Sabata C. Lund

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

Gary D Bader, Joseph T. Glessner, Stephen J. Guter, 2010, Nature.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

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

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Multiple Recurrent De Novo Copy Number Variations , Including Duplications of the 7 q 11 . 23 Williams-Beuren Syndrome Region , Are Associated with Autism

Rebecca, Michael J. DiCola, Stephan J Sanders, 2011 .

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

Subcategories of Restricted and Repetitive Behaviors in Children with Autism Spectrum Disorders

Andreas Buja, Andrew Pickles, Catherine Lord, 2013, Journal of autism and developmental disorders.

Exploring the Relationship Between Anxiety and Insistence on Sameness in Autism Spectrum Disorders

A. Buja, Vanessa Hus, C. Lord, 2013, Autism research : official journal of the International Society for Autism Research.

Subcategories of Restricted and Repetitive Behaviors in Children with Autism Spectrum Disorders

A. Buja, Vanessa Hus, C. Lord, 2012, Journal of Autism and Developmental Disorders.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.