Publications:

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Polymorphisms in the HTR2A and HTR3A Genes Contribute to Pain in TMD Myalgia.

Frontiers In Oral Health

Louca Jounger, Sofia S; Christidis, Nikolaos N; Hedenberg-Magnusson, Britt B; List, Thomas T; Svensson, Peter P; Schalling, Martin M; Ernberg, Malin M

Publication Date: 2021

Variant appearance in text: rs174697

PubMed Link: 35047998

Variant Present in the following documents:

• Main text
• froh-02-647924.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: rs174697

PubMed Link: 32399466

Variant Present in the following documents:

• Main text

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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: rs174697

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: rs174697

PubMed Link: 30165727

Variant Present in the following documents:

• Main text

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Biological Predictors of Clozapine Response: A Systematic Review.

Frontiers In Psychiatry

Samanaite, Ruta R; Gillespie, Amy A; Sendt, Kyra-Verena KV; McQueen, Grant G; MacCabe, James H JH; Egerton, Alice A

Publication Date: 2018

Variant appearance in text: rs174697

PubMed Link: 30093869

Variant Present in the following documents:

• fpsyt-09-00327.pdf

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Sensorimotor gating in healthy adults tested over a 15 year period.

Biological Psychology

Swerdlow, Neal R NR; Bhakta, Savita G SG; Rana, Brinda K BK; Kei, Justin J; Chou, Hsun-Hua HH; Talledo, Jo A JA

Publication Date: 2017-02

Variant appearance in text: rs174697

PubMed Link: 28027936

Variant Present in the following documents:

• Main text

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Towards a systems view of IBS.

Nature Reviews. Gastroenterology & Hepatology

Mayer, Emeran A EA; Labus, Jennifer S JS; Tillisch, Kirsten K; Cole, Steven W SW; Baldi, Pierre P

Publication Date: 2015-10

Variant appearance in text: rs174697

PubMed Link: 26303675

Variant Present in the following documents:

• Main text

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Catecholaminergic Gene Polymorphisms Are Associated with GI Symptoms and Morphological Brain Changes in Irritable Bowel Syndrome.

Plos One

Orand, Alexa A; Gupta, Arpana A; Shih, Wendy W; Presson, Angela P AP; Hammer, Christian C; Niesler, Beate B; Heendeniya, Nuwanthi N; Mayer, Emeran A EA; Chang, Lin L

Publication Date: 2015

Variant appearance in text: rs174697

PubMed Link: 26288143

Variant Present in the following documents:

• Main text
• pone.0135910.pdf

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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: rs174697

PubMed Link: 26207649

Variant Present in the following documents:

• Main text

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Association of COMT and COMT-DRD2 interaction with creative potential.

Frontiers In Human Neuroscience

Zhang, Shun S; Zhang, Muzi M; Zhang, Jinghuan J

Publication Date: 2014

Variant appearance in text: rs174697

PubMed Link: 24782743

Variant Present in the following documents:

• Main text
• fnhum-08-00216.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: rs174697

PubMed Link: 23963787

Variant Present in the following documents:

• Main text

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Potential genetic risk factors for chronic TMD: genetic associations from the OPPERA case control study.

The Journal Of Pain

Smith, Shad B SB; Maixner, Dylan W DW; Greenspan, Joel D JD; Dubner, Ronald R; Fillingim, Roger B RB; Ohrbach, Richard R; Knott, Charles C; Slade, Gary D GD; Bair, Eric E; Gibson, Dustin G DG; Zaykin, Dmitri V DV; Weir, Bruce S BS; Maixner, William W; Diatchenko, Luda L

Publication Date: 2011-11

Variant appearance in text: rs174697

PubMed Link: 22074755

Variant Present in the following documents:

• Main text

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Gender-stratified gene and gene-treatment interactions in smoking cessation.

The Pharmacogenomics Journal

Lee, W W; Bergen, A W AW; Swan, G E GE; Li, D D; Liu, J J; Thomas, P P; Tyndale, R F RF; Benowitz, N L NL; Lerman, C C; Conti, D V DV

Publication Date: 2012-12

Variant appearance in text: rs174697

PubMed Link: 21808284

Variant Present in the following documents:

• NIHMS305090-supplement-3.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: rs174697

PubMed Link: 21656904

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: rs174697

PubMed Link: 20551675

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: rs174697

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: rs174697

PubMed Link: 19673036

Variant Present in the following documents:

• Main text

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