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Items: 1 to 20 of 389

1.

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
2.

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
3.

New copy number variations in schizophrenia.

Magri C, Sacchetti E, Traversa M, Valsecchi P, Gardella R, Bonvicini C, Minelli A, Gennarelli M, Barlati S.

PLoS One. 2010 Oct 13;5(10):e13422. doi: 10.1371/journal.pone.0013422.

4.

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.

5.

Penetrance for copy number variants associated with schizophrenia.

Vassos E, Collier DA, Holden S, Patch C, Rujescu D, St Clair D, Lewis CM.

Hum Mol Genet. 2010 Sep 1;19(17):3477-81. doi: 10.1093/hmg/ddq259. Epub 2010 Jun 29.

PMID:
20587603
6.

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

Kirov G, Pocklington AJ, Holmans P, Ivanov D, Ikeda M, Ruderfer D, Moran J, Chambert K, Toncheva D, Georgieva L, Grozeva D, Fjodorova M, Wollerton R, Rees E, Nikolov I, van de Lagemaat LN, Bayés A, Fernandez E, Olason PI, Böttcher Y, Komiyama NH, Collins MO, Choudhary J, Stefansson K, Stefansson H, Grant SG, Purcell S, Sklar P, O'Donovan MC, Owen MJ.

Mol Psychiatry. 2012 Feb;17(2):142-53. doi: 10.1038/mp.2011.154. Epub 2011 Nov 15.

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 and 'schizophrenia'].

Neyndorff JP, de Winter RF, Blom JD.

Tijdschr Psychiatr. 2014;56(2):86-94. Review. Dutch.

9.

Copy number variation in schizophrenia in the Japanese population.

Ikeda M, Aleksic B, Kirov G, Kinoshita Y, Yamanouchi Y, Kitajima T, Kawashima K, Okochi T, Kishi T, Zaharieva I, Owen MJ, O'Donovan MC, Ozaki N, Iwata N.

Biol Psychiatry. 2010 Feb 1;67(3):283-6. doi: 10.1016/j.biopsych.2009.08.034. Epub 2009 Oct 31.

PMID:
19880096
10.

Copy number variation in schizophrenia in Sweden.

Szatkiewicz JP, O'Dushlaine C, Chen G, Chambert K, Moran JL, Neale BM, Fromer M, Ruderfer D, Akterin S, Bergen SE, Kähler A, Magnusson PK, Kim Y, Crowley JJ, Rees E, Kirov G, O'Donovan MC, Owen MJ, Walters J, Scolnick E, Sklar P, Purcell S, Hultman CM, McCarroll SA, Sullivan PF.

Mol Psychiatry. 2014 Jul;19(7):762-73. doi: 10.1038/mp.2014.40. Epub 2014 Apr 29.

11.

Case history and genome-wide scans for copy number variants in a family with patient having 15q11.1-q11.2 duplication and 22q11.2 deletion, and schizophrenia.

Takahashi S, Suzuki T, Nakamura-Tomizuka S, Osaki K, Sotome Y, Sagawa T, Uchiyama M.

Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):229-35. doi: 10.1002/ajmg.b.32307. Epub 2015 Mar 16.

PMID:
25776014
12.

Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.

Buizer-Voskamp JE, Muntjewerff JW; Genetic Risk and Outcome in Psychosis (GROUP) Consortium Members., Strengman E, Sabatti C, Stefansson H, Vorstman JA, Ophoff RA.

Biol Psychiatry. 2011 Oct 1;70(7):655-62. doi: 10.1016/j.biopsych.2011.02.015. Epub 2011 Apr 13.

13.

Schizophrenia genetics: advancing on two fronts.

Owen MJ, Williams HJ, O'Donovan MC.

Curr Opin Genet Dev. 2009 Jun;19(3):266-70. doi: 10.1016/j.gde.2009.02.008. Epub 2009 Apr 1. Review.

PMID:
19345090
14.

Copy number variation and psychiatric disease risk.

Levy RJ, Xu B, Gogos JA, Karayiorgou M.

Methods Mol Biol. 2012;838:97-113. doi: 10.1007/978-1-61779-507-7_4.

PMID:
22228008
15.

Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems.

Sahoo T, Theisen A, Rosenfeld JA, Lamb AN, Ravnan JB, Schultz RA, Torchia BS, Neill N, Casci I, Bejjani BA, Shaffer LG.

Genet Med. 2011 Oct;13(10):868-80. doi: 10.1097/GIM.0b013e3182217a06.

PMID:
21792059
16.

A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.

Rudd DS, Axelsen M, Epping EA, Andreasen NC, Wassink TH.

Am J Med Genet B Neuropsychiatr Genet. 2014 Dec;165B(8):619-26. doi: 10.1002/ajmg.b.32266. Epub 2014 Sep 16.

PMID:
25228354
17.

Analysis of copy number variations in brain DNA from patients with schizophrenia and other psychiatric disorders.

Ye T, Lipska BK, Tao R, Hyde TM, Wang L, Li C, Choi KH, Straub RE, Kleinman JE, Weinberger DR.

Biol Psychiatry. 2012 Oct 15;72(8):651-4. doi: 10.1016/j.biopsych.2012.06.014. Epub 2012 Jul 15.

18.

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.

PMID:
22228009
19.

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.

20.

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.

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