Stephan J. Sanders · researcher · YYNN

Stephan J. Sanders

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researcher

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Works
5

Common genetic variants, acting additively, are a major source of risk for autism

scientific article

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

scientific article (publication date: June 2011)

Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism

scientific article published on 14 December 2011

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

scientific article published on 13 February 2017

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