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Results: 1 to 20 of 60

1.

Intercellular protein-protein interactions at synapses.

Yang X, Hou D, Jiang W, Zhang C.

Protein Cell. 2014 Jun;5(6):420-44. doi: 10.1007/s13238-014-0054-z. Epub 2014 Apr 23.

PMID:
24756565
[PubMed - in process]
Free PMC Article
2.

Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon.

Lin M, Zhao D, Hrabovsky A, Pedrosa E, Zheng D, Lachman HM.

PLoS One. 2014 Apr 15;9(4):e94968. doi: 10.1371/journal.pone.0094968. eCollection 2014.

PMID:
24736721
[PubMed - in process]
Free PMC Article
3.

Novel implications of Lingo-1 and its signaling partners in schizophrenia.

Fernandez-Enright F, Andrews JL, Newell KA, Pantelis C, Huang XF.

Transl Psychiatry. 2014 Jan 21;4:e348. doi: 10.1038/tp.2013.121.

PMID:
24448210
[PubMed - in process]
Free PMC Article
4.

Clinical significance of MYT1L gene polymorphisms in Chinese patients with gastric cancer.

Zhang Y, Zhu H, Zhang X, Gu D, Zhou X, Wang M, Cao C, Zhang X, Wu X, Gong W, Tang Y, Zhou J, Tang C, Zhang Z, Chen J.

PLoS One. 2013 Aug 28;8(8):e71979. doi: 10.1371/journal.pone.0071979. eCollection 2013.

PMID:
24015200
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Advances in osteoarthritis genetics.

Panoutsopoulou K, Zeggini E.

J Med Genet. 2013 Nov;50(11):715-24. doi: 10.1136/jmedgenet-2013-101754. Epub 2013 Jul 18.

PMID:
23868913
[PubMed - in process]
Free PMC Article
6.

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.

Nag A, Bochukova EG, Kremeyer B, Campbell DD, Muller H, Valencia-Duarte AV, Cardona J, Rivas IC, Mesa SC, Cuartas M, Garcia J, Bedoya G, Cornejo W, Herrera LD, Romero R, Fournier E, Reus VI, Lowe TL, Farooqi IS; Tourette Syndrome Association International Consortium for Genetics, Mathews CA, McGrath LM, Yu D, Cook E, Wang K, Scharf JM, Pauls DL, Freimer NB, Plagnol V, Ruiz-Linares A.

PLoS One. 2013;8(3):e59061. doi: 10.1371/journal.pone.0059061. Epub 2013 Mar 22.

PMID:
23533600
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs.

Chen X, Shen Y, Zhang F, Chiang C, Pillalamarri V, Blumenthal I, Talkowski M, Wu BL, Gusella JF.

Am J Hum Genet. 2013 Mar 7;92(3):375-86. doi: 10.1016/j.ajhg.2013.02.006.

PMID:
23472757
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A genome-wide association study of brain lesion distribution in multiple sclerosis.

Gourraud PA, Sdika M, Khankhanian P, Henry RG, Beheshtian A, Matthews PM, Hauser SL, Oksenberg JR, Pelletier D, Baranzini SE.

Brain. 2013 Apr;136(Pt 4):1012-24. doi: 10.1093/brain/aws363. Epub 2013 Feb 13.

PMID:
23412934
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Autism risk factors: genes, environment, and gene-environment interactions.

Chaste P, Leboyer M.

Dialogues Clin Neurosci. 2012 Sep;14(3):281-92. Review.

PMID:
23226953
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.

Fanous AH, Zhou B, Aggen SH, Bergen SE, Amdur RL, Duan J, Sanders AR, Shi J, Mowry BJ, Olincy A, Amin F, Cloninger CR, Silverman JM, Buccola NG, Byerley WF, Black DW, Freedman R, Dudbridge F, Holmans PA, Ripke S, Gejman PV, Kendler KS, Levinson DF; Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium.

Am J Psychiatry. 2012 Dec 1;169(12):1309-17. doi: 10.1176/appi.ajp.2012.12020218.

PMID:
23212062
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Targeted pharmacogenetic analysis of antipsychotic response in the CATIE study.

Liu Q, Jamba M, Patrick C 3rd, Padmanabhan S, Brennan MD.

Pharmacogenomics. 2012 Aug;13(11):1227-37. doi: 10.2217/pgs.12.105.

PMID:
22920393
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.

Need AC, McEvoy JP, Gennarelli M, Heinzen EL, Ge D, Maia JM, Shianna KV, He M, Cirulli ET, Gumbs CE, Zhao Q, Campbell CR, Hong L, Rosenquist P, Putkonen A, Hallikainen T, Repo-Tiihonen E, Tiihonen J, Levy DL, Meltzer HY, Goldstein DB.

Am J Hum Genet. 2012 Aug 10;91(2):303-12. doi: 10.1016/j.ajhg.2012.06.018. Epub 2012 Aug 2.

PMID:
22863191
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genetic regulation of Nrxn1 [corrected] expression: an integrative cross-species analysis of schizophrenia candidate genes.

Mozhui K, Wang X, Chen J, Mulligan MK, Li Z, Ingles J, Chen X, Lu L, Williams RW.

Transl Psychiatry. 2011 Jul 26;1:e25. doi: 10.1038/tp.2011.24. Erratum in: Transl Psychiatry. 2011;1:e38.

PMID:
22832527
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Severe Intellectual Disability Associated with Recessive Defects in CNTNAP2 and NRXN1.

Zweier C.

Mol Syndromol. 2012 Apr;2(3-5):181-185. Epub 2011 Sep 8.

PMID:
22670139
[PubMed]
Free PMC Article
15.

Phenotypic spectrum and genotype-phenotype correlations of NRXN1 exon deletions.

Schaaf CP, Boone PM, Sampath S, Williams C, Bader PI, Mueller JM, Shchelochkov OA, Brown CW, Crawford HP, Phalen JA, Tartaglia NR, Evans P, Campbell WM, Tsai AC, Parsley L, Grayson SW, Scheuerle A, Luzzi CD, Thomas SK, Eng PA, Kang SH, Patel A, Stankiewicz P, Cheung SW.

Eur J Hum Genet. 2012 Dec;20(12):1240-7. doi: 10.1038/ejhg.2012.95. Epub 2012 May 23.

PMID:
22617343
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

ASTN1 and alcohol dependence: family-based association analysis in multiplex alcohol dependence families.

Hill SY, Weeks DE, Jones BL, Zezza N, Stiffler S.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jun;159B(4):445-55. doi: 10.1002/ajmg.b.32048. Epub 2012 Apr 9.

PMID:
22488871
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Modeling psychiatric disorders at the cellular and network levels.

Brennand KJ, Simone A, Tran N, Gage FH.

Mol Psychiatry. 2012 Dec;17(12):1239-53. doi: 10.1038/mp.2012.20. Epub 2012 Apr 3. Review.

PMID:
22472874
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes.

de Jong S, van Eijk KR, Zeegers DW, Strengman E, Janson E, Veldink JH, van den Berg LH, Cahn W, Kahn RS, Boks MP, Ophoff RA; PGC Schizophrenia (GWAS) Consortium.

Eur J Hum Genet. 2012 Sep;20(9):1004-8. doi: 10.1038/ejhg.2012.38. Epub 2012 Mar 21.

PMID:
22433715
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Sex-dependent novelty response in neurexin-1α mutant mice.

Laarakker MC, Reinders NR, Bruining H, Ophoff RA, Kas MJ.

PLoS One. 2012;7(2):e31503. doi: 10.1371/journal.pone.0031503. Epub 2012 Feb 13.

PMID:
22348092
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

Leblond CS, Heinrich J, Delorme R, Proepper C, Betancur C, Huguet G, Konyukh M, Chaste P, Ey E, Rastam M, Anckarsäter H, Nygren G, Gillberg IC, Melke J, Toro R, Regnault B, Fauchereau F, Mercati O, Lemière N, Skuse D, Poot M, Holt R, Monaco AP, Järvelä I, Kantojärvi K, Vanhala R, Curran S, Collier DA, Bolton P, Chiocchetti A, Klauck SM, Poustka F, Freitag CM, Waltes R, Kopp M, Duketis E, Bacchelli E, Minopoli F, Ruta L, Battaglia A, Mazzone L, Maestrini E, Sequeira AF, Oliveira B, Vicente A, Oliveira G, Pinto D, Scherer SW, Zelenika D, Delepine M, Lathrop M, Bonneau D, Guinchat V, Devillard F, Assouline B, Mouren MC, Leboyer M, Gillberg C, Boeckers TM, Bourgeron T.

PLoS Genet. 2012 Feb;8(2):e1002521. doi: 10.1371/journal.pgen.1002521. Epub 2012 Feb 9.

PMID:
22346768
[PubMed - indexed for MEDLINE]
Free PMC Article

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