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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

186 related articles for article (PubMed ID: 20370803)

  • 21. 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]  

  • 22. TNF-alpha polymorphisms are associated with obsessive-compulsive disorder.
    Hounie AG; Cappi C; Cordeiro Q; Sampaio AS; Moraes I; Rosário MC; Palácios SA; Goldberg AC; Vallada HP; Machado-Lima A; Nakano E; Kalil J; Pauls D; Pereira CA; Guilherme L; Miguel EC
    Neurosci Lett; 2008 Sep; 442(2):86-90. PubMed ID: 18639610
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Association of a glutamate (NMDA) subunit receptor gene (GRIN2B) with obsessive-compulsive disorder: a preliminary study.
    Arnold PD; Rosenberg DR; Mundo E; Tharmalingam S; Kennedy JL; Richter MA
    Psychopharmacology (Berl); 2004 Aug; 174(4):530-8. PubMed ID: 15083261
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Glutamate system genes and brain volume alterations in pediatric obsessive-compulsive disorder: a preliminary study.
    Wu K; Hanna GL; Easter P; Kennedy JL; Rosenberg DR; Arnold PD
    Psychiatry Res; 2013 Mar; 211(3):214-20. PubMed ID: 23154099
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Role of GAD2 and HTR1B genes in early-onset obsessive-compulsive disorder: results from transmission disequilibrium study.
    Mas S; Pagerols M; Gassó P; Ortiz A; Rodriguez N; Morer A; Plana MT; Lafuente A; Lazaro L
    Genes Brain Behav; 2014 Apr; 13(4):409-17. PubMed ID: 24571444
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.
    Stewart SE; Mayerfeld C; Arnold PD; Crane JR; O'Dushlaine C; Fagerness JA; Yu D; Scharf JM; Chan E; Kassam F; Moya PR; Wendland JR; Delorme R; Richter MA; Kennedy JL; Veenstra-VanderWeele J; Samuels J; Greenberg BD; McCracken JT; Knowles JA; Fyer AJ; Rauch SL; Riddle MA; Grados MA; Bienvenu OJ; Cullen B; Wang Y; Shugart YY; Piacentini J; Rasmussen S; Nestadt G; Murphy DL; Jenike MA; Cook EH; Pauls DL; Hanna GL; Mathews CA
    Am J Med Genet B Neuropsychiatr Genet; 2013 Jun; 162B(4):367-79. PubMed ID: 23606572
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates.
    Lochner C; Hemmings SM; Kinnear CJ; Niehaus DJ; Nel DG; Corfield VA; Moolman-Smook JC; Seedat S; Stein DJ
    Compr Psychiatry; 2005; 46(1):14-9. PubMed ID: 15714189
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 5-HT3 receptor influences the washing phenotype and visual organization in obsessive-compulsive disorder supporting 5-HT3 receptor antagonists as novel treatment option.
    Lennertz L; Wagner M; Grabe HJ; Franke PE; Guttenthaler V; Rampacher F; Schulze-Rauschenbach S; Vogeley A; Benninghoff J; Ruhrmann S; Pukrop R; Klosterkötter J; Falkai P; Maier W; Mössner R
    Eur Neuropsychopharmacol; 2014 Jan; 24(1):86-94. PubMed ID: 23928294
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Modification of the association between early adversity and obsessive-compulsive disorder by polymorphisms in the MAOA, MAOB and COMT genes.
    McGregor NW; Hemmings SMJ; Erdman L; Calmarza-Font I; Stein DJ; Lochner C
    Psychiatry Res; 2016 Dec; 246():527-532. PubMed ID: 27821364
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Association study of polymorphisms in the GluR6 kainate receptor gene (GRIK2) with schizophrenia.
    Shibata H; Shibata A; Ninomiya H; Tashiro N; Fukumaki Y
    Psychiatry Res; 2002 Dec; 113(1-2):59-67. PubMed ID: 12467946
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association study between BDNF gene variants and Mexican patients with obsessive-compulsive disorder.
    Márquez L; Camarena B; Hernández S; Lóyzaga C; Vargas L; Nicolini H
    Eur Neuropsychopharmacol; 2013 Nov; 23(11):1600-5. PubMed ID: 23999029
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder.
    Mössner R; Walitza S; Geller F; Scherag A; Gutknecht L; Jacob C; Bogusch L; Remschmidt H; Simons M; Herpertz-Dahlmann B; Fleischhaker C; Schulz E; Warnke A; Hinney A; Wewetzer C; Lesch KP
    Int J Neuropsychopharmacol; 2006 Aug; 9(4):437-42. PubMed ID: 16146581
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Association of the functional serotonin transporter haplotype with familial form of obsessive compulsive disorder in Iranian patients.
    Rashidi FS; Ahmadipour E; Shiravand S; Ahmadiani A; Asadi S; Shams J
    Int J Psychiatry Clin Pract; 2018 Mar; 22(1):47-53. PubMed ID: 28691545
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Association between genetic variants of serotonergic and glutamatergic pathways and the concentration of neurometabolites of the anterior cingulate cortex in paediatric patients with obsessive-compulsive disorder.
    Ortiz AE; Gassó P; Mas S; Falcon C; Bargalló N; Lafuente A; Lázaro L
    World J Biol Psychiatry; 2016 Aug; 17(5):394-404. PubMed ID: 26505676
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genome-wide linkage analysis of obsessive-compulsive disorder implicates chromosome 1p36.
    Mathews CA; Badner JA; Andresen JM; Sheppard B; Himle JA; Grant JE; Williams KA; Chavira DA; Azzam A; Schwartz M; Reus VI; Kim SW; Cook EH; Hanna GL
    Biol Psychiatry; 2012 Oct; 72(8):629-36. PubMed ID: 22633946
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Genetic meta-analysis of obsessive-compulsive disorder and self-report compulsive symptoms.
    Smit DJA; Cath D; Zilhão NR; Ip HF; Denys D; den Braber A; de Geus EJC; Verweij KJH; Hottenga JJ; Boomsma DI
    Am J Med Genet B Neuropsychiatr Genet; 2020 Jun; 183(4):208-216. PubMed ID: 31891238
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Polymorphisms within the neuronal cadherin (CDH2) gene are associated with obsessive-compulsive disorder (OCD) in a South African cohort.
    McGregor NW; Lochner C; Stein DJ; Hemmings SM
    Metab Brain Dis; 2016 Feb; 31(1):191-6. PubMed ID: 26093892
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Glutamate receptors genes polymorphism and the risk of paranoid schizophrenia in Russians and tatars from the Republic of Bashkortostan].
    Gareeva AE; Khusnutdinova EK
    Mol Biol (Mosk); 2014; 48(5):771-81. PubMed ID: 25842862
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.