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Items: 9

1.

Myt1L Promotes Differentiation of Oligodendrocyte Precursor Cells and is Necessary for Remyelination After Lysolecithin-Induced Demyelination.

Shi Y, Shao Q, Li Z, Gonzalez GA, Lu F, Wang D, Pu Y, Huang A, Zhao C, He C, Cao L.

Neurosci Bull. 2018 Apr;34(2):247-260. doi: 10.1007/s12264-018-0207-9. Epub 2018 Feb 3.

PMID:
29397565
2.

Genetic variants in Nogo receptor signaling pathways may be associated with early life adversity in schizophrenia susceptibility.

Andrews JL, Fernandez-Enright F.

BBA Clin. 2014 Dec 9;3:36-43. doi: 10.1016/j.bbacli.2014.11.008. eCollection 2015 Jun.

3.

Identification of rare copy number variants in high burden schizophrenia families.

Van Den Bossche MJ, Strazisar M, Cammaerts S, Liekens AM, Vandeweyer G, Depreeuw V, Mattheijssens M, Lenaerts AS, De Zutter S, De Rijk P, Sabbe B, Del-Favero J.

Am J Med Genet B Neuropsychiatr Genet. 2013 Apr;162B(3):273-82. doi: 10.1002/ajmg.b.32146. Epub 2013 Mar 15.

PMID:
23505263
4.

Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia.

Lee Y, Mattai A, Long R, Rapoport JL, Gogtay N, Addington AM.

Psychiatr Genet. 2012 Aug;22(4):206-9. doi: 10.1097/YPG.0b013e328353ae3d.

5.

Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism.

Meyer KJ, Axelsen MS, Sheffield VC, Patil SR, Wassink TH.

Psychiatr Genet. 2012 Jun;22(3):137-40. doi: 10.1097/YPG.0b013e32834dc3f5.

6.

MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions.

Stevens SJ, van Ravenswaaij-Arts CM, Janssen JW, Klein Wassink-Ruiter JS, van Essen AJ, Dijkhuizen T, van Rheenen J, Heuts-Vijgen R, Stegmann AP, Smeets EE, Engelen JJ.

Am J Med Genet A. 2011 Nov;155A(11):2739-45. doi: 10.1002/ajmg.a.34274. Epub 2011 Oct 11.

PMID:
21990140
7.

Association study of myelin transcription factor 1-like polymorphisms with schizophrenia in Han Chinese population.

Li W, Wang X, Zhao J, Lin J, Song XQ, Yang Y, Jiang C, Xiao B, Yang G, Zhang HX, Lv LX.

Genes Brain Behav. 2012 Feb;11(1):87-93. doi: 10.1111/j.1601-183X.2011.00734.x. Epub 2011 Oct 19.

8.

Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample.

Riley B, Thiselton D, Maher BS, Bigdeli T, Wormley B, McMichael GO, Fanous AH, Vladimirov V, O'Neill FA, Walsh D, Kendler KS.

Mol Psychiatry. 2010 Jan;15(1):29-37. doi: 10.1038/mp.2009.109. Epub 2009 Oct 20.

9.

Recurrent CNVs disrupt three candidate genes in schizophrenia patients.

Vrijenhoek T, Buizer-Voskamp JE, van der Stelt I, Strengman E; Genetic Risk and Outcome in Psychosis (GROUP) Consortium, Sabatti C, Geurts van Kessel A, Brunner HG, Ophoff RA, Veltman JA.

Am J Hum Genet. 2008 Oct;83(4):504-10. doi: 10.1016/j.ajhg.2008.09.011.

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