COMT c.615+310C>T

Variant ID: 22-19952132-C-T

NM_000754.3(COMT):c.615+310C>T

This variant was identified in 46 publications

View GRCh38 version.




Publications:


Pharmacogenetic Analysis Enables Optimization of Pain Therapy: A Case Report of Ineffective Oxycodone Therapy.

Journal Of Personalized Medicine
Wiss, Florine M FM; Stäuble, Céline K CK; Meyer Zu Schwabedissen, Henriette E HE; Allemann, Samuel S SS; Lampert, Markus L ML
Publication Date: 2023-05-13

Variant appearance in text: rs4646316
PubMed Link: 37240999
Variant Present in the following documents:
  • jpm-13-00829.pdf
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A Missense Variant in COMT Associated with Hearing Loss among Young Adults: The National Longitudinal Study of Adolescent to Adult Health (Add Health).

Biomedicines
Li, Chuan-Ming CM; Chen, Le L; Chen, Guanjie G; Zhang, Jianhua J; Hoffman, Howard J HJ
Publication Date: 2022-10-31

Variant appearance in text: rs4646316
PubMed Link: 36359276
Variant Present in the following documents:
  • Main text
  • biomedicines-10-02756.pdf
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Genome-Wide Association Study Identifies Candidate Loci Associated with Opioid Analgesic Requirements in the Treatment of Cancer Pain.

Cancers
Nishizawa, Daisuke D; Terui, Takeshi T; Ishitani, Kunihiko K; Kasai, Shinya S; Hasegawa, Junko J; Nakayama, Kyoko K; Ebata, Yuko Y; Ikeda, Kazutaka K
Publication Date: 2022-09-27

Variant appearance in text: rs4646316
PubMed Link: 36230616
Variant Present in the following documents:
  • Main text
  • cancers-14-04692.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: rs4646316
PubMed Link: 35848345
Variant Present in the following documents:
  • Main text
  • 10.1177_17455057221111315.pdf
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Brain Radiotoxicity-Related 15CAcBRT Gene Expression Signature Predicts Survival Prognosis of Glioblastoma Patients.

Neuro-Oncology
Reyes-González, Jesús J; Barajas-Olmos, Francisco F; García-Ortiz, Humberto H; Magraner-Pardo, Lorena L; Pons, Tirso T; Moreno, Sergio S; Aguirre-Cruz, Lucinda L; Reyes-Abrahantes, Andy A; Martínez-Hernández, Angélica A; Contreras-Cubas, Cecilia C; Barrios-Payan, Jorge J; Ruiz-Garcia, Henry J HJ; Hernandez-Pando, Rogelio R; Quiñones-Hinojosa, Alfredo A; Orozco, Lorena L; Abrahantes-Pérez, María Del Carmen MDC
Publication Date: 2022-07-08

Variant appearance in text: rs4646316
PubMed Link: 35802478
Variant Present in the following documents:
  • Main text
  • noac171.pdf
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Cannabinoid Hyperemesis Syndrome Survey and Genomic Investigation.

Cannabis And Cannabinoid Research
Russo, Ethan B EB; Spooner, Chris C; May, Len L; Leslie, Ryan R; Whiteley, Venetia L VL
Publication Date: 2022-06

Variant appearance in text: rs4646316
PubMed Link: 34227878
Variant Present in the following documents:
  • Main text
  • can.2021.0046.pdf
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Pharmacogenomics as a Tool to Limit Acute and Long-Term Adverse Effects of Chemotherapeutics: An Update in Pediatric Oncology.

Frontiers In Pharmacology
Bernsen, Emma C EC; Hagleitner, Melanie M MM; Kouwenberg, Theodorus W TW; Hanff, Lidwien M LM
Publication Date: 2020

Variant appearance in text: rs4646316
PubMed Link: 32848787
Variant Present in the following documents:
  • Table_1.pdf
View BVdb publication page



Pharmacogenomics and Pharmacogenetics in Osteosarcoma: Translational Studies and Clinical Impact.

International Journal Of Molecular Sciences
Hattinger, Claudia Maria CM; Patrizio, Maria Pia MP; Luppi, Silvia S; Serra, Massimo M
Publication Date: 2020-06-30

Variant appearance in text: rs4646316
PubMed Link: 32629971
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4646316
PubMed Link: 32533012
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_65332.pdf
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FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders.

Brain And Behavior
Zhou, Binbin B; Wang, Huan H; Cai, Yu Y; Wen, Han H; Wang, Lulu L; Zhu, Min M; Chen, Yunqing Y; Yu, Yanyan Y; Lu, Xi X; Zhou, Meihong M; Fang, Pu P; Li, Xiaobing X; Hong, Daojun D
Publication Date: 2020-06

Variant appearance in text: COMT: 615+310C>T; rs4646316
PubMed Link: 32307925
Variant Present in the following documents:
  • BRB3-10-e01625-s001.xlsx, sheet 1
View BVdb publication page



Understanding the Physiological Links Between Physical Frailty and Cognitive Decline.

Aging And Disease
Ma, Lina L; Chan, Piu P
Publication Date: 2020-04

Variant appearance in text: rs4646316
PubMed Link: 32257550
Variant Present in the following documents:
  • Main text
  • ad-11-2-405.pdf
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Influence of Genetic Variation in COMT on Cisplatin-Induced Nephrotoxicity in Cancer Patients.

Genes
Agema, Bram C BC; Koolen, Stijn L W SLW; With, Mirjam de M; Doorn, Nadia van NV; Heersche, Niels N; Hoop, Esther Oomen-de EO; Visser, Sabine S; Aerts, Joachim G J V JGJV; Bins, Sander S; Schaik, Ron H N van RHNV; Mathijssen, Ron H J RHJ
Publication Date: 2020-03-27

Variant appearance in text: rs4646316
PubMed Link: 32230800
Variant Present in the following documents:
  • 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: rs4646316
PubMed Link: 32133580
Variant Present in the following documents:
  • Main text
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Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy (The PRONE Study).

Cancers
Driessen, Chantal M CM; Ham, Janneke C JC; Te Loo, Maroeska M; van Meerten, Esther E; van Lamoen, Maurits M; Hakobjan, Marina H MH; Takes, Robert P RP; van der Graaf, Winette T WT; Kaanders, Johannes H JH; Coenen, Marieke J H MJH; van Herpen, Carla M CM
Publication Date: 2019-04-17

Variant appearance in text: rs4646316
PubMed Link: 30999660
Variant Present in the following documents:
  • Main text
  • cancers-11-00551.pdf
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The genetic vulnerability to cisplatin ototoxicity: a systematic review.

Scientific Reports
Tserga, Evangelia E; Nandwani, Tara T; Edvall, Niklas K NK; Bulla, Jan J; Patel, Poulam P; Canlon, Barbara B; Cederroth, Christopher R CR; Baguley, David M DM
Publication Date: 2019-03-05

Variant appearance in text: rs4646316
PubMed Link: 30837596
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_40138.pdf
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Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology.

The Journal Of Molecular Diagnostics : Jmd
Swart, Marelize M; Stansberry, Wesley M WM; Pratt, Victoria M VM; Medeiros, Elizabeth B EB; Kiel, Patrick J PJ; Shen, Fei F; Schneider, Bryan P BP; Skaar, Todd C TC
Publication Date: 2019-05

Variant appearance in text: COMT: 615+310C>T; rs4646316
PubMed Link: 30794985
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: rs4646316
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Shared biological pathways for frailty and cognitive impairment: A systematic review.

Ageing Research Reviews
Sargent, Lana L; Nalls, Mike M; Starkweather, Angela A; Hobgood, Sarah S; Thompson, Holly H; Amella, Elaine J EJ; Singleton, Andrew A
Publication Date: 2018-11

Variant appearance in text: rs4646316
PubMed Link: 30102995
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: rs4646316
PubMed Link: 30093869
Variant Present in the following documents:
  • fpsyt-09-00327.pdf
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Genetic Risk for Age-Related Cognitive Impairment Does Not Predict Cognitive Performance in Middle Age.

Journal Of Alzheimer'S Disease : Jad
Korthauer, Laura E LE; Awe, Elizabeth E; Frahmand, Marijam M; Driscoll, Ira I
Publication Date: 2018

Variant appearance in text: rs4646316
PubMed Link: 29865048
Variant Present in the following documents:
  • Main text
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Pharmacogenetic analysis of irreversible severe cisplatin-induced nephropathy: a case report of a 27-year-old woman.

British Journal Of Clinical Pharmacology
de Jong, Corine C; Sanders, Stefan S; Creemers, Geert-Jan GJ; Burylo, Artur M AM; Taks, Margot M; Schellens, Jan H M JHM; Deenen, Maarten J MJ
Publication Date: 2017-09

Variant appearance in text: rs4646316
PubMed Link: 28560854
Variant Present in the following documents:
  • Main text
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TPMT, COMT and ACYP2 genetic variants in paediatric cancer patients with cisplatin-induced ototoxicity.

Pharmacogenetics And Genomics
Thiesen, Signe S; Yin, Peng P; Jorgensen, Andrea L AL; Zhang, Jieying Eunice JE; Manzo, Valentina V; McEvoy, Laurence L; Barton, Christopher C; Picton, Susan S; Bailey, Simon S; Brock, Penelope P; Vyas, Harish H; Walker, David D; Makin, Guy G; Bandi, Srinivas S; Pizer, Barry B; Hawcutt, Daniel B DB; Pirmohamed, Munir M
Publication Date: 2017-06

Variant appearance in text: rs4646316
PubMed Link: 28445188
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: rs4646316
PubMed Link: 27217152
Variant Present in the following documents:
  • Main text
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Pharmacogenomics in Pediatric Patients: Towards Personalized Medicine.

Paediatric Drugs
Maagdenberg, Hedy H; Vijverberg, Susanne J H SJ; Bierings, Marc B MB; Carleton, Bruce C BC; Arets, Hubertus G M HG; de Boer, Anthonius A; Maitland-van der Zee, Anke H AH
Publication Date: 2016-08

Variant appearance in text: rs4646316
PubMed Link: 27142473
Variant Present in the following documents:
  • Main text
  • 40272_2016_Article_176.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: rs4646316
PubMed Link: 27091610
Variant Present in the following documents:
  • Main text
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Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study.

Schizophrenia Research
Greenwood, Tiffany A TA; Lazzeroni, Laura C LC; Calkins, Monica E ME; Freedman, Robert R; Green, Michael F MF; Gur, Raquel E RE; Gur, Ruben C RC; Light, Gregory A GA; Nuechterlein, Keith H KH; Olincy, Ann A; Radant, Allen D AD; Seidman, Larry J LJ; Siever, Larry J LJ; Silverman, Jeremy M JM; Stone, William S WS; Sugar, Catherine A CA; Swerdlow, Neal R NR; Tsuang, Debby W DW; Tsuang, Ming T MT; Turetsky, Bruce I BI; Braff, David L DL
Publication Date: 2016-01

Variant appearance in text: rs4646316
PubMed Link: 26597662
Variant Present in the following documents:
  • Main text
View BVdb publication page



Proinflammatory genotype is associated with the frailty phenotype in the English Longitudinal Study of Ageing.

Aging Clinical And Experimental Research
Mekli, Krisztina K; Nazroo, James Y JY; Marshall, Alan D AD; Kumari, Meena M; Pendleton, Neil N
Publication Date: 2016-06

Variant appearance in text: rs4646316
PubMed Link: 26248682
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4646316
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: rs4646316
PubMed Link: 25793616
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts.

Plos One
Hagleitner, Melanie M MM; Coenen, Marieke J H MJ; Patino-Garcia, Ana A; de Bont, Eveline S J M ES; Gonzalez-Neira, Anna A; Vos, Hanneke I HI; van Leeuwen, Frank N FN; Gelderblom, Hans H; Hoogerbrugge, Peter M PM; Guchelaar, Henk-Jan HJ; Te Loo, Maroeska W M MW
Publication Date: 2014

Variant appearance in text: rs4646316
PubMed Link: 25551397
Variant Present in the following documents:
  • Main text
  • pone.0115869.pdf
View BVdb publication page



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: rs4646316
PubMed Link: 24639636
Variant Present in the following documents:
  • Main text
  • fnbeh-08-00071.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: rs4646316
PubMed Link: 24343288
Variant Present in the following documents:
  • Main text
View BVdb publication page



The role of inherited TPMT and COMT genetic variation in cisplatin-induced ototoxicity in children with cancer.

Clinical Pharmacology And Therapeutics
Yang, J J JJ; Lim, J Y S JY; Huang, J J; Bass, J J; Wu, J J; Wang, C C; Fang, J J; Stewart, E E; Harstead, E H EH; E, S S; Robinson, G W GW; Evans, W E WE; Pappo, A A; Zuo, J J; Relling, M V MV; Onar-Thomas, A A; Gajjar, A A; Stewart, C F CF
Publication Date: 2013-08

Variant appearance in text: rs4646316
PubMed Link: 23820299
Variant Present in the following documents:
  • Main text
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Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children.

Clinical Pharmacology And Therapeutics
Pussegoda, K K; Ross, C J CJ; Visscher, H H; Yazdanpanah, M M; Brooks, B B; Rassekh, S R SR; Zada, Y F YF; Dubé, M-P MP; Carleton, B C BC; Hayden, M R MR; ,
Publication Date: 2013-08

Variant appearance in text: rs4646316
PubMed Link: 23588304
Variant Present in the following documents:
  • Main text
View BVdb publication page



Chemotherapy refractory testicular germ cell tumor is associated with a variant in Armadillo Repeat gene deleted in Velco-Cardio-Facial syndrome (ARVCF).

Frontiers In Endocrinology
Fung, Chunkit C; Vaughn, David J DJ; Mitra, Nandita N; Ciosek, Stephanie L SL; Vardhanabhuti, Saran S; Nathanson, Katherine L KL; Kanetsky, Peter A PA
Publication Date: 2012

Variant appearance in text: rs4646316
PubMed Link: 23248619
Variant Present in the following documents:
  • Main text
  • fendo-03-00163.pdf
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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: rs4646316
PubMed Link: 22963606
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4646316
PubMed Link: 22021758
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs4646316
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



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: rs4646316
PubMed Link: 21656904
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: rs4646316
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: rs4646316
PubMed Link: 20551675
Variant Present in the following documents:
  • Main text
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Association of COMT haplotypes and breast cancer risk in caucasian women.

Anticancer Research
Peterson, Neeraja B NB; Trentham-Dietz, Amy A; Garcia-Closas, Montserrat M; Newcomb, Polly A PA; Titus-Ernstoff, Linda L; Huang, Yifan Y; Chanock, Stephen J SJ; Haines, Jonathan L JL; Egan, Kathleen M KM
Publication Date: 2010-01

Variant appearance in text: rs4646316
PubMed Link: 20150638
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: rs4646316
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: rs4646316
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: rs4646316
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: rs4646316
PubMed Link: 18663369
Variant Present in the following documents:
  • Main text
View BVdb publication page