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Items: 7


Induced pluripotent stem cells derived from a schizophrenia patient with ASTN2 deletion.

Arioka Y, Kushima I, Kubo H, Mori D, Ozaki N.

Stem Cell Res. 2018 Jul;30:81-84. doi: 10.1016/j.scr.2018.05.013. Epub 2018 May 19.


Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.

Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium.

Mol Autism. 2017 May 22;8:21. doi: 10.1186/s13229-017-0137-9. eCollection 2017.


Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation.

Gazzellone MJ, Zarrei M, Burton CL, Walker S, Uddin M, Shaheen SM, Coste J, Rajendram R, Schachter RJ, Colasanto M, Hanna GL, Rosenberg DR, Soreni N, Fitzgerald KD, Marshall CR, Buchanan JA, Merico D, Arnold PD, Scherer SW.

J Neurodev Disord. 2016 Oct 18;8:36. doi: 10.1186/s11689-016-9170-9. eCollection 2016.


Polymorphisms within ASTN2 gene are associated with age at onset of Alzheimer's disease.

Wang KS, Tonarelli S, Luo X, Wang L, Su B, Zuo L, Mao C, Rubin L, Briones D, Xu C.

J Neural Transm (Vienna). 2015 May;122(5):701-8. doi: 10.1007/s00702-014-1306-z. Epub 2014 Nov 21.


A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.

Wang KS, Liu XF, Aragam N.

Schizophr Res. 2010 Dec;124(1-3):192-9. doi: 10.1016/j.schres.2010.09.002.


Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.

Adkins DE, Aberg K, McClay JL, Bukszár J, Zhao Z, Jia P, Stroup TS, Perkins D, McEvoy JP, Lieberman JA, Sullivan PF, van den Oord EJ.

Mol Psychiatry. 2011 Mar;16(3):321-32. doi: 10.1038/mp.2010.14. Epub 2010 Mar 2.


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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