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Items: 1 to 20 of 149

1.

RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function.

Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG.

Biol Psychiatry. 2008 Nov 1;64(9):789-96. doi: 10.1016/j.biopsych.2008.04.035. Epub 2008 Jun 20.

PMID:
18571626
2.

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
3.

More evidence supports the association of PPP3CC with schizophrenia.

Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Hung SI, Yu SL, Hwang TJ, Hsieh MH, Liu CC, Tsuang MM, Wu JY, Jou YS, Faraone SV, Tsuang MT, Chen WJ, Hwu HG.

Mol Psychiatry. 2007 Oct;12(10):966-74. Epub 2007 Mar 6.

PMID:
17339875
4.

HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.

Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Wu JY, Hung SI, Chan HY, Chen JJ, Hsieh MH, Hwang TJ, Faraone SV, Tsuang MT, Chen WJ, Hwu HG.

Psychiatr Genet. 2007 Dec;17(6):333-8.

PMID:
18075473
5.

ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function.

Liu CM, Fann CS, Chen CY, Liu YL, Oyang YJ, Yang WC, Chang CC, Wen CC, Chen WJ, Hwang TJ, Hsieh MH, Liu CC, Faraone SV, Tsuang MT, Hwu HG.

Biol Psychiatry. 2011 Jul 1;70(1):51-8. doi: 10.1016/j.biopsych.2011.02.033. Epub 2011 Apr 30.

PMID:
21531385
6.

Further evidence for the involvement of MYH9 in the etiology of non-syndromic cleft lip with or without cleft palate.

Birnbaum S, Reutter H, Mende M, de Assis NA, Diaz-Lacava A, Herms S, Scheer M, Lauster C, Braumann B, Schmidt G, Martini M, Hemprich A, Pötzsch S, Knapp M, Nöthen MM, Kramer FJ, Mangold E.

Eur J Oral Sci. 2009 Apr;117(2):200-3. doi: 10.1111/j.1600-0722.2008.00604.x.

PMID:
19320731
7.

[Interest of a new instrument to assess cognition in schizophrenia: The Brief Assessment of Cognition in Schizophrenia (BACS)].

Bralet MC, Navarre M, Eskenazi AM, Lucas-Ross M, Falissard B.

Encephale. 2008 Dec;34(6):557-62. doi: 10.1016/j.encep.2007.12.005. Epub 2008 Jul 9. French.

PMID:
19081451
8.

Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.

Puri V, McQuillin A, Datta S, Choudhury K, Pimm J, Thirumalai S, Krasucki R, Lawrence J, Quested D, Bass N, Crombie C, Fraser G, Walker N, Moorey H, Ray MK, Sule A, Curtis D, St Clair D, Gurling H.

Eur J Hum Genet. 2008 Oct;16(10):1275-82. doi: 10.1038/ejhg.2008.76. Epub 2008 Apr 16.

9.

NCAM1 and neurocognition in schizophrenia.

Sullivan PF, Keefe RS, Lange LA, Lange EM, Stroup TS, Lieberman J, Maness PF.

Biol Psychiatry. 2007 Apr 1;61(7):902-10. Epub 2006 Dec 8.

PMID:
17161382
10.

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.

PMID:
17823922
11.

Failure to find an association between myosin heavy chain 9, non-muscle (MYH9) and schizophrenia: a three-stage case-control association study.

Amagane H, Watanabe Y, Kaneko N, Nunokawa A, Muratake T, Ishiguro H, Arinami T, Ujike H, Inada T, Iwata N, Kunugi H, Sasaki T, Hashimoto R, Itokawa M, Ozaki N, Someya T.

Schizophr Res. 2010 May;118(1-3):106-12. doi: 10.1016/j.schres.2010.01.023. Epub 2010 Feb 26.

PMID:
20188514
12.

Human QKI, a new candidate gene for schizophrenia involved in myelination.

Aberg K, Saetre P, Lindholm E, Ekholm B, Pettersson U, Adolfsson R, Jazin E.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):84-90.

PMID:
16342280
13.

Sustained attention deficits in nonpsychotic relatives of schizophrenic patients: a recurrence risk ratio analysis.

Chen WJ, Chang CH, Liu SK, Hwang TJ, Hwu HG; Multidimensional Psychopathology Group Research Project.

Biol Psychiatry. 2004 May 15;55(10):995-1000.

PMID:
15121483
14.

Potential linkage disequilibrium between schizophrenia and locus D22S278 on the long arm of chromosome 22.

Moises HW, Yang L, Li T, Havsteen B, Fimmers R, Baur MP, Liu X, Gottesman II.

Am J Med Genet. 1995 Oct 9;60(5):465-7.

PMID:
8546164
15.

Impact of schizophrenia candidate genes on schizotypy and cognitive endophenotypes at the population level.

Stefanis NC, Trikalinos TA, Avramopoulos D, Smyrnis N, Evdokimidis I, Ntzani EE, Ioannidis JP, Stefanis CN.

Biol Psychiatry. 2007 Oct 1;62(7):784-92. Epub 2007 Mar 6.

PMID:
17336946
16.

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K.

Hum Genet. 2010 Sep;128(3):345-50. doi: 10.1007/s00439-010-0861-0. Epub 2010 Jul 16.

17.

Clustering by neurocognition for fine mapping of the schizophrenia susceptibility loci on chromosome 6p.

Lin SH, Liu CM, Liu YL, Shen-Jang Fann C, Hsiao PC, Wu JY, Hung SI, Chen CH, Wu HM, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, Faraone SV, Tsuang MT, Hwu HG, Chen WJ.

Genes Brain Behav. 2009 Nov;8(8):785-94. doi: 10.1111/j.1601-183X.2009.00523.x. Epub 2009 Jul 21.

18.

Evaluation of RGS4 as a candidate gene for schizophrenia.

Liu YL, Shen-Jang Fann C, Liu CM, Wu JY, Hung SI, Chan HY, Chen JJ, Lin CY, Liu SK, Hsieh MH, Hwang TJ, Ouyang WC, Chen CY, Lin JJ, Chou FH, Chueh CM, Liu WM, Tsuang MM, Faraone SV, Tsuang MT, Chen WJ, Hwu HG.

Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):418-20.

PMID:
16526029
19.

Support for NRG1 as a susceptibility factor for schizophrenia in a northern Swedish isolated population.

Alaerts M, Ceulemans S, Forero D, Moens LN, De Zutter S, Heyrman L, Lenaerts AS, Norrback KF, De Rijk P, Nilsson LG, Goossens D, Adolfsson R, Del-Favero J.

Arch Gen Psychiatry. 2009 Aug;66(8):828-37. doi: 10.1001/archgenpsychiatry.2009.82.

PMID:
19652122
20.

Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.

Ohtsuki T, Horiuchi Y, Koga M, Ishiguro H, Inada T, Iwata N, Ozaki N, Ujike H, Watanabe Y, Someya T, Arinami T.

Neurosci Lett. 2008 Apr 25;435(3):194-7. doi: 10.1016/j.neulet.2008.02.053. Epub 2008 Feb 29.

PMID:
18384956

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