Publications:

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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: rs460700

PubMed Link: 35237725

Variant Present in the following documents:

• Main text
• 10.1177_23982128221079548.pdf

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The dopamine transporter gene SLC6A3: multidisease risks.

Molecular Psychiatry

Reith, Maarten E A MEA; Kortagere, Sandhya S; Wiers, Corinde E CE; Sun, Hui H; Kurian, Manju A MA; Galli, Aurelio A; Volkow, Nora D ND; Lin, Zhicheng Z

Publication Date: 2022-02

Variant appearance in text: rs460700

PubMed Link: 34650206

Variant Present in the following documents:

• 41380_2021_1341_MOESM1_ESM.pdf

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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: rs460700

PubMed Link: 32133580

Variant Present in the following documents:

• Main text

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Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

Bmc Cancer

Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F

Publication Date: 2017-05-12

Variant appearance in text: rs460700

PubMed Link: 28499365

Variant Present in the following documents:

• 12885_2017_3314_MOESM1_ESM.xls, sheet 1

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The SLC6A3 gene possibly affects susceptibility to late-onset alcohol dependence but not specific personality traits in a Han Chinese population.

Plos One

Huang, Chang-Chih CC; Kuo, Shin-Chang SC; Yeh, Yi-Wei YW; Chen, Chun-Yen CY; Yen, Che-Hung CH; Liang, Chih-Sung CS; Ho, Pei-Shen PS; Lu, Ru-Band RB; Huang, San-Yuan SY

Publication Date: 2017

Variant appearance in text: rs460700

PubMed Link: 28182634

Variant Present in the following documents:

• Main text
• pone.0171170.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: rs460700

PubMed Link: 27217152

Variant Present in the following documents:

• Main text
• mp201674a.pdf

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Fine-mapping reveals novel alternative splicing of the dopamine transporter.

American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics

Talkowski, Michael E ME; McCann, Kathleen L KL; Chen, Michael M; McClain, Lora L; Bamne, Mikhil M; Wood, Joel J; Chowdari, Kodavali V KV; Watson, Annie A; Prasad, Konasale M KM; Kirov, George G; Georgieva, Lyudmilla L; Toncheva, Draga D; Mansour, Hader H; Lewis, David A DA; Owen, Michael M; O'Donovan, Michael M; Papasaikas, Panagiotis P; Sullivan, Patrick P; Ruderfer, Douglas D; Yao, Jeffrey K JK; Leonard, Sherry S; Thomas, Pramod P; Miyajima, Fabio F; Quinn, John J; Lopez, A Javier AJ; Nimgaonkar, Vishwajit L VL

Publication Date: 2010-12-05

Variant appearance in text: rs460700

PubMed Link: 20957647

Variant Present in the following documents:

• Main text

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Chromosome 5p Region SNPs Are Associated with Risk of NSCLC among Women.

Journal Of Cancer Epidemiology

Van Dyke, Alison L AL; Cote, Michele L ML; Wenzlaff, Angela S AS; Abrams, Judith J; Land, Susan S; Iyer, Priyanka P; Schwartz, Ann G AG

Publication Date: 2009

Variant appearance in text: rs460700

PubMed Link: 20445798

Variant Present in the following documents:

• Main text
• JCE2009-242151.pdf

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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: rs460700

PubMed Link: 18821566

Variant Present in the following documents:

• Main text

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