Publications:

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Simultaneous selection of multiple important single nucleotide polymorphisms in familial genome wide association studies data.

Scientific Reports

Majumdar, Subhabrata S; Basu, Saonli S; McGue, Matt M; Chatterjee, Snigdhansu S

Publication Date: 2023-05-25

Variant appearance in text: rs165774

PubMed Link: 37231056

Variant Present in the following documents:

• Main text
• 41598_2023_Article_35379.pdf
• 41598_2023_35379_MOESM1_ESM.pdf

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Suicide-Related Single Nucleotide Polymorphisms, rs4918918 and rs10903034: Association with Dementia in Older Adults.

Genes

Abramova, Olga O; Soloveva, Kristina K; Zorkina, Yana Y; Gryadunov, Dmitry D; Ikonnikova, Anna A; Fedoseeva, Elena E; Emelyanova, Marina M; Ochneva, Aleksandra A; Andriushchenko, Nika N; Pavlov, Konstantin K; Pavlova, Olga O; Ushakova, Valeriya V; Syunyakov, Timur T; Andryushchenko, Alisa A; Karpenko, Olga O; Savilov, Victor V; Kurmishev, Marat M; Andreuyk, Denis D; Gurina, Olga O; Chekhonin, Vladimir V; Kostyuk, Georgy G; Morozova, Anna A

Publication Date: 2022-11-21

Variant appearance in text: rs165774

PubMed Link: 36421848

Variant Present in the following documents:

• Main text
• genes-13-02174.pdf

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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: rs165774

PubMed Link: 35848345

Variant Present in the following documents:

• Main text
• 10.1177_17455057221111315.pdf

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Altered Cerebral Curvature in Preterm Infants Is Associated with the Common Genetic Variation Related to Autism Spectrum Disorder and Lipid Metabolism.

Journal Of Clinical Medicine

Kim, Hyuna H; Ahn, Ja-Hye JH; Lee, Joo Young JY; Jang, Yong Hun YH; Kim, Young-Eun YE; Kim, Johanna Inhyang JI; Kim, Bung-Nyun BN; Lee, Hyun Ju HJ

Publication Date: 2022-05-31

Variant appearance in text: rs165774

PubMed Link: 35683524

Variant Present in the following documents:

• jcm-11-03135.pdf

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Genetic and epigenetic mechanisms influencing acute to chronic postsurgical pain transitions in pediatrics: Preclinical to clinical evidence.

Canadian Journal Of Pain = Revue Canadienne De La Douleur

Dourson, Adam J AJ; Willits, Adam A; Raut, Namrata G R NGR; Kader, Leena L; Young, Erin E; Jankowski, Michael P MP; Chidambaran, Vidya V

Publication Date: 2022

Variant appearance in text: rs165774

PubMed Link: 35572362

Variant Present in the following documents:

• Main text
• UCJP_6_2021799.pdf

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Central Nervous System Plasticity Influences Language and Cognitive Recovery in Adult Glioma.

Neurosurgery

Krishna, Saritha S; Kakaizada, Sofia S; Almeida, Nyle N; Brang, David D; Hervey-Jumper, Shawn S

Publication Date: 2021-09-15

Variant appearance in text: rs165774

PubMed Link: 33476391

Variant Present in the following documents:

• Main text

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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: rs165774

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: rs165774

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: rs165774

PubMed Link: 32399466

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• 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: rs165774

PubMed Link: 32133580

Variant Present in the following documents:

• Main text

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Genetic variants and cognitive functions in patients with brain tumors.

Neuro-Oncology

Correa, Denise D DD; Satagopan, Jaya J; Martin, Axel A; Braun, Erica E; Kryza-Lacombe, Maria M; Cheung, Kenneth K; Sharma, Ajay A; Dimitriadoy, Sofia S; O'Connell, Kelli K; Leong, Siok S; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I

Publication Date: 2019-10-09

Variant appearance in text: rs165774

PubMed Link: 31123752

Variant Present in the following documents:

• Main text

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Genetic Variants Associated with Cancer Pain and Response to Opioid Analgesics: Implications for Precision Pain Management.

Seminars In Oncology Nursing

Yang, Gee Su GS; Barnes, Natalie M NM; Lyon, Debra E DE; Dorsey, Susan G SG

Publication Date: 2019-06

Variant appearance in text: rs165774

PubMed Link: 31085105

Variant Present in the following documents:

• Main text

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A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study.

International Journal Of Geriatric Psychiatry

Driscoll, Ira I; Snively, Beverly M BM; Espeland, Mark A MA; Shumaker, Sally A SA; Rapp, Stephen R SR; Goveas, Joseph S JS; Casanova, Ramon L RL; Wactawski-Wende, Jean J; Manson, JoAnn E JE; Rossom, Rebecca R; Brooks, Janet J; Hernandez, Dena G DG; Singleton, Andrew B AB; Resnick, Susan M SM

Publication Date: 2019-05

Variant appearance in text: rs165774

PubMed Link: 30706571

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: rs165774

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

Human Genetics

Liu, Jiaqi J; Zhou, Yangzhong Y; Liu, Sen S; Song, Xiaofei X; Yang, Xin-Zhuang XZ; Fan, Yanhui Y; Chen, Weisheng W; Akdemir, Zeynep Coban ZC; Yan, Zihui Z; Zuo, Yuzhi Y; Du, Renqian R; Liu, Zhenlei Z; Yuan, Bo B; Zhao, Sen S; Liu, Gang G; Chen, Yixin Y; Zhao, Yanxue Y; Lin, Mao M; Zhu, Qiankun Q; Niu, Yuchen Y; Liu, Pengfei P; Ikegawa, Shiro S; Song, You-Qiang YQ; Posey, Jennifer E JE; Qiu, Guixing G; , ; Zhang, Feng F; Wu, Zhihong Z; Lupski, James R JR; Wu, Nan N

Publication Date: 2018-07

Variant appearance in text: rs165774

PubMed Link: 30019117

Variant Present in the following documents:

• Main text

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Potential link between genetic polymorphisms of catechol-O-methyltransferase and dopamine receptors and treatment efficacy of risperidone on schizophrenia.

Neuropsychiatric Disease And Treatment

Han, Jiyang J; Li, Yan Y; Wang, Xumei X

Publication Date: 2017

Variant appearance in text: rs165774

PubMed Link: 29255361

Variant Present in the following documents:

• Main text
• ndt-13-2935.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: rs165774

PubMed Link: 27521242

Variant Present in the following documents:

• Main text
• pyw070.pdf

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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: rs165774

PubMed Link: 27217152

Variant Present in the following documents:

• Main text
• mp201674a.pdf

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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: rs165774

PubMed Link: 27091610

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: rs165774

PubMed Link: 26207649

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: rs165774

PubMed Link: 25929431

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: rs165774

PubMed Link: 25793616

Variant Present in the following documents:

• Main text

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Is the experience of thermal pain genetics dependent?

Biomed Research International

Horjales-Araujo, Emilia E; Dahl, Joergen B JB

Publication Date: 2015

Variant appearance in text: rs165774

PubMed Link: 25699274

Variant Present in the following documents:

• Main text
• BMRI2015-349584.pdf

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Polymorphisms in genes implicated in dopamine, serotonin and noradrenalin metabolism suggest association with cerebrospinal fluid monoamine metabolite concentrations in psychosis.

Behavioral And Brain Functions : Bbf

Andreou, Dimitrios D; Söderman, Erik E; Axelsson, Tomas T; Sedvall, Göran C GC; Terenius, Lars L; Agartz, Ingrid I; Jönsson, Erik G EG

Publication Date: 2014-07-29

Variant appearance in text: rs165774

PubMed Link: 25073638

Variant Present in the following documents:

• Main text
• 1744-9081-10-26.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: rs165774

PubMed Link: 24639636

Variant Present in the following documents:

• Main text
• fnbeh-08-00071.pdf

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Genetic association analysis of 300 genes identifies a risk haplotype in SLC18A2 for post-traumatic stress disorder in two independent samples.

Neuropsychopharmacology : Official Publication Of The American College Of Neuropsychopharmacology

Solovieff, Nadia N; Roberts, Andrea L AL; Ratanatharathorn, Andrew A; Haloosim, Michelle M; De Vivo, Immaculata I; King, Anthony P AP; Liberzon, Israel I; Aiello, Allison A; Uddin, Monica M; Wildman, Derek E DE; Galea, Sandro S; Smoller, Jordan W JW; Purcell, Shaun M SM; Koenen, Karestan C KC

Publication Date: 2014-07

Variant appearance in text: rs165774

PubMed Link: 24525708

Variant Present in the following documents:

• Main text

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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: rs165774

PubMed Link: 24343288

Variant Present in the following documents:

• Main text

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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: rs165774

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: rs165774

PubMed Link: 23880798

Variant Present in the following documents:

• Main text

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No association of catechol-O-methyltransferase polymorphisms with schizophrenia in the Han Chinese population.

Genetic Testing And Molecular Biomarkers

Zhang, Fuquan F; Liu, Chenxing C; Chen, Yaguang Y; Wang, Lifang L; Lu, Tianlan T; Yan, Hao H; Ruan, Yanyan Y; Yue, Weihua W; Zhang, Dai D

Publication Date: 2012-09

Variant appearance in text: rs165774

PubMed Link: 22963606

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: rs165774

PubMed Link: 22956598

Variant Present in the following documents:

• annrheumdis-2012-201742-s1.pdf

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A novel SNP in COMT is associated with alcohol dependence but not opiate or nicotine dependence: a case control study.

Behavioral And Brain Functions : Bbf

Voisey, Joanne J; Swagell, Christopher D CD; Hughes, Ian P IP; Lawford, Bruce R BR; Young, Ross M D RM; Morris, C Phillip CP

Publication Date: 2011-12-31

Variant appearance in text: rs165774

PubMed Link: 22208661

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: rs165774

PubMed Link: 22021758

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: rs165774

PubMed Link: 21808284

Variant Present in the following documents:

• NIHMS305090-supplement-3.pdf

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Pharmacogenetics of antidepressant response.

Journal Of Psychiatry & Neuroscience : Jpn

Porcelli, Stefano S; Drago, Antonio A; Fabbri, Chiara C; Gibiino, Sara S; Calati, Raffaella R; Serretti, Alessandro A

Publication Date: 2011-03

Variant appearance in text: rs165774

PubMed Link: 21172166

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: rs165774

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: rs165774

PubMed Link: 20551675

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• 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: rs165774

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: rs165774

PubMed Link: 19673036

Variant Present in the following documents:

• Main text

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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: rs165774

PubMed Link: 18937309

Variant Present in the following documents:

• Main text

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