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Results: 11

Related Articles by Review for PubMed (Select 23325106)


Implication of a rare deletion at distal 16p11.2 in schizophrenia.

Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK, Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nöthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G; Molecular Genetics of Schizophrenia Consortium; Wellcome Trust Case Control Consortium 2.

JAMA Psychiatry. 2013 Mar;70(3):253-60. doi: 10.1001/2013.jamapsychiatry.71.


Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation.

Guilmatre A, Dubourg C, Mosca AL, Legallic S, Goldenberg A, Drouin-Garraud V, Layet V, Rosier A, Briault S, Bonnet-Brilhault F, Laumonnier F, Odent S, Le Vacon G, Joly-Helas G, David V, Bendavid C, Pinoit JM, Henry C, Impallomeni C, Germano E, Tortorella G, Di Rosa G, Barthelemy C, Andres C, Faivre L, Frébourg T, Saugier Veber P, Campion D.

Arch Gen Psychiatry. 2009 Sep;66(9):947-56. doi: 10.1001/archgenpsychiatry.2009.80. Review.


The role of copy number variation in schizophrenia.

Kirov G.

Expert Rev Neurother. 2010 Jan;10(1):25-32. doi: 10.1586/ern.09.133. Review.


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.


Genetic relationships between schizophrenia, bipolar disorder, and schizoaffective disorder.

Cardno AG, Owen MJ.

Schizophr Bull. 2014 May;40(3):504-15. doi: 10.1093/schbul/sbu016. Epub 2014 Feb 24. Review.


[Influence of paternal age in schizophrenia].

Hubert A, Szöke A, Leboyer M, Schürhoff F.

Encephale. 2011 Jun;37(3):199-206. doi: 10.1016/j.encep.2010.12.005. Epub 2011 Apr 2. Review. French.


Copy number variants in obesity-related syndromes: review and perspectives on novel molecular approaches.

D'Angelo CS, Koiffmann CP.

J Obes. 2012;2012:845480. doi: 10.1155/2012/845480. Epub 2012 Dec 17. Review.


Animal models of psychiatric disorders that reflect human copy number variation.

Nomura J, Takumi T.

Neural Plast. 2012;2012:589524. doi: 10.1155/2012/589524. Epub 2012 Jul 30. Review.


Detection and characterization of copy number variation in autism spectrum disorder.

Marshall CR, Scherer SW.

Methods Mol Biol. 2012;838:115-35. doi: 10.1007/978-1-61779-507-7_5. Review.


Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

Schreiner MJ, Lazaro MT, Jalbrzikowski M, Bearden CE.

Neuropharmacology. 2013 May;68:157-73. doi: 10.1016/j.neuropharm.2012.09.012. Epub 2012 Oct 23. Review.


Rare structural variants in schizophrenia: one disorder, multiple mutations; one mutation, multiple disorders.

Sebat J, Levy DL, McCarthy SE.

Trends Genet. 2009 Dec;25(12):528-35. doi: 10.1016/j.tig.2009.10.004. Epub 2009 Oct 31. Review.

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