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Items: 1 to 20 of 698

1.

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
2.

Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.

Gothelf D, Schaer M, Eliez S.

Dev Disabil Res Rev. 2008;14(1):59-68. doi: 10.1002/ddrr.9. Review.

PMID:
18636637
3.

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
4.

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.

5.

Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects.

Carmel M, Zarchi O, Michaelovsky E, Frisch A, Patya M, Green T, Gothelf D, Weizman A.

J Psychiatr Res. 2014 Sep;56:28-35. doi: 10.1016/j.jpsychires.2014.04.019. Epub 2014 May 9.

PMID:
24853458
6.

Genetic abnormalities of chromosome 22 and the development of psychosis.

Williams NM, Owen MJ.

Curr Psychiatry Rep. 2004 Jun;6(3):176-82. Review.

PMID:
15142470
7.

Schizophrenia-like neurophysiological abnormalities in 22q11.2 deletion syndrome and their association to COMT and PRODH genotypes.

Zarchi O, Carmel M, Avni C, Attias J, Frisch A, Michaelovsky E, Patya M, Green T, Weinberger R, Weizman A, Gothelf D.

J Psychiatr Res. 2013 Nov;47(11):1623-9. doi: 10.1016/j.jpsychires.2013.07.004. Epub 2013 Aug 1.

PMID:
23910792
8.

An association study between the genetic polymorphisms within TBX1 and schizophrenia in the Chinese population.

Ma G, Shi Y, Tang W, He Z, Huang K, Li Z, He G, Feng G, Li H, He L.

Neurosci Lett. 2007 Oct 2;425(3):146-50. Epub 2007 Aug 15.

PMID:
17850965
9.

[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
10.

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.

Arinami T.

J Hum Genet. 2006;51(12):1037-45. Epub 2006 Sep 13. Review.

PMID:
16969581
11.

Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).

McQuade L, Christodoulou J, Budarf M, Sachdev R, Wilson M, Emanuel B, Colley A.

Am J Med Genet. 1999 Sep 3;86(1):27-33.

PMID:
10440825
12.

Abnormal cortical activation during response inhibition in 22q11.2 deletion syndrome.

Gothelf D, Hoeft F, Hinard C, Hallmayer JF, Stoecker JV, Antonarakis SE, Morris MA, Reiss AL.

Hum Brain Mapp. 2007 Jun;28(6):533-42.

PMID:
17427209
13.

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
14.

[Chromosome 22q11 and schizophrenia].

Agatsuma S, Hiroi N.

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

PMID:
16220657
15.

Differential gene expression in the hippocampus of the Df1/+ mice: a model for 22q11.2 deletion syndrome and schizophrenia.

Sivagnanasundaram S, Fletcher D, Hubank M, Illingworth E, Skuse D, Scambler P.

Brain Res. 2007 Mar 30;1139:48-59. Epub 2007 Jan 10.

PMID:
17292336
16.

Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.

Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR.

Biol Psychiatry. 2014 Mar 1;75(5):406-13. doi: 10.1016/j.biopsych.2013.07.021. Epub 2013 Aug 28.

17.

Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.

Shashi V, Keshavan MS, Howard TD, Berry MN, Basehore MJ, Lewandowski E, Kwapil TR.

Clin Genet. 2006 Mar;69(3):234-8.

PMID:
16542388
19.

[22q11.2 deletion syndrome].

Ishikawa T.

Nihon Rinsho. 2006 Jun 28;Suppl 2:70-3. Review. Japanese. No abstract available.

PMID:
16817353
20.

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.

Gothelf D, Eliez S, Thompson T, Hinard C, Penniman L, Feinstein C, Kwon H, Jin S, Jo B, Antonarakis SE, Morris MA, Reiss AL.

Nat Neurosci. 2005 Nov;8(11):1500-2. Epub 2005 Oct 23.

PMID:
16234808

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