Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 9


Mouse models of autism: testing hypotheses about molecular mechanisms.

Roullet FI, Crawley JN.

Curr Top Behav Neurosci. 2011;7:187-212. doi: 10.1007/7854_2010_113.


Characterization of the proteome, diseases and evolution of the human postsynaptic density.

Bayés A, van de Lagemaat LN, Collins MO, Croning MD, Whittle IR, Choudhary JS, Grant SG.

Nat Neurosci. 2011 Jan;14(1):19-21. doi: 10.1038/nn.2719. Epub 2010 Dec 19.


Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.

Betancur C.

Brain Res. 2011 Mar 22;1380:42-77. doi: 10.1016/j.brainres.2010.11.078. Epub 2010 Dec 1. Review.


The genetics of autism: key issues, recent findings, and clinical implications.

El-Fishawy P, State MW.

Psychiatr Clin North Am. 2010 Mar;33(1):83-105. doi: 10.1016/j.psc.2009.12.002. Review.


Systems approach to explore components and interactions in the presynapse.

Abul-Husn NS, Bushlin I, Morón JA, Jenkins SL, Dolios G, Wang R, Iyengar R, Ma'ayan A, Devi LA.

Proteomics. 2009 Jun;9(12):3303-15. doi: 10.1002/pmic.200800767.


Improved human disease candidate gene prioritization using mouse phenotype.

Chen J, Xu H, Aronow BJ, Jegga AG.

BMC Bioinformatics. 2007 Oct 16;8:392.


Molecular characterization and comparison of the components and multiprotein complexes in the postsynaptic proteome.

Collins MO, Husi H, Yu L, Brandon JM, Anderson CN, Blackstock WP, Choudhary JS, Grant SG.

J Neurochem. 2006 Apr;97 Suppl 1:16-23.


The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information.

Smith CL, Goldsmith CA, Eppig JT.

Genome Biol. 2005;6(1):R7. Epub 2004 Dec 15.


Autism as a paradigmatic complex genetic disorder.

Veenstra-Vanderweele J, Christian SL, Cook EH Jr.

Annu Rev Genomics Hum Genet. 2004;5:379-405. Review.


Supplemental Content

Support Center