COMT c.-92+689T>C

Variant ID: 22-19930109-T-C

NM_000754.4(COMT):c.-92+689T>C

This variant was identified in 29 publications

View GRCh38 version.




Publications:


Effect of Catechol-O-Methyltransferase Genotype Polymorphism on Neurological and Psychiatric Disorders: Progressing Towards Personalized Medicine.

Cureus
Srivastava, Kosha K; Ochuba, Olive O; Sandhu, Jasmine K JK; Alkayyali, Tasnim T; Ruo, Sheila W SW; Waqar, Ahsan A; Jain, Ashish A; Joseph, Christine C; Poudel, Sujan S
Publication Date: 2021-09

Variant appearance in text: rs737866
PubMed Link: 34725583
Variant Present in the following documents:
  • Main text
  • cureus-0013-00000018311.pdf
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Oxidative Stress Genes in Diabetes Mellitus Type 2: Association with Diabetic Kidney Disease.

Oxidative Medicine And Cellular Longevity
Roumeliotis, Athanasios A; Roumeliotis, Stefanos S; Tsetsos, Fotis F; Georgitsi, Marianthi M; Georgianos, Panagiotis I PI; Stamou, Aikaterini A; Vasilakou, Anna A; Kotsa, Kalliopi K; Tsekmekidou, Xanthippi X; Paschou, Peristera P; Panagoutsos, Stylianos S; Liakopoulos, Vassilios V
Publication Date: 2021

Variant appearance in text: rs737866
PubMed Link: 34545296
Variant Present in the following documents:
  • Main text
  • OMCL2021-2531062.pdf
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Similarity-driven multi-view embeddings from high-dimensional biomedical data.

Nature Computational Science
Avants, Brian B BB; Tustison, Nicholas J NJ; Stone, James R JR
Publication Date: 2021-02

Variant appearance in text: rs737866
PubMed Link: 33796865
Variant Present in the following documents:
  • NIHMS1664982-supplement-1.pdf
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Prediction of age at onset in Parkinson's disease using objective specific neuroimaging genetics based on a sparse canonical correlation analysis.

Scientific Reports
Won, Ji Hye JH; Kim, Mansu M; Youn, Jinyoung J; Park, Hyunjin H
Publication Date: 2020-07-15

Variant appearance in text: rs737866
PubMed Link: 32669683
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_68301.pdf
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Neuropharmacological and Neurogenetic Correlates of Opioid Use Disorder (OUD) As a Function of Ethnicity: Relevance to Precision Addiction Medicine.

Current Neuropharmacology
Abijo, Tomilowo T; Blum, Kenneth K; Gondré-Lewis, Marjorie C MC
Publication Date: 2020

Variant appearance in text: rs737866
PubMed Link: 31744450
Variant Present in the following documents:
  • Main text
  • CN-18-578.pdf
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Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits.

The Pharmacogenomics Journal
Li, Jin J; Wei, Zhi Z; Zhang, Jie J; Hakonarson, Hakon H; Cook-Sather, Scott D SD
Publication Date: 2019-12

Variant appearance in text: rs737866
PubMed Link: 30760877
Variant Present in the following documents:
  • Main text
  • nihms-1517353.pdf
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Pain polymorphisms and opioids: An evidence based review.

Molecular Medicine Reports
Vieira, Cláudia Margarida Pereira CMP; Fragoso, Rosa Maria RM; Pereira, Deolinda D; Medeiros, Rui R
Publication Date: 2019-03

Variant appearance in text: rs737866
PubMed Link: 30592275
Variant Present in the following documents:
  • Main text
  • mmr-19-03-1423.pdf
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Association of Polymorphisms in Pharmacogenetic Candidate Genes with Propofol Susceptibility.

Scientific Reports
Zhong, Qi Q; Chen, Xiangdong X; Zhao, Yan Y; Liu, Ru R; Yao, Shanglong S
Publication Date: 2017-06-13

Variant appearance in text: rs737866
PubMed Link: 28611364
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_3229.pdf
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Overlapping dopaminergic pathway genetic susceptibility to heroin and cocaine addictions in African Americans.

Annals Of Human Genetics
Levran, Orna O; Randesi, Matthew M; da Rosa, Joel Correa JC; Ott, Jurg J; Rotrosen, John J; Adelson, Miriam M; Kreek, Mary Jeanne MJ
Publication Date: 2015-05

Variant appearance in text: rs737866
PubMed Link: 25875614
Variant Present in the following documents:
  • Main text
View BVdb publication page



A review of pharmacogenetic studies of substance-related disorders.

Drug And Alcohol Dependence
Jones, Jermaine D JD; Comer, Sandra D SD
Publication Date: 2015-07-01

Variant appearance in text: rs737866
PubMed Link: 25819021
Variant Present in the following documents:
  • Main text
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COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.

Plos One
Sampaio, Aline Santos AS; Hounie, Ana Gabriela AG; Petribú, Kátia K; Cappi, Carolina C; Morais, Ivanil I; Vallada, Homero H; do Rosário, Maria Conceição MC; Stewart, S Evelyn SE; Fargeness, Jesen J; Mathews, Carol C; Arnold, Paul P; Hanna, Gregory L GL; Richter, Margaret M; Kennedy, James J; Fontenelle, Leonardo L; de Bragança Pereira, Carlos Alberto CA; Pauls, David L DL; Miguel, Eurípedes Constantino EC
Publication Date: 2015

Variant appearance in text: rs737866
PubMed Link: 25793616
Variant Present in the following documents:
  • Main text
  • pone.0119592.pdf
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Oxidative stress in susceptibility to breast cancer: study in Spanish population.

Bmc Cancer
Rodrigues, Patricia P; de Marco, Griselda G; Furriol, Jessica J; Mansego, Maria Luisa ML; Pineda-Alonso, Mónica M; Gonzalez-Neira, Anna A; Martin-Escudero, Juan Carlos JC; Benitez, Javier J; Lluch, Ana A; Chaves, Felipe J FJ; Eroles, Pilar P
Publication Date: 2014-11-21

Variant appearance in text: rs737866
PubMed Link: 25416100
Variant Present in the following documents:
  • Main text
  • 12885_2014_Article_5048.pdf
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Advances in genetic studies of substance abuse in China.

Shanghai Archives Of Psychiatry
Sun, Yan Y; Meng, Shiqiu S; Li, Jiali J; Shi, Jie J; Lu, Lin L
Publication Date: 2013-08

Variant appearance in text: rs737866
PubMed Link: 24991158
Variant Present in the following documents:
  • Main text
  • sap-25-04-199.pdf
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Gene-sex interactions in schizophrenia: focus on dopamine neurotransmission.

Frontiers In Behavioral Neuroscience
Godar, Sean C SC; Bortolato, Marco M
Publication Date: 2014

Variant appearance in text: rs737866
PubMed Link: 24639636
Variant Present in the following documents:
  • Main text
  • fnbeh-08-00071.pdf
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Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.

Anesthesiology
Kambur, Oleg O; Kaunisto, Mari A MA; Tikkanen, Emmi E; Leal, Suzanne M SM; Ripatti, Samuli S; Kalso, Eija A EA
Publication Date: 2013-12

Variant appearance in text: rs737866
PubMed Link: 24343288
Variant Present in the following documents:
  • Main text
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Pharmacogenetics of chronic pain and its treatment.

Mediators Of Inflammation
Světlík, Svatopluk S; Hronová, Karolína K; Bakhouche, Hana H; Matoušková, Olga O; Slanař, Ondřej O
Publication Date: 2013

Variant appearance in text: rs737866
PubMed Link: 23766564
Variant Present in the following documents:
  • Main text
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Perspective: Identification of genetic variants associated with dopaminergic compensatory mechanisms in early Parkinson's disease.

Frontiers In Neuroscience
Greenbaum, Lior L; Lorberboym, Mordechai M; Melamed, Eldad E; Rigbi, Amihai A; Barhum, Yael Y; Kohn, Yoav Y; Khlebtovsky, Alexander A; Lerer, Bernard B; Djaldetti, Ruth R
Publication Date: 2013

Variant appearance in text: rs737866
PubMed Link: 23596382
Variant Present in the following documents:
  • Main text
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Pathways to age of onset of heroin use: a structural model approach exploring the relationship of the COMT gene, impulsivity and childhood trauma.

Plos One
Li, Ting T; Du, Jiang J; Yu, Shunying S; Jiang, Haifeng H; Fu, Yingmei Y; Wang, Dongxiang D; Sun, Haiming H; Chen, Hanhui H; Zhao, Min M
Publication Date: 2012

Variant appearance in text: rs737866
PubMed Link: 23155402
Variant Present in the following documents:
  • Main text
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Genetic predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis.

Plos Medicine
Tansey, Katherine E KE; Guipponi, Michel M; Perroud, Nader N; Bondolfi, Guido G; Domenici, Enrico E; Evans, David D; Hall, Stephanie K SK; Hauser, Joanna J; Henigsberg, Neven N; Hu, Xiaolan X; Jerman, Borut B; Maier, Wolfgang W; Mors, Ole O; O'Donovan, Michael M; Peters, Tim J TJ; Placentino, Anna A; Rietschel, Marcella M; Souery, Daniel D; Aitchison, Katherine J KJ; Craig, Ian I; Farmer, Anne A; Wendland, Jens R JR; Malafosse, Alain A; Holmans, Peter P; Lewis, Glyn G; Lewis, Cathryn M CM; Stensbøl, Tine Bryan TB; Kapur, Shitij S; McGuffin, Peter P; Uher, Rudolf R
Publication Date: 2012

Variant appearance in text: rs737866
PubMed Link: 23091423
Variant Present in the following documents:
  • pmed.1001326.s001.pdf
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Custom genotyping for substance addiction susceptibility genes in Jordanians of Arab descent.

Bmc Research Notes
Al-Eitan, Laith N LN; Jaradat, Saied A SA; Hulse, Gary K GK; Tay, Guan K GK
Publication Date: 2012-09-10

Variant appearance in text: rs737866
PubMed Link: 22963930
Variant Present in the following documents:
  • Main text
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Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort.

Bmj Open
Nyman, Emma S ES; Sulkava, Sonja S; Soronen, Pia P; Miettunen, Jouko J; Loukola, Anu A; Leppä, Virpi V; Joukamaa, Matti M; Mäki, Pirjo P; Järvelin, Marjo-Riitta MR; Freimer, Nelson N; Peltonen, Leena L; Veijola, Juha J; Paunio, Tiina T
Publication Date: 2011-08-27

Variant appearance in text: rs737866
PubMed Link: 22021758
Variant Present in the following documents:
  • Main text
  • bmjopen-2011-000087.draft_revisions.pdf
  • bmjopen-2011-000087.pdf
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Role of novelty seeking personality traits as mediator of the association between COMT and onset age of drug use in Chinese heroin dependent patients.

Plos One
Li, Ting T; Yu, Shunying S; Du, Jiang J; Chen, Hanhui H; Jiang, Haifeng H; Xu, Ke K; Fu, Yingmei Y; Wang, Dongxiang D; Zhao, Min M
Publication Date: 2011

Variant appearance in text: rs737866
PubMed Link: 21857968
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Ittiwut, Rungnapa R; Listman, Jennifer B JB; Ittiwut, Chupong C; Cubells, Joseph F JF; Weiss, Roger D RD; Brady, Kathleen K; Oslin, David D; Farrer, Lindsay A LA; Kranzler, Henry R HR; Gelernter, Joel J
Publication Date: 2011-09

Variant appearance in text: rs737866
PubMed Link: 21656904
Variant Present in the following documents:
  • Main text
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Epistasis between neurochemical gene polymorphisms and risk for ADHD.

European Journal Of Human Genetics : Ejhg
Segurado, Ricardo R; Bellgrove, Mark A MA; Manconi, Francesca F; Gill, Michael M; Hawi, Ziarah Z
Publication Date: 2011-05

Variant appearance in text: rs737866
PubMed Link: 21368917
Variant Present in the following documents:
  • Main text
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Catechol O-methyltransferase pharmacogenomics and selective serotonin reuptake inhibitor response.

The Pharmacogenomics Journal
Ji, Y Y; Biernacka, J J; Snyder, K K; Drews, M M; Pelleymounter, L L LL; Colby, C C; Wang, L L; Mrazek, D A DA; Weinshilboum, R M RM
Publication Date: 2012-02

Variant appearance in text: rs737866
PubMed Link: 20877297
Variant Present in the following documents:
  • Main text
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Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.

Human Heredity
Fridley, Brooke L BL; Jenkins, Gregory D GD
Publication Date: 2010

Variant appearance in text: rs737866
PubMed Link: 20551675
Variant Present in the following documents:
  • Main text
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Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.

Pharmacogenetics And Genomics
Zhang, Jianping J; Ji, Yuan Y; Moon, Irene I; Pelleymounter, Linda L LL; Ezequel Salavaggione, Oreste O; Wu, Yanhong Y; Jenkins, Gregory D GD; Batzler, Anthony J AJ; Schaid, Daniel J DJ; Weinshilboum, Richard M RM
Publication Date: 2009-08

Variant appearance in text: rs737866
PubMed Link: 19641441
Variant Present in the following documents:
  • Main text
View BVdb publication page



Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Biederman, Joseph J; Kim, Jang Woo JW; Doyle, Alysa E AE; Mick, Eric E; Fagerness, Jesen J; Smoller, Jordan W JW; Faraone, Stephen V SV
Publication Date: 2008-12-05

Variant appearance in text: rs737866
PubMed Link: 18937309
Variant Present in the following documents:
  • Main text
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Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).

Molecular Psychiatry
Strug, L J LJ; Suresh, R R; Fyer, A J AJ; Talati, A A; Adams, P B PB; Li, W W; Hodge, S E SE; Gilliam, T C TC; Weissman, M M MM
Publication Date: 2010-02

Variant appearance in text: rs737866
PubMed Link: 18663369
Variant Present in the following documents:
  • Main text
View BVdb publication page