scholarly article | Q13442814 |
P356 | DOI | 10.1038/TPJ.2012.32 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/tpj.2012.32 |
P932 | PMC publication ID | 3941038 |
P698 | PubMed publication ID | 22907730 |
P5875 | ResearchGate publication ID | 230711930 |
P50 | author | Yu-Bo Chai | Q73806612 |
P2093 | author name string | R M Weinshilboum | |
Y Nakamura | |||
N Kamatani | |||
Y Ji | |||
K A Snyder | |||
M Kubo | |||
D Flockhart | |||
Z Desta | |||
A Batzler | |||
J M Biernacka | |||
T Mushiroda | |||
D Schaid | |||
D A Mrazek | |||
M S Drews | |||
G D Jenkins | |||
S Hebbring | |||
P2860 | cites work | Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia | Q24308818 |
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G protein-coupled receptor kinase 5 regulates beta 1-adrenergic receptor association with PSD-95 | Q28204363 | ||
Homocysteine, folate and vitamin B12 in neuropsychiatric diseases: review and treatment recommendations | Q28259237 | ||
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose | Q28475004 | ||
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Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines | Q34239148 | ||
Association of G72/G30 with schizophrenia in the Chinese population | Q34326702 | ||
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The thermolabile variant of MTHFR is associated with depression in the British Women's Heart and Health Study and a meta-analysis | Q34482845 | ||
Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors | Q34488758 | ||
Polymorphisms in genes coding for GRK2 and GRK5 and response differences in antihypertensive-treated patients | Q34527912 | ||
Glycine and a glycine dehydrogenase (GLDC) SNP as citalopram/escitalopram response biomarkers in depression: pharmacometabolomics-informed pharmacogenomics | Q34555598 | ||
Review and meta-analysis of antidepressant pharmacogenetic findings in major depressive disorder | Q34871885 | ||
Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response | Q35040545 | ||
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A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression | Q35737324 | ||
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A GRK5 polymorphism that inhibits beta-adrenergic receptor signaling is protective in heart failure | Q37000342 | ||
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SSRI response in depression may be influenced by SNPs in HTR1B and HTR1A. | Q37437784 | ||
Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promises | Q37914472 | ||
Differential regulation of dopamine D1A receptor responsiveness by various G protein-coupled receptor kinases | Q41227485 | ||
Reduced platelet G protein-coupled receptor kinase 2 in major depressive disorder: antidepressant treatment-induced upregulation of GRK2 protein discriminates between responder and non-responder patients | Q42471862 | ||
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project | Q42655084 | ||
Dietary folate, riboflavin, vitamin B-6, and vitamin B-12 and depressive symptoms in early adolescence: the Ryukyus Child Health Study | Q42934810 | ||
One-carbon metabolism disturbances in affective disorders. A preliminary report | Q45394158 | ||
Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified | Q47664212 | ||
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The HTR1A and HTR1B receptor genes influence stress-related information processing. | Q49122883 | ||
Interactive effects of DAOA (G72) and catechol-O-methyltransferase on neurophysiology in prefrontal cortex. | Q51024502 | ||
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder. | Q51034630 | ||
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P433 | issue | 5 | |
P921 | main subject | major depressive disorder | Q42844 |
serotonin | Q167934 | ||
genomics | Q222046 | ||
functional genomics | Q1068690 | ||
genome-wide association study | Q1098876 | ||
pharmacogenomics | Q1152227 | ||
P304 | page(s) | 456-463 | |
P577 | publication date | 2012-08-21 | |
P1433 | published in | The Pharmacogenomics Journal | Q10534704 |
P1476 | title | Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics | |
P478 | volume | 13 |
Q28597255 | A genome-wide association study of antidepressant response in Koreans |
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Q89581651 | Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial |
Q38540142 | BDNF/TRKB/P75NTR polymorphisms and their consequences on antidepressant efficacy in depressed patients. |
Q47659995 | Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics. |
Q34065310 | Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations |
Q40269228 | Detecting Associations between Major Depressive Disorder Treatment and Essential Hypertension using Electronic Health Records |
Q90816200 | Dual Roles for the TSPYL Family in Mediating Serotonin Transport and the Metabolism of Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder |
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Q28083508 | Ethical and public policy challenges for pharmacogenomics |
Q31104563 | Evaluation of methodology for the analysis of 'time-to-event' data in pharmacogenomic genome-wide association studies |
Q37199719 | FKBP5 genetic variation: association with selective serotonin reuptake inhibitor treatment outcomes in major depressive disorder |
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Q101237251 | Genome-wide association studies of antidepressant class response and treatment-resistant depression |
Q34254863 | Increased G protein-coupled receptor kinase (GRK) expression in the anterior cingulate cortex in schizophrenia |
Q93012838 | Influence of GRK5 gene polymorphisms on ritodrine efficacy and adverse drug events in preterm labor treatment |
Q30885784 | Metabolic Profiling and Phenotyping of Central Nervous System Diseases: Metabolites Bring Insights into Brain Dysfunctions |
Q91622024 | Metabolomic signature of exposure and response to citalopram/escitalopram in depressed outpatients |
Q47118154 | MicroRNA-Mediated Regulation of ITGB3 and CHL1 Is Implicated in SSRI Action |
Q47572666 | Multivariate generalized linear model for genetic pleiotropy. |
Q47436767 | New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. |
Q35040224 | PDYN rs2281285 variant association with drinking to avoid emotional or somatic discomfort |
Q38657429 | Peripheral biomarkers of major depression and antidepressant treatment response: Current knowledge and future outlooks |
Q90224430 | Pharmacogenomics-Driven Prediction of Antidepressant Treatment Outcomes: A Machine-Learning Approach With Multi-trial Replication |
Q37158262 | Pharmacometabolomics informs Pharmacogenomics |
Q35032056 | Pharmacometabolomics: implications for clinical pharmacology and systems pharmacology. |
Q57303389 | Polygenic risk scores for major depressive disorder and neuroticism as predictors of antidepressant response: Meta-analysis of three treatment cohorts |
Q47666907 | Progress in Elucidating Biomarkers of Antidepressant Pharmacological Treatment Response: A Systematic Review and Meta-analysis of the Last 15 Years |
Q47796188 | Serotonin in psychiatry: in vitro disease modeling using patient-derived neurons |
Q45022135 | Summaries of plenary, symposia, and oral sessions at the XXII World Congress of Psychiatric Genetics, Copenhagen, Denmark, 12-16 October 2014. |
Q64249357 | Systems Approach to Identify Common Genes and Pathways Associated with Response to Selective Serotonin Reuptake Inhibitors and Major Depression Risk |
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Q37213132 | TSPAN5, ERICH3 and selective serotonin reuptake inhibitors in major depressive disorder: pharmacometabolomics-informed pharmacogenomics |
Q35715254 | The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response. |
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