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Items: 1 to 20 of 105

1.

Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder.

Veenstra-VanderWeele J, Kim SJ, Gonen D, Hanna GL, Leventhal BL, Cook EH Jr.

Mol Psychiatry. 2001 Mar;6(2):160-7.

2.

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 Jr, Hanna GL.

Arch Gen Psychiatry. 2006 Jul;63(7):778-85.

PMID:
16818867
3.

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
4.

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 5;144B(8):1027-33.

PMID:
17894418
5.

Mutation screening of human 5-HT(2B)receptor gene in early-onset obsessive-compulsive disorder.

Kim SJ, Veenstra-VanderWeele J, Hanna GL, Gonen D, Leventhal BL, Cook EH Jr.

Mol Cell Probes. 2000 Feb;14(1):47-52.

PMID:
10722792
6.

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 5;150B(6):886-92. doi: 10.1002/ajmg.b.30914.

PMID:
19152386
7.

A screen of SLC1A1 for OCD-related alleles.

Wang Y, Adamczyk A, Shugart YY, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Bienvenu OJ, Riddle M, Liang KY, Valle D, Wang T, Nestadt G.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):675-9. doi: 10.1002/ajmg.b.31001.

PMID:
19569082
8.

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. doi: 10.1001/archgenpsychiatry.2009.6.

9.

Association of the glutamate transporter gene SLC1A1 with atypical antipsychotics-induced obsessive-compulsive symptoms.

Kwon JS, Joo YH, Nam HJ, Lim M, Cho EY, Jung MH, Choi JS, Kim B, Kang DH, Oh S, Park T, Hong KS.

Arch Gen Psychiatry. 2009 Nov;66(11):1233-41. doi: 10.1001/archgenpsychiatry.2009.155.

PMID:
19884611
10.

Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands.

Hanna GL, Veenstra-VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC, Leventhal BL, Cook EH Jr.

Am J Med Genet. 2002 Jul 8;114(5):541-52.

PMID:
12116192
11.

Novel mutations of the extraneuronal monoamine transporter gene in children and adolescents with obsessive-compulsive disorder.

Lazar A, Walitza S, Jetter A, Gerlach M, Warnke A, Herpertz-Dahlmann B, Gründemann D, Grimberg G, Schulz E, Remschmidt H, Wewetzer C, Schömig E.

Int J Neuropsychopharmacol. 2008 Feb;11(1):35-48. Epub 2007 May 4.

PMID:
17477885
12.

Sequence variants of the brain-derived neurotrophic factor (BDNF) gene are strongly associated with obsessive-compulsive disorder.

Hall D, Dhilla A, Charalambous A, Gogos JA, Karayiorgou M.

Am J Hum Genet. 2003 Aug;73(2):370-6. Epub 2003 Jun 27.

13.

Frequency and transmission of glutamate receptors GRIK2 and GRIK3 polymorphisms in patients with obsessive compulsive disorder.

Delorme R, Krebs MO, Chabane N, Roy I, Millet B, Mouren-Simeoni MC, Maier W, Bourgeron T, Leboyer M.

Neuroreport. 2004 Mar 22;15(4):699-702.

PMID:
15094479
14.

Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive-compulsive disorder with compulsive hoarding.

Liang KY, Wang Y, Shugart YY, Grados M, Fyer AJ, Rauch S, Murphy D, McCracken J, Rasmussen S, Cullen B, Hoehn-Saric R, Greenberg B, Pinto A, Knowles J, Piacentini J, Pauls D, Bienvenu O, Riddle M, Samuels J, Nestadt G.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):1000-2. doi: 10.1002/ajmg.b.30713.

PMID:
18286588
15.

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. doi: 10.1002/ajmg.b.32137. Epub 2013 Apr 18.

PMID:
23606572
16.

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. Epub 2005 Sep 7.

PMID:
16146581
17.

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.

PMID:
22617815
18.

Interaction between genetic variants of DLGAP3 and SLC1A1 affecting the risk of atypical antipsychotics-induced obsessive-compulsive symptoms.

Ryu S, Oh S, Cho EY, Nam HJ, Yoo JH, Park T, Joo YH, Kwon JS, Hong KS.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):949-59. doi: 10.1002/ajmg.b.31242. Epub 2011 Oct 11.

PMID:
21990008
19.

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12.

PMID:
15108191
20.

Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.

Alonso P, Gratacòs M, Menchón JM, Saiz-Ruiz J, Segalàs C, Baca-García E, Labad J, Fernández-Piqueras J, Real E, Vaquero C, Pérez M, Dolengevich H, González JR, Bayés M, de Cid R, Vallejo J, Estivill X.

Biol Psychiatry. 2008 Mar 15;63(6):619-28. Epub 2007 Sep 19.

PMID:
17884018
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