CYP450 2D6 and 2C19 genotypes in ADHD: not related with treatment resistance but with over-representation of 2C19 ultra-metabolizers
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A. Tufan | M. Kutuk | Z. Topal | Ufuk Acikbas | G. Guler | B. Karakaş | H. Basaga | F. Kılıçaslan | E. Altıntaş | Yeliz Aka | O. Kutuk | Bahriye Karakaş
[1] J. Stingl,et al. CYP2D6 in the Brain: Potential Impact on Adverse Drug Reactions in the Central Nervous System—Results From the ADRED Study , 2021, Frontiers in Pharmacology.
[2] Xiao-dong Liu,et al. Alterations of Cytochrome P450s and UDP-Glucuronosyltransferases in Brain Under Diseases and Their Clinical Significances , 2021, Frontiers in Pharmacology.
[3] W. Daniel,et al. Cytochrome P450 expression and regulation in the brain , 2020, Drug metabolism reviews.
[4] J. Stingl,et al. Genetic polymorphism of CYP2C19 and subcortical variability in the human adult brain , 2020, bioRxiv.
[5] J. Stingl,et al. Effects of genetic variability of CYP2D6 on neural substrates of sustained attention during on-task activity , 2019, bioRxiv.
[6] C. Bousman,et al. Commercial Pharmacogenetic Tests in Psychiatry: Do they Facilitate the Implementation of Pharmacogenetic Dosing Guidelines? , 2019, Pharmacopsychiatry.
[7] Lisa J. Martin,et al. Influence of CYP2C19 Metabolizer Status on Escitalopram/Citalopram Tolerability and Response in Youth With Anxiety and Depressive Disorders , 2019, Front. Pharmacol..
[8] S. Faraone,et al. Genetics of attention deficit hyperactivity disorder , 2018, Molecular Psychiatry.
[9] G. Özhan,et al. CYP2C9, CYPC19 and CYP2D6 gene profiles and gene susceptibility to drug response and toxicity in Turkish population , 2016, Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society.
[10] Ian R. McGrane,et al. Pharmacogenetics of Cytochrome P450 Enzymes in American Indian and Caucasian Children Admitted to a Psychiatric Hospital. , 2016, Journal of child and adolescent psychopharmacology.
[11] E. Gillam,et al. Differential Expression of Cytochrome P450 Enzymes from the CYP2C Subfamily in the Human Brain , 2015, Drug Metabolism and Disposition.
[12] M. Ingelman-Sundberg,et al. Pharmacogenomics of Cytochrome P450 Dependent Metabolism of Endogenous Compounds: Implications for Behavior, Psychopathology and Treatment , 2014 .
[13] A. Llerena,et al. CYP2D6 variation, behaviour and psychopathology: implications for pharmacogenomics-guided clinical trials. , 2014, British journal of clinical pharmacology.
[14] G. Schulte,et al. Decreased hippocampal volume and increased anxiety in a transgenic mouse model expressing the human CYP2C19 gene , 2013, Molecular Psychiatry.
[15] M. Schwab,et al. Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. , 2013, Pharmacology & therapeutics.
[16] J. Brockmöller,et al. Genetic variability of drug-metabolizing enzymes: the dual impact on psychiatric therapy and regulation of brain function , 2013, Molecular Psychiatry.
[17] U. Yasar,et al. Evaluation of lansoprazole as a probe for assessing cytochrome P450 2C19 activity and genotype–phenotype correlation in childhood , 2012, European Journal of Clinical Pharmacology.
[18] R. Tyndale,et al. Cytochrome P450 enzymes in the brain: emerging evidence of biological significance. , 2011, Trends in pharmacological sciences.
[19] E. Bromek,et al. Cytochrome P450 mediates dopamine formation in the brain in vivo , 2011, Journal of neurochemistry.
[20] J Kirchheiner,et al. CYP2D6 in the brain: genotype effects on resting brain perfusion , 2011, Molecular Psychiatry.
[21] D. Nelson. The Cytochrome P450 Homepage , 2009, Human Genomics.
[22] M. Loriot,et al. Xenobiotic-Metabolizing Enzymes and Transporters in the Normal Human Brain: Regional and Cellular Mapping as a Basis for Putative Roles in Cerebral Function , 2009, Drug Metabolism and Disposition.
[23] Deborah C. Mash,et al. Induction of the drug metabolizing enzyme CYP2D in monkey brain by chronic nicotine treatment , 2008, Neuropharmacology.
[24] M. Sikora,et al. The Endocannabinoid Anandamide Is a Substrate for the Human Polymorphic Cytochrome P450 2D6 , 2008, Journal of Pharmacology and Experimental Therapeutics.
[25] Wei Duan,et al. Clinical pharmacogenetics and potential application in personalized medicine. , 2008, Current drug metabolism.
[26] M. Ingelman-Sundberg,et al. Influence of cytochrome P450 polymorphisms on drug therapies: pharmacogenetic, pharmacoepigenetic and clinical aspects. , 2007, Pharmacology & therapeutics.
[27] A. Seeringer,et al. Clinical implications of pharmacogenetics of cytochrome P450 drug metabolizing enzymes. , 2007, Biochimica et biophysica acta.
[28] D. Patel,et al. Attention deficit hyperactivity disorder across the lifespan: the child, adolescent, and adult. , 2007, Disease-a-month : DM.
[29] J. McCracken,et al. CYP2D6 and clinical response to atomoxetine in children and adolescents with ADHD. , 2007, Journal of the American Academy of Child and Adolescent Psychiatry.
[30] K. Otani,et al. CYP2C19 polymorphism affects personality traits of Japanese females , 2007, Neuroscience Letters.
[31] E. Begg,et al. Pharmacogenetics, Drug-Metabolizing Enzymes, and Clinical Practice , 2006, Pharmacological Reviews.
[32] U. Ozbek,et al. CYP2D6 and CYP1A1 mutations in the Turkish population , 2005, Cell biochemistry and function.
[33] D. Murry,et al. Methylphenidate Is Stereoselectively Hydrolyzed by Human Carboxylesterase CES1A1 , 2004, Journal of Pharmacology and Experimental Therapeutics.
[34] P. Joyce,et al. Association between cytochrome P450 2D6 genotype and harm avoidance , 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[35] N. Thuerauf,et al. CYP2D6 Genotype: Impact on Adverse Effects and Nonresponse During Treatment with Antidepressants—a Pilot Study , 2004, Clinical pharmacology and therapeutics.
[36] P. du Souich,et al. 5‐Hydroxytryptamine is biotransformed by CYP2C9, 2C19 and 2B6 to hydroxylamine, which is converted into nitric oxide , 2004, British journal of pharmacology.
[37] K. Miczek,et al. Neurosteroids, GABAA receptors, and escalated aggressive behavior , 2003, Hormones and Behavior.
[38] Sharon Miksys,et al. Regional and cellular expression of CYP2D6 in human brain: higher levels in alcoholics , 2002, Journal of neurochemistry.
[39] S. Imaoka,et al. Progesterone oxidation by cytochrome P450 2D isoforms in the brain. , 2001, Endocrinology.
[40] M. Eichelbaum,et al. Cellular localization and regional distribution of CYP2D6 mRNA and protein expression in human brain. , 2001, Pharmacogenetics.
[41] M. Schwartz,et al. Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia) , 2000, European Journal of Human Genetics.
[42] G. Murray,et al. Cytochrome P450 in normal human brain and brain tumours. , 1997, Biochemical Society transactions.
[43] N. Ryan,et al. Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data. , 1997, Journal of the American Academy of Child and Adolescent Psychiatry.
[44] E. Spina,et al. Clinical applications of CYP genotyping in psychiatry , 2014, Journal of Neural Transmission.
[45] Scott C Armstrong,et al. Clinical guidelines for psychiatrists for the use of pharmacogenetic testing for CYP450 2D6 and CYP450 2C19. , 2006, Psychosomatics.
[46] J. Prince. Pharmacotherapy of attention-deficit hyperactivity disorder in children and adolescents: update on new stimulant preparations, atomoxetine, and novel treatments. , 2006, Child and adolescent psychiatric clinics of North America.
[47] M Ingelman-Sundberg,et al. Genetic polymorphisms of cytochrome P450 2D6 (CYP2D6): clinical consequences, evolutionary aspects and functional diversity , 2005, The Pharmacogenomics Journal.
[48] A. Daly. Development of analytical technology in pharmacogenetic research , 2004, Naunyn-Schmiedeberg's Archives of Pharmacology.
[49] L. Bertilsson,et al. Increased incidence of CYP2D6 gene duplication in patients with persistent mood disorders: ultrarapid metabolism of antidepressants as a cause of nonresponse. A pilot study , 2003, European Journal of Clinical Pharmacology.