Andrew D. Paterson · researcher (ORCID 0000-0002-9169-118X) · YYNN

Andrew D. Paterson

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researcher (ORCID 0000-0002-9169-118X)

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Works
8

Functional impact of global rare copy number variation in autism spectrum disorders

scientific article published on 15 July 2010

Sixth World Congress of Psychiatric Genetics X chromosome workshop

Type 1 diabetes in the BB rat: a polygenic disease

scientific article published on 23 January 2009

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

scientific article

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

scientific article

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

scientific article (publication date: 30 December 2005)

Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort

scientific article

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

scientific article

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Websitesickkids.ca

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