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Items: 1 to 20 of 96

1.

Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways.

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

PLoS One. 2017 Aug 7;12(8):e0182778. doi: 10.1371/journal.pone.0182778. eCollection 2017.

2.

Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition.

Breuss MW, Hansen AH, Landler L, Keays DA.

Behav Brain Res. 2017 Apr 14;323:47-55. doi: 10.1016/j.bbr.2017.01.029. Epub 2017 Jan 25.

3.

Association of CACNA1C and SYNE1 in offspring of patients with psychiatric disorders.

Gassó P, Sánchez-Gistau V, Mas S, Sugranyes G, Rodríguez N, Boloc D, de la Serna E, Romero S, Moreno D, Moreno C, Díaz-Caneja CM, Lafuente A, Castro-Fornieles J.

Psychiatry Res. 2016 Nov 30;245:427-435. doi: 10.1016/j.psychres.2016.08.058. Epub 2016 Sep 2.

PMID:
27620326
4.

Variation in CACNA1C is Associated with Amygdala Structure and Function in Adolescents.

Sumner JA, Sheridan MA, Drury SS, Esteves KC, Walsh K, Koenen KC, McLaughlin KA.

J Child Adolesc Psychopharmacol. 2015 Nov;25(9):701-10. doi: 10.1089/cap.2015.0047. Epub 2015 Sep 24.

5.

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

Rees E, Kirov G, Walters JT, Richards AL, Howrigan D, Kavanagh DH, Pocklington AJ, Fromer M, Ruderfer DM, Georgieva L, Carrera N, Gormley P, Palta P, Williams H, Dwyer S, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Tsuang MT, Glatt SJ, Chen WJ, Hwu HG; Taiwanese Trios Exome Sequencing Consortium, Neale BM, Palotie A, Sklar P, Purcell SM, McCarroll SA, Holmans P, Owen MJ, O'Donovan MC.

Transl Psychiatry. 2015 Jul 21;5:e607. doi: 10.1038/tp.2015.99.

6.

Altered CSMD1 Expression Alters Cocaine-Conditioned Place Preference: Mutual Support for a Complex Locus from Human and Mouse Models.

Drgonova J, Walther D, Singhal S, Johnson K, Kessler B, Troncoso J, Uhl GR.

PLoS One. 2015 Jul 14;10(7):e0120908. doi: 10.1371/journal.pone.0120908. eCollection 2015.

7.

ZNF804A rs1344706 is associated with cortical thickness, surface area, and cortical volume of the unmedicated first episode schizophrenia and healthy controls.

Wei Q, Li M, Kang Z, Li L, Diao F, Zhang R, Wang J, Zheng L, Wen X, Zhang J, Zhao J, Huang R.

Am J Med Genet B Neuropsychiatr Genet. 2015 Jun;168B(4):265-73. doi: 10.1002/ajmg.b.32308. Epub 2015 Apr 29.

PMID:
25921517
8.

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia.

Ruderfer DM, Lim ET, Genovese G, Moran JL, Hultman CM, Sullivan PF, McCarroll SA, Holmans P, Sklar P, Purcell SM.

Eur J Hum Genet. 2015 Apr;23(4):555-7. doi: 10.1038/ejhg.2014.228. Epub 2014 Nov 5.

9.

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.

Melhem NM, Lu C, Dresbold C, Middleton FA, Klei L, Wood S, Faraone SV, Vinogradov S, Tiobech J, Yano V, Roeder K, Byerley W, Myles-Worsley M, Devlin B.

Am J Med Genet B Neuropsychiatr Genet. 2014 Sep;165B(6):521-30. doi: 10.1002/ajmg.b.32255. Epub 2014 Jul 1.

10.

[The effect of the serotonin transporter 5-HTTLPR polymorphism on the recognition of facial emotions in schizophrenia].

Alfimova MV, Golimbet VE, Korovaitseva GI, Lezheiko TV, Abramova LI, Aksenova EV, Bolgov MI.

Zh Nevrol Psikhiatr Im S S Korsakova. 2014;114(1):42-8. Russian.

PMID:
24637816
11.

Metabotropic glutamate receptor 3 is associated with heroin dependence but not depression or schizophrenia in a Chinese population.

Jia W, Zhang R, Wu B, Dai ZX, Zhu YS, Li PP, Zhu F.

PLoS One. 2014 Jan 31;9(1):e87247. doi: 10.1371/journal.pone.0087247. eCollection 2014.

12.

The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function.

Walton E, Geisler D, Hass J, Liu J, Turner J, Yendiki A, Smolka MN, Ho BC, Manoach DS, Gollub RL, Roessner V, Calhoun VD, Ehrlich S.

PLoS One. 2013 Oct 2;8(10):e76815. doi: 10.1371/journal.pone.0076815. eCollection 2013.

13.

A molecular genetic approach to uncovering the differential functions of dopamine D2 receptor isoforms.

Wang Y, Sasaoka T, Dang MT.

Methods Mol Biol. 2013;964:181-200. doi: 10.1007/978-1-62703-251-3_11.

PMID:
23296784
14.

Paradoxical downregulation of HLA-A expression by IFNγ associated with schizophrenia and noncoding genes.

Gu S, Fellerhoff B, Müller N, Laumbacher B, Wank R.

Immunobiology. 2013 May;218(5):738-44. doi: 10.1016/j.imbio.2012.08.275. Epub 2012 Sep 18.

PMID:
23083632
15.

Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia.

Wassink TH, Epping EA, Rudd D, Axelsen M, Ziebell S, Fleming FW, Monson E, Ho BC, Andreasen NC.

Arch Gen Psychiatry. 2012 Sep;69(9):885-92. doi: 10.1001/archgenpsychiatry.2011.2116.

16.

zCall: a rare variant caller for array-based genotyping: genetics and population analysis.

Goldstein JI, Crenshaw A, Carey J, Grant GB, Maguire J, Fromer M, O'Dushlaine C, Moran JL, Chambert K, Stevens C; Swedish Schizophrenia Consortium; ARRA Autism Sequencing Consortium, Sklar P, Hultman CM, Purcell S, McCarroll SA, Sullivan PF, Daly MJ, Neale BM.

Bioinformatics. 2012 Oct 1;28(19):2543-5. Epub 2012 Jul 27.

17.

Role of the apolipoprotein E and catechol-O-methyltransferase genes in prospective and retrospective memory traits.

Dongés B, Haupt LM, Lea RA, Chan RC, Shum DH, Griffiths LR.

Gene. 2012 Sep 10;506(1):135-40. doi: 10.1016/j.gene.2012.06.067. Epub 2012 Jul 3.

PMID:
22771913
18.

Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain.

Malhotra AK, Correll CU, Chowdhury NI, Müller DJ, Gregersen PK, Lee AT, Tiwari AK, Kane JM, Fleischhacker WW, Kahn RS, Ophoff RA, Meltzer HY, Lencz T, Kennedy JL.

Arch Gen Psychiatry. 2012 Sep;69(9):904-12.

19.

Runs of homozygosity implicate autozygosity as a schizophrenia risk factor.

Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF; Schizophrenia Psychiatric Genome-Wide Association Study Consortium.

PLoS Genet. 2012;8(4):e1002656. doi: 10.1371/journal.pgen.1002656. Epub 2012 Apr 12.

20.

The impact of serotonin transporter (5-HTTLPR) genotype on the development of resting-state functional connectivity in children and adolescents: a preliminary report.

Wiggins JL, Bedoyan JK, Peltier SJ, Ashinoff S, Carrasco M, Weng SJ, Welsh RC, Martin DM, Monk CS.

Neuroimage. 2012 Feb 1;59(3):2760-70. doi: 10.1016/j.neuroimage.2011.10.030. Epub 2011 Oct 18.

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