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Items: 1 to 20 of 24

1.

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.

2.

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.

3.

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.

4.

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.

5.

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.

6.

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.

7.

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.

8.

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.

9.

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.

10.

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.

11.

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.

12.

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.

13.

Serotonin transporter gene polymorphism, childhood trauma, and cognition in patients with psychotic disorders.

Aas M, Djurovic S, Athanasiu L, Steen NE, Agartz I, Lorentzen S, Sundet K, Andreassen OA, Melle I.

Schizophr Bull. 2012 Jan;38(1):15-22. doi: 10.1093/schbul/sbr113. Epub 2011 Sep 9.

14.

Association between TCF4 and schizophrenia does not exert its effect by common nonsynonymous variation or by influencing cis-acting regulation of mRNA expression in adult human brain.

Williams HJ, Moskvina V, Smith RL, Dwyer S, Russo G, Owen MJ, O'Donovan MC.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(7):781-4. doi: 10.1002/ajmg.b.31219. Epub 2011 Aug 2.

15.

ATA homozigosity in the IL-10 gene promoter is a risk factor for schizophrenia in Spanish females: a case control study.

Almoguera B, Riveiro-Alvarez R, Lopez-Castroman J, Dorado P, Lopez-Rodriguez R, Fernandez-Navarro P, Baca-García E, Fernandez-Piqueras J, Dal-Ré R, Abad-Santos F, Llerena A, Ayuso C; Spanish Consortium of Pharmacogenetics Research in Schizophrenia..

BMC Med Genet. 2011 Jun 9;12:81. doi: 10.1186/1471-2350-12-81.

16.

Anhedonia as a phenotype for the Val158Met COMT polymorphism in relatives of patients with schizophrenia.

Docherty AR, Sponheim SR.

J Abnorm Psychol. 2008 Nov;117(4):788-98. doi: 10.1037/a0013745.

17.

Differential association of the COMT Val158Met polymorphism with clinical phenotypes in schizophrenia and bipolar disorder.

Goghari VM, Sponheim SR.

Schizophr Res. 2008 Aug;103(1-3):186-91. doi: 10.1016/j.schres.2008.05.015. Epub 2008 Jun 20.

18.

Analysis of protocadherin alpha gene enhancer polymorphism in bipolar disorder and schizophrenia.

Pedrosa E, Stefanescu R, Margolis B, Petruolo O, Lo Y, Nolan K, Novak T, Stopkova P, Lachman HM.

Schizophr Res. 2008 Jul;102(1-3):210-9. doi: 10.1016/j.schres.2008.04.013. Epub 2008 May 27.

19.

Genetic variation in catechol-O-methyltransferase: effects on working memory in schizophrenic patients, their siblings, and healthy controls.

Diaz-Asper CM, Goldberg TE, Kolachana BS, Straub RE, Egan MF, Weinberger DR.

Biol Psychiatry. 2008 Jan 1;63(1):72-9. Epub 2007 Aug 20.

20.

Cytochrome P4502D6 genotype does not determine response to clozapine.

Arranz MJ, Dawson E, Shaikh S, Sham P, Sharma T, Aitchison K, Crocq MA, Gill M, Kerwin R, Collier DA.

Br J Clin Pharmacol. 1995 Apr;39(4):417-20.

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