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Results: 1 to 20 of 28

1.

Characterization of SLITRK1 variation in obsessive-compulsive disorder.

Ozomaro U, Cai G, Kajiwara Y, Yoon S, Makarov V, Delorme R, Betancur C, Ruhrmann S, Falkai P, Grabe HJ, Maier W, Wagner M, Lennertz L, Moessner R, Murphy DL, Buxbaum JD, Züchner S, Grice DE.

PLoS One. 2013 Aug 21;8(8):e70376. doi: 10.1371/journal.pone.0070376. eCollection 2013.

PMID:
23990902
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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
[PubMed - indexed for MEDLINE]
3.

The genetic basis of Gilles de la Tourette Syndrome.

Paschou P.

Neurosci Biobehav Rev. 2013 Jul;37(6):1026-39. doi: 10.1016/j.neubiorev.2013.01.016. Epub 2013 Jan 17. Review.

PMID:
23333760
[PubMed - indexed for MEDLINE]
4.

Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder.

Greenwood TA; Bipolar Genome Study (BiGS) Consortium, Kelsoe JR.

PLoS One. 2013;8(1):e53804. doi: 10.1371/journal.pone.0053804. Epub 2013 Jan 10.

PMID:
23326512
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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 30;211(3):214-20. doi: 10.1016/j.pscychresns.2012.07.003. Epub 2012 Nov 13.

PMID:
23154099
[PubMed - indexed for MEDLINE]
6.

Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood.

Davies MN, Volta M, Pidsley R, Lunnon K, Dixit A, Lovestone S, Coarfa C, Harris RA, Milosavljevic A, Troakes C, Al-Sarraj S, Dobson R, Schalkwyk LC, Mill J.

Genome Biol. 2012 Jun 15;13(6):R43. doi: 10.1186/gb-2012-13-6-r43.

PMID:
22703893
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Novel candidate genes of thyroid tumourigenesis identified in Trk-T1 transgenic mice.

Heiliger KJ, Hess J, Vitagliano D, Salerno P, Braselmann H, Salvatore G, Ugolini C, Summerer I, Bogdanova T, Unger K, Thomas G, Santoro M, Zitzelsberger H.

Endocr Relat Cancer. 2012 May 24;19(3):409-21. doi: 10.1530/ERC-11-0387. Print 2012 Jun.

PMID:
22454401
[PubMed - indexed for MEDLINE]
Free Article
8.

Slitrks as emerging candidate genes involved in neuropsychiatric disorders.

Proenca CC, Gao KP, Shmelkov SV, Rafii S, Lee FS.

Trends Neurosci. 2011 Mar;34(3):143-53. doi: 10.1016/j.tins.2011.01.001. Review.

PMID:
21315458
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Additional support for the association of SLITRK1 var321 and Tourette syndrome.

O'Roak BJ, Morgan TM, Fishman DO, Saus E, Alonso P, Gratacòs M, Estivill X, Teltsh O, Kohn Y, Kidd KK, Cho J, Lifton RP, State MW.

Mol Psychiatry. 2010 May;15(5):447-50. doi: 10.1038/mp.2009.105. Epub 2010 Mar 30. No abstract available.

PMID:
20351724
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The genetics of Tourette syndrome: a review.

O'Rourke JA, Scharf JM, Yu D, Pauls DL.

J Psychosom Res. 2009 Dec;67(6):533-45. doi: 10.1016/j.jpsychores.2009.06.006. Epub 2009 Sep 30. Review.

PMID:
19913658
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

SLITRK1 binds 14-3-3 and regulates neurite outgrowth in a phosphorylation-dependent manner.

Kajiwara Y, Buxbaum JD, Grice DE.

Biol Psychiatry. 2009 Nov 15;66(10):918-25. doi: 10.1016/j.biopsych.2009.05.033. Epub 2009 Jul 29.

PMID:
19640509
[PubMed - indexed for MEDLINE]
12.

Analysis of DNA methylation of multiple genes in microdissected cells from formalin-fixed and paraffin-embedded tissues.

Dietrich D, Lesche R, Tetzner R, Krispin M, Dietrich J, Haedicke W, Schuster M, Kristiansen G.

J Histochem Cytochem. 2009 May;57(5):477-89. doi: 10.1369/jhc.2009.953026. Epub 2009 Jan 19.

PMID:
19153192
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome.

Stillman AA, Krsnik Z, Sun J, Rasin MR, State MW, Sestan N, Louvi A.

J Comp Neurol. 2009 Mar 1;513(1):21-37. doi: 10.1002/cne.21919.

PMID:
19105198
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

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
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
16.

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
[PubMed - indexed for MEDLINE]
17.

SERT Ileu425Val in autism, Asperger syndrome and obsessive-compulsive disorder.

Wendland JR, DeGuzman TB, McMahon F, Rudnick G, Detera-Wadleigh SD, Murphy DL.

Psychiatr Genet. 2008 Feb;18(1):31-9. doi: 10.1097/YPG.0b013e3282f08a06.

PMID:
18197083
[PubMed - indexed for MEDLINE]
18.

Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.

Speed WC, O'Roak BJ, Tárnok Z, Barta C, Pakstis AJ, State MW, Kidd KK.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):463-6.

PMID:
18004766
[PubMed - indexed for MEDLINE]
19.

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
[PubMed - indexed for MEDLINE]
20.

Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene.

Orth M, Djarmati A, Bäumer T, Winkler S, Grünewald A, Lohmann-Hedrich K, Kabakci K, Hagenah J, Klein C, Münchau A.

Mov Disord. 2007 Oct 31;22(14):2090-6.

PMID:
17702041
[PubMed - indexed for MEDLINE]

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