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Items: 1 to 20 of 26

1.

Interstitial deletion within 7q31.1q31.3 in a woman with mild intellectual disability and schizophrenia.

Akahoshi K, Yamamoto T.

Neuropsychiatr Dis Treat. 2018 Jul 5;14:1773-1778. doi: 10.2147/NDT.S168469. eCollection 2018.

2.

Building a schizophrenia genetic network: Transcription Factor 4 regulates genes involved in neuronal development and schizophrenia risk.

Xia H, Jahr FM, Kim NK, Xie L, Shabalin AA, Bryois J, Sweet DH, Kronfol MM, Palasuberniam P, McRae M, Riley BP, Sullivan PF, van den Oord EJ, McClay JL.

Hum Mol Genet. 2018 Jun 14. doi: 10.1093/hmg/ddy222. [Epub ahead of print]

PMID:
29905862
3.

Meta-analysis of FOXP2 rs10447760 polymorphism with schizophrenia.

Chen Y, Fang X, Wang Y, Zhang C.

Asian J Psychiatr. 2018 Jun;35:50-51. doi: 10.1016/j.ajp.2018.05.012. Epub 2018 May 18. No abstract available.

PMID:
29783134
4.

No association between FOXP2 rs10447760 and schizophrenia in a replication study of the Chinese Han population.

Yin J, Jia N, Liu Y, Jin C, Zhang F, Yu S, Wang J, Yuan J.

Psychiatr Genet. 2018 Apr;28(2):19-23. doi: 10.1097/YPG.0000000000000193.

PMID:
29346177
5.

Autoimmunity as a Driving Force of Cognitive Evolution.

Nataf S.

Front Neurosci. 2017 Oct 26;11:582. doi: 10.3389/fnins.2017.00582. eCollection 2017.

6.

The FOXP2-Driven Network in Developmental Disorders and Neurodegeneration.

Oswald F, Klöble P, Ruland A, Rosenkranz D, Hinz B, Butter F, Ramljak S, Zechner U, Herlyn H.

Front Cell Neurosci. 2017 Jul 26;11:212. doi: 10.3389/fncel.2017.00212. eCollection 2017.

7.

Association between forkhead-box P2 gene polymorphism and clinical symptoms in chronic schizophrenia in a Chinese population.

Rao W, Du X, Zhang Y, Yu Q, Hui L, Yu Y, Kou C, Yin G, Zhu X, Man L, Soares JC, Zhang XY.

J Neural Transm (Vienna). 2017 Jul;124(7):891-897. doi: 10.1007/s00702-017-1723-x. Epub 2017 Apr 18.

PMID:
28421313
8.

Risperidone and NAP protect cognition and normalize gene expression in a schizophrenia mouse model.

Vaisburd S, Shemer Z, Yeheskel A, Giladi E, Gozes I.

Sci Rep. 2015 Nov 10;5:16300. doi: 10.1038/srep16300.

9.

Understanding Language from a Genomic Perspective.

Graham SA, Fisher SE.

Annu Rev Genet. 2015;49:131-60. doi: 10.1146/annurev-genet-120213-092236. Epub 2015 Oct 5. Review.

PMID:
26442845
10.

Genetic and Developmental Perspective of Language Abnormality in Autism and Schizophrenia: One Disease Occurring at Different Ages in Humans?

Wang HG, Jeffries JJ, Wang TF.

Neuroscientist. 2016 Apr;22(2):119-31. doi: 10.1177/1073858415572078. Epub 2015 Feb 16.

PMID:
25686622
11.

Decoding the molecular evolution of human cognition using comparative genomics.

Usui N, Co M, Konopka G.

Brain Behav Evol. 2014;84(2):103-16. doi: 10.1159/000365182. Epub 2014 Sep 20.

12.

Left brain, right brain: facts and fantasies.

Corballis MC.

PLoS Biol. 2014 Jan;12(1):e1001767. doi: 10.1371/journal.pbio.1001767. Epub 2014 Jan 21.

13.

Preliminary evidence of an interaction between the FOXP2 gene and childhood emotional abuse predicting likelihood of auditory verbal hallucinations in schizophrenia.

McCarthy-Jones S, Green MJ, Scott RJ, Tooney PA, Cairns MJ, Wu JQ, Oldmeadow C, Carr V; Australian Schizophrenia Research Bank.

J Psychiatr Res. 2014 Mar;50:66-72. doi: 10.1016/j.jpsychires.2013.11.012. Epub 2013 Dec 7.

14.

Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.

Park Y, Won S, Nam M, Chung JH, Kwack K.

J Child Neurol. 2014 Dec;29(12):NP207-11. doi: 10.1177/0883073813511301. Epub 2013 Dec 18.

PMID:
24356376
15.

Sequencing of five left-right cerebral asymmetry genes in a cohort of schizophrenia and schizotypal disorder patients from Russia.

Levchenko A, Davtian S, Petrova N, Malashichev Y.

Psychiatr Genet. 2014 Apr;24(2):75-80. doi: 10.1097/YPG.0000000000000021.

PMID:
24322325
16.

Transcriptome comparison of human neurons generated using induced pluripotent stem cells derived from dental pulp and skin fibroblasts.

Chen J, Lin M, Foxe JJ, Pedrosa E, Hrabovsky A, Carroll R, Zheng D, Lachman HM.

PLoS One. 2013 Oct 3;8(10):e75682. doi: 10.1371/journal.pone.0075682. eCollection 2013.

17.

The DISC1 promoter: characterization and regulation by FOXP2.

Walker RM, Hill AE, Newman AC, Hamilton G, Torrance HS, Anderson SM, Ogawa F, Derizioti P, Nicod J, Vernes SC, Fisher SE, Thomson PA, Porteous DJ, Evans KL.

Hum Mol Genet. 2012 Jul 1;21(13):2862-72. doi: 10.1093/hmg/dds111. Epub 2012 Mar 20.

PMID:
22434823
18.

FoxP2 is significantly associated with schizophrenia and major depression in the Chinese Han population.

Li T, Zeng Z, Zhao Q, Wang T, Huang K, Li J, Li Y, Liu J, Wei Z, Wang Y, Feng G, He L, Shi Y.

World J Biol Psychiatry. 2013 Mar;14(2):146-50. doi: 10.3109/15622975.2011.615860. Epub 2012 Mar 9.

PMID:
22404659
19.

Genetic influences of cortical gray matter in language-related regions in healthy controls and schizophrenia.

Jamadar S, Powers NR, Meda SA, Gelernter J, Gruen JR, Pearlson GD.

Schizophr Res. 2011 Jul;129(2-3):141-8. doi: 10.1016/j.schres.2011.03.027. Epub 2011 Apr 20.

20.

Genetic variation in FOXP2 alters grey matter concentrations in schizophrenia patients.

Španiel F, Horáček J, Tintěra J, Ibrahim I, Novák T, Čermák J, Klírová M, Höschl C.

Neurosci Lett. 2011 Apr 15;493(3):131-5. doi: 10.1016/j.neulet.2011.02.024. Epub 2011 Feb 18.

PMID:
21334420

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