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Items: 1 to 20 of 31

1.

A Schizophrenia-Related Genetic-Brain-Cognition Pathway Revealed in a Large Chinese Population.

Luo N, Sui J, Chen J, Zhang F, Tian L, Lin D, Song M, Calhoun VD, Cui Y, Vergara VM, Zheng F, Liu J, Yang Z, Zuo N, Fan L, Xu K, Liu S, Li J, Xu Y, Liu S, Lv L, Chen J, Chen Y, Guo H, Li P, Lu L, Wan P, Wang H, Wang H, Yan H, Yan J, Yang Y, Zhang H, Zhang D, Jiang T.

EBioMedicine. 2018 Nov;37:471-482. doi: 10.1016/j.ebiom.2018.10.009. Epub 2018 Oct 16.

2.

Genetic Variants in CSMD1 Gene Are Associated with Cognitive Performance in Normal Elderly Population.

Stepanov V, Marusin A, Vagaitseva K, Bocharova A, Makeeva O.

Genet Res Int. 2017;2017:6293826. doi: 10.1155/2017/6293826. Epub 2017 Dec 12.

3.

[Association study of genetic markers of schizophrenia and its cognitive endophenotypes].

Bocharova AV, Stepanov VA, Marusin AV, Kharkov VN, Vagaitseva KV, Fedorenko OY, Bokhan NA, Semke AV, Ivanova SA.

Genetika. 2017 Jan;53(1):100-8. Russian.

PMID:
29372809
4.

Perinatal Asphyxia in Rat Alters Expression of Novel Schizophrenia Risk Genes.

Paparelli A, Iwata K, Wakuda T, Iyegbe C, Murray RM, Takei N.

Front Mol Neurosci. 2017 Oct 27;10:341. doi: 10.3389/fnmol.2017.00341. eCollection 2017.

5.

Genome-Wide Supported Risk Variants in MIR137, CACNA1C, CSMD1, DRD2, and GRM3 Contribute to Schizophrenia Susceptibility in Pakistani Population.

Fatima A, Farooq M, Abdullah U, Tariq M, Mustafa T, Iqbal M, Tommerup N, Mahmood Baig S.

Psychiatry Investig. 2017 Sep;14(5):687-692. doi: 10.4306/pi.2017.14.5.687. Epub 2017 Sep 11.

6.

Genome-Wide Association Study of Psychosis Proneness in the Finnish Population.

Ortega-Alonso A, Ekelund J, Sarin AP, Miettunen J, Veijola J, Järvelin MR, Hennah W.

Schizophr Bull. 2017 Oct 21;43(6):1304-1314. doi: 10.1093/schbul/sbx006.

7.

Large-scale interaction effects reveal missing heritability in schizophrenia, bipolar disorder and posttraumatic stress disorder.

Woo HJ, Yu C, Kumar K, Reifman J.

Transl Psychiatry. 2017 Apr 11;7(4):e1089. doi: 10.1038/tp.2017.61.

8.

Replicated association between the European GWAS locus rs10503253 at CSMD1 and schizophrenia in Asian population.

Liu W, Liu F, Xu X, Bai Y.

Neurosci Lett. 2017 Apr 24;647:122-128. doi: 10.1016/j.neulet.2017.03.039. Epub 2017 Mar 24.

PMID:
28344127
9.

A genetic association study of CSMD1 and CSMD2 with cognitive function.

Athanasiu L, Giddaluru S, Fernandes C, Christoforou A, Reinvang I, Lundervold AJ, Nilsson LG, Kauppi K, Adolfsson R, Eriksson E, Sundet K, Djurovic S, Espeseth T, Nyberg L, Steen VM, Andreassen OA, Le Hellard S.

Brain Behav Immun. 2017 Mar;61:209-216. doi: 10.1016/j.bbi.2016.11.026. Epub 2016 Nov 25.

10.

A Novel Relationship for Schizophrenia, Bipolar, and Major Depressive Disorder. Part 8: a Hint from Chromosome 8 High Density Association Screen.

Chen X, Long F, Cai B, Chen X, Qin L, Chen G.

Mol Neurobiol. 2017 Oct;54(8):5868-5882. doi: 10.1007/s12035-016-0102-1. Epub 2016 Sep 22.

PMID:
27660274
11.

No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population.

Liu Y, Cheng Z, Wang J, Jin C, Yuan J, Wang G, Zhang F, Zhao X.

BMC Psychiatry. 2016 Jul 4;16:206. doi: 10.1186/s12888-016-0923-5.

12.

Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks.

Sherva R, Wang Q, Kranzler H, Zhao H, Koesterer R, Herman A, Farrer LA, Gelernter J.

JAMA Psychiatry. 2016 May 1;73(5):472-80. doi: 10.1001/jamapsychiatry.2016.0036.

13.

Genetics of structural connectivity and information processing in the brain.

Giddaluru S, Espeseth T, Salami A, Westlye LT, Lundquist A, Christoforou A, Cichon S, Adolfsson R, Steen VM, Reinvang I, Nilsson LG, Le Hellard S, Nyberg L.

Brain Struct Funct. 2016 Dec;221(9):4643-4661. Epub 2016 Feb 6.

14.

Individual risk alleles of susceptibility to schizophrenia are associated with poor clinical and social outcomes.

Sakamoto S, Takaki M, Okahisa Y, Mizuki Y, Inagaki M, Ujike H, Mitsuhashi T, Takao S, Ikeda M, Uchitomi Y, Iwata N, Yamada N.

J Hum Genet. 2016 Apr;61(4):329-34. doi: 10.1038/jhg.2015.153. Epub 2015 Dec 17.

PMID:
26674612
15.

Genetic assessment of additional endophenotypes from the Consortium on the Genetics of Schizophrenia Family Study.

Greenwood TA, Lazzeroni LC, Calkins ME, Freedman R, Green MF, Gur RE, Gur RC, Light GA, Nuechterlein KH, Olincy A, Radant AD, Seidman LJ, Siever LJ, Silverman JM, Stone WS, Sugar CA, Swerdlow NR, Tsuang DW, Tsuang MT, Turetsky BI, Braff DL.

Schizophr Res. 2016 Jan;170(1):30-40. doi: 10.1016/j.schres.2015.11.008. Epub 2015 Nov 18. Review.

16.

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.

17.

Neuroinformatic analyses of common and distinct genetic components associated with major neuropsychiatric disorders.

Lotan A, Fenckova M, Bralten J, Alttoa A, Dixson L, Williams RW, van der Voet M.

Front Neurosci. 2014 Nov 6;8:331. doi: 10.3389/fnins.2014.00331. eCollection 2014.

18.

The CSMD1 genome-wide associated schizophrenia risk variant rs10503253 affects general cognitive ability and executive function in healthy males.

Koiliari E, Roussos P, Pasparakis E, Lencz T, Malhotra A, Siever LJ, Giakoumaki SG, Bitsios P.

Schizophr Res. 2014 Apr;154(1-3):42-7. doi: 10.1016/j.schres.2014.02.017. Epub 2014 Mar 11.

PMID:
24630139
19.

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Mol Autism. 2014 Jan 10;5(1):1. doi: 10.1186/2040-2392-5-1.

20.

Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1.

Xu W, Cohen-Woods S, Chen Q, Noor A, Knight J, Hosang G, Parikh SV, De Luca V, Tozzi F, Muglia P, Forte J, McQuillin A, Hu P, Gurling HM, Kennedy JL, McGuffin P, Farmer A, Strauss J, Vincent JB.

BMC Med Genet. 2014 Jan 4;15:2. doi: 10.1186/1471-2350-15-2.

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