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Items: 18

1.

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.

Priebe L, Degenhardt FA, Herms S, Haenisch B, Mattheisen M, Nieratschker V, Weingarten M, Witt S, Breuer R, Paul T, Alblas M, Moebus S, Lathrop M, Leboyer M, Schreiber S, Grigoroiu-Serbanescu M, Maier W, Propping P, Rietschel M, Nöthen MM, Cichon S, Mühleisen TW.

Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1.

PMID:
21358712
2.

Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.

Striano P, Coppola A, Paravidino R, Malacarne M, Gimelli S, Robbiano A, Traverso M, Pezzella M, Belcastro V, Bianchi A, Elia M, Falace A, Gazzerro E, Ferlazzo E, Freri E, Galasso R, Gobbi G, Molinatto C, Cavani S, Zuffardi O, Striano S, Ferrero GB, Silengo M, Cavaliere ML, Benelli M, Magi A, Piccione M, Dagna Bricarelli F, Coviello DA, Fichera M, Minetti C, Zara F.

Arch Neurol. 2012 Mar;69(3):322-30. doi: 10.1001/archneurol.2011.1999. Epub 2011 Nov 14. Review.

PMID:
22083797
3.

Copy variations in schizophrenia and bipolar disorder.

Lachman HM.

Cytogenet Genome Res. 2008;123(1-4):27-35. doi: 10.1159/000184689. Epub 2009 Mar 11. Review.

4.

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
5.

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
6.

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
7.

Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.

Weiss LA.

Expert Rev Mol Diagn. 2009 Nov;9(8):795-803. doi: 10.1586/erm.09.59. Review.

PMID:
19895225
8.

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
9.

The genetics of early-onset bipolar disorder: A systematic review.

Kennedy KP, Cullen KR, DeYoung CG, Klimes-Dougan B.

J Affect Disord. 2015 Sep 15;184:1-12. doi: 10.1016/j.jad.2015.05.017. Epub 2015 May 15. Review.

PMID:
26057335
10.

[DNA polymorphisms].

Suehiro Y, Furuya T, Sasaki K, Hinota Y.

Rinsho Byori. 2013 Nov;61(11):1001-7. Review. Japanese.

PMID:
24450105
11.

Risk counselling for family members in bipolar disorder and schizophrenia.

Gershon ES.

Int J Neuropsychopharmacol. 2013 Apr;16(3):713-4. doi: 10.1017/S1461145712001150. Epub 2012 Nov 9. Review.

PMID:
23137787
12.

[Genetics of schizophrenia].

Jitoku D, Yoshikawa T.

Nihon Rinsho. 2013 Apr;71(4):599-604. Review. Japanese.

PMID:
23678585
13.

Developmental psychopathology: the role of structural variation in the genome.

Gill M.

Dev Psychopathol. 2012 Nov;24(4):1319-34. doi: 10.1017/S0954579412000739. Review.

PMID:
23062300
14.

[Copy number variations and 'schizophrenia'].

Neyndorff JP, de Winter RF, Blom JD.

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

15.

The impact of human copy number variation on gene expression.

Gamazon ER, Stranger BE.

Brief Funct Genomics. 2015 Sep;14(5):352-7. doi: 10.1093/bfgp/elv017. Epub 2015 Apr 27. Review.

PMID:
25922366
16.

Properties and rates of germline mutations in humans.

Campbell CD, Eichler EE.

Trends Genet. 2013 Oct;29(10):575-84. doi: 10.1016/j.tig.2013.04.005. Epub 2013 May 16. Review.

17.

CNVs in Epilepsy.

Mefford HC.

Curr Genet Med Rep. 2014 Jun 28;2:162-167. eCollection 2014. Review.

18.

Whole-genome analyses of whole-brain data: working within an expanded search space.

Medland SE, Jahanshad N, Neale BM, Thompson PM.

Nat Neurosci. 2014 Jun;17(6):791-800. doi: 10.1038/nn.3718. Epub 2014 May 27. Review.

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