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Paper Details

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Genet Med
108
2019
.1 deletion, 16p11, 16p12, AUTS2, CNVs, NRXN1, SETD5, autism, cognitive impairment, complex disorders, disease genes, disease-associated genes, disease-associated variants, pathogenic CNVs
Author NameAffiliation
Arjun KrishnanMichigan State University
Arjun KrishnanMichigan State University
Francesca MariUniversity of Siena
Francesca MariAzienda Ospedaliera Universitaria Senese
Emanuela AvolaOasi Research Institute-IRCCS
Claire Beneteau
Cindy Skinner
Alessandra RenieriUniversity of Siena
Alessandra RenieriAzienda Ospedaliera Universitaria Senese
Alexandre ReymondCenter for Integrative Genomics, University of Lausanne
Charles E Schwartz
Santhosh GirirajanThe Pennsylvania State University, University Park
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