Dong, Shan
University of California, San Francisco
9 papers on CoChatORCID 0000-0001-9130-0225
Most cited papers
- Verified
The contribution of de novo coding mutations to autism spectrum disorder
Iossifov, I., O’Roak, B. J., Sanders, S. J., Ronemus, M., Krumm, N., Levy, D., Stessman, H. A., Witherspoon, K. T., Vives, L., Patterson, K. E., et al. (2014) · Nature
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,585
- Verified
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism
Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2018) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,323
- Verified
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Satterstrom, F. K., Kosmicki, J. A., Wang, J., Breen, M. S., De Rubeis, S., An, J.-Y., Peng, M., Collins, R., Grove, J., Klei, L., et al. (2020) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 2,321
- Verified
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci
Sanders, S. J., He, X., Willsey, A. J., Ercan-Sencicek, A. G., Samocha, K. E., Cicek, A. E., Murtha, M. T., Bal, V. H., Bishop, S. L., Dong, S., et al. (2015) · Neuron
Autism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalities
Cited by 1,430
- Verified
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
Willsey, A. J., Sanders, S. J., Li, M., Dong, S., Tebbenkamp, A. T., Muhle, R. A., Reilly, S. K., Lin, L., Fertuzinhos, S., Miller, J. A., et al. (2013) · Cell
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 934
- Verified
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Fu, J. M., Satterstrom, F. K., Peng, M., Brand, H., Collins, R. L., Dong, S., Wamsley, B., Klei, L., Wang, L., Hao, S. P., et al. (2022) · Nature Genetics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 640
- Verified
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
An, J.-Y., Lin, K., Zhu, L., Werling, D. M., Dong, S., Brand, H., Wang, H. Z., Zhao, X., Schwartz, G. B., Collins, R. L., et al. (2018) · Science
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 316
- Verified
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
Werling, D. M., Brand, H., An, J.-Y., Stone, M. R., Zhu, L., Glessner, J. T., Collins, R. L., Dong, S., Layer, R. M., Markenscoff-Papadimitriou, E., et al. (2018) · Nature Genetics
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 293
- Verified
The female protective effect in autism spectrum disorder is not mediated by a single genetic locus
Gockley, J., Willsey, A. J., Dong, S., Dougherty, J. D., Constantino, J. N., & Sanders, S. J. (2015) · Molecular Autism
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 61
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