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Items: 1 to 20 of 87

1.

Functional analysis of polymorphisms in the promoter regions of genes on 22q11.

Hoogendoorn B, Coleman SL, Guy CA, Smith SK, O'Donovan MC, Buckland PR.

Hum Mutat. 2004 Jul;24(1):35-42.

PMID:
15221787
2.

Promoter polymorphisms in glutathione-S-transferase genes affect transcription.

Guy CA, Hoogendoorn B, Smith SK, Coleman S, O'Donovan MC, Buckland PR.

Pharmacogenetics. 2004 Jan;14(1):45-51.

PMID:
15128050
3.

Functional analysis of human promoter polymorphisms.

Hoogendoorn B, Coleman SL, Guy CA, Smith K, Bowen T, Buckland PR, O'Donovan MC.

Hum Mol Genet. 2003 Sep 15;12(18):2249-54. Epub 2003 Jul 22.

PMID:
12915441
4.

Lack of functional promoter polymorphisms in genes involved in glutamate neurotransmission.

Smith SK, Hoogendoorn B, Guy CA, Coleman SL, O'Donovan MC, Buckland PR.

Psychiatr Genet. 2003 Dec;13(4):193-9.

PMID:
14639045
5.

Genomic disorders on 22q11.

McDermid HE, Morrow BE.

Am J Hum Genet. 2002 May;70(5):1077-88. Epub 2002 Mar 29. Review.

6.

Streamlined approach to functional analysis of promoter-region polymorphisms.

Coleman SL, Hoogendoorn B, Guy C, Smith SK, O'Donovan MC, Buckland PR.

Biotechniques. 2002 Aug;33(2):412, 414, 416 passim.

PMID:
12188194
7.

Detailed analysis of PRODH and PsPRODH reveals no association with schizophrenia.

Williams HJ, Williams N, Spurlock G, Norton N, Zammit S, Kirov G, Owen MJ, O'Donovan MC.

Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):42-6.

PMID:
12815738
8.

Genetic variation in COMT and PRODH is associated with brain anatomy in patients with schizophrenia.

Zinkstok J, Schmitz N, van Amelsvoort T, Moeton M, Baas F, Linszen D.

Genes Brain Behav. 2008 Feb;7(1):61-9. Epub 2007 May 14.

9.

Hyperprolinemia is a risk factor for schizoaffective disorder.

Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, D'Amato T, Petit M, Thibaut F, Frébourg T, Campion D.

Mol Psychiatry. 2005 May;10(5):479-85.

PMID:
15494707
10.

Evidence for association between novel polymorphisms in the PRODH gene and schizophrenia in a Chinese population.

Li T, Ma X, Sham PC, Sun X, Hu X, Wang Q, Meng H, Deng W, Liu X, Murray RM, Collier DA.

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):13-5.

PMID:
15274030
11.

Polymorphism in SNAP29 gene promoter region associated with schizophrenia.

Saito T, Guan F, Papolos DF, Rajouria N, Fann CS, Lachman HM.

Mol Psychiatry. 2001 Mar;6(2):193-201. Erratum in: Mol Psychiatry 2001 Sep;6(5):605.

12.

[In search of susceptibility genes for schizophrenia].

Schosser A, Aschauer HN.

Wien Klin Wochenschr. 2004 Dec 30;116(24):827-33. Review. German.

PMID:
15690966
13.

Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome.

Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, Drouin-Garraud V, Lemarchand M, Philip N, Gérard-Desplanches A, Carlier M, Philippe A, Nolen MC, Heron D, Sarda P, Lacombe D, Coizet C, Alembik Y, Layet V, Afenjar A, Hannequin D, Demily C, Petit M, Thibaut F, Frebourg T, Campion D.

Hum Mol Genet. 2007 Jan 1;16(1):83-91. Epub 2006 Nov 29.

PMID:
17135275
14.

22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome.

Maynard TM, Haskell GT, Lieberman JA, LaMantia AS.

Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):407-19. Review.

PMID:
12175881
15.

Single nucleotide polymorphisms in the human interleukin-1B gene affect transcription according to haplotype context.

Chen H, Wilkins LM, Aziz N, Cannings C, Wyllie DH, Bingle C, Rogus J, Beck JD, Offenbacher S, Cork MJ, Rafie-Kolpin M, Hsieh CM, Kornman KS, Duff GW.

Hum Mol Genet. 2006 Feb 15;15(4):519-29. Epub 2006 Jan 6.

PMID:
16399797
16.

Association of functional polymorphisms of the human tryptophan hydroxylase 2 gene with risk for bipolar disorder in Han Chinese.

Lin YM, Chao SC, Chen TM, Lai TJ, Chen JS, Sun HS.

Arch Gen Psychiatry. 2007 Sep;64(9):1015-24.

PMID:
17768266
17.

[Chromosome 22q11 and schizophrenia].

Agatsuma S, Hiroi N.

Nihon Shinkei Seishin Yakurigaku Zasshi. 2005 Apr;25(2):79-84. Review. Japanese.

PMID:
16220657
18.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
20.

No evidence for an association between variants at the proline dehydrogenase locus and schizophrenia or bipolar affective disorder.

Abou Jamra R, Schumacher J, Becker T, Dahdouh F, Ohlraun S, Suliman H, Schulze TG, Tullius M, Kovalenko S, Maier W, Rietschel M, Propping P, Nöthen MM, Cichon S.

Psychiatr Genet. 2005 Sep;15(3):195-8.

PMID:
16094254

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