TXNRD2 c.103+340G>A

Variant ID: 22-19928884-C-T

NM_006440.3(TXNRD2):c.103+340G>A

This variant was identified in 39 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: rs2020917
PubMed Link: 35848345
Variant Present in the following documents:
  • Main text
  • 10.1177_17455057221111315.pdf
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Genetic and Clinical Factors Associated with Opioid Response in Chinese Han Patients with Cancer Pain: An Exploratory Cross-Sectional Study.

Pain And Therapy
Shi, Chen C; Liu, Jinmei J; Hu, Jianli J; Chen, Xu X; Xie, Jiyi J; Luo, Juan J; Wang, Cong C; Wang, Hanxiang H; Yuan, Qi Q; Zhu, Haixia H; Gong, Weijing W; Li, Shijun S; Zhou, Hong H; Wang, Leiyun L; Wang, Hui H; Zhang, Yu Y
Publication Date: 2022-03

Variant appearance in text: rs2020917
PubMed Link: 35107781
Variant Present in the following documents:
  • Main text
  • 40122_2022_Article_353.pdf
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Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.

European Journal Of Human Genetics : Ejhg
Publication Date: 2020-12

Variant appearance in text: rs2020917
PubMed Link: 33262486
Variant Present in the following documents:
  • Main text
  • 41431_2020_Article_741.pdf
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The association of catechol-O-methyltransferase (COMT) rs4680 polymorphisms and generalized anxiety disorder in the Chinese Han population.

International Journal Of Clinical And Experimental Pathology
He, Qianqian Q; Shen, Zhongxia Z; Ren, Lie L; Wang, Xing X; Qian, Mincai M; Zhu, Jianying J; Shen, Xinhua X
Publication Date: 2020

Variant appearance in text: rs2020917
PubMed Link: 32782694
Variant Present in the following documents:
  • Main text
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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: rs2020917
PubMed Link: 32533012
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_65332.pdf
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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: rs2020917
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: rs2020917
PubMed Link: 30692067
Variant Present in the following documents:
  • Main text
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Analysis of the relationship between COMT polymorphisms and endometriosis susceptibility.

Medicine
Zhai, Jiajia J; Jiang, Lei L; Wen, Aiping A; Jia, Jingde J; Zhu, Lili L; Fan, Bo B
Publication Date: 2019-01

Variant appearance in text: rs2020917
PubMed Link: 30608422
Variant Present in the following documents:
  • Main text
  • medi-98-e13933.pdf
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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: rs2020917
PubMed Link: 30178121
Variant Present in the following documents:
  • Main text
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Association between COMT gene rs165599 SNP and schizophrenia: A meta-analysis of case-control studies.

Molecular Genetics & Genomic Medicine
Gozukara Bag, Harika Gozde HG
Publication Date: 2018-09

Variant appearance in text: rs2020917
PubMed Link: 30165727
Variant Present in the following documents:
  • Main text
  • MGG3-6-845.pdf
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Prediction of opioid dose in cancer pain patients using genetic profiling: not yet an option with support vector machine learning.

Bmc Research Notes
Olesen, Anne Estrup AE; Grønlund, Debbie D; Gram, Mikkel M; Skorpen, Frank F; Drewes, Asbjørn Mohr AM; Klepstad, Pål P
Publication Date: 2018-01-27

Variant appearance in text: rs2020917
PubMed Link: 29374492
Variant Present in the following documents:
  • Main text
  • 13104_2018_Article_3194.pdf
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Decoding emotion of the other differs among schizophrenia patients and schizoaffective patients: A pilot study.

Schizophrenia Research. Cognition
Tadmor, Hagar H; Levin, Maya M; Dadon, Tzameret T; Meiman, Meital E ME; Ajameeh, Alaa A; Mazzawi, Hosam H; Rigbi, Amihai A; Kremer, Ilana I; Golani, Idit I; Shamir, Alon A
Publication Date: 2016-09

Variant appearance in text: rs2020917
PubMed Link: 28740812
Variant Present in the following documents:
  • Main text
  • main.pdf
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TPH-2 Polymorphisms Interact with Early Life Stress to Influence Response to Treatment with Antidepressant Drugs.

The International Journal Of Neuropsychopharmacology
Xu, Zhi Z; Reynolds, Gavin P GP; Yuan, Yonggui Y; Shi, Yanyan Y; Pu, Mengjia M; Zhang, Zhijun Z
Publication Date: 2016-11

Variant appearance in text: rs2020917
PubMed Link: 27521242
Variant Present in the following documents:
  • Main text
  • pyw070.pdf
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Genetic variation and cognitive dysfunction in opioid-treated patients with cancer.

Brain And Behavior
Kurita, Geana Paula GP; Ekholm, Ola O; Kaasa, Stein S; Klepstad, Pål P; Skorpen, Frank F; Sjøgren, Per P
Publication Date: 2016-07

Variant appearance in text: rs2020917
PubMed Link: 27247849
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: rs2020917
PubMed Link: 27217152
Variant Present in the following documents:
  • Main text
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COMT, BDNF, and DTNBP1 polymorphisms and cognitive functions in patients with brain tumors.

Neuro-Oncology
Correa, Denise D DD; Satagopan, Jaya J; Cheung, Kenneth K; Arora, Arshi K AK; Kryza-Lacombe, Maria M; Xu, Youming Y; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I
Publication Date: 2016-10

Variant appearance in text: rs2020917
PubMed Link: 27091610
Variant Present in the following documents:
  • Main text
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Serotonin and Dopamine Gene Variation and Theory of Mind Decoding Accuracy in Major Depression: A Preliminary Investigation.

Plos One
Zahavi, Arielle Y AY; Sabbagh, Mark A MA; Washburn, Dustin D; Mazurka, Raegan R; Bagby, R Michael RM; Strauss, John J; Kennedy, James L JL; Ravindran, Arun A; Harkness, Kate L KL
Publication Date: 2016

Variant appearance in text: rs2020917
PubMed Link: 26974654
Variant Present in the following documents:
  • Main text
  • pone.0150872.pdf
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Genetic influences on insight problem solving: the role of catechol-O-methyltransferase (COMT) gene polymorphisms.

Frontiers In Psychology
Jiang, Weili W; Shang, Siyuan S; Su, Yanjie Y
Publication Date: 2015

Variant appearance in text: rs2020917
PubMed Link: 26528222
Variant Present in the following documents:
  • Main text
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COMT gene locus: new functional variants.

Pain
Meloto, Carolina B CB; Segall, Samantha K SK; Smith, Shad S; Parisien, Marc M; Shabalina, Svetlana A SA; Rizzatti-Barbosa, Célia M CM; Gauthier, Josée J; Tsao, Douglas D; Convertino, Marino M; Piltonen, Marjo H MH; Slade, Gary Dmitri GD; Fillingim, Roger B RB; Greenspan, Joel D JD; Ohrbach, Richard R; Knott, Charles C; Maixner, William W; Zaykin, Dmitri D; Dokholyan, Nikolay V NV; Reenilä, Ilkka I; Männistö, Pekka T PT; Diatchenko, Luda L
Publication Date: 2015-10

Variant appearance in text: rs2020917
PubMed Link: 26207649
Variant Present in the following documents:
  • Main text
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Genetic and Non-genetic Factors Associated With Constipation in Cancer Patients Receiving Opioids.

Clinical And Translational Gastroenterology
Laugsand, Eivor A EA; Skorpen, Frank F; Kaasa, Stein S; Sabatowski, Rainer R; Strasser, Florian F; Fayers, Peter P; Klepstad, Pål P
Publication Date: 2015-06-18

Variant appearance in text: rs2020917
PubMed Link: 26087058
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: rs2020917
PubMed Link: 25929431
Variant Present in the following documents:
  • Main text
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Genetic variants and early cigarette smoking and nicotine dependence phenotypes in adolescents.

Plos One
O'Loughlin, Jennifer J; Sylvestre, Marie-Pierre MP; Labbe, Aurélie A; Low, Nancy C NC; Roy-Gagnon, Marie-Hélène MH; Dugas, Erika N EN; Karp, Igor I; Engert, James C JC
Publication Date: 2014

Variant appearance in text: rs2020917
PubMed Link: 25545355
Variant Present in the following documents:
  • Main text
  • pone.0115716.pdf
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Clinical and genetic factors related to cancer-induced bone pain and bone pain relief.

The Oncologist
Scarpi, Emanuela E; Calistri, Daniele D; Klepstad, Pål P; Kaasa, Stein S; Skorpen, Frank F; Habberstad, Ragnhild R; Nanni, Oriana O; Amadori, Dino D; Maltoni, Marco M
Publication Date: 2014-12

Variant appearance in text: rs2020917
PubMed Link: 25342315
Variant Present in the following documents:
  • Main text
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The genetic interacting landscape of 63 candidate genes in Major Depressive Disorder: an explorative study.

Biodata Mining
Lekman, Magnus M; Hössjer, Ola O; Andrews, Peter P; Källberg, Henrik H; Uvehag, Daniel D; Charney, Dennis D; Manji, Husseini H; Rush, John A JA; McMahon, Francis J FJ; Moore, Jason H JH; Kockum, Ingrid I
Publication Date: 2014

Variant appearance in text: rs2020917
PubMed Link: 25279001
Variant Present in the following documents:
  • Main text
  • 1756-0381-7-19.pdf
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Complex multilocus effects of catechol-O-methyltransferase haplotypes predict pain and pain interference 6 weeks after motor vehicle collision.

Neuromolecular Medicine
Bortsov, Andrey V AV; Diatchenko, Luda L; McLean, Samuel A SA
Publication Date: 2014-03

Variant appearance in text: rs2020917
PubMed Link: 23963787
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: rs2020917
PubMed Link: 23880798
Variant Present in the following documents:
  • Main text
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Catechol-O-methyltransferase: characteristics, polymorphisms and role in breast cancer.

Drug Discovery Today. Disease Mechanisms
Yager, James D JD
Publication Date: 2012-06-01

Variant appearance in text: rs2020917
PubMed Link: 23734165
Variant Present in the following documents:
  • Main text
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Investigating the genetic basis of theory of mind (ToM): the role of catechol-O-methyltransferase (COMT) gene polymorphisms.

Plos One
Xia, Haiwei H; Wu, Nan N; Su, Yanjie Y
Publication Date: 2012

Variant appearance in text: rs2020917
PubMed Link: 23209597
Variant Present in the following documents:
  • Main text
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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.

Annals Of The Rheumatic Diseases
Peters, Marjolein J MJ; Broer, Linda L; Willemen, Hanneke L D M HL; Eiriksdottir, Gudny G; Hocking, Lynne J LJ; Holliday, Kate L KL; Horan, Michael A MA; Meulenbelt, Ingrid I; Neogi, Tuhina T; Popham, Maria M; Schmidt, Carsten O CO; Soni, Anushka A; Valdes, Ana M AM; Amin, Najaf N; Dennison, Elaine M EM; Eijkelkamp, Niels N; Harris, Tamara B TB; Hart, Deborah J DJ; Hofman, Albert A; Huygen, Frank J P M FJ; Jameson, Karen A KA; Jones, Gareth T GT; Launer, Lenore J LJ; Kerkhof, Hanneke J M HJ; de Kruijf, Marjolein M; McBeth, John J; Kloppenburg, Margreet M; Ollier, William E WE; Oostra, Ben B; Payton, Antony A; Rivadeneira, Fernando F; Smith, Blair H BH; Smith, Albert V AV; Stolk, Lisette L; Teumer, Alexander A; Thomson, Wendy W; Uitterlinden, André G AG; Wang, Ke K; van Wingerden, Sophie H SH; Arden, Nigel K NK; Cooper, Cyrus C; Felson, David D; Gudnason, Vilmundur V; Macfarlane, Gary J GJ; Pendleton, Neil N; Slagboom, P Eline PE; Spector, Tim D TD; Völzke, Henry H; Kavelaars, Annemieke A; van Duijn, Cornelia M CM; Williams, Frances M K FM; van Meurs, Joyce B J JB
Publication Date: 2013-03

Variant appearance in text: rs2020917
PubMed Link: 22956598
Variant Present in the following documents:
  • Main text
  • annrheumdis-2012-201742-s1.pdf
  • annrheumdis-2012-201742.pdf
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Genetic variation in selenoprotein genes, lifestyle, and risk of colon and rectal cancer.

Plos One
Slattery, Martha L ML; Lundgreen, Abbie A; Welbourn, Bill B; Corcoran, Christopher C; Wolff, Roger K RK
Publication Date: 2012

Variant appearance in text: rs2020917
PubMed Link: 22615972
Variant Present in the following documents:
  • Main text
  • pone.0037312.pdf
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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: rs2020917
PubMed Link: 20877297
Variant Present in the following documents:
  • Main text
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A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry.

Schizophrenia Research
Strohmaier, Jana J; Frank, Josef J; Wendland, Jens R JR; Schumacher, Johannes J; Jamra, Rami Abou RA; Treutlein, Jens J; Nieratschker, Vanessa V; Breuer, René R; Mattheisen, Manuel M; Herms, Stefan S; Mühleisen, Thomas W TW; Maier, Wolfgang W; Nöthen, Markus M MM; Cichon, Sven S; Rietschel, Marcella M; Schulze, Thomas G TG
Publication Date: 2010-05

Variant appearance in text: rs2020917
PubMed Link: 20083391
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: rs2020917
PubMed Link: 19673036
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: rs2020917
PubMed Link: 19641441
Variant Present in the following documents:
  • Main text
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Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms.

Cancer Research
Ji, Yuan Y; Olson, Janet J; Zhang, Jianping J; Hildebrandt, Michelle M; Wang, Liewei L; Ingle, James J; Fredericksen, Zachary Z; Sellers, Thomas T; Miller, William W; Dixon, J Michael JM; Brauch, Hiltrud H; Eichelbaum, Michel M; Justenhoven, Christina C; Hamann, Ute U; Ko, Yon Y; Brüning, Thomas T; Chang-Claude, Jenny J; Wang-Gohrke, Shan S; Schaid, Daniel D; Weinshilboum, Richard R
Publication Date: 2008-07-15

Variant appearance in text: rs2020917
PubMed Link: 18632656
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: rs2020917
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: rs2020917
PubMed Link: 16882734
Variant Present in the following documents:
  • Main text
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Interactions between genes involved in the antioxidant defence system and breast cancer risk.

British Journal Of Cancer
Oestergaard, M Z MZ; Tyrer, J J; Cebrian, A A; Shah, M M; Dunning, A M AM; Ponder, B A J BA; Easton, D F DF; Pharoah, P D P PD
Publication Date: 2006-08-21

Variant appearance in text: rs2020917
PubMed Link: 16868544
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: rs2020917
PubMed Link: 16848906
Variant Present in the following documents:
  • Main text
  • 1744-8069-2-24.pdf
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