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Items: 1 to 20 of 22

1.

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.

Levinson DF, Duan J, Oh S, Wang K, Sanders AR, Shi J, Zhang N, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Kendler KS, Freedman R, Dudbridge F, Pe'er I, Hakonarson H, Bergen SE, Fanous AH, Holmans PA, Gejman PV.

Am J Psychiatry. 2011 Mar;168(3):302-16. doi: 10.1176/appi.ajp.2010.10060876. Epub 2011 Feb 1.

2.

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
3.

Copy number variations in schizophrenia: critical review and new perspectives on concepts of genetics and disease.

Bassett AS, Scherer SW, Brzustowicz LM.

Am J Psychiatry. 2010 Aug;167(8):899-914. doi: 10.1176/appi.ajp.2009.09071016. Epub 2010 May 3. Review.

4.

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.

PMID:
20021318
5.

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
6.

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.

7.

Genome-wide investigation of rare structural variants identifies VIPR2 as a new candidate gene for schizophrenia.

Nieratschker V, Meyer-Lindenberg A, Witt SH.

Expert Rev Neurother. 2011 Jul;11(7):937-41. doi: 10.1586/ern.11.84. Review.

PMID:
21721910
8.

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
9.

Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: a systematic review of literature and meta-analysis.

Giaroli G, Bass N, Strydom A, Rantell K, McQuillin A.

Schizophr Res. 2014 Nov;159(2-3):340-6. doi: 10.1016/j.schres.2014.09.025. Epub 2014 Oct 11. Review.

10.

The unexpected role of copy number variations in juvenile myoclonic epilepsy.

Helbig I, Hartmann C, Mefford HC.

Epilepsy Behav. 2013 Jul;28 Suppl 1:S66-8. doi: 10.1016/j.yebeh.2012.07.005. Review.

PMID:
23756484
11.

Recent genomic advances in schizophrenia.

Doherty JL, O'Donovan MC, Owen MJ.

Clin Genet. 2012 Feb;81(2):103-9. doi: 10.1111/j.1399-0004.2011.01773.x. Epub 2011 Oct 5. Review.

PMID:
21895634
12.

Developments in schizophrenia genetics: from linkage to microchips, deletions and duplications.

Haraldsson HM, Ettinger U, Sigurdsson E.

Nord J Psychiatry. 2011 Apr;65(2):82-8. doi: 10.3109/08039488.2011.552734. Epub 2011 Jan 28. Review.

PMID:
21271949
13.

Copy number variants are frequent in genetic generalized epilepsy with intellectual disability.

Mullen SA, Carvill GL, Bellows S, Bayly MA, Trucks H, Lal D, Sander T, Berkovic SF, Dibbens LM, Scheffer IE, Mefford HC.

Neurology. 2013 Oct 22;81(17):1507-14. doi: 10.1212/WNL.0b013e3182a95829. Epub 2013 Sep 25. Review. Erratum in: Neurology. 2013 Dec 10;81(24):2148. Trucks, Holger [added]; Lal, Dennis [added]; Sander, Thoman [added].

14.

Disentangling the myriad genomics of complex disorders, specifically focusing on autism, epilepsy, and schizophrenia.

Poot M, van der Smagt JJ, Brilstra EH, Bourgeron T.

Cytogenet Genome Res. 2011;135(3-4):228-40. doi: 10.1159/000334064. Epub 2011 Nov 12. Review.

PMID:
22085975
15.

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, Fr├ębourg T, Saugier Veber P, Campion D.

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

16.

Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.

Hiroi N, Takahashi T, Hishimoto A, Izumi T, Boku S, Hiramoto T.

Mol Psychiatry. 2013 Nov;18(11):1153-65. doi: 10.1038/mp.2013.92. Epub 2013 Aug 6. Review.

17.

Gene discovery and functional assessment of rare copy-number variants in neurodevelopmental disorders.

Iyer J, Girirajan S.

Brief Funct Genomics. 2015 Sep;14(5):315-28. doi: 10.1093/bfgp/elv018. Epub 2015 May 13. Review.

PMID:
25971441
18.

After GWAS: searching for genetic risk for schizophrenia and bipolar disorder.

Gershon ES, Alliey-Rodriguez N, Liu C.

Am J Psychiatry. 2011 Mar;168(3):253-6. doi: 10.1176/appi.ajp.2010.10091340. Epub 2011 Feb 1. Review.

PMID:
21285144
19.

Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.

Torres F, Barbosa M, Maciel P.

J Med Genet. 2016 Feb;53(2):73-90. doi: 10.1136/jmedgenet-2015-103366. Epub 2015 Oct 26. Review.

PMID:
26502893
20.

The human clinical phenotypes of altered CHRNA7 copy number.

Gillentine MA, Schaaf CP.

Biochem Pharmacol. 2015 Oct 15;97(4):352-62. doi: 10.1016/j.bcp.2015.06.012. Epub 2015 Jun 18. Review.

PMID:
26095975
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