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Items: 1 to 20 of 49


Genetic Consideration of Schizotypal Traits: A Review.

Walter EE, Fernandez F, Snelling M, Barkus E.

Front Psychol. 2016 Nov 15;7:1769. eCollection 2016. Review.


Genetic association of single nucleotide polymorphisms in dystrobrevin binding protein 1 gene with schizophrenia in a Malaysian population.

Tan GK, Tee SF, Tang PY.

Genet Mol Biol. 2015 May;38(2):138-46. doi: 10.1590/S1415-4757382220140142. Epub 2015 May 1.


The Schizophrenia-Related Protein Dysbindin-1A Is Degraded and Facilitates NF-Kappa B Activity in the Nucleus.

Fu C, Chen D, Chen R, Hu Q, Wang G.

PLoS One. 2015 Jul 14;10(7):e0132639. doi: 10.1371/journal.pone.0132639. eCollection 2015.


Can genomics help usher schizophrenia into the age of RDoC and DSM-6?

Fanous AH.

Schizophr Bull. 2015 May;41(3):535-41. doi: 10.1093/schbul/sbv029. No abstract available.


Autonomy and Enhancement.

Schaefer GO, Kahane G, Savulescu J.

Neuroethics. 2014;7:123-136. Epub 2013 Aug 17.


Genetics of schizophrenia: What do we know?

Zhang JP, Malhotra AK.

Curr Psychiatr. 2013 Mar 1;12(3):24-33. No abstract available.


Epistatic interaction between COMT and DTNBP1 modulates prefrontal function in mice and in humans.

Papaleo F, Burdick MC, Callicott JH, Weinberger DR.

Mol Psychiatry. 2014 Mar;19(3):311-6. doi: 10.1038/mp.2013.133. Epub 2013 Oct 22.


Genes and schizophrenia: from a Festschrift Seminar honoring William T. Carpenter Jr, MD.

Malhotra AK.

Schizophr Bull. 2014 Mar;40 Suppl 2:S117-22. doi: 10.1093/schbul/sbt135. Epub 2013 Oct 10.


Empirical support for DSM-IV schizoaffective disorder: clinical and cognitive validators from a large patient sample.

DeRosse P, Burdick KE, Lencz T, Siris SG, Malhotra AK.

PLoS One. 2013 May 30;8(5):e63734. doi: 10.1371/journal.pone.0063734. Print 2013.


Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.

Barøy T, Misceo D, Strømme P, Stray-Pedersen A, Holmgren A, Rødningen OK, Blomhoff A, Helle JR, Stormyr A, Tvedt B, Fannemel M, Frengen E.

Orphanet J Rare Dis. 2013 Jan 7;8:3. doi: 10.1186/1750-1172-8-3.


Loss of dysbindin-1 in mice impairs reward-based operant learning by increasing impulsive and compulsive behavior.

Carr GV, Jenkins KA, Weinberger DR, Papaleo F.

Behav Brain Res. 2013 Mar 15;241:173-84. doi: 10.1016/j.bbr.2012.12.021. Epub 2012 Dec 20.


Losing your inhibition: linking cortical GABAergic interneurons to schizophrenia.

Inan M, Petros TJ, Anderson SA.

Neurobiol Dis. 2013 May;53:36-48. doi: 10.1016/j.nbd.2012.11.013. Epub 2012 Nov 29. Review.


Glutamatergic synaptic dysregulation in schizophrenia: therapeutic implications.

Coyle JT, Basu A, Benneyworth M, Balu D, Konopaske G.

Handb Exp Pharmacol. 2012;(213):267-95. doi: 10.1007/978-3-642-25758-2_10. Review.


Reduced expression of STOP/MAP6 in mice leads to cognitive deficits.

Volle J, Brocard J, Saoud M, Gory-Faure S, Brunelin J, Andrieux A, Suaud-Chagny MF.

Schizophr Bull. 2013 Sep;39(5):969-78. doi: 10.1093/schbul/sbs113. Epub 2012 Sep 20.


Prenatal whole genome sequencing: just because we can, should we?

Donley G, Hull SC, Berkman BE.

Hastings Cent Rep. 2012 Jul-Aug;42(4):28-40. doi: 10.1002/hast.50. Epub 2012 Jun 20. No abstract available.


Common variants in MAGI2 gene are associated with increased risk for cognitive impairment in schizophrenic patients.

Koide T, Banno M, Aleksic B, Yamashita S, Kikuchi T, Kohmura K, Adachi Y, Kawano N, Kushima I, Nakamura Y, Okada T, Ikeda M, Ohi K, Yasuda Y, Hashimoto R, Inada T, Ujike H, Iidaka T, Suzuki M, Takeda M, Iwata N, Ozaki N.

PLoS One. 2012;7(5):e36836. doi: 10.1371/journal.pone.0036836. Epub 2012 May 23. Erratum in: PLoS One. 2012;7(9). doi:10.1371/annotation/47ca9c23-9fdd-47f6-9d36-db0a31769f22.


Genetic influence on the working memory circuitry: behavior, structure, function and extensions to illness.

Karlsgodt KH, Bachman P, Winkler AM, Bearden CE, Glahn DC.

Behav Brain Res. 2011 Dec 1;225(2):610-22. doi: 10.1016/j.bbr.2011.08.016. Epub 2011 Aug 22. Review.


Synaptic dysbindin-1 reductions in schizophrenia occur in an isoform-specific manner indicating their subsynaptic location.

Talbot K, Louneva N, Cohen JW, Kazi H, Blake DJ, Arnold SE.

PLoS One. 2011 Mar 1;6(3):e16886. doi: 10.1371/journal.pone.0016886.


The ATXN1 and TRIM31 genes are related to intelligence in an ADHD background: evidence from a large collaborative study totaling 4,963 subjects.

Rizzi TS, Arias-Vasquez A, Rommelse N, Kuntsi J, Anney R, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Ruano D, Van der Sluis S, Markunas CA, Garrett ME, Ashley-Koch AE, Kollins SH, Anastopoulos AD, Hansell NK, Wright MJ, Montgomery GW, Martin NG, Harris SE, Davies G, Tenesa A, Porteous DJ, Starr JM, Deary IJ, St Pourcain B, Davey Smith G, Timpson NJ, Evans DM, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Faraone SV, Franke B, Posthuma D.

Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):145-57. doi: 10.1002/ajmg.b.31149. Epub 2010 Dec 16.

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