Cecilia Kim

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

Identification of ALK as a major familial neuroblastoma predisposition gene

Yaël P. Mossé, Marci Laudenslager, Luca Longo et al. · Nature · 2008 · 1.4K citations · Full text

Genetic Disorder, Genetics, Pathology +3

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Marc E. Rothenberg, Jonathan M. Spergel, Joseph D. Sherrill et al. · Nature Genetics · 2010 · 436 citations

Esophagus, Allergy, Pathogenesis +8

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

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

Richard Anney, Lambertus Klei, Dalila Pinto et al. · Human Molecular Genetics · 2012 · 372 citations · Full text