These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
181 related articles for article (PubMed ID: 20155310)
1. Glutamate transporter gene (SLC1A1) single nucleotide polymorphism (rs301430) and repetitive behaviors and anxiety in children with autism spectrum disorder. Gadow KD; Roohi J; DeVincent CJ; Kirsch S; Hatchwell E J Autism Dev Disord; 2010 Sep; 40(9):1139-45. PubMed ID: 20155310 [TBL] [Abstract][Full Text] [Related]
2. Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorder. Gadow KD; DeVincent CJ; Pisarevskaya V; Olvet DM; Xu W; Mendell NR; Finch SJ; Hatchwell E Prog Neuropsychopharmacol Biol Psychiatry; 2010 Oct; 34(7):1208-14. PubMed ID: 20600463 [TBL] [Abstract][Full Text] [Related]
3. A single nucleotide polymorphism in SLC1A1 gene is associated with age of onset of obsessive-compulsive disorder. Dallaspezia S; Mazza M; Lorenzi C; Benedetti F; Smeraldi E Eur Psychiatry; 2014 Jun; 29(5):301-3. PubMed ID: 24768158 [TBL] [Abstract][Full Text] [Related]
4. Family-Based Association Testing of OCD-associated SNPs of SLC1A1 in an autism sample. Brune CW; Kim SJ; Hanna GL; Courchesne E; Lord C; Leventhal BL; Cook EH Autism Res; 2008 Apr; 1(2):108-13. PubMed ID: 19360657 [TBL] [Abstract][Full Text] [Related]
5. Association of DRD4 polymorphism with severity of oppositional defiant disorder, separation anxiety disorder and repetitive behaviors in children with autism spectrum disorder. Gadow KD; Devincent CJ; Olvet DM; Pisarevskaya V; Hatchwell E Eur J Neurosci; 2010 Sep; 32(6):1058-65. PubMed ID: 20731709 [TBL] [Abstract][Full Text] [Related]
6. Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder. Dickel DE; Veenstra-VanderWeele J; Cox NJ; Wu X; Fischer DJ; Van Etten-Lee M; Himle JA; Leventhal BL; Cook EH; Hanna GL Arch Gen Psychiatry; 2006 Jul; 63(7):778-85. PubMed ID: 16818867 [TBL] [Abstract][Full Text] [Related]
7. A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder. Wendland JR; Moya PR; Timpano KR; Anavitarte AP; Kruse MR; Wheaton MG; Ren-Patterson RF; Murphy DL Arch Gen Psychiatry; 2009 Apr; 66(4):408-16. PubMed ID: 19349310 [TBL] [Abstract][Full Text] [Related]
9. Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder. Stewart SE; Fagerness JA; Platko J; Smoller JW; Scharf JM; Illmann C; Jenike E; Chabane N; Leboyer M; Delorme R; Jenike MA; Pauls DL Am J Med Genet B Neuropsychiatr Genet; 2007 Dec; 144B(8):1027-33. PubMed ID: 17894418 [TBL] [Abstract][Full Text] [Related]
10. Allele-specific associations of 5-HTTLPR/rs25531 with ADHD and autism spectrum disorder. Gadow KD; DeVincent CJ; Siegal VI; Olvet DM; Kibria S; Kirsch SF; Hatchwell E Prog Neuropsychopharmacol Biol Psychiatry; 2013 Jan; 40():292-7. PubMed ID: 23123360 [TBL] [Abstract][Full Text] [Related]
11. Association of the candidate gene SLC1A1 and obsessive-compulsive disorder in Han Chinese population. Wu H; Wang X; Yu S; Wang D; Chen J; Jiang K; Zhu L; Xiao Z; Fralick D Psychiatry Res; 2013 Oct; 209(3):737-9. PubMed ID: 23411042 [TBL] [Abstract][Full Text] [Related]
12. Association of COMT (Val158Met) and BDNF (Val66Met) gene polymorphisms with anxiety, ADHD and tics in children with autism spectrum disorder. Gadow KD; Roohi J; DeVincent CJ; Kirsch S; Hatchwell E J Autism Dev Disord; 2009 Nov; 39(11):1542-51. PubMed ID: 19582565 [TBL] [Abstract][Full Text] [Related]
13. Association between glutamate transporter gene polymorphisms and obsessive-compulsive disorder/trait empathy in a Korean population. Kim HW; Kang JI; Hwang EH; Kim SJ PLoS One; 2018; 13(1):e0190593. PubMed ID: 29304071 [TBL] [Abstract][Full Text] [Related]
14. Sensory processing and stereotypical and repetitive behaviour in children with autism and intellectual disability. Joosten AV; Bundy AC Aust Occup Ther J; 2010 Dec; 57(6):366-72. PubMed ID: 21091701 [TBL] [Abstract][Full Text] [Related]
15. Functional studies and rare variant screening of SLC1A1/EAAC1 in males with obsessive-compulsive disorder. Veenstra-VanderWeele J; Xu T; Ruggiero AM; Anderson LR; Jones ST; Himle JA; Kennedy JL; Richter MA; Hanna GL; Arnold PD Psychiatr Genet; 2012 Oct; 22(5):256-60. PubMed ID: 22617815 [TBL] [Abstract][Full Text] [Related]
16. A family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder in 378 families. Shugart YY; Wang Y; Samuels JF; Grados MA; Greenberg BD; Knowles JA; McCracken JT; Rauch SL; Murphy DL; Rasmussen SA; Cullen B; Hoehn-Saric R; Pinto A; Fyer AJ; Piacentini J; Pauls DL; Bienvenu OJ; Riddle MA; Liang KY; Nestadt G Am J Med Genet B Neuropsychiatr Genet; 2009 Sep; 150B(6):886-92. PubMed ID: 19152386 [TBL] [Abstract][Full Text] [Related]
17. Interaction of SLC1A1 gene variants and life stress on pharmacological resistance in obsessive-compulsive disorder. Real E; Gratacòs M; Labad J; Alonso P; Escaramís G; Segalàs C; Subirà M; López-Solà C; Estivill X; Menchón JM Pharmacogenomics J; 2013 Oct; 13(5):470-5. PubMed ID: 22776887 [TBL] [Abstract][Full Text] [Related]
18. Presentation and Correlates of Hoarding Behaviors in Children with Autism Spectrum Disorders and Comorbid Anxiety or Obsessive-Compulsive Symptoms. La Buissonnière-Ariza V; Wood JJ; Kendall PC; McBride NM; Cepeda SL; Small BJ; Lewin AB; Kerns C; Storch EA J Autism Dev Disord; 2018 Dec; 48(12):4167-4178. PubMed ID: 29974314 [TBL] [Abstract][Full Text] [Related]
19. Short report: Relationships between sensory processing, repetitive behaviors, anxiety, and intolerance of uncertainty in autism spectrum disorder and Williams syndrome. Glod M; Riby DM; Rodgers J Autism Res; 2019 May; 12(5):759-765. PubMed ID: 30919599 [TBL] [Abstract][Full Text] [Related]
20. Comprehensive family-based association study of the glutamate transporter gene SLC1A1 in obsessive-compulsive disorder. Samuels J; Wang Y; Riddle MA; Greenberg BD; Fyer AJ; McCracken JT; Rauch SL; Murphy DL; Grados MA; Knowles JA; Piacentini J; Cullen B; Bienvenu OJ; Rasmussen SA; Geller D; Pauls DL; Liang KY; Shugart YY; Nestadt G Am J Med Genet B Neuropsychiatr Genet; 2011 Jun; 156B(4):472-7. PubMed ID: 21445956 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]