Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 61 Records) |
Query Trace: Attention and SLC6A3[original query] |
---|
Positive effects of methylphenidate on hyperactivity are moderated by monoaminergic gene variants in children with autism spectrum disorders. The pharmacogenomics journal 2014 Jun 14 (3): 295-302. McCracken J T, Badashova K K, Posey D J, Aman M G, Scahill L, Tierney E, Arnold L E, Vitiello B, Whelan F, Chuang S Z, Davies M, Shah B, McDougle C J, Nurmi E |
Meta-analysis of the association between dopamine transporter genotype and response to methylphenidate treatment in ADHD. The pharmacogenomics journal 2014 Feb 14 (1): 77-84. Kambeitz J, Romanos M, Ettinger |
Differential associations of dopamine-related polymorphisms with discrete components of reaction time variability: relevance for attention deficit/hyperactivity disorder. Neuropsychobiology 2014 69 (4): 220-6. Grant Phillip, Kuepper Yvonne, Wielpuetz Catrin, Hennig Jürg |
Association of dopamine gene variants, emotion dysregulation and ADHD in autism spectrum disorder. Research in developmental disabilities 2014 Jul 35 (7): 1658-65. Gadow Kenneth D, Pinsonneault Julia K, Perlman Greg, Sadee Wolfga |
Dopamine transporter genotype and stimulant dose-response in youth with attention-deficit/hyperactivity disorder. Journal of child and adolescent psychopharmacology 2014 Jun 24 (5): 238-44. Stein Mark A, Waldman Irwin, Newcorn Jeffrey, Bishop Jeffrey, Kittles Rick, Cook Edwin |
Further evidence for the association between a polymorphism in the promoter region of SLC6A3/DAT1 and ADHD: findings from a sample of adults. European archives of psychiatry and clinical neuroscience 2014 Aug 264 (5): 401-8. de Azeredo Lucas A, Rovaris Diego L, Mota Nina R, Polina Evelise R, Marques Francine Z, Contini Verônica, Vitola Eduardo S, Belmonte-de-Abreu Paulo, Rohde Luis A, Grevet Eugenio H, Bau Claiton H |
Influence of DAT1 and COMT variants on neural activation during response inhibition in adolescents with attention-deficit/hyperactivity disorder and healthy controls. Psychological medicine 2015 Jun 1-12. van Rooij D, Hoekstra P J, Bralten J, Hakobjan M, Oosterlaan J, Franke B, Rommelse N, Buitelaar J K, Hartman C |
An association between a dopamine transporter gene (SLC6A3) haplotype and ADHD symptom measures in nonclinical adults. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Mar 168B (2): 89-96. Tong Janette H S, Cummins Tarrant D R, Johnson Beth P, McKinley Leigh-Anne, Pickering Hayley E, Fanning Peter, Stefanac Nicole R, Newman Daniel P, Hawi Ziarih, Bellgrove Mark |
Genetic associations with reflexive visual attention in infancy and childhood. Developmental science 2015 Nov . Lundwall Rebecca A, Dannemiller James L, Goldsmith H Hi |
Meta-analysis of the association of the SLC6A3 3'-UTR VNTR with cognition. Neuroscience and biobehavioral reviews 2015 Nov . Ettinger Ulrich, Merten Natascha, Kambeitz Jose |
The molecular genetic architecture of attention deficit hyperactivity disorder. Molecular psychiatry 2015 Mar 20 (3): 289-97. Hawi Z, Cummins T D R, Tong J, Johnson B, Lau R, Samarrai W, Bellgrove M |
MAOA Influences the Trajectory of Attentional Development. Frontiers in human neuroscience 2016 10 424. Lundwall Rebecca A, Rasmussen Claudia |
Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies. Molecular psychiatry 2016 May . Bonvicini C, Faraone S V, Scassellati |
Enlarged striatal volume in adults with ADHD carrying the 9-6 haplotype of the dopamine transporter gene DAT1. Journal of neural transmission (Vienna, Austria : 1996) 2016 Mar . Onnink A Marten H, Franke Barbara, van Hulzen Kimm, Zwiers Marcel P, Mostert Jeanette C, Schene Aart H, Heslenfeld Dirk J, Oosterlaan Jaap, Hoekstra Pieter J, Hartman Catharina A, Vasquez Alejandro Arias, Kan Cornelis C, Buitelaar Jan, Hoogman Marti |
Attention deficit hyperactivity disorder: genetic association study in a cohort of Spanish children. Behavioral and brain functions : BBF 2016 12 (1): 2. Gomez-Sanchez Clara I, Riveiro-Alvarez Rosa, Soto-Insuga Victor, Rodrigo Maria, Tirado-Requero Pilar, Mahillo-Fernandez Ignacio, Abad-Santos Francisco, Carballo Juan J, Dal-Ré Rafael, Ayuso Carm |
Pharmacogenetics of methylphenidate in childhood attention-deficit/hyperactivity disorder: long-term effects. Scientific reports 2017 Sep 7 (1): 10391. Gomez-Sanchez Clara I, Carballo Juan J, Riveiro-Alvarez Rosa, Soto-Insuga Victor, Rodrigo Maria, Mahillo-Fernandez Ignacio, Abad-Santos Francisco, Dal-Ré Rafael, Ayuso Carm |
No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs. Attention deficit and hyperactivity disorders 2017 Feb . Geissler Julia M, , Romanos Marcel, Gerlach Manfred, Berg Daniela, Schulte Claud |
Pharmacogenetics predictors of methylphenidate efficacy in childhood ADHD. Molecular psychiatry 2017 Dec . Myer N M, Boland J R, Faraone S |
SLC6A3 polymorphism and response to methylphenidate in children with ADHD: A systematic review and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 04 177 (3): 287-300. Soleimani Robabeh, Salehi Zivar, Soltanipour Soheil, Hasandokht Tolou, Jalali Mir Mohamm |
Testing genetic modifiers of behavior and response to atomoxetine in autism spectrum disorder with ADHD. Journal of developmental and physical disabilities 2018 Jun 30 (3): 355-371. Barrie Elizabeth S, Pinsonneault Julia K, Sadee Wolfgang, Hollway Jill A, Handen Benjamin L, Smith Tristram, Arnold L Eugene, Butter Eric, Hansen-Kiss Emily, Herman Gail E, Aman Michael |
Neuropsychiatric disease-associated genetic variants of the dopamine transporter display heterogeneous molecular phenotypes. The Journal of biological chemistry 2018 05 293 (19): 7250-7262. Herborg Freja, Andreassen Thorvald F, Berlin Frida, Loland Claus J, Gether Ulr |
Dopaminergic gene analysis indicates influence of inattention but not IQ in executive dysfunction of Indian ADHD probands. Journal of neurogenetics 2019 10 33 (4): 209-217. Maitra Subhamita, Chatterjee Mahasweta, Sinha Swagata, Mukhopadhyay Kanch |
[Polymorphisms in Sleep and Cognitive Function Related Genes are Associated with Vehicle Crash History in Shift Working Bus Drivers]. Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova 2019 1 67 (1): 49-54. Dorokhov V B, Puchkova A N, Taranov A O, Ermolayev V V, Tupitsyna T V, Slominsky P A, Dementiyenko V |
[The combined effect of genetic factors and attention deficit hyperactivity disorder on the development of dependence on synthetic cannabinoids]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2020 120 (2): 15-21. Gareeva A E, Sharafiev R R, Akhmetova E A, Nasibullin T R, Fakhurtdinova Z R, Yuldashev V L, Asadullin A |
The SLC6A3 gene polymorphism is related to the development of attentional functions but not to ADHD. Scientific reports 2020 Apr 10 (1): 6176. Kuc Katarzyna, Bielecki Maksymilian, Racicka-Pawlukiewicz Ewa, Czerwinski Micha? B, Cybulska-Klosowicz Ani |
The dopamine transporter gene SLC6A3: multidisease risks. Molecular psychiatry 2021 10 27 (2): 1031-1046. Reith Maarten E A, Kortagere Sandhya, Wiers Corinde E, Sun Hui, Kurian Manju A, Galli Aurelio, Volkow Nora D, Lin Zhiche |
Specific dopaminergic genetic variants influence impulsivity, cognitive deficit, and disease severity of Indian ADHD probands. Molecular biology reports 2022 May . Maitra Subhamita, Chatterjee Mahasweta, Roychowdhury Anirban, Panda Chinmay Kumar, Sinha Swagata, Mukhopadhyay Kanch |
Study of changes in rs2283265 polymorphisms in dopamine receptor D2 and rs27072 in dopamine transporter gene (SLC6A3) in patients with attention-deficit hyperactivity disorder. Iranian journal of child neurology 2022 16 (3): 121-132. Safavi Parvin, Soleimani Farsani Hossein, Farrokhi Effat, Malekpour Tehrani Afsaneh, Khoshdel Nika, Khoshdel Abolfa |
Correlation research of susceptibility single nucleotide polymorphisms and the severity of clinical symptoms in attention deficit hyperactivity disorder. Frontiers in psychiatry 2022 10 13 1003542. Xu Yunyu, Lin Shuangxiang, Tao Jiejie, Liu Xinmiao, Zhou Ronghui, Chen Shuangli, Vyas Punit, Yang Chuang, Chen Bicheng, Qian Andan, Wang Meih |
Gene Interaction of Dopaminergic Synaptic Pathway Genes in Attention-Deficit Hyperactivity Disorder: a Case-Control Study in Chinese Children. Molecular neurobiology 2023 8 . Lin Zhong, Hongyao He, Jing Zhang, Xiaoyan Gao, Feifei Yin, Pengxiang Zuo, Ranran So |
- Page last reviewed:Feb 1, 2024
- Content source: