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Results: 1 to 20 of 22

1.

MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome.

Merico D, Costain G, Butcher NJ, Warnica W, Ogura L, Alfred SE, Brzustowicz LM, Bassett AS.

Front Neurol. 2014 Nov 21;5:238. doi: 10.3389/fneur.2014.00238. eCollection 2014.

PMID:
25484875
[PubMed]
Free PMC Article
2.

Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice.

Doherty JL, Owen MJ.

Genome Med. 2014 Apr 28;6(4):29. doi: 10.1186/gm546. eCollection 2014. Review.

PMID:
24944580
[PubMed]
Free PMC Article
3.

Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon.

Lin M, Zhao D, Hrabovsky A, Pedrosa E, Zheng D, Lachman HM.

PLoS One. 2014 Apr 15;9(4):e94968. doi: 10.1371/journal.pone.0094968. eCollection 2014.

PMID:
24736721
[PubMed - in process]
Free PMC Article
4.

CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome.

Abekhoukh S, Bardoni B.

Front Cell Neurosci. 2014 Mar 27;8:81. doi: 10.3389/fncel.2014.00081. eCollection 2014. Review.

PMID:
24733999
[PubMed]
Free PMC Article
5.

Prevalence of selected genomic deletions and duplications in a French-Canadian population-based sample of newborns.

Tucker T, Giroux S, Clément V, Langlois S, Friedman JM, Rousseau F.

Mol Genet Genomic Med. 2013 Jul;1(2):87-97. doi: 10.1002/mgg3.12. Epub 2013 May 21.

PMID:
24498606
[PubMed]
Free PMC Article
6.

Analysis of copy number variations at 15 schizophrenia-associated loci.

Rees E, Walters JT, Georgieva L, Isles AR, Chambert KD, Richards AL, Mahoney-Davies G, Legge SE, Moran JL, McCarroll SA, O'Donovan MC, Owen MJ, Kirov G.

Br J Psychiatry. 2014 Feb;204(2):108-14. doi: 10.1192/bjp.bp.113.131052. Epub 2013 Dec 5.

PMID:
24311552
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Parent-of-origin Effect in Schizophrenia and Non-affective Psychoses: Evidence from Dermatoglyphics.

Divakaran A, Narayanaswamy JC, Kalmadi SV, Narayan V, Rao NP, Venkatasubramanian G.

Indian J Psychol Med. 2013 Jul;35(3):260-7. doi: 10.4103/0253-7176.119481.

PMID:
24249928
[PubMed]
Free PMC Article
8.

Channelopathy pathogenesis in autism spectrum disorders.

Schmunk G, Gargus JJ.

Front Genet. 2013 Nov 5;4:222. doi: 10.3389/fgene.2013.00222. Review.

PMID:
24204377
[PubMed]
Free PMC Article
9.

AKAPs integrate genetic findings for autism spectrum disorders.

Poelmans G, Franke B, Pauls DL, Glennon JC, Buitelaar JK.

Transl Psychiatry. 2013 Jun 11;3:e270. doi: 10.1038/tp.2013.48.

PMID:
23756379
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

The human imprintome: regulatory mechanisms, methods of ascertainment, and roles in disease susceptibility.

Skaar DA, Li Y, Bernal AJ, Hoyo C, Murphy SK, Jirtle RL.

ILAR J. 2012;53(3-4):341-58. doi: 10.1093/ilar.53.3-4.341. Review.

PMID:
23744971
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Pescosolido MF, Gamsiz ED, Nagpal S, Morrow EM.

J Am Acad Child Adolesc Psychiatry. 2013 Apr;52(4):414-430.e14. doi: 10.1016/j.jaac.2013.01.003. Review.

PMID:
23582872
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Molecular characteristics of Human Endogenous Retrovirus type-W in schizophrenia and bipolar disorder.

Perron H, Hamdani N, Faucard R, Lajnef M, Jamain S, Daban-Huard C, Sarrazin S, LeGuen E, Houenou J, Delavest M, Moins-Teisserenc H, Bengoufa D, Yolken R, Madeira A, Garcia-Montojo M, Gehin N, Burgelin I, Ollagnier G, Bernard C, Dumaine A, Henrion A, Gombert A, Le Dudal K, Charron D, Krishnamoorthy R, Tamouza R, Leboyer M.

Transl Psychiatry. 2012 Dec 4;2:e201. doi: 10.1038/tp.2012.125. Erratum in: Transl Psychiatry. 2013;3:e226. Moins-Teiserenc, H [corrected to Moins-Teisserenc, H].

PMID:
23212585
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk.

Chapman J, Rees E, Harold D, Ivanov D, Gerrish A, Sims R, Hollingworth P, Stretton A; GERAD1 Consortium, Holmans P, Owen MJ, O'Donovan MC, Williams J, Kirov G.

Hum Mol Genet. 2013 Feb 15;22(4):816-24. doi: 10.1093/hmg/dds476. Epub 2012 Nov 11.

PMID:
23148125
[PubMed - indexed for MEDLINE]
Free PMC Article
14.
15.

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Coughlin CR 2nd, Scharer GH, Shaikh TH.

Genome Med. 2012 Oct 30;4(10):80. doi: 10.1186/gm381. eCollection 2012. Review.

PMID:
23114084
[PubMed]
Free PMC Article
16.

Association testing of copy number variants in schizophrenia and autism spectrum disorders.

Crespi BJ, Crofts HJ.

J Neurodev Disord. 2012 May 30;4(1):15. doi: 10.1186/1866-1955-4-15.

PMID:
22958593
[PubMed]
Free PMC Article
17.

Allele-biased expression in differentiating human neurons: implications for neuropsychiatric disorders.

Lin M, Hrabovsky A, Pedrosa E, Wang T, Zheng D, Lachman HM.

PLoS One. 2012;7(8):e44017. doi: 10.1371/journal.pone.0044017. Epub 2012 Aug 30.

PMID:
22952857
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

High frequency of known copy number abnormalities and maternal duplication 15q11-q13 in patients with combined schizophrenia and epilepsy.

Stewart LR, Hall AL, Kang SH, Shaw CA, Beaudet AL.

BMC Med Genet. 2011 Nov 25;12:154. doi: 10.1186/1471-2350-12-154.

PMID:
22118685
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

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.

PMID:
22083728
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

RNA-Seq of human neurons derived from iPS cells reveals candidate long non-coding RNAs involved in neurogenesis and neuropsychiatric disorders.

Lin M, Pedrosa E, Shah A, Hrabovsky A, Maqbool S, Zheng D, Lachman HM.

PLoS One. 2011;6(9):e23356. doi: 10.1371/journal.pone.0023356. Epub 2011 Sep 7.

PMID:
21915259
[PubMed - indexed for MEDLINE]
Free PMC Article
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