Clara Lajonchere

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

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei et al. · Nature · 2010 · 2K citations · Full text

Autism Spectrum Disorders, Syndromic Autism, Genetics +4

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Kai Wang, Haitao Zhang, Deqiong Ma et al. · Nature · 2009 · 968 citations · Full text

Neurodevelopmental Disorders, Syndromic Autism, Genetic Disorder +7

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

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2010 · 585 citations · Full text

Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing

Yong‐hui Jiang, Ryan K. C. Yuen, Xin Jin et al. · The American Journal of Human Genetics · 2013 · 491 citations · Full text

Whole-genome Sequencing, Sequencing, Engineering +13

Genome-Wide Analyses of Exonic Copy Number Variants in a Family-Based Study Point to Novel Autism Susceptibility Genes

Maja Bućan, Brett S. Abrahams, Kai Wang et al. · PLoS Genetics · 2009 · 432 citations · Full text