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Behavioral, Neurophysiological, and Synaptic Impairment in a Transgenic Neuregulin1 (NRG1-IV) Murine Schizophrenia Model.

Papaleo F, Yang F, Paterson C, Palumbo S, Carr GV, Wang Y, Floyd K, Huang W, Thomas CJ, Chen J, Weinberger DR, Law AJ.

J Neurosci. 2016 Apr 27;36(17):4859-75. doi: 10.1523/JNEUROSCI.4632-15.2016.


Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling.

Liu Y, Pham X, Zhang L, Chen PL, Burzynski G, McGaughey DM, He S, McGrath JA, Wolyniec P, Fallin MD, Pierce MS, McCallion AS, Pulver AE, Avramopoulos D, Valle D.

G3 (Bethesda). 2014 Nov 20;5(1):61-72. doi: 10.1534/g3.114.015636.


Heritability and genome-wide SNP linkage analysis of temperament in bipolar disorder.

Greenwood TA, Badner JA, Byerley W, Keck PE, McElroy SL, Remick RA, Sadovnick AD, Akiskal HS, Kelsoe JR.

J Affect Disord. 2013 Sep 25;150(3):1031-40. doi: 10.1016/j.jad.2013.05.035.


Multiple variants aggregate in the neuregulin signaling pathway in a subset of schizophrenia patients.

Hatzimanolis A, McGrath JA, Wang R, Li T, Wong PC, Nestadt G, Wolyniec PS, Valle D, Pulver AE, Avramopoulos D.

Transl Psychiatry. 2013 May 28;3:e264. doi: 10.1038/tp.2013.33.


Personalized medicine in psychiatry: problems and promises.

Ozomaro U, Wahlestedt C, Nemeroff CB.

BMC Med. 2013 May 16;11:132. doi: 10.1186/1741-7015-11-132. Review.


Targeted deletion of the mouse α2 nicotinic acetylcholine receptor subunit gene (Chrna2) potentiates nicotine-modulated behaviors.

Lotfipour S, Byun JS, Leach P, Fowler CD, Murphy NP, Kenny PJ, Gould TJ, Boulter J.

J Neurosci. 2013 May 1;33(18):7728-41. doi: 10.1523/JNEUROSCI.4731-12.2013.


Expression of the G72/G30 gene in transgenic mice induces behavioral changes.

Cheng L, Hattori E, Nakajima A, Woehrle NS, Opal MD, Zhang C, Grennan K, Dulawa SC, Tang YP, Gershon ES, Liu C.

Mol Psychiatry. 2014 Feb;19(2):175-83. doi: 10.1038/mp.2012.185.


FKBP5 genetic variation: association with selective serotonin reuptake inhibitor treatment outcomes in major depressive disorder.

Ellsworth KA, Moon I, Eckloff BW, Fridley BL, Jenkins GD, Batzler A, Biernacka JM, Abo R, Brisbin A, Ji Y, Hebbring S, Wieben ED, Mrazek DA, Weinshilboum RM, Wang L.

Pharmacogenet Genomics. 2013 Mar;23(3):156-66. doi: 10.1097/FPC.0b013e32835dc133.


Linkage replication for chromosomal region 13q32 in schizophrenia: evidence from a Brazilian pilot study on early onset schizophrenia families.

Gadelha A, Ota VK, Cano JP, Melaragno MI, Smith MA, de Jesus Mari J, Bressan RA, Belangero SI, Breen G.

PLoS One. 2012;7(12):e52262. doi: 10.1371/journal.pone.0052262.


A structure-function mechanism for schizophrenia.

Vadakkan KI.

Front Psychiatry. 2012 Dec 28;3:108. doi: 10.3389/fpsyt.2012.00108.


Is pre-psychotic intervention of schizophrenia realistic ?

Salleh MR.

Malays J Med Sci. 2002 Jul;9(2):1-6. No abstract available.


Deletion of PLCB1 gene in schizophrenia-affected patients.

Lo Vasco VR, Cardinale G, Polonia P.

J Cell Mol Med. 2012 Apr;16(4):844-51. doi: 10.1111/j.1582-4934.2011.01363.x.


Methamphetamine-associated psychosis.

Grant KM, LeVan TD, Wells SM, Li M, Stoltenberg SF, Gendelman HE, Carlo G, Bevins RA.

J Neuroimmune Pharmacol. 2012 Mar;7(1):113-39. doi: 10.1007/s11481-011-9288-1. Review.


Evidence of overlapping genetic diathesis of panic attacks and gastrointestinal disorders in a sample of male twin pairs.

Logue MW, Bauver SR, Kremen WS, Franz CE, Eisen SA, Tsuang MT, Grant MD, Lyons MJ.

Twin Res Hum Genet. 2011 Feb;14(1):16-24. doi: 10.1375/twin.14.1.16.


Genetics of major mood disorders.

Berrettini W.

Psychiatry (Edgmont). 2004 Sep;1(2):38-48.


Genome-wide linkage scan of bipolar disorder in a Colombian population isolate replicates Loci on chromosomes 7p21-22, 1p31, 16p12 and 21q21-22 and identifies a novel locus on chromosome 12q.

Kremeyer B, García J, Müller H, Burley MW, Herzberg I, Parra MV, Duque C, Vega J, Montoya P, López MC, Bedoya G, Reus V, Palacio C, López C, Ospina-Duque J, Freimer NB, Ruiz-Linares A.

Hum Hered. 2010;70(4):255-68. doi: 10.1159/000320914.


Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans.

Xu B, Woodroffe A, Rodriguez-Murillo L, Roos JL, van Rensburg EJ, Abecasis GR, Gogos JA, Karayiorgou M.

Proc Natl Acad Sci U S A. 2009 Sep 29;106(39):16746-51. doi: 10.1073/pnas.0908584106.

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