Publications:

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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: rs174696

PubMed Link: 35683524

Variant Present in the following documents:

• jcm-11-03135.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: rs174696

PubMed Link: 34725583

Variant Present in the following documents:

• Main text
• cureus-0013-00000018311.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: rs174696

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: rs174696

PubMed Link: 32782694

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: rs174696

PubMed Link: 31123752

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: rs174696

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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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: rs174696

PubMed Link: 30178121

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: rs174696

PubMed Link: 30093869

Variant Present in the following documents:

• fpsyt-09-00327.pdf

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The Genetics of Treatment-Resistant Depression: A Critical Review and Future Perspectives.

The International Journal Of Neuropsychopharmacology

Fabbri, Chiara C; Corponi, Filippo F; Souery, Daniel D; Kasper, Siegfried S; Montgomery, Stuart S; Zohar, Joseph J; Rujescu, Dan D; Mendlewicz, Julien J; Serretti, Alessandro A

Publication Date: 2019-02-01

Variant appearance in text: rs174696

PubMed Link: 29688548

Variant Present in the following documents:

• Main text
• pyy024.pdf

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Association of Polymorphisms in Pharmacogenetic Candidate Genes with Propofol Susceptibility.

Scientific Reports

Zhong, Qi Q; Chen, Xiangdong X; Zhao, Yan Y; Liu, Ru R; Yao, Shanglong S

Publication Date: 2017-06-13

Variant appearance in text: rs174696

PubMed Link: 28611364

Variant Present in the following documents:

• Main text
• 41598_2017_Article_3229.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: rs174696

PubMed Link: 28027936

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: rs174696

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: rs174696

PubMed Link: 27091610

Variant Present in the following documents:

• Main text

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Peer Influence, Genetic Propensity, and Binge Drinking: A Natural Experiment and a Replication.

Ajs; American Journal Of Sociology

Guo, Guang G; Li, Yi Y; Wang, Hongyu H; Cai, Tianji T; Duncan, Greg J GJ

Publication Date: 2015-11

Variant appearance in text: rs174696

PubMed Link: 26900620

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: rs174696

PubMed Link: 25929431

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: rs174696

PubMed Link: 25819021

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: rs174696

PubMed Link: 25545355

Variant Present in the following documents:

• Main text
• pone.0115716.pdf

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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: rs174696

PubMed Link: 24343288

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: rs174696

PubMed Link: 23880798

Variant Present in the following documents:

• Main text

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Multifaceted genomic risk for brain function in schizophrenia.

Neuroimage

Chen, Jiayu J; Calhoun, Vince D VD; Pearlson, Godfrey D GD; Ehrlich, Stefan S; Turner, Jessica A JA; Ho, Beng-Choon BC; Wassink, Thomas H TH; Michael, Andrew M AM; Liu, Jingyu J

Publication Date: 2012-07-16

Variant appearance in text: rs174696

PubMed Link: 22440650

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: rs174696

PubMed Link: 21857968

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: rs174696

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: rs174696

PubMed Link: 21656904

Variant Present in the following documents:

• Main text

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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: rs174696

PubMed Link: 21172166

Variant Present in the following documents:

• Main text

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A candidate gene association study of alcohol consumption in young women.

Alcoholism, Clinical And Experimental Research

Agrawal, Arpana A; Lynskey, Michael T MT; Todorov, Alexandre A AA; Schrage, Andrew J AJ; Littlefield, Andrew K AK; Grant, Julia D JD; Zhu, Qin Q; Nelson, Elliot C EC; Madden, Pamela A F PA; Bucholz, Kathleen K KK; Sher, Kenneth J KJ; Heath, Andrew C AC

Publication Date: 2011-03

Variant appearance in text: rs174696

PubMed Link: 21143251

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: rs174696

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: rs174696

PubMed Link: 20551675

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: rs174696

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: rs174696

PubMed Link: 18937309

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: rs174696

PubMed Link: 18663369

Variant Present in the following documents:

• Main text

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A network of dopaminergic gene variations implicated as risk factors for schizophrenia.

Human Molecular Genetics

Talkowski, Michael E ME; Kirov, George G; Bamne, Mikhil M; Georgieva, Lyudmila L; Torres, Gonzalo G; Mansour, Hader H; Chowdari, Kodavali V KV; Milanova, Vihra V; Wood, Joel J; McClain, Lora L; Prasad, Konasale K; Shirts, Brian B; Zhang, Jianping J; O'Donovan, Michael C MC; Owen, Michael J MJ; Devlin, Bernie B; Nimgaonkar, Vishwajit L VL

Publication Date: 2008-03-01

Variant appearance in text: rs174696

PubMed Link: 18045777

Variant Present in the following documents:

• Main text

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