COMT c.-92+1987T>C

Variant ID: 22-19931407-T-C

NM_000754.4(COMT):c.-92+1987T>C

This variant was identified in 32 publications

View GRCh38 version.




Publications:


Sex hormone-related polymorphisms in endometriosis and migraine: A narrative review.

Women'S Health (London, England)
van der Vaart, Joy-Fleur JF; Merki-Feld, Gabriele Susanne GS
Publication Date: 2022

Variant appearance in text: rs933271
PubMed Link: 35848345
Variant Present in the following documents:
  • Main text
  • 10.1177_17455057221111315.pdf
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Genetic Variants and Their Associations to Type 2 Diabetes Mellitus Complications in the United Arab Emirates.

Frontiers In Endocrinology
ElHajj Chehadeh, Sarah S; Sayed, Noura S NS; Abdelsamad, Hanin S HS; Almahmeed, Wael W; Khandoker, Ahsan H AH; Jelinek, Herbert F HF; Alsafar, Habiba S HS
Publication Date: 2021

Variant appearance in text: rs933271
PubMed Link: 35069435
Variant Present in the following documents:
  • Main text
  • fendo-12-751885.pdf
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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: rs933271
PubMed Link: 34725583
Variant Present in the following documents:
  • Main text
  • cureus-0013-00000018311.pdf
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Genetic variations in catechol-O-methyltransferase gene are associated with levodopa response variability in Chinese patients with Parkinson's disease.

Scientific Reports
Zhao, Cuiping C; Wang, Yihua Y; Zhang, Bin B; Yue, Yaoxian Y; Zhang, Jianyuan J
Publication Date: 2020-06-12

Variant appearance in text: rs933271
PubMed Link: 32533012
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_65332.pdf
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Pharmacogenetics of Antipsychotic Drug Treatment: Update and Clinical Implications.

Molecular Neuropsychiatry
Yoshida, Kazunari K; Müller, Daniel J DJ
Publication Date: 2020-04

Variant appearance in text: rs933271
PubMed Link: 32399466
Variant Present in the following documents:
  • Main text
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Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research.

Cns Drugs
Elsayed, Nada A NA; Yamamoto, Kaila M KM; Froehlich, Tanya E TE
Publication Date: 2020-04

Variant appearance in text: rs933271
PubMed Link: 32133580
Variant Present in the following documents:
  • Main text
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[Postpartum depression: association with genetic polymorphisms of noradrenaline metabolic enzymes and the risk factors].

Nan Fang Yi Ke Da Xue Xue Bao = Journal Of Southern Medical University
Ma, Jiahui J; Huang, Zhengdong Z; Wang, Saiying S; Zheng, Shanshan S; Duan, Kaiming K
Publication Date: 2019-01-30

Variant appearance in text: rs933271
PubMed Link: 30692067
Variant Present in the following documents:
  • Main text
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Neuroplasticity, Neurotransmission and Brain-Related Genes in Major Depression and Bipolar Disorder: Focus on Treatment Outcomes in an Asiatic Sample.

Advances In Therapy
Calabrò, Marco M; Mandelli, Laura L; Crisafulli, Concetta C; Lee, Soo-Jung SJ; Jun, Tae-Youn TY; Wang, Sheng-Min SM; Patkar, Ashwin A AA; Masand, Prakash S PS; Benedetti, Francesco F; Han, Changsu C; Pae, Chi-Un CU; Serretti, Alessandro A
Publication Date: 2018-10

Variant appearance in text: rs933271
PubMed Link: 30178121
Variant Present in the following documents:
  • Main text
  • 12325_2018_Article_781.pdf
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Attempts to replicate genetic associations with schizophrenia in a cohort from north India.

Npj Schizophrenia
Prasad, Suman S; Bhatia, Triptish T; Kukshal, Prachi P; Nimgaonkar, Vishwajit L VL; Deshpande, Smita N SN; Thelma, B K BK
Publication Date: 2017-08-30

Variant appearance in text: rs933271
PubMed Link: 28855605
Variant Present in the following documents:
  • Main text
  • 41537_2017_Article_30.pdf
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A systematic review of the association between fatigue and genetic polymorphisms.

Brain, Behavior, And Immunity
Wang, Tengteng T; Yin, Jie J; Miller, Andrew H AH; Xiao, Canhua C
Publication Date: 2017-05

Variant appearance in text: rs933271
PubMed Link: 28089639
Variant Present in the following documents:
  • Main text
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Genetic polymorphisms in genes related to risk-taking behaviours predicting body mass index trajectory among Mexican American adolescents.

Pediatric Obesity
Zhao, Hua H; Wilkinson, Anna A; Shen, Jie J; Wu, Xifeng X; Chow, Wong-Ho WH
Publication Date: 2017-10

Variant appearance in text: rs933271
PubMed Link: 27228958
Variant Present in the following documents:
  • Main text
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Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry
Bonvicini, C C; Faraone, S V SV; Scassellati, C C
Publication Date: 2016-07

Variant appearance in text: rs933271
PubMed Link: 27217152
Variant Present in the following documents:
  • Main text
  • mp201674a.pdf
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Gene network analysis shows immune-signaling and ERK1/2 as novel genetic markers for multiple addiction phenotypes: alcohol, smoking and opioid addiction.

Bmc Systems Biology
Reyes-Gibby, Cielito C CC; Yuan, Christine C; Wang, Jian J; Yeung, Sai-Ching J SC; Shete, Sanjay S
Publication Date: 2015-06-05

Variant appearance in text: rs933271
PubMed Link: 26044620
Variant Present in the following documents:
  • Main text
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Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study.

The Journal Of Headache And Pain
De Marchis, Maria Laura ML; Barbanti, Piero P; Palmirotta, Raffaele R; Egeo, Gabriella G; Aurilia, Cinzia C; Fofi, Luisa L; Piroso, Serena S; Ialongo, Cristiano C; Della-Morte, David D; D'Andrea, Giovanni G; Ferroni, Patrizia P; Guadagni, Fiorella F
Publication Date: 2015

Variant appearance in text: rs933271
PubMed Link: 25929431
Variant Present in the following documents:
  • Main text
  • 10194_2015_Article_520.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: rs933271
PubMed Link: 25875614
Variant Present in the following documents:
  • Main text
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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: rs933271
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: rs933271
PubMed Link: 25793616
Variant Present in the following documents:
  • Main text
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No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women.

Menopause (New York, N.Y.)
Passarelli, Michael N MN; Newcomb, Polly A PA; Makar, Karen W KW; Burnett-Hartman, Andrea N AN; Phipps, Amanda I AI; David, Sean P SP; Hsu, Li L; Harrison, Tabitha A TA; Hutter, Carolyn M CM; Duggan, David J DJ; White, Emily E; Chan, Andrew T AT; Peters, Ulrike U
Publication Date: 2014-04

Variant appearance in text: rs933271
PubMed Link: 23880798
Variant Present in the following documents:
  • Main text
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Associations between maternal genotypes and metabolites implicated in congenital heart defects.

Molecular Genetics And Metabolism
Chowdhury, Shimul S; Hobbs, Charlotte A CA; MacLeod, Stewart L SL; Cleves, Mario A MA; Melnyk, Stepan S; James, S Jill SJ; Hu, Ping P; Erickson, Stephen W SW
Publication Date: 2012-11

Variant appearance in text: rs933271
PubMed Link: 23059056
Variant Present in the following documents:
  • Main text
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Identification of significant genes in genomics using Bayesian variable selection methods.

Advances And Applications In Bioinformatics And Chemistry : Aabc
Lin, Eugene E; Huang, Lung-Cheng LC
Publication Date: 2008

Variant appearance in text: rs933271
PubMed Link: 21918603
Variant Present in the following documents:
  • Main text
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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: rs933271
PubMed Link: 21857968
Variant Present in the following documents:
  • Main text
  • pone.0022923.pdf
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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: rs933271
PubMed Link: 21656904
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: rs933271
PubMed Link: 20877297
Variant Present in the following documents:
  • Main text
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Predicting sensation seeking from dopamine genes. A candidate-system approach.

Psychological Science
Derringer, Jaime J; Krueger, Robert F RF; Dick, Danielle M DM; Saccone, Scott S; Grucza, Richard A RA; Agrawal, Arpana A; Lin, Peng P; Almasy, Laura L; Edenberg, Howard J HJ; Foroud, Tatiana T; Nurnberger, John I JI; Hesselbrock, Victor M VM; Kramer, John R JR; Kuperman, Samuel S; Porjesz, Bernice B; Schuckit, Marc A MA; Bierut, Laura J LJ; ,
Publication Date: 2010-09

Variant appearance in text: rs933271
PubMed Link: 20732903
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: rs933271
PubMed Link: 20551675
Variant Present in the following documents:
  • Main text
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A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.

Journal Of Translational Medicine
Huang, Lung-Cheng LC; Hsu, Sen-Yen SY; Lin, Eugene E
Publication Date: 2009-09-22

Variant appearance in text: rs933271
PubMed Link: 19772600
Variant Present in the following documents:
  • Main text
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Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.

Croatian Medical Journal
Pal, Prodipto P; Mihanović, Mate M; Molnar, Sven S; Xi, Huifeng H; Sun, Guangyun G; Guha, Saurav S; Jeran, Nina N; Tomljenović, Andrea A; Malnar, Ana A; Missoni, Sasa S; Deka, Ranjan R; Rudan, Pavao P
Publication Date: 2009-08

Variant appearance in text: rs933271
PubMed Link: 19673036
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: rs933271
PubMed Link: 18663369
Variant Present in the following documents:
  • Main text
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High throughput automated allele frequency estimation by pyrosequencing.

Plos One
Doostzadeh, Julie J; Shokralla, Shadi S; Absalan, Farnaz F; Jalili, Roxana R; Mohandessi, Sharareh S; Langston, James W JW; Davis, Ronald W RW; Ronaghi, Mostafa M; Gharizadeh, Baback B
Publication Date: 2008-07-16

Variant appearance in text: rs933271
PubMed Link: 18628978
Variant Present in the following documents:
  • Main text
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The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.

Molecular Psychiatry
Mukherjee, N N; Kidd, K K KK; Pakstis, A J AJ; Speed, W C WC; Li, H H; Tarnok, Z Z; Barta, C C; Kajuna, S L B SL; Kidd, J R JR
Publication Date: 2010-02

Variant appearance in text: rs933271
PubMed Link: 18574484
Variant Present in the following documents:
  • Main text
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Genetic predictors for acute experimental cold and heat pain sensitivity in humans.

Journal Of Medical Genetics
Kim, H H; Mittal, D P DP; Iadarola, M J MJ; Dionne, R A RA
Publication Date: 2006-08

Variant appearance in text: rs933271
PubMed Link: 16882734
Variant Present in the following documents:
  • Main text
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Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.

Molecular Pain
Kim, Hyungsuk H; Lee, Hyewon H; Rowan, Janet J; Brahim, Jaime J; Dionne, Raymond A RA
Publication Date: 2006-07-18

Variant appearance in text: rs933271
PubMed Link: 16848906
Variant Present in the following documents:
  • Main text
  • 1744-8069-2-24.pdf
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