COMT c.*764C>G

Variant ID: 22-19957023-C-G

NM_000754.3(COMT):c.*764C>G

This variant was identified in 24 publications

View GRCh38 version.




Publications:


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: rs165728
PubMed Link: 33796865
Variant Present in the following documents:
  • NIHMS1664982-supplement-1.pdf
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Association of Genetic Variation in the 3'UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome.

Frontiers In Neurology
Pagliaroli, Luca L; Vereczkei, Andrea A; Padmanabhuni, Shanmukha Sampath SS; Tarnok, Zsanett Z; Farkas, Luca L; Nagy, Peter P; Rizzo, Renata R; Wolanczyk, Tomasz T; Szymanska, Urszula U; Kapisyzi, Mira M; Basha, Entela E; Koumoula, Anastasia A; Androutsos, Christos C; Tsironi, Vaia V; Karagiannidis, Iordanis I; Paschou, Peristera P; Barta, Csaba C
Publication Date: 2020

Variant appearance in text: rs165728
PubMed Link: 32922348
Variant Present in the following documents:
  • Main text
  • fneur-11-00803.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: rs165728
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: rs165728
PubMed Link: 32399466
Variant Present in the following documents:
  • Main text
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The Computational Analysis Conducted on miRNA Target Sites in Association with SNPs at 3'UTR of ADHD-implicated Genes.

Central Nervous System Agents In Medicinal Chemistry
Abdi, Adel A; Zafarpiran, Mina M; Farsani, Zeinab S ZS
Publication Date: 2020

Variant appearance in text: rs165728
PubMed Link: 31660846
Variant Present in the following documents:
  • Main text
  • CNSAMC-20-58.pdf
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Association of GDNF and CNTNAP2 gene variants with gambling.

Journal Of Behavioral Addictions
Das, Arundhuti A; Pagliaroli, Luca L; Vereczkei, Andrea A; Kotyuk, Eszter E; Langstieh, Banrida B; Demetrovics, Zsolt Z; Barta, Csaba C
Publication Date: 2019-09-01

Variant appearance in text: rs165728
PubMed Link: 31446765
Variant Present in the following documents:
  • Main text
  • jba-08-03-40.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: rs165728
PubMed Link: 30592275
Variant Present in the following documents:
  • Main text
  • mmr-19-03-1423.pdf
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs165728
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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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: rs165728
PubMed Link: 30165727
Variant Present in the following documents:
  • Main text
View BVdb publication page



A common polymorphism of COMT was associated with symptomatic lumbar disc herniation based on a large sample with Chinese Han ancestry.

Scientific Reports
Liu, Hongliang H; Zhao, Hongmou H; Li, Zhong Z; Xue, Hanzhong H; Lu, Jun J; Ma, Wei W
Publication Date: 2018-08-29

Variant appearance in text: rs165728
PubMed Link: 30158547
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_31240.pdf
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Novel human genome variants associated with alcohol use disorders identified in a Lithuanian cohort.

Acta Medica Lituanica
Baronas, Karolis K; Rančelis, Tautvydas T; Pranculis, Aidas A; Domarkienė, Ingrida I; Ambrozaitytė, Laima L; Kučinskas, Vaidutis V
Publication Date: 2018

Variant appearance in text: rs165728
PubMed Link: 29928152
Variant Present in the following documents:
  • Main text
  • aml-25-007.pdf
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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: rs165728
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 1
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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: rs165728
PubMed Link: 28855605
Variant Present in the following documents:
  • Main text
  • 41537_2017_Article_30.pdf
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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs165728
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Association study of MiRSNPs with schizophrenia, tardive dyskinesia and cognition.

Schizophrenia Research
John, Jibin J; Bhatia, Triptish T; Kukshal, Prachi P; Chandna, Puneet P; Nimgaonkar, Vishwajit L VL; Deshpande, Smita N SN; Thelma, B K BK
Publication Date: 2016-07

Variant appearance in text: rs165728
PubMed Link: 27106592
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs165728
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
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Association of the catechol-o-methyltransferase gene polymorphisms with Korean autism spectrum disorders.

Journal Of Korean Medical Science
Yoo, Hee Jeong HJ; Cho, In Hee IH; Park, Mira M; Yang, So Young SY; Kim, Soon Ae SA
Publication Date: 2013-09

Variant appearance in text: rs165728
PubMed Link: 24015051
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs165728
PubMed Link: 23766564
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs165728
PubMed Link: 22956598
Variant Present in the following documents:
  • annrheumdis-2012-201742-s1.pdf
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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: rs165728
PubMed Link: 19673036
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms in estrogen- and androgen-metabolizing genes and the risk of gastric cancer.

Carcinogenesis
Freedman, Neal D ND; Ahn, Jiyoung J; Hou, Lifang L; Lissowska, Jolanta J; Zatonski, Witold W; Yeager, Meredith M; Chanock, Stephen J SJ; Chow, Wong Ho WH; Abnet, Christian C CC
Publication Date: 2009-01

Variant appearance in text: rs165728
PubMed Link: 19015200
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: rs165728
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: rs165728
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: rs165728
PubMed Link: 16848906
Variant Present in the following documents:
  • Main text
  • 1744-8069-2-24.pdf
View BVdb publication page