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Items: 1 to 20 of 126

1.

Association of DISC1 with autism and Asperger syndrome.

Kilpinen H, Ylisaukko-Oja T, Hennah W, Palo OM, Varilo T, Vanhala R, Nieminen-von Wendt T, von Wendt L, Paunio T, Peltonen L.

Mol Psychiatry. 2008 Feb;13(2):187-96.

PMID:
17579608
2.

A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.

Hennah W, Tuulio-Henriksson A, Paunio T, Ekelund J, Varilo T, Partonen T, Cannon TD, Lönnqvist J, Peltonen L.

Mol Psychiatry. 2005 Dec;10(12):1097-103.

PMID:
16103888
3.

Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects.

Hennah W, Varilo T, Kestilä M, Paunio T, Arajärvi R, Haukka J, Parker A, Martin R, Levitzky S, Partonen T, Meyer J, Lönnqvist J, Peltonen L, Ekelund J.

Hum Mol Genet. 2003 Dec 1;12(23):3151-9.

4.

Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory.

Cannon TD, Hennah W, van Erp TG, Thompson PM, Lonnqvist J, Huttunen M, Gasperoni T, Tuulio-Henriksson A, Pirkola T, Toga AW, Kaprio J, Mazziotta J, Peltonen L.

Arch Gen Psychiatry. 2005 Nov;62(11):1205-13.

PMID:
16275808
5.

Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.

Hennah W, Tomppo L, Hiekkalinna T, Palo OM, Kilpinen H, Ekelund J, Tuulio-Henriksson A, Silander K, Partonen T, Paunio T, Terwilliger JD, Lönnqvist J, Peltonen L.

Hum Mol Genet. 2007 Mar 1;16(5):453-62.

6.

Evidence for association between Disrupted-in-Schizophrenia 1 (DISC1) gene polymorphisms and autism in Chinese Han population: a family-based association study.

Zheng F, Wang L, Jia M, Yue W, Ruan Y, Lu T, Liu J, Li J, Zhang D.

Behav Brain Funct. 2011 May 15;7:14. doi: 10.1186/1744-9081-7-14.

7.

Association between the TRAX/DISC locus and both bipolar disorder and schizophrenia in the Scottish population.

Thomson PA, Wray NR, Millar JK, Evans KL, Hellard SL, Condie A, Muir WJ, Blackwood DH, Porteous DJ.

Mol Psychiatry. 2005 Jul;10(7):657-68, 616.

PMID:
15838535
8.

A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention.

Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Ouyang WC, Chan HY, Chen JJ, Yang WC, Lin CY, Lee SF, Hwu HG.

Biol Psychiatry. 2006 Sep 15;60(6):554-62.

PMID:
16997000
9.

Replication of 1q42 linkage in Finnish schizophrenia pedigrees.

Ekelund J, Hennah W, Hiekkalinna T, Parker A, Meyer J, Lönnqvist J, Peltonen L.

Mol Psychiatry. 2004 Nov;9(11):1037-41.

PMID:
15197400
10.

Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.

Palo OM, Antila M, Silander K, Hennah W, Kilpinen H, Soronen P, Tuulio-Henriksson A, Kieseppä T, Partonen T, Lönnqvist J, Peltonen L, Paunio T.

Hum Mol Genet. 2007 Oct 15;16(20):2517-28.

11.

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.

Auranen M, Varilo T, Alen R, Vanhala R, Ayers K, Kempas E, Ylisaukko-Oja T, Peltonen L, Järvelä I.

Mol Psychiatry. 2003 Oct;8(10):879-84.

PMID:
14515138
12.

Limited association between Disrupted in Schizophrenia 1 (DISC1) gene and bipolar disorder in the Chinese population.

Xiao Y, Zhang J, Wang Y, Wang P, Li X, Ji J, Yang F, Feng G, He L, He G.

Psychiatr Genet. 2011 Feb;21(1):42-6.

PMID:
21222298
13.

Genetic association between schizophrenia and the DISC1 gene in the Scottish population.

Zhang F, Sarginson J, Crombie C, Walker N, St Clair D, Shaw D.

Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):155-9. Erratum in: Am J Med Genet B Neuropsychiatr Genet. 2007 Sep 5;144(6):840.

PMID:
16389590
14.

DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness.

Millar JK, James R, Brandon NJ, Thomson PA.

Ann Med. 2004;36(5):367-78. Review.

PMID:
15478311
15.

Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism.

Turunen JA, Rehnström K, Kilpinen H, Kuokkanen M, Kempas E, Ylisaukko-Oja T.

Autism Res. 2008 Jun;1(3):189-92. doi: 10.1002/aur.25.

PMID:
19360665
16.

Evidence for the involvement of genetic variation in the oxytocin receptor gene (OXTR) in the etiology of autistic disorders on high-functioning level.

Wermter AK, Kamp-Becker I, Hesse P, Schulte-Körne G, Strauch K, Remschmidt H.

Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):629-39. doi: 10.1002/ajmg.b.31032.

PMID:
19777562
17.

Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.

Chien YL, Wu YY, Chiu YN, Liu SK, Tsai WC, Lin PI, Chen CH, Gau SS, Chien WH.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Aug 1;35(6):1512-7. doi: 10.1016/j.pnpbp.2011.04.010.

PMID:
21575668
18.

DISC1 duplication in two brothers with autism and mild mental retardation.

Crepel A, Breckpot J, Fryns JP, De la Marche W, Steyaert J, Devriendt K, Peeters H.

Clin Genet. 2010 Apr;77(4):389-94. doi: 10.1111/j.1399-0004.2009.01318.x.

PMID:
20002455
19.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79.

20.

Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD).

Kantojärvi K, Kotala I, Rehnström K, Ylisaukko-Oja T, Vanhala R, von Wendt TN, von Wendt L, Järvelä I.

Autism Res. 2011 Jun;4(3):228-33. doi: 10.1002/aur.187.

PMID:
21384559
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