Stephan Sanders
University of California, San Francisco(US)University of Oxford(GB)
Publications by Year
Research Areas
Autism Spectrum Disorder Research, Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Congenital heart defects research
Most-Cited Works
- → Synaptic, transcriptional and chromatin genes disrupted in autism(2014)2,891 cited
- → Predicting Splicing from Primary Sequence with Deep Learning(2019)2,751 cited
- → The contribution of de novo coding mutations to autism spectrum disorder(2014)2,750 cited
- → De novo mutations revealed by whole-exome sequencing are strongly associated with autism(2012)2,152 cited
- → Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci(2015)1,524 cited
- → Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism(2011)1,287 cited