Su H. Chu

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

Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus et al. · Neuron · 2011 · 1.3K citations · Full text

Neurodevelopmental Disorders, Williams Syndrome Region, Syndromic Autism +10

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

Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism

Thomas Fernandez, Stephan Sanders, Ilana R. Yurkiewicz et al. · Biological Psychiatry · 2011 · 203 citations · Full text

Syndromic Autism, Genetic Disorder, Genetics +8

Genome-wide Transcriptome Profiling Reveals the Functional Impact of Rare De Novo and Recurrent CNVs in Autism Spectrum Disorders

Rui Luo, Stephan Sanders, Yuan Tian et al. · The American Journal of Human Genetics · 2012 · 174 citations · Full text

Functional Genomics, Autism Spectrum Disorders, Syndromic Autism +9

Associations of Neighborhood Opportunity and Social Vulnerability With Trajectories of Childhood Body Mass Index and Obesity Among US Children

Izzuddin M. Aris, Wei Perng, Dana Dabelea et al. · JAMA Network Open · 2022 · 102 citations · Full text