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Items: 1 to 20 of 111

1.

Trio study and meta-analysis support the association of genetic variation at the serotonin transporter with early-onset obsessive-compulsive disorder.

Walitza S, Marinova Z, Grünblatt E, Lazic SE, Remschmidt H, Vloet TD, Wendland JR.

Neurosci Lett. 2014 Sep 19;580:100-3. doi: 10.1016/j.neulet.2014.07.038.

2.

Association of the serotonin transporter polymorphism and obsessive-compulsive disorder: systematic review.

Bloch MH, Landeros-Weisenberger A, Sen S, Dombrowski P, Kelmendi B, Coric V, Pittenger C, Leckman JF.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):850-8. doi: 10.1002/ajmg.b.30699. Review.

PMID:
18186076
3.

Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder.

Dickel DE, Veenstra-VanderWeele J, Bivens NC, Wu X, Fischer DJ, Van Etten-Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL.

Biol Psychiatry. 2007 Feb 1;61(3):322-9.

PMID:
17241828
4.

Is serotonin transporter polymorphism (5-HTTLPR) allele status a predictor for obsessive-compulsive disorder? A meta-analysis.

Mak L, Streiner DL, Steiner M.

Arch Womens Ment Health. 2015 Jun;18(3):435-45. doi: 10.1007/s00737-015-0526-z. Review.

PMID:
25896187
5.

Molecular genetics of obsessive-compulsive disorder: a comprehensive meta-analysis of genetic association studies.

Taylor S.

Mol Psychiatry. 2013 Jul;18(7):799-805. doi: 10.1038/mp.2012.76.

PMID:
22665263
6.

Association between serotonergic candidate genes and specific phenotypes of obsessive compulsive disorder.

Denys D, Van Nieuwerburgh F, Deforce D, Westenberg HG.

J Affect Disord. 2006 Mar;91(1):39-44.

PMID:
16443280
7.

Genetic Polymorphism of the Serotonin Transporter Gene, SLC6A4 rs16965628, Is Associated with Obsessive Compulsive Disorder.

Cengiz M, Okutan SN, Bayoglu B, Sakalli Kani A, Bayar R, Kocabasoglu N.

Genet Test Mol Biomarkers. 2015 May;19(5):228-34. doi: 10.1089/gtmb.2014.0319.

PMID:
25751280
8.

Association of serotonin transporter gene polymorphisms with obsessive-compulsive disorder (OCD) in a south Indian population.

Tibrewal P, Kumar HB, Shubha GN, Subhashree D, Purushottam M, Thennarasu K, Reddy YC, Jain S.

Indian J Med Res. 2010 Dec;132:690-5.

9.

Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.

Moya PR, Wendland JR, Rubenstein LM, Timpano KR, Heiman GA, Tischfield JA, King RA, Andrews AM, Ramamoorthy S, McMahon FJ, Murphy DL.

Mov Disord. 2013 Aug;28(9):1263-70. doi: 10.1002/mds.25460.

10.

Meta-analysis of the association of serotonin transporter gene polymorphism with obsessive-compulsive disorder.

Lin PY.

Prog Neuropsychopharmacol Biol Psychiatry. 2007 Apr 13;31(3):683-9.

PMID:
17291658
11.

A large case-control study of common functional SLC6A4 and BDNF variants in obsessive-compulsive disorder.

Wendland JR, Kruse MR, Cromer KR, Murphy DL.

Neuropsychopharmacology. 2007 Dec;32(12):2543-51. Erratum in: Neuropsychopharmacology. 2008 May;33(6):1476. Cromer, Kiara C [corrected to Cromer, Kiara R].

12.

Serotonin transporter promoter gain-of-function genotypes are linked to obsessive-compulsive disorder.

Hu XZ, Lipsky RH, Zhu G, Akhtar LA, Taubman J, Greenberg BD, Xu K, Arnold PD, Richter MA, Kennedy JL, Murphy DL, Goldman D.

Am J Hum Genet. 2006 May;78(5):815-26.

13.

A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorder.

Wendland JR, Moya PR, Kruse MR, Ren-Patterson RF, Jensen CL, Timpano KR, Murphy DL.

Hum Mol Genet. 2008 Mar 1;17(5):717-23.

PMID:
18055562
14.

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.

PMID:
16146581
15.

Association of SLC6A4 variants with obsessive-compulsive disorder in a large multicenter US family study.

Voyiaziakis E, Evgrafov O, Li D, Yoon HJ, Tabares P, Samuels J, Wang Y, Riddle MA, Grados MA, Bienvenu OJ, Shugart YY, Liang KY, Greenberg BD, Rasmussen SA, Murphy DL, Wendland JR, McCracken JT, Piacentini J, Rauch SL, Pauls DL, Nestadt G, Fyer AJ, Knowles JA.

Mol Psychiatry. 2011 Jan;16(1):108-20. doi: 10.1038/mp.2009.100.

PMID:
19806148
16.

Association study of the serotonin transporter gene polymorphism in obsessive-compulsive disorder.

Camarena B, Rinetti G, Cruz C, Hernández S, de la Fuente JR, Nicolini H.

Int J Neuropsychopharmacol. 2001 Sep;4(3):269-72.

PMID:
11602033
17.

Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway.

Walitza S, Wewetzer C, Gerlach M, Klampfl K, Geller F, Barth N, Hahn F, Herpertz-Dahlmann B, Gössler M, Fleischhaker C, Schulz E, Hebebrand J, Warnke A, Hinney A.

J Neural Transm (Vienna). 2004 Jul;111(7):817-25.

PMID:
15206000
18.

Lack of evidence for association between serotonin transporter gene (5-HTTLPR) and obsessive-compulsive disorder by case control and family association study in humans.

Chabane N, Millet B, Delorme R, Lichtermann D, Mathieu F, Laplanche JL, Roy I, Mouren MC, Hankard R, Maier W, Launay JM, Leboyer M.

Neurosci Lett. 2004 Jun 10;363(2):154-6.

PMID:
15172105
19.

The current status of association studies in obsessive-compulsive disorder.

Hemmings SM, Stein DJ.

Psychiatr Clin North Am. 2006 Jun;29(2):411-44. Review.

PMID:
16650716
20.

Glutamate transporter gene SLC1A1 associated with obsessive-compulsive disorder.

Arnold PD, Sicard T, Burroughs E, Richter MA, Kennedy JL.

Arch Gen Psychiatry. 2006 Jul;63(7):769-76.

PMID:
16818866
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