DBH c.340-1149T>C

Variant ID: 9-136503819-T-C

NM_000787.3(DBH):c.340-1149T>C

This variant was identified in 11 publications

View GRCh38 version.




Publications:


Multi-ancestry meta-analysis of tobacco use disorders based on electronic health record data prioritizes novel candidate risk genes and reveals associations with numerous health outcomes.

Medrxiv : The Preprint Server For Health Sciences
Toikumo, Sylvanus S; Jennings, Mariela V MV; Pham, Benjamin B; Lee, Hyunjoon H; Mallard, Travis T TT; Bianchi, Sevim B SB; Meredith, John J JJ; Vilar-Rib, Laura L; Xu, Heng H; Hatoum, Alexander S AS; Johnson, Emma C EC; Pazdernik, Vanessa V; Jinwala, Zeal Z; Leger, Brittany S BS; Niarchou, Maria M; Ehinmowo, Michael M; BioBank, Penn Medicine PM; Veteran, Million M; Jenkins, Greg D GD; Batzler, Anthony A; Pendegraft, Richard R; Palmer, Abraham A AA; Zhou, Hang H; Biernacka, Joanna M JM; Coombes, Brandon J BJ; Gelernter, Joel J; Xu, Ke K; Hancock, Dana B DB; Cox, Nancy J NJ; Smoller, Jordan W JW; Davis, Lea K LK; Justice, Amy C AC; Kranzler, Henry R HR; Kember, Rachel L RL; Sanchez-Roige, Sandra S
Publication Date: 2023-03-29

Variant appearance in text: rs2007153
PubMed Link: 37034728
Variant Present in the following documents:
  • Main text
  • nihpp-2023.03.27.23287713v1.pdf
View BVdb publication page



Factors in the neurodevelopment of negative urgency: Findings from a community-dwelling sample.

Brain And Neuroscience Advances
Evans, Casey L CL; Sawyer, Kayle S KS; Levy, Sarah A SA; Conklin, Jessica P JP; McDonough, EmilyKate E; Gansler, David A DA
Publication Date: 2022

Variant appearance in text: rs2007153
PubMed Link: 35237725
Variant Present in the following documents:
  • Main text
  • 10.1177_23982128221079548.pdf
View BVdb publication page



Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment.

Behavioural Neurology
Li, Lanlan L; Yang, Yeying Y; Zhang, Qi Q; Wang, Jiao J; Jiang, Jiehui J; Neuroimaging Initiative, Alzheimer's Disease AD
Publication Date: 2021

Variant appearance in text: rs2007153
PubMed Link: 34336000
Variant Present in the following documents:
  • Main text
  • BN2021-3359103.pdf
View BVdb publication page



Association Analyses of SNAP25, HNMT, FCHSD1, and DBH Single-Nucleotide Polymorphisms with Parkinson's Disease in a Northern Chinese Population.

Neuropsychiatric Disease And Treatment
Dai, Cuiyun C; Zhang, Yichi Y; Zhan, Xiaoni X; Tian, Meihui M; Pang, Hao H
Publication Date: 2021

Variant appearance in text: rs2007153
PubMed Link: 34079266
Variant Present in the following documents:
  • Main text
  • ndt-17-1689.pdf
View BVdb publication page



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: rs2007153
PubMed Link: 32133580
Variant Present in the following documents:
  • Main text
View BVdb publication page



Roles of Response Inhibition and Gene-Environment Interplay in Pathways to Adolescents' Externalizing Problems.

Journal Of Research On Adolescence : The Official Journal Of The Society For Research On Adolescence
Wang, Frances L FL; Chassin, Laurie L; Lee, Matthew M; Haller, Moira M; King, Kevin K
Publication Date: 2017-06

Variant appearance in text: rs2007153
PubMed Link: 28876522
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs2007153
PubMed Link: 27217152
Variant Present in the following documents:
View BVdb publication page



Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer.

Genetic Epidemiology
Poirier, Julia G JG; Brennan, Paul P; McKay, James D JD; Spitz, Margaret R MR; Bickeböller, Heike H; Risch, Angela A; Liu, Geoffrey G; Le Marchand, Loic L; Tworoger, Shelley S; McLaughlin, John J; Rosenberger, Albert A; Heinrich, Joachim J; Brüske, Irene I; Muley, Thomas T; Henderson, Brian E BE; Wilkens, Lynne R LR; Zong, Xuchen X; Li, Yafang Y; Hao, Ke K; Timens, Wim W; Bossé, Yohan Y; Sin, Don D DD; Obeidat, Ma'en M; Amos, Christopher I CI; Hung, Rayjean J RJ
Publication Date: 2015-03

Variant appearance in text: rs2007153
PubMed Link: 25644374
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: rs2007153
PubMed Link: 21808284
Variant Present in the following documents:
  • NIHMS305090-supplement-3.pdf
View BVdb publication page



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: rs2007153
PubMed Link: 19673036
Variant Present in the following documents:
  • Main text
View BVdb publication page



SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE
Publication Date: 2008-12-05

Variant appearance in text: rs2007153
PubMed Link: 18821566
Variant Present in the following documents:
  • Main text
View BVdb publication page