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Items: 1 to 20 of 139

1.

Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome.

Chou IC, Wan L, Liu SC, Tsai CH, Tsai FJ.

Pediatr Neurol. 2007 Dec;37(6):404-6.

PMID:
18021920
2.

Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome.

Deng H, Le WD, Xie WJ, Jankovic J.

Acta Neurol Scand. 2006 Dec;114(6):400-2.

PMID:
17083340
3.

Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder.

Zimprich A, Hatala K, Riederer F, Stogmann E, Aschauer HN, Stamenkovic M.

Psychiatr Genet. 2008 Dec;18(6):308-9. doi: 10.1097/YPG.0b013e3283060f6f.

PMID:
19018236
4.

Sequence variants in SLITRK1 are associated with Tourette's syndrome.

Abelson JF, Kwan KY, O'Roak BJ, Baek DY, Stillman AA, Morgan TM, Mathews CA, Pauls DL, Rasin MR, Gunel M, Davis NR, Ercan-Sencicek AG, Guez DH, Spertus JA, Leckman JF, Dure LS 4th, Kurlan R, Singer HS, Gilbert DL, Farhi A, Louvi A, Lifton RP, Sestan N, State MW.

Science. 2005 Oct 14;310(5746):317-20.

5.

Association of SLITRK1 to Gilles de la Tourette Syndrome.

Miranda DM, Wigg K, Kabia EM, Feng Y, Sandor P, Barr CL.

Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):483-6. doi: 10.1002/ajmg.b.30840.

PMID:
18698576
6.

Tourette syndrome is not caused by mutations in the central cannabinoid receptor (CNR1) gene.

Gadzicki D, Müller-Vahl KR, Heller D, Ossege S, Nöthen MM, Hebebrand J, Stuhrmann M.

Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):97-103.

PMID:
15108190
7.

Tourette syndrome and the norepinephrine transporter gene: results of a systematic mutation screening.

Stöber G, Hebebrand J, Cichon S, Brüss M, Bönisch H, Lehmkuhl G, Poustka F, Schmidt M, Remschmidt H, Propping P, Nöthen MM.

Am J Med Genet. 1999 Apr 16;88(2):158-63.

PMID:
10206236
8.

Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region.

Miranda DM, Wigg K, Feng Y, Sandor P, Barr CL.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 5;147B(1):68-72.

PMID:
17671968
9.

Sequence analysis of SLITRK1 for var321 in Danish patients with Tourette syndrome and review of the literature.

Yasmeen S, Melchior L, Bertelsen B, Skov L, Mol Debes N, Tümer Z.

Psychiatr Genet. 2013 Jun;23(3):130-3. doi: 10.1097/YPG.0b013e328360c880. Review.

PMID:
23528612
10.

A large Italian family with Gilles de la Tourette syndrome: clinical study and analysis of the SLITRK1 gene.

Fabbrini G, Pasquini M, Aurilia C, Berardelli I, Breedveld G, Oostra BA, Bonifati V, Berardelli A.

Mov Disord. 2007 Nov 15;22(15):2229-34.

PMID:
17712845
11.

Dopamine receptor D2 gene polymorphisms are associated in Taiwanese children with Tourette syndrome.

Lee CC, Chou IC, Tsai CH, Wang TR, Li TC, Tsai FJ.

Pediatr Neurol. 2005 Oct;33(4):272-6.

PMID:
16194726
12.

Genetic and clinical analysis of a large Dutch Gilles de la Tourette family.

Verkerk AJ, Cath DC, van der Linde HC, Both J, Heutink P, Breedveld G, Aulchenko YS, Oostra BA.

Mol Psychiatry. 2006 Oct;11(10):954-64. Epub 2006 Aug 8.

PMID:
16894393
13.

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Keen-Kim D, Mathews CA, Reus VI, Lowe TL, Herrera LD, Budman CL, Gross-Tsur V, Pulver AE, Bruun RD, Erenberg G, Naarden A, Sabatti C, Freimer NB.

Hum Mol Genet. 2006 Nov 15;15(22):3324-8. Epub 2006 Oct 11.

PMID:
17035247
14.

Systematic screening for mutations in the promoter and the coding region of the 5-HT1A gene.

Erdmann J, Shimron-Abarbanell D, Cichon S, Albus M, Maier W, Lichtermann D, Minges J, Reuner U, Franzek E, Ertl MA, et al.

Am J Med Genet. 1995 Oct 9;60(5):393-9.

PMID:
8546152
15.

A new gene for Tourette's syndrome: a window into causal mechanisms?

Grados MA, Walkup JT.

Trends Genet. 2006 Jun;22(6):291-3. Epub 2006 May 4.

PMID:
16678301
16.

Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome.

Belloso JM, Bache I, Guitart M, Caballin MR, Halgren C, Kirchhoff M, Ropers HH, Tommerup N, Tümer Z.

Eur J Hum Genet. 2007 Jun;15(6):711-3. Epub 2007 Mar 28.

17.

Psychopathological features of obsessive-compulsive disorder in an Italian family with Gilles de la Tourette syndrome not linked to the SLITRK1 gene.

Pasquini M, Fabbrini G, Berardelli I, Bonifati V, Biondi M, Berardelli A.

Psychiatry Res. 2008 Oct 30;161(1):109-11. doi: 10.1016/j.psychres.2008.02.012. Epub 2008 Aug 21.

PMID:
18722020
18.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
19.

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians.

Xiong L, Levchenko A, Montplaisir J, Rivière JB, Thibodeau P, St-Onge J, Gaspar C, Desautels A, Lespérance P, Chouinard S, Turecki G, Rouleau GA.

Sleep Med. 2008 Mar;9(3):273-82. Epub 2007 Jul 17.

PMID:
17644423
20.

Genetic and functional studies of a missense variant in a glutamate transporter, SLC1A3, in Tourette syndrome.

Adamczyk A, Gause CD, Sattler R, Vidensky S, Rothstein JD, Singer H, Wang T.

Psychiatr Genet. 2011 Apr;21(2):90-7. doi: 10.1097/YPG.0b013e328341a307.

PMID:
21233784

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