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Results: 1 to 20 of 37

Related Articles by Review for PubMed (Select 18806272)

1.

Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.

Bassett AS, Marshall CR, Lionel AC, Chow EW, Scherer SW.

Hum Mol Genet. 2008 Dec 15;17(24):4045-53. doi: 10.1093/hmg/ddn307. Epub 2008 Sep 20. Erratum in: Hum Mol Genet. 2009 May 1;18(9):1717.

2.

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
3.

Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.

Demczuk S, Lévy A, Aubry M, Croquette MF, Philip N, Prieur M, Sauer U, Bouvagnet P, Rouleau GA, Thomas G, et al.

Hum Genet. 1995 Jul;96(1):9-13. Review.

PMID:
7607662
4.

Schizophrenia and 22q11.2 deletion syndrome.

Bassett AS, Chow EW.

Curr Psychiatry Rep. 2008 Apr;10(2):148-57. Review.

5.

Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?

Hosak L, Silhan P, Hosakova J.

Neuro Endocrinol Lett. 2012;33(2):183-90. Review.

PMID:
22592199
6.

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
7.

22q11.2 deletion syndrome: DiGeorge, velocardiofacial, and conotruncal anomaly face syndromes.

Cuneo BF.

Curr Opin Pediatr. 2001 Oct;13(5):465-72. Review. Erratum in: Curr Opin Pediatr 2002 Apr;14(2):286.

PMID:
11801894
8.

The role of DNA copy number variation in schizophrenia.

Tam GW, Redon R, Carter NP, Grant SG.

Biol Psychiatry. 2009 Dec 1;66(11):1005-12. doi: 10.1016/j.biopsych.2009.07.027. Epub 2009 Sep 12. Review.

PMID:
19748074
9.

The 22q11.2 deletion syndrome.

Emanuel BS, McDonald-McGinn D, Saitta SC, Zackai EH.

Adv Pediatr. 2001;48:39-73. Review.

PMID:
11480765
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.

22q11 deletion syndrome: a genetic subtype of schizophrenia.

Bassett AS, Chow EW.

Biol Psychiatry. 1999 Oct 1;46(7):882-91. Review.

12.

Understanding the role of Tbx1 as a candidate gene for 22q11.2 deletion syndrome.

Gao S, Li X, Amendt BA.

Curr Allergy Asthma Rep. 2013 Dec;13(6):613-21. doi: 10.1007/s11882-013-0384-6. Review.

13.

Neuroimaging correlates of 22q11.2 deletion syndrome: implications for schizophrenia research.

Boot E, van Amelsvoort TA.

Curr Top Med Chem. 2012;12(21):2303-13. Review.

PMID:
23279171
14.

Genomic disorders on chromosome 22.

Yu S, Graf WD, Shprintzen RJ.

Curr Opin Pediatr. 2012 Dec;24(6):665-71. doi: 10.1097/MOP.0b013e328358acd0. Review.

PMID:
23111679
15.

The 22q11.2 deletion syndrome as a window into complex neuropsychiatric disorders over the lifespan.

Jonas RK, Montojo CA, Bearden CE.

Biol Psychiatry. 2014 Mar 1;75(5):351-60. doi: 10.1016/j.biopsych.2013.07.019. Epub 2013 Aug 28. Review.

16.

Molecular mechanisms in 22q11 deletion syndrome.

Williams NM.

Schizophr Bull. 2011 Sep;37(5):882-9. doi: 10.1093/schbul/sbr095. Review.

17.

Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: patterning, proliferation, and mitochondrial functions of 22q11 genes.

Meechan DW, Maynard TM, Tucker ES, LaMantia AS.

Int J Dev Neurosci. 2011 May;29(3):283-94. doi: 10.1016/j.ijdevneu.2010.08.005. Epub 2010 Sep 15. Review.

18.

Cognitive, behavioural and psychiatric phenotype in 22q11.2 deletion syndrome.

Philip N, Bassett A.

Behav Genet. 2011 May;41(3):403-12. doi: 10.1007/s10519-011-9468-z. Epub 2011 May 15. Review.

19.

Copy number variations in neurodevelopmental disorders.

Grayton HM, Fernandes C, Rujescu D, Collier DA.

Prog Neurobiol. 2012 Oct;99(1):81-91. doi: 10.1016/j.pneurobio.2012.07.005. Epub 2012 Jul 17. Review.

PMID:
22813947
20.

The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.

Drew LJ, Crabtree GW, Markx S, Stark KL, Chaverneff F, Xu B, Mukai J, Fenelon K, Hsu PK, Gogos JA, Karayiorgou M.

Int J Dev Neurosci. 2011 May;29(3):259-81. doi: 10.1016/j.ijdevneu.2010.09.007. Epub 2010 Oct 8. Review.

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