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Best matches for tbx1 schizophrenia:

Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia. Ping LY et al. Genes (Basel). (2016)

Genome-wide association study of schizophrenia in Ashkenazi Jews. Goes FS et al. Am J Med Genet B Neuropsychiatr Genet. (2015)

Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome. Flore G et al. Cereb Cortex. (2017)

Search results

Items: 1 to 20 of 24

1.

Copy number elevation of 22q11.2 genes arrests the developmental maturation of working memory capacity and adult hippocampal neurogenesis.

Boku S, Izumi T, Abe S, Takahashi T, Nishi A, Nomaru H, Naka Y, Kang G, Nagashima M, Hishimoto A, Enomoto S, Duran-Torres G, Tanigaki K, Zhang J, Ye K, Kato S, Männistö PT, Kobayashi K, Hiroi N.

Mol Psychiatry. 2018 Apr;23(4):985-992. doi: 10.1038/mp.2017.158. Epub 2017 Aug 22.

2.

Screening for Mutations in the TBX1 Gene on Chromosome 22q11.2 in Schizophrenia.

Ping LY, Chuang YA, Hsu SH, Tsai HY, Cheng MC.

Genes (Basel). 2016 Nov 22;7(11). pii: E102.

3.

Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome.

Flore G, Cioffi S, Bilio M, Illingworth E.

Cereb Cortex. 2017 Mar 1;27(3):2210-2225. doi: 10.1093/cercor/bhw076.

PMID:
27005988
4.

Genome-wide association study of schizophrenia in Ashkenazi Jews.

Goes FS, McGrath J, Avramopoulos D, Wolyniec P, Pirooznia M, Ruczinski I, Nestadt G, Kenny EE, Vacic V, Peters I, Lencz T, Darvasi A, Mulle JG, Warren ST, Pulver AE.

Am J Med Genet B Neuropsychiatr Genet. 2015 Dec;168(8):649-59. doi: 10.1002/ajmg.b.32349. Epub 2015 Jul 21.

PMID:
26198764
5.

Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms.

Guna A, Butcher NJ, Bassett AS.

J Neurodev Disord. 2015;7(1):18. doi: 10.1186/s11689-015-9113-x. Epub 2015 Jul 1.

6.

Whole-Genome Sequencing and Integrative Genomic Analysis Approach on Two 22q11.2 Deletion Syndrome Family Trios for Genotype to Phenotype Correlations.

Chung JH, Cai J, Suskin BG, Zhang Z, Coleman K, Morrow BE.

Hum Mutat. 2015 Aug;36(8):797-807. doi: 10.1002/humu.22814. Epub 2015 Jul 2.

7.

Evidence for involvement of GNB1L in autism.

Chen YZ, Matsushita M, Girirajan S, Lisowski M, Sun E, Sul Y, Bernier R, Estes A, Dawson G, Minshew N, Shellenberg GD, Eichler EE, Rieder MJ, Nickerson DA, Tsuang DW, Tsuang MT, Wijsman EM, Raskind WH, Brkanac Z.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):61-71. doi: 10.1002/ajmg.b.32002. Epub 2011 Nov 16.

8.

Expression of the NR2B-NMDA receptor subunit and its Tbr-1/CINAP regulatory proteins in postmortem brain suggest altered receptor processing in schizophrenia.

Kristiansen LV, Patel SA, Haroutunian V, Meador-Woodruff JH.

Synapse. 2010 Jul;64(7):495-502. doi: 10.1002/syn.20754.

PMID:
20175224
9.

Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.

Meechan DW, Tucker ES, Maynard TM, LaMantia AS.

Proc Natl Acad Sci U S A. 2009 Sep 22;106(38):16434-45. doi: 10.1073/pnas.0905696106. Epub 2009 Sep 10.

10.

Supportive evidence for reduced expression of GNB1L in schizophrenia.

Ishiguro H, Koga M, Horiuchi Y, Noguchi E, Morikawa M, Suzuki Y, Arai M, Niizato K, Iritani S, Itokawa M, Inada T, Iwata N, Ozaki N, Ujike H, Kunugi H, Sasaki T, Takahashi M, Watanabe Y, Someya T, Kakita A, Takahashi H, Nawa H, Arinami T.

Schizophr Bull. 2010 Jul;36(4):756-65. doi: 10.1093/schbul/sbn160. Epub 2008 Nov 14.

11.

Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.

Prasad SE, Howley S, Murphy KC.

Dev Disabil Res Rev. 2008;14(1):26-34. doi: 10.1002/ddrr.5. Review.

PMID:
18636634
12.

Strong evidence that GNB1L is associated with schizophrenia.

Williams NM, Glaser B, Norton N, Williams H, Pierce T, Moskvina V, Monks S, Del Favero J, Goossens D, Rujescu D, Giegling I, Kirov G, Craddock N, Murphy KC, O'Donovan MC, Owen MJ.

Hum Mol Genet. 2008 Feb 15;17(4):555-66. Epub 2007 Nov 13.

PMID:
18003636
13.

An association study between the genetic polymorphisms within TBX1 and schizophrenia in the Chinese population.

Ma G, Shi Y, Tang W, He Z, Huang K, Li Z, He G, Feng G, Li H, He L.

Neurosci Lett. 2007 Oct 2;425(3):146-50. Epub 2007 Aug 15.

PMID:
17850965
14.

Analysis of TBX1 variation in patients with psychotic and affective disorders.

Funke BH, Lencz T, Finn CT, DeRosse P, Poznik GD, Plocik AM, Kane J, Rogus J, Malhotra AK, Kucherlapati R.

Mol Med. 2007 Jul-Aug;13(7-8):407-14.

15.

Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome.

Weksberg R, Stachon AC, Squire JA, Moldovan L, Bayani J, Meyn S, Chow E, Bassett AS.

Hum Genet. 2007 Feb;120(6):837-45. Epub 2006 Oct 7.

16.

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia.

Arinami T.

J Hum Genet. 2006;51(12):1037-45. Epub 2006 Sep 13. Review.

PMID:
16969581
17.

Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome.

Long JM, LaPorte P, Merscher S, Funke B, Saint-Jore B, Puech A, Kucherlapati R, Morrow BE, Skoultchi AI, Wynshaw-Boris A.

Neurogenetics. 2006 Nov;7(4):247-57. Epub 2006 Aug 10.

PMID:
16900388
18.

Chromosome 22 deletion syndrome and schizophrenia.

Williams NM, O'Donovan MC, Owen MJ.

Int Rev Neurobiol. 2006;73:1-27. Review. No abstract available.

PMID:
16737900
19.

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Scambler PJ, Lindsay E.

Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34. Epub 2006 May 9.

20.

Mouse models of 22q11 deletion syndrome.

Paylor R, Lindsay E.

Biol Psychiatry. 2006 Jun 15;59(12):1172-9. Epub 2006 Apr 17. Review.

PMID:
16616724

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