity: opioid withdrawal (abstinence) syndrome with emphasis on pharmacogenomics and respiratory depression.
Baldo BA
Archives of Toxicology, 2023
Should we start integrating genetic data in decision-making on device-aided therapies in Parkinson disease? A point of view.
Salles PA et al.
Parkinsonism & Related Disorders, 2021
The genetics and epigenetics of Neonatal Abstinence Syndrome.
Wachman EM et al.
Seminars in Fetal & Neonatal Medicine, 2019
Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity.
Wachman EM et al.
The American Journal on Addictions, 2017
Correlations Between Methionine Cycle Metabolism, COMT Genotype, and Polyneuropathy in L-Dopa Treated Parkinson's Disease: A Preliminary Cross-Sectional Study.
Andréasson M et al.
Journal of Parkinson's Disease, 2017
Genetics of pain perception, COMT and postoperative pain management in children.
Sadhasivam S et al.
Pharmacogenomics, 2014
Association of OPRM1 and COMT single-nucleotide polymorphisms with hospital length of stay and treatment of neonatal abstinence syndrome.
Wachman EM et al.
Jama, 2013
Role of the apolipoprotein E and catechol-O-methyltransferase genes in prospective and retrospective memory traits.
Dongés B et al.
Gene, 2012
Polymorphism of the catechol-O-methyltransferase gene in Han Chinese patients with psoriasis vulgaris.
Gao L et al.
Genetics and Molecular Biology, 2009
Gene-environment interactions in sporadic Parkinson's disease.
Benmoyal-Segal L et al.
Journal of Neurochemistry, 2006
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