AGP Research: Publications (2)
1. AGP Publications:
2. Publications acknowledging the AGP:
2011:
- 27th April 2011:
"Gene-ontology enrichment analysis in
two independent family-based samples highlights biologically
plausible processes for autism spectrum disorders".
European Journal of Human Genetics. Ric Anney et al. (Free to access
and download).
- 11th January 2011: "Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism". Journal of Neurdevelopmental Disorders. Veronica Vieland et al. (Free to access and download).
2010:
- 23rd October 2010: Rare familial 16q21 microdeletions under linkage peak implicate cadherin 8 ( CDH8) in susceptibility to autism and learning disability, Alistair T Pagnamenta, Hameed
Khan, Susan Walker, et al. Journal of Medical Genetics. (Free to
access and download).
- 15th September 2010: Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability, Abdul Noor, Annabel Whibley, Christian R. Marshall et al. Science Translational Medicine. (Abstract free to access).
2009:
-
"Chromosomal Copy Number Variation in Psychiatric Disorders",
A. Pagnamenta and A. Monaco, European Psychiatric Review,
2009, 2(1): 8-12.
- 8th October 2009: Hopkins autism study:
- "A genome-wide linkage and association scan reveals novel loci for autism", Weiss L.A., Arking D.E., the Gene Discovery Project of Johns Hopkins, the Autism Consortium, Daly M.J., Nature 461, 802-808. PMID: 19812673.
- See also: media coverage
3. AGP Presentations and posters: